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<title>Most recent issue published online for the International Journal of Nanotechnology.</title>
<description>International Journal of Nanotechnology</description>
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<dc:publisher>Inderscience Publishers Ltd</dc:publisher>
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<title>International Journal of Nanotechnology</title>
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<link>http://www.inderscience.com/browse/index.php?journalID=54&amp;year=2012&amp;vol=9&amp;issue=3/4/5/6/7</link>
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<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045324">
<title>Editorial&#58; Nanoscience and Nanotechnology in Provence&#45;Alpes&#45;C&#244;te d&#39;Azur</title>
<link>http://www.inderscience.com/link.php?id=45324</link>
<description>An overview over activities in nanoscience and nanotechnology in France and specifically the Provence&#45;Alpes&#45;C&#244;te d&#39;Azur Region is given. Nanoscience activities are organised and funded in France by several institutions. A dedicated national programme, called C&#39;Nano and which is coordinated by the French National Center for Scientific Research &#150; CNRS, assures the animation. Project funding comes on the national level from the French Ministry for Higher Education and the French National Research Agency &#40;ANR&#41; or regionally from Universities and Regional and Local Councils. The activities and initiatives in nanoscience are accompanied by dedicated teaching and educational programmes.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45324"><b>Editorial&#58; Nanoscience and Nanotechnology in Provence&#45;Alpes&#45;C&#244;te d&#39;Azur</b></A><br />Margrit Hanb&#252;cken; Michel Lannoo; Wilfried Blanc; Thierry Djenizian; Lionel Santinacci<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 163 - 166</i><br />An overview over activities in nanoscience and nanotechnology in France and specifically the Provence&#45;Alpes&#45;C&#244;te d&#39;Azur Region is given. Nanoscience activities are organised and funded in France by several institutions. A dedicated national programme, called C&#39;Nano and which is coordinated by the French National Center for Scientific Research &#150; CNRS, assures the animation. Project funding comes on the national level from the French Ministry for Higher Education and the French National Research Agency &#40;ANR&#41; or regionally from Universities and Regional and Local Councils. The activities and initiatives in nanoscience are accompanied by dedicated teaching and educational programmes.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045324</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 163 - 166</dc:source>
<dc:creator>Margrit Hanb&#252;cken; Michel Lannoo; Wilfried Blanc; Thierry Djenizian; Lionel Santinacci</dc:creator>
<dc:contributor>C&#39;Nano PACA, Campus Luminy &#150; Case 913, F&#45;13288 Marseille, France. &#39; C&#39;Nano PACA, Campus Luminy &#150; Case 913, F&#45;13288 Marseille, France. &#39; C&#39;Nano PACA, Campus Luminy &#150; Case 913, F&#45;13288 Marseille, France. &#39; C&#39;Nano PACA, Campus Luminy &#150; Case 913, F&#45;13288 Marseille, France. &#39; C&#39;Nano PACA, Campus Luminy &#150; Case 913, F&#45;13288 Marseille, France</dc:contributor>
<dc:subject>C&#39</dc:subject>
<dc:subject>Nano PACA</dc:subject>
<dc:subject>biotechnology</dc:subject>
<dc:subject>bioelectronics</dc:subject>
<dc:subject>nanomaterials</dc:subject>
<dc:subject>sustainable energy</dc:subject>
<dc:subject>instrumentation</dc:subject>
<dc:subject>environment</dc:subject>
<dc:subject>electronic devices</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>nanoscience</dc:subject>
<dc:subject>sustainability</dc:subject>
<dc:subject>research</dc:subject>
<dc:subject>teaching</dc:subject>
<dc:subject>education.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
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<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045325">
<title>Environmental fate of nanoparticles&#58; physical chemical and biological aspects &#150; a few snapshots</title>
<link>http://www.inderscience.com/link.php?id=45325</link>
<description>The environmental risk that nanomaterials can undergo is a major problem, which could prevent the commercial development of nanoproducts, especially in technology domains corresponding to large distribution&#58; cosmetics, composite materials, civil engineering materials and leisure materials. The risk assessment is based on a complex approach, which implies the knowledge of the degradation mechanisms of the nanoproducts in aquatic media &#40;kinetics and chemical change&#41;, the quantities that are distributed in the different ecosystem compartments and the biological effects on various targets &#40;bacterial micro&#45;organisms, primary and secondary predators&#41;. The paper aims at showing the unique surface properties of nanomaterials and especially when the size is decreasing largely less than 100 nm, the stability and the eventual degradation of intermediate nanomaterials, e.g., some composites used in sunscreens. The biological effects of the nanomaterials depends on their unique properties and especially the large surface tension as the size decreases, the defects within the bulk and on the surface at the origin of the production of ROS. The molecular mechanisms underlying the toxicity are described especially in terms of oxidation&#45;reduction reactions owing to surface reactivity, surface atoms dissolution, oxidative dissolution and dissolution.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45325"><b>Environmental fate of nanoparticles&#58; physical chemical and biological aspects &#150; a few snapshots</b></A><br />Armand Masion; M&#233;lanie Auffan; J&#233;r&#244;me Labille; C&#233;line Botta; Natalia Solovitch; J&#233;r&#244;me Rose; Jean&#45;Yves Bottero<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 167 - 180</i><br />The environmental risk that nanomaterials can undergo is a major problem, which could prevent the commercial development of nanoproducts, especially in technology domains corresponding to large distribution&#58; cosmetics, composite materials, civil engineering materials and leisure materials. The risk assessment is based on a complex approach, which implies the knowledge of the degradation mechanisms of the nanoproducts in aquatic media &#40;kinetics and chemical change&#41;, the quantities that are distributed in the different ecosystem compartments and the biological effects on various targets &#40;bacterial micro&#45;organisms, primary and secondary predators&#41;. The paper aims at showing the unique surface properties of nanomaterials and especially when the size is decreasing largely less than 100 nm, the stability and the eventual degradation of intermediate nanomaterials, e.g., some composites used in sunscreens. The biological effects of the nanomaterials depends on their unique properties and especially the large surface tension as the size decreases, the defects within the bulk and on the surface at the origin of the production of ROS. The molecular mechanisms underlying the toxicity are described especially in terms of oxidation&#45;reduction reactions owing to surface reactivity, surface atoms dissolution, oxidative dissolution and dissolution.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045325</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 167 - 180</dc:source>
<dc:creator>Armand Masion; M&#233;lanie Auffan; J&#233;r&#244;me Labille; C&#233;line Botta; Natalia Solovitch; J&#233;r&#244;me Rose; Jean&#45;Yves Bottero</dc:creator>
<dc:contributor>CEREGE, UMR6635 CNRS Aix&#45;Marseille Universit&#233;, Europole de l&#39;Arbois; BP 80, 13545 Aix&#45;en&#45;Provence Cedex 04, France. &#39; CEREGE, UMR6635 CNRS Aix&#45;Marseille Universit&#233;, Europole de l&#39;Arbois; BP 80, 13545 Aix&#45;en&#45;Provence Cedex 04, France. &#39; CEREGE, UMR6635 CNRS Aix&#45;Marseille Universit&#233;, Europole de l&#39;Arbois; BP 80, 13545 Aix&#45;en&#45;Provence Cedex 04, France. &#39; CEREGE, UMR6635 CNRS Aix&#45;Marseille Universit&#233;, Europole de l&#39;Arbois; BP 80, 13545 Aix&#45;en&#45;Provence Cedex 04, France. &#39; CEREGE, UMR6635 CNRS Aix&#45;Marseille Universit&#233;, Europole de l&#39;Arbois; BP 80, 13545 Aix&#45;en&#45;Provence Cedex 04, France. &#39; CEREGE, UMR6635 CNRS Aix&#45;Marseille Universit&#233;, Europole de l&#39;Arbois; BP 80, 13545 Aix&#45;en&#45;Provence Cedex 04, France. &#39; CEREGE, UMR6635 CNRS Aix&#45;Marseille Universit&#233;, Europole de l&#39;Arbois; BP 80, 13545 Aix&#45;en&#45;Provence Cedex 04, France</dc:contributor>
<dc:subject>nanomaterials</dc:subject>
<dc:subject>mobility</dc:subject>
<dc:subject>ecotoxicity</dc:subject>
<dc:subject>toxicity</dc:subject>
<dc:subject>aging</dc:subject>
<dc:subject>porous media</dc:subject>
<dc:subject>physical chemical properties</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>nanoparticles</dc:subject>
<dc:subject>environmental risk</dc:subject>
<dc:subject>dissolution</dc:subject>
<dc:subject>risk assessment</dc:subject>
<dc:subject>aquatic media</dc:subject>
<dc:subject>kinetics</dc:subject>
<dc:subject>chemical change</dc:subject>
<dc:subject>ecosystems</dc:subject>
<dc:subject>biological effects</dc:subject>
<dc:subject>surface properties</dc:subject>
<dc:subject>biological effects</dc:subject>
<dc:subject>surface tension.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>167</prism:startingPage>
<prism:endingPage>180</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045326">
<title>Effects of metallic and metal oxide nanoparticles in aquatic and terrestrial food chains. Biomarkers responses in invertebrates and bacteria</title>
<link>http://www.inderscience.com/link.php?id=45326</link>
<description>Although the market of nanoparticles &#40;NPs&#41; is rapidly expanding, the environmental and health impact of manufactured NPs and nanomaterials is still poorly understood and predictable. Hence, several laboratories of the PACA region have unified their skills to address this issue with an interdisciplinary approach. We present an outline of the ecological impact of metallic and metal oxide NPs span from the surface atoms of NPs, to unicellular organisms, such as bacteria, and organism levels. On multicellular organisms, we focus on biomarkers reporting on stress, central nervous system endpoints and antioxidative balance assessment. On bacteria, which are key players in NPs transfer, we study not only the impact of NPs on cells, at the microbial community, cell and molecular level, but also the effect of cells on NPs. Our priority is through our collaborations, to surpass case&#45;by&#45;case studies and develop aquatic and terrestrial mesocosms, to get information at an integrative level on the trophic links and ecosystemic consequences of NPs.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45326"><b>Effects of metallic and metal oxide nanoparticles in aquatic and terrestrial food chains. Biomarkers responses in invertebrates and bacteria</b></A><br />A. Thi&#233;ry; L. De Jong; J. Issartel; X. Moreau; G. Saez; P. Barth&#233;l&#233;my; I. Bestel; C. Santaella; W. Achouak; M. Auffan; J. Rose; J&#45;Y. Bottero<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 181 - 203</i><br />Although the market of nanoparticles &#40;NPs&#41; is rapidly expanding, the environmental and health impact of manufactured NPs and nanomaterials is still poorly understood and predictable. Hence, several laboratories of the PACA region have unified their skills to address this issue with an interdisciplinary approach. We present an outline of the ecological impact of metallic and metal oxide NPs span from the surface atoms of NPs, to unicellular organisms, such as bacteria, and organism levels. On multicellular organisms, we focus on biomarkers reporting on stress, central nervous system endpoints and antioxidative balance assessment. On bacteria, which are key players in NPs transfer, we study not only the impact of NPs on cells, at the microbial community, cell and molecular level, but also the effect of cells on NPs. Our priority is through our collaborations, to surpass case&#45;by&#45;case studies and develop aquatic and terrestrial mesocosms, to get information at an integrative level on the trophic links and ecosystemic consequences of NPs.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045326</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 181 - 203</dc:source>
<dc:creator>A. Thi&#233;ry; L. De Jong; J. Issartel; X. Moreau; G. Saez; P. Barth&#233;l&#233;my; I. Bestel; C. Santaella; W. Achouak; M. Auffan; J. Rose; J&#45;Y. Bottero</dc:creator>
<dc:contributor>UMR&#45;CNRS&#47;IRD 6116&#47;GDRi iCEINT &#40;CNRS&#45;CEA&#41;, Institut M&#233;diterran&#233;en d&#39;Ecologie et de Pal&#233;o&#233;cologie, &#233;quipe &#39;Biomarqueurs et Bioindicateurs Environnementaux&#39;, D&#233;partement Organisation et Vuln&#233;rabilit&#233; des Syst&#232;mes Ecologiques, Aix&#45;Marseille Universit&#233;, 3 place Victor Hugo, Case 97, 13331 Marseille Cedex 3, France. &#39; UMR&#45;CNRS&#47;IRD 6116&#47;GDRi iCEINT &#40;CNRS&#45;CEA&#41;, Institut M&#233;diterran&#233;en d&#39;Ecologie et de Pal&#233;o&#233;cologie, &#233;quipe &#39;Biomarqueurs et Bioindicateurs Environnementaux&#39;, D&#233;partement Organisation et Vuln&#233;rabilit&#233; des Syst&#232;mes Ecologiques, Aix&#45;Marseille Universit&#233;, 3 place Victor Hugo, Case 97, 13331 Marseille Cedex 3, France. &#39; UMR&#45;CNRS&#47;IRD 6116&#47;GDRi iCEINT &#40;CNRS&#45;CEA&#41;, Institut M&#233;diterran&#233;en d&#39;Ecologie et de Pal&#233;o&#233;cologie, &#233;quipe &#39;Biomarqueurs et Bioindicateurs Environnementaux&#39;, D&#233;partement Organisation et Vuln&#233;rabilit&#233; des Syst&#232;mes Ecologiques, Aix&#45;Marseille Universit&#233;, 3 place Victor Hugo, Case 97, 13331 Marseille Cedex 3, France. &#39; UMR&#45;CNRS&#47;IRD 6116&#47;GDRi iCEINT &#40;CNRS&#45;CEA&#41;, Institut M&#233;diterran&#233;en d&#39;Ecologie et de Pal&#233;o&#233;cologie, &#233;quipe &#39;Biomarqueurs et Bioindicateurs Environnementaux&#39;, D&#233;partement Organisation et Vuln&#233;rabilit&#233; des Syst&#232;mes Ecologiques, Aix&#45;Marseille Universit&#233;, 3 place Victor Hugo, Case 97, 13331 Marseille Cedex 3, France. &#39; UMR&#45;CNRS&#47;IRD 6116&#47;GDRi iCEINT &#40;CNRS&#45;CEA&#41;, Institut M&#233;diterran&#233;en d&#39;Ecologie et de Pal&#233;o&#233;cologie, &#233;quipe &#39;Biomarqueurs et Bioindicateurs Environnementaux&#39;, D&#233;partement Organisation et Vuln&#233;rabilit&#233; des Syst&#232;mes Ecologiques, Aix&#45;Marseille Universit&#233;, 3 place Victor Hugo, Case 97, 13331 Marseille Cedex 3, France. &#39; INSERM, U869, Univ. Bordeaux, ARNA Laboratory, 33000 Bordeaux, France. &#39; INSERM, U869, Univ. Bordeaux, ARNA Laboratory, 33000 Bordeaux, France. &#39; UMR 6191 CNRS&#45;CEA&#45;Aix&#45;Marseille University&#47;GDRi iCEINT &#40;CNRS&#45;CEA&#41;, LEMIRE Laboratory of Microbial Ecology and Extreme Environments, CEA Cadarache, 13108 Saint&#45;Paul&#45;Lez&#45;Durance, France. &#39; UMR 6191 CNRS&#45;CEA&#45;Aix&#45;Marseille University&#47;GDRi iCEINT &#40;CNRS&#45;CEA&#41;, LEMIRE Laboratory of Microbial Ecology and Extreme Environments, CEA Cadarache, 13108 Saint&#45;Paul&#45;Lez&#45;Durance, France. &#39; CNRS, CEREGE, UMR 6635, 13545 Aix en Provence, France; GDRi iCEINT internationnal Consortium for the Environmental Implications of NanoTechnology &#40;CNRS&#45;CEA&#41;, Aix&#45;Marseille Univ, CEREGE, UMR 6635, 13545 Aix&#45;en&#45;Provence, France. &#39; CNRS, CEREGE, UMR 6635, 13545 Aix en Provence, France; GDRi iCEINT internationnal Consortium for the Environmental Implications of NanoTechnology &#40;CNRS&#45;CEA&#41;, Aix&#45;Marseille Univ, CEREGE, UMR 6635, 13545 Aix&#45;en&#45;Provence, France. &#39; CNRS, CEREGE, UMR 6635, 13545 Aix en Provence, France; GDRi iCEINT internationnal Consortium for the Environmental Implications of NanoTechnology &#40;CNRS&#45;CEA&#41;, Aix&#45;Marseille Univ, CEREGE, UMR 6635, 13545 Aix&#45;en&#45;Provence, France</dc:contributor>
<dc:subject>aquatic food chain</dc:subject>
<dc:subject>terrestrial food chain</dc:subject>
<dc:subject>biomarkers</dc:subject>
<dc:subject>invertebrates</dc:subject>
<dc:subject>bacteria</dc:subject>
<dc:subject>metal oxide nanoparticles</dc:subject>
<dc:subject>mesocosms</dc:subject>
<dc:subject>biofilm</dc:subject>
<dc:subject>surface reactivity</dc:subject>
<dc:subject>biotransformation</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>environmental impact</dc:subject>
<dc:subject>health impact</dc:subject>
<dc:subject>nanomaterials</dc:subject>
<dc:subject>trophic links</dc:subject>
<dc:subject>ecosystems.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>181</prism:startingPage>
<prism:endingPage>203</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045327">
<title>Adsorption of nickel and arsenic from aqueous solution on natural sepiolite</title>
<link>http://www.inderscience.com/link.php?id=45327</link>
<description>The adsorption capacity of a natural nanostructured clay &#40;sepiolite&#41; for the inorganic species&#58; Ni&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;2&#43;&amp;lt;&#47;SUP&amp;gt; and As&#40;V&#41; has been studied using a batch method. The different parameters affecting sorption such as the mass of adsorbent, contact time, sorbate concentration or pH have been investigated and optimal experimental conditions have been determined. Langmuir and Freundlich equations, which are commonly used to describe sorption equilibrium, were applied to model experimental results. The maximum sorption capacity of sepiolite towards Ni&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;2&#43;&amp;lt;&#47;SUP&amp;gt; and As&#40;V&#41; was 2.236 mg  g&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt; and 0.006 mg  g&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt;, respectively. The differences between the sorption capacities could be explained by different parameters like the charge of the ions or the free energy of hydration. The conclusion of this study is that natural sepiolite can adsorb cationic heavy metal and anionic metalloid species, which can have interesting applications in environmental applications such as the removal of these species from polluted waters.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45327"><b>Adsorption of nickel and arsenic from aqueous solution on natural sepiolite</b></A><br />S. Ansanay&#45;Alex; C. Lomenech; C. Hurel; N. Marmier<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 204 - 215</i><br />The adsorption capacity of a natural nanostructured clay &#40;sepiolite&#41; for the inorganic species&#58; Ni&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;2&#43;&amp;lt;&#47;SUP&amp;gt; and As&#40;V&#41; has been studied using a batch method. The different parameters affecting sorption such as the mass of adsorbent, contact time, sorbate concentration or pH have been investigated and optimal experimental conditions have been determined. Langmuir and Freundlich equations, which are commonly used to describe sorption equilibrium, were applied to model experimental results. The maximum sorption capacity of sepiolite towards Ni&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;2&#43;&amp;lt;&#47;SUP&amp;gt; and As&#40;V&#41; was 2.236 mg  g&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt; and 0.006 mg  g&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt;, respectively. The differences between the sorption capacities could be explained by different parameters like the charge of the ions or the free energy of hydration. The conclusion of this study is that natural sepiolite can adsorb cationic heavy metal and anionic metalloid species, which can have interesting applications in environmental applications such as the removal of these species from polluted waters.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045327</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 204 - 215</dc:source>
<dc:creator>S. Ansanay&#45;Alex; C. Lomenech; C. Hurel; N. Marmier</dc:creator>
<dc:contributor>University of Nice Sophia Antipolis, Laboratory of Radiochemistry, Analytical Sciences and Environment, Parc Valrose, 28 avenue Valrose, 06108 Nice cedex 2, France. &#39; University of Nice Sophia Antipolis, Laboratory of Radiochemistry, Analytical Sciences and Environment, Parc Valrose, 28 avenue Valrose, 06108 Nice cedex 2, France. &#39; University of Nice Sophia Antipolis, Laboratory of Radiochemistry, Analytical Sciences and Environment, Parc Valrose, 28 avenue Valrose, 06108 Nice cedex 2, France. &#39; University of Nice Sophia Antipolis, Laboratory of Radiochemistry, Analytical Sciences and Environment, Parc Valrose, 28 avenue Valrose, 06108 Nice cedex 2, France</dc:contributor>
<dc:subject>natural nanostructured solids</dc:subject>
<dc:subject>sepiolite</dc:subject>
<dc:subject>clay</dc:subject>
<dc:subject>adsorption capacity</dc:subject>
<dc:subject>nickel</dc:subject>
<dc:subject>arsenic</dc:subject>
<dc:subject>wastewater treatment</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>water pollution</dc:subject>
<dc:subject>cationic heavy metals</dc:subject>
<dc:subject>anionic metalloid species.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>204</prism:startingPage>
<prism:endingPage>215</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045328">
<title>Functionalisation through periodically arranged nanostructures</title>
<link>http://www.inderscience.com/link.php?id=45328</link>
<description>The controlled fabrication of uniform nanostructure arrays and their subsequent use for selective functionalisations of substrates is of increasing interest for controlled applications in nanotechnology. Fabrication of nanostructures via epitaxial growth has turned out to be an interesting alternative to standard lithography methods. In this work, we present the elaboration and fabrication of ordered, regular arrays of identical nanostructures, arranged in either one or two dimensions, obtained through different experimental bottom&#45;up and top&#45;down approaches. These nanostructures can be grown in different sizes and various shapes like nanoparticles, nanodiscs or nanostripes. One&#45;dimensional nanostructure arrangements are obtained through the controlled growth on previously nanopatterned templates like vicinal Si&#40;111&#41; substrates or structured Ag&#40;110&#41; surfaces. Two&#45;dimensional nanostructure arrangements are obtained by deposition of the adsorbate material through the openings of a nanoporous alumina membrane, serving in this case as an evaporation mask. A local functionalisation of substrates can be obtained in specific cases like growth of magnetic material on silicon or catalytic matter and graphene on silicon carbide and will be described.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45328"><b>Functionalisation through periodically arranged nanostructures</b></A><br />Houda Sahaf; Eric Moyen; Magali Mac&#233;; Laurence Masson; Margrit Hanb&#252;cken; Lukas Gerhard; Wulf Wulfhekel<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 216 - 229</i><br />The controlled fabrication of uniform nanostructure arrays and their subsequent use for selective functionalisations of substrates is of increasing interest for controlled applications in nanotechnology. Fabrication of nanostructures via epitaxial growth has turned out to be an interesting alternative to standard lithography methods. In this work, we present the elaboration and fabrication of ordered, regular arrays of identical nanostructures, arranged in either one or two dimensions, obtained through different experimental bottom&#45;up and top&#45;down approaches. These nanostructures can be grown in different sizes and various shapes like nanoparticles, nanodiscs or nanostripes. One&#45;dimensional nanostructure arrangements are obtained through the controlled growth on previously nanopatterned templates like vicinal Si&#40;111&#41; substrates or structured Ag&#40;110&#41; surfaces. Two&#45;dimensional nanostructure arrangements are obtained by deposition of the adsorbate material through the openings of a nanoporous alumina membrane, serving in this case as an evaporation mask. A local functionalisation of substrates can be obtained in specific cases like growth of magnetic material on silicon or catalytic matter and graphene on silicon carbide and will be described.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045328</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 216 - 229</dc:source>
<dc:creator>Houda Sahaf; Eric Moyen; Magali Mac&#233;; Laurence Masson; Margrit Hanb&#252;cken; Lukas Gerhard; Wulf Wulfhekel</dc:creator>
<dc:contributor>CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus Luminy, Case 913, Marseille 13288, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus Luminy, Case 913, Marseille 13288, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus Luminy, Case 913, Marseille 13288, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus Luminy, Case 913, Marseille 13288, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus Luminy, Case 913, Marseille 13288, France. &#39; Physikalisches Institut, Karlsruhe Institute of Technology, Wolfgang Gaede Str. 1, 76131 Karlsruhe, Germany. &#39; Physikalisches Institut, Karlsruhe Institute of Technology, Wolfgang Gaede Str. 1, 76131 Karlsruhe, Germany</dc:contributor>
<dc:subject>nanopatterning</dc:subject>
<dc:subject>self&#45;assembly</dc:subject>
<dc:subject>chemical functionalisation</dc:subject>
<dc:subject>nanopatterned templates</dc:subject>
<dc:subject>silicon nanostripes</dc:subject>
<dc:subject>magnetic nanostructures</dc:subject>
<dc:subject>graphene</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>uniform nanostructure arrays</dc:subject>
<dc:subject>nanostructure fabrication</dc:subject>
<dc:subject>nanoparticles</dc:subject>
<dc:subject>nanodiscs</dc:subject>
<dc:subject>nanoporous alumina membrane</dc:subject>
<dc:subject>silicon carbide.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>216</prism:startingPage>
<prism:endingPage>229</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045329">
<title>Laser&#45;ablative nanostructuring of surfaces</title>
<link>http://www.inderscience.com/link.php?id=45329</link>
<description>We present an overview of laser methods for nanostructuring of surfaces that are in the focus of ongoing research activities of our Institute &#40;LP3&#41;. The methods imply the removal of material by laser radiation to provide either spontaneous nanostructuring of laser&#45;illuminated surface or its controlled nano&#45;modification. Here, the desired relief or architecture is achieved through a proper selection of radiation characteristics &#40;pulse duration and wavelength&#41; and parameters of environment &#40;pressure of ambient gas, etc.&#41;. Examples of formed nano&#45;architectures include penguin&#45;like structures of black Si with enhanced light absorption in the visible, semiconductor &#40;Si, Ge, ZnO, etc.&#41; quantum dot nanostructures with UV&#47;visible fluorescence, as well as periodic plasmonic nanoarrays. Exhibiting a series of unique properties, these structures are of importance for photovoltaics, optoelectronics and biological sensing applications.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45329"><b>Laser&#45;ablative nanostructuring of surfaces</b></A><br />A.V. Kabashin; T. Sarnet; D. Grojo; Ph. Delaporte; L. Charmasson; P. Blandin; R. Torres; T.J&#45;Y. Derrien; M. Sentis<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 230 - 245</i><br />We present an overview of laser methods for nanostructuring of surfaces that are in the focus of ongoing research activities of our Institute &#40;LP3&#41;. The methods imply the removal of material by laser radiation to provide either spontaneous nanostructuring of laser&#45;illuminated surface or its controlled nano&#45;modification. Here, the desired relief or architecture is achieved through a proper selection of radiation characteristics &#40;pulse duration and wavelength&#41; and parameters of environment &#40;pressure of ambient gas, etc.&#41;. Examples of formed nano&#45;architectures include penguin&#45;like structures of black Si with enhanced light absorption in the visible, semiconductor &#40;Si, Ge, ZnO, etc.&#41; quantum dot nanostructures with UV&#47;visible fluorescence, as well as periodic plasmonic nanoarrays. Exhibiting a series of unique properties, these structures are of importance for photovoltaics, optoelectronics and biological sensing applications.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045329</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 230 - 245</dc:source>
<dc:creator>A.V. Kabashin; T. Sarnet; D. Grojo; Ph. Delaporte; L. Charmasson; P. Blandin; R. Torres; T.J&#45;Y. Derrien; M. Sentis</dc:creator>
<dc:contributor>Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France. &#39; Lasers, Plasmas et Proc&#233;d&#233;s Photoniques &#40;LP3, UMR 6182 CNRS&#41;, Universit&#233; de la M&#233;diterran&#233;e, Campus de Luminy case 917, 13288 Marseille cedex 9, France</dc:contributor>
<dc:subject>laser nanofabrication</dc:subject>
<dc:subject>laser ablation</dc:subject>
<dc:subject>semiconductor nanostructures</dc:subject>
<dc:subject>plasmonics nanostructures</dc:subject>
<dc:subject>black silicon</dc:subject>
<dc:subject>colloidal nanoparticles</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>quantum dots</dc:subject>
<dc:subject>nanoarrays</dc:subject>
<dc:subject>photovoltaics</dc:subject>
<dc:subject>optoelectronics</dc:subject>
<dc:subject>biological sensing</dc:subject>
<dc:subject>biosensors</dc:subject>
<dc:subject>enhanced light absorption.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>230</prism:startingPage>
<prism:endingPage>245</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045330">
<title>Anodic 3D nanostructuring for tailored applications</title>
<link>http://www.inderscience.com/link.php?id=45330</link>
<description>Electrochemistry can be used to fabricate different three dimensional objects on the nanometre scale. Porous anodic aluminium oxide &#40;AAO&#41; membranes with varying but controlled morphologies are used in several complementary experiments in physics and biology. The present paper gives a description of the membrane fabrication procedure and presents a selection of applications based on the use of the membranes as evaporation masks in crystal growth experiments, as masks in reactive ion etching experiments or as moulds to fabricate arrays of ordered polymer nanopillars. Applications in energy storage are also briefly mentioned. Finally the fabrication of TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes &#40;TNT&#41; is described. Their anodic formation is very close to that of the AAO membranes and TNTs offer additional perspectives for applications.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45330"><b>Anodic 3D nanostructuring for tailored applications</b></A><br />Eric Moyen; Lionel Santinacci; Laurence Masson; Houda Sahaf; Magali Mac&#233;; Lo&#239;c Assaud; Margrit Hanb&#252;cken<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 246 - 259</i><br />Electrochemistry can be used to fabricate different three dimensional objects on the nanometre scale. Porous anodic aluminium oxide &#40;AAO&#41; membranes with varying but controlled morphologies are used in several complementary experiments in physics and biology. The present paper gives a description of the membrane fabrication procedure and presents a selection of applications based on the use of the membranes as evaporation masks in crystal growth experiments, as masks in reactive ion etching experiments or as moulds to fabricate arrays of ordered polymer nanopillars. Applications in energy storage are also briefly mentioned. Finally the fabrication of TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes &#40;TNT&#41; is described. Their anodic formation is very close to that of the AAO membranes and TNTs offer additional perspectives for applications.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045330</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 246 - 259</dc:source>
<dc:creator>Eric Moyen; Lionel Santinacci; Laurence Masson; Houda Sahaf; Magali Mac&#233;; Lo&#239;c Assaud; Margrit Hanb&#252;cken</dc:creator>
<dc:contributor>CINaM&#45;CNRS, Aix&#45;Marseille University, Campus Luminy &#150; Case 913 &#150; 13288 Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille University, Campus Luminy &#150; Case 913 &#150; 13288 Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille University, Campus Luminy &#150; Case 913 &#150; 13288 Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille University, Campus Luminy &#150; Case 913 &#150; 13288 Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille University, Campus Luminy &#150; Case 913 &#150; 13288 Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille University, Campus Luminy &#150; Case 913 &#150; 13288 Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille University, Campus Luminy &#150; Case 913 &#150; 13288 Marseille, France</dc:contributor>
<dc:subject>nanoporosity</dc:subject>
<dc:subject>nanoarrays</dc:subject>
<dc:subject>nanopatterning</dc:subject>
<dc:subject>nanostructures</dc:subject>
<dc:subject>TiO nanotubes</dc:subject>
<dc:subject>self&#45;assembly</dc:subject>
<dc:subject>templates</dc:subject>
<dc:subject>chemical functionalisation</dc:subject>
<dc:subject>nanoreservoirs</dc:subject>
<dc:subject>electrochemistry</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>porous AAO</dc:subject>
<dc:subject>anodic aluminium oxide</dc:subject>
<dc:subject>AAO membranes</dc:subject>
<dc:subject>evaporation masks</dc:subject>
<dc:subject>polymer nanopillars</dc:subject>
<dc:subject>titanium oxide.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>246</prism:startingPage>
<prism:endingPage>259</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045331">
<title>Novel fabrication technologies of 1D TiO2 nanotubes, vertical tin and iron&#45;based nanowires for Li&#45;ion microbatteries</title>
<link>http://www.inderscience.com/link.php?id=45331</link>
<description>We present the combination of anodisation, sputtering and electrodeposition processes as a novel technology to fabricate nanoarchitectured materials. Titania nanotubes are successfully fabricated using Ti foils and Ti film on Si wafers; by simply varying the anodisation parameters a 600&#45;900 nm range of tube length and a 50&#45;150 nm range of tube diameter can be obtained. Iron and tin oxides nanowires, microballs, microcubes or with sponge&#45;like morphology are obtained showing that the crystallinity can be tuned by optional heat treatment, but the initial morphology is preserved. We investigate all these materials as alternative electrodes for lithium&#45;ion batteries and microbatteries. It should be highlighted the fabrication of vertical nanowires using a template&#45;free approach exhibits some advantages because the electroactive species are fabricated directly onto the current collector, ensuring good electrical contact between titania nanotube layers and the current collector, and tackle the use of additives such as binder and conductive agents. Thus, Sn on an amorphous titania matrix and SnO nanowires on a crystalline titania matrix with a particular geometry &#40;2 &#181;m of tin&#47;tin oxide length&#41; have a remarkable reversible capacity of about 140 &#181;A h cm&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;2&amp;lt;&#47;SUP&amp;gt; &#40;675 mA h g&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt; and 70 &#181;A h cm&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;2&amp;lt;&#47;SUP&amp;gt; &#181;m&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt;&#41; which is kept about 85&#37; over 50 cycles. The matrix presented here can allow the volume expansion of lithium&#45;tin alloys and thus enhances the electrochemical performances as compared with usual tin&#45;based electrodes. In the text is also described the electrochemistry of a series of samples such as a 3 &#181;m thick nanocomposite made of vertical iron oxide nanowires with quite regular form and diameters ranging between 20 nm and 150 nm grown on a matrix of self&#45;organised TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes. The obtained capacities compare very favourably with the best literature data for Li&#45;ion microbatteries.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45331"><b>Novel fabrication technologies of 1D TiO2 nanotubes, vertical tin and iron&#45;based nanowires for Li&#45;ion microbatteries</b></A><br />Gregorio F. Ortiz; Ilie Hanzu; Pedro Lavela; Philippe Knauth; Thierry Djenizian; Jos&#233; L. Tirado<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 260 - 294</i><br />We present the combination of anodisation, sputtering and electrodeposition processes as a novel technology to fabricate nanoarchitectured materials. Titania nanotubes are successfully fabricated using Ti foils and Ti film on Si wafers; by simply varying the anodisation parameters a 600&#45;900 nm range of tube length and a 50&#45;150 nm range of tube diameter can be obtained. Iron and tin oxides nanowires, microballs, microcubes or with sponge&#45;like morphology are obtained showing that the crystallinity can be tuned by optional heat treatment, but the initial morphology is preserved. We investigate all these materials as alternative electrodes for lithium&#45;ion batteries and microbatteries. It should be highlighted the fabrication of vertical nanowires using a template&#45;free approach exhibits some advantages because the electroactive species are fabricated directly onto the current collector, ensuring good electrical contact between titania nanotube layers and the current collector, and tackle the use of additives such as binder and conductive agents. Thus, Sn on an amorphous titania matrix and SnO nanowires on a crystalline titania matrix with a particular geometry &#40;2 &#181;m of tin&#47;tin oxide length&#41; have a remarkable reversible capacity of about 140 &#181;A h cm&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;2&amp;lt;&#47;SUP&amp;gt; &#40;675 mA h g&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt; and 70 &#181;A h cm&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;2&amp;lt;&#47;SUP&amp;gt; &#181;m&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt;&#41; which is kept about 85&#37; over 50 cycles. The matrix presented here can allow the volume expansion of lithium&#45;tin alloys and thus enhances the electrochemical performances as compared with usual tin&#45;based electrodes. In the text is also described the electrochemistry of a series of samples such as a 3 &#181;m thick nanocomposite made of vertical iron oxide nanowires with quite regular form and diameters ranging between 20 nm and 150 nm grown on a matrix of self&#45;organised TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes. The obtained capacities compare very favourably with the best literature data for Li&#45;ion microbatteries.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045331</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 260 - 294</dc:source>
<dc:creator>Gregorio F. Ortiz; Ilie Hanzu; Pedro Lavela; Philippe Knauth; Thierry Djenizian; Jos&#233; L. Tirado</dc:creator>
<dc:contributor>Inorganic Chemistry Lab, University of Cordoba, Marie Curie Building, Campus of Rabanales, 14071 Cordoba, Spain; ALISTORE&#45;European Research Institute, F&#233;d&#233;ration de Recherche CNRS no. 3104, 33, rue Saint Leu, 80039 Amiens Cedex, France. &#39; Institut f&#252;r Physikalische Chemie und Elektrochemie, Lebniz Universit&#228;t Hannover, Callinstra&#223;e 3a, 30167 Hannover, Germany; ALISTORE&#45;European Research Institute, F&#233;d&#233;ration de Recherche CNRS no. 3104, 33, rue Saint Leu, 80039 Amiens Cedex, France. &#39; Inorganic Chemistry Lab, University of Cordoba, Marie Curie Building, Campus of Rabanales, 14071 Cordoba, Spain; ALISTORE&#45;European Research Institute, F&#233;d&#233;ration de Recherche CNRS no. 3104, 33, rue Saint Leu, 80039 Amiens Cedex, France. &#39; Laboratoire Chimie Provence &#40;UMR 6264&#41;, Electrochemistry of Materials Research Group, University of Aix&#45;Marseille I, II, III&#45;CNRS Centre Saint&#45;J&#233;r&#244;me, F&#45;13397 Marseille Cedex 20, France; ALISTORE&#45;European Research Institute, F&#233;d&#233;ration de Recherche CNRS no. 3104, 33, rue Saint Leu, 80039 Amiens Cedex, France. &#39; Laboratoire Chimie Provence &#40;UMR 6264&#41;, Electrochemistry of Materials Research Group, University of Aix&#45;Marseille I, II, III&#45;CNRS Centre Saint&#45;J&#233;r&#244;me, F&#45;13397 Marseille Cedex 20, France; ALISTORE&#45;European Research Institute, F&#233;d&#233;ration de Recherche CNRS no. 3104, 33, rue Saint Leu, 80039 Amiens Cedex, France &#39; Inorganic Chemistry Lab, University of Cordoba, Marie Curie Building, Campus of Rabanales, 14071 Cordoba, Spain; ALISTORE&#45;European Research Institute, F&#233;d&#233;ration de Recherche CNRS no. 3104, 33, rue Saint Leu, 80039 Amiens Cedex, France.</dc:contributor>
<dc:subject>thin films</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>titania</dc:subject>
<dc:subject>nanotubes</dc:subject>
<dc:subject>tin oxide</dc:subject>
<dc:subject>nanowires</dc:subject>
<dc:subject>iron oxide</dc:subject>
<dc:subject>silicon</dc:subject>
<dc:subject>lithium batteries</dc:subject>
<dc:subject>microbatteries</dc:subject>
<dc:subject>energy storage</dc:subject>
<dc:subject>nanomaterials</dc:subject>
<dc:subject>anodisation</dc:subject>
<dc:subject>sputtering</dc:subject>
<dc:subject>electrodeposition.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>260</prism:startingPage>
<prism:endingPage>294</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045333">
<title>Electrochemical fabrication of oriented ZnO nanorods on TiO2 nanotubes</title>
<link>http://www.inderscience.com/link.php?id=45333</link>
<description>We report the ability to use TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotube as a guide layer to achieve the vertical growth of ZnO nanorods, in additive&#45;free bath. First, we focused on the anodisation conditions &#40;cell voltage and anodisation time&#41; to produce TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotube thin films grown from a 1.5 &#181;m thick Ti layer sputtered onto Si. Highly organised titania nanotubes were obtained in glycerol viscous electrolyte. In a second step, the electrochemical growth of ZnO grains has been investigated from a zinc nitrate bath at 70&#176;C on both Ti foil and TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes. ZnO deposition mechanism has been highlighted through the electrochemical experiments in conjunction with XRD technique and scanning electron microscopy &#40;SEM&#41; examinations. On Ti foils, we show that addition of additives is required to obtain a highly oriented nanostructured ZnO deposit. On TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes, additives are not necessary to obtain such a deposit&#58; Titania nanotubes can be used to guide the vertical growth of hybrid nanoarchitectured ZnO&#47;TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 electrode.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45333"><b>Electrochemical fabrication of oriented ZnO nanorods on TiO2 nanotubes</b></A><br />Marielle Eyraud; G. Jimenez&#45;Cadena; C. Chassigneux; F. Vacandio; E. Comini; G. Sberveglieri; T. Djenizian<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 295 - 311</i><br />We report the ability to use TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotube as a guide layer to achieve the vertical growth of ZnO nanorods, in additive&#45;free bath. First, we focused on the anodisation conditions &#40;cell voltage and anodisation time&#41; to produce TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotube thin films grown from a 1.5 &#181;m thick Ti layer sputtered onto Si. Highly organised titania nanotubes were obtained in glycerol viscous electrolyte. In a second step, the electrochemical growth of ZnO grains has been investigated from a zinc nitrate bath at 70&#176;C on both Ti foil and TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes. ZnO deposition mechanism has been highlighted through the electrochemical experiments in conjunction with XRD technique and scanning electron microscopy &#40;SEM&#41; examinations. On Ti foils, we show that addition of additives is required to obtain a highly oriented nanostructured ZnO deposit. On TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 nanotubes, additives are not necessary to obtain such a deposit&#58; Titania nanotubes can be used to guide the vertical growth of hybrid nanoarchitectured ZnO&#47;TiO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2 electrode.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045333</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 295 - 311</dc:source>
<dc:creator>Marielle Eyraud; G. Jimenez&#45;Cadena; C. Chassigneux; F. Vacandio; E. Comini; G. Sberveglieri; T. Djenizian</dc:creator>
<dc:contributor>Aix&#45;Marseille Univ CNRS, Laboratoire Chimie Provence, Electrochemistry of Materials Research Group, Centre Saint Jerome 13397 Marseille Cedex 20, France. &#39; INFM&#45;CNR SENSOR, Lab and University of Brescia, Via Valotti 9, 25133 Brescia, Italy. &#39; Aix&#45;Marseille Univ CNRS, Laboratoire Chimie Provence, Electrochemistry of Materials Research Group, Centre Saint Jerome 13397 Marseille Cedex 20, France. &#39; Aix&#45;Marseille Univ CNRS, Laboratoire Chimie Provence, Electrochemistry of Materials Research Group, Centre Saint Jerome 13397 Marseille Cedex 20, France. &#39; SENSOR, University of Brescia and CNR&#45;IDASC, Via Valotti 9, 25133 Brescia, Italy. &#39; SENSOR, University of Brescia and CNR&#45;IDASC, Via Valotti 9, 25133 Brescia, Italy. &#39; Aix&#45;Marseille Univ CNRS, Laboratoire Chimie Provence, Electrochemistry of Materials Research Group, Centre Saint Jerome 13397 Marseille Cedex 20, France</dc:contributor>
<dc:subject>zinc oxide</dc:subject>
<dc:subject>ZnO nanorods</dc:subject>
<dc:subject>titania nanotubes</dc:subject>
<dc:subject>TiO2</dc:subject>
<dc:subject>composite nanoarchitectured electrodes</dc:subject>
<dc:subject>electrochemical methods</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>anodisation</dc:subject>
<dc:subject>thin films.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>295</prism:startingPage>
<prism:endingPage>311</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045336">
<title>Dry and wet methods of silicon dioxide surface functionalisation with 3&#45;aminopropyl trimethoxysilane&#58; application to fullerene C60 anchoring</title>
<link>http://www.inderscience.com/link.php?id=45336</link>
<description>In this work, we have studied the formation of self&#45;assembled monolayers &#40;SAM&#41; of 3&#45;aminopropyltrimethoxysilane &#40;APTMS&#41;, chemically bound to silicon dioxide surface, prepared using a deposition from both solution and a new solvent&#45;free process, using contact angle measurements, ellipsometry, ATR&#45;FTIR spectroscopy and AFM imaging. In the first part, we have analysed the grafting kinetics of APTMS SAMs to control the formation of a single monolayer. Results show that with the dry deposition method about 4 h are needed to obtain a complete APTMS single monolayer. In parallel, the ordering kinetics of the SAM has been monitored by ATR&#45;FTIR spectroscopy, showing that the monolayer reaches its final order before grafting. The possibility of using the as&#45;obtained APTMS SAMs from wet and dry methods for anchoring functional molecular moieties is then probed with fullerene C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60 molecules deposited from a solution. The grafting kinetics of C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60 is studied on wetly deposited APTMS, showing a first step at about two monolayers. At last, comparative analysis of C60 grafted on either dryly or wetly deposited APTMS shows that the latter allows obtaining more homogeneous C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60 layer. Such results could help in paving the way to the preparation of hybrid C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60&#45;based molecular devices on silicon through a bottom&#45;up approach.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45336"><b>Dry and wet methods of silicon dioxide surface functionalisation with 3&#45;aminopropyl trimethoxysilane&#58; application to fullerene C60 anchoring</b></A><br />A.Gr&#233;gory Delafosse; Lionel Patrone; Didier Goguenheim<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 312 - 324</i><br />In this work, we have studied the formation of self&#45;assembled monolayers &#40;SAM&#41; of 3&#45;aminopropyltrimethoxysilane &#40;APTMS&#41;, chemically bound to silicon dioxide surface, prepared using a deposition from both solution and a new solvent&#45;free process, using contact angle measurements, ellipsometry, ATR&#45;FTIR spectroscopy and AFM imaging. In the first part, we have analysed the grafting kinetics of APTMS SAMs to control the formation of a single monolayer. Results show that with the dry deposition method about 4 h are needed to obtain a complete APTMS single monolayer. In parallel, the ordering kinetics of the SAM has been monitored by ATR&#45;FTIR spectroscopy, showing that the monolayer reaches its final order before grafting. The possibility of using the as&#45;obtained APTMS SAMs from wet and dry methods for anchoring functional molecular moieties is then probed with fullerene C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60 molecules deposited from a solution. The grafting kinetics of C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60 is studied on wetly deposited APTMS, showing a first step at about two monolayers. At last, comparative analysis of C60 grafted on either dryly or wetly deposited APTMS shows that the latter allows obtaining more homogeneous C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60 layer. Such results could help in paving the way to the preparation of hybrid C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;60&#45;based molecular devices on silicon through a bottom&#45;up approach.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045336</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 312 - 324</dc:source>
<dc:creator>A.Gr&#233;gory Delafosse; Lionel Patrone; Didier Goguenheim</dc:creator>
<dc:contributor>Aix&#45;Marseille Universit&#233;, IM2NP; CNRS, IM2NP &#40;UMR 6242&#41;; Institut Sup&#233;rieur de l&#39;Electronique et du Num&#233;rique, IM2NP, Maison des Technologies, Place Georges Pompidou, 83000 Toulon, France. &#39; Aix&#45;Marseille Universit&#233;, IM2NP; CNRS, IM2NP &#40;UMR 6242&#41;; Institut Sup&#233;rieur de l&#39;Electronique et du Num&#233;rique, IM2NP, Maison des Technologies, Place Georges Pompidou, 83000 Toulon, France. &#39; CNRS, IM2NP &#40;UMR 6242&#41;; Institut Sup&#233;rieur de l&#39;Electronique et du Num&#233;rique, IM2NP, Maison des Technologies, Place Georges Pompidou, 83000 Toulon, France</dc:contributor>
<dc:subject>self&#45;assembled monolayers</dc:subject>
<dc:subject>aminopropyltrimethoxysilane</dc:subject>
<dc:subject>APTMS</dc:subject>
<dc:subject>fullerene C60</dc:subject>
<dc:subject>silicon oxide</dc:subject>
<dc:subject>grafting kinetics</dc:subject>
<dc:subject>silicon dioxide</dc:subject>
<dc:subject>surface functionalisation</dc:subject>
<dc:subject>ordering kinetics</dc:subject>
<dc:subject>nanotechnology.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>312</prism:startingPage>
<prism:endingPage>324</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045337">
<title>Self&#45;organised growth of molecular arrays at surfaces</title>
<link>http://www.inderscience.com/link.php?id=45337</link>
<description>The autonomous ordering and assembly of atoms and molecules on atomically well&#45;defined surfaces allow creating a wide range of surface nanostructures, opening an alternative &#145;bottom&#45;up&#146; route to the traditional &#145;top&#45;down&#146; fabrication methods of the microelectronics industry now approaching their fundamental limits. This review summarises some recent efforts of our team to grow molecular arrays on metal, insulating or semiconductor surfaces. In a fundamental approach, two&#45;dimensional surface arrays of nanometre size have been obtained under ultrahigh vacuum by evaporation of molecules, functionalised to favour the intermolecular links rather than molecule&amp;&#45;substrate ones. Intermolecular links such as hydrogen bonds, covalent or coordination bonding were profitably used to create various molecular networks. Alternatively, we also investigated molecular self&#45;assembly from the solution whose architectures are mainly fixed by the molecule&#45;substrate adsorption forces. Molecular assemblies were characterised using Scanning Near&#45;Field Microscopies &#40;Scanning Tunnelling Microscopy, non&#45;contact&#45;Atomic Force Microscopy&#41;, whereas electronic and vibrational properties were investigated by surface spectroscopy such as Ultra&#45;Violet and X&#45;ray Photoelectron Spectroscopy, infrared or Surface&#45;Enhanced Raman Spectroscopy.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45337"><b>Self&#45;organised growth of molecular arrays at surfaces</b></A><br />L. Porte; M. Abel; P. Amsalem; F. Bocquet; F.C. Bocquet; V. Chevallier; S. Clair; G. Delafosse; S. Desbief; V. Gadenne; L. Giovanelli; M. Koudia; Y. Ksari; C. Loppacher; A. Merlen; L. Nony; O. Ourdjini; L. Patrone; R. Pawlak; J. Romann; J&#45;C. Valmalette; J&#45;M. Themlin<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 325 - 354</i><br />The autonomous ordering and assembly of atoms and molecules on atomically well&#45;defined surfaces allow creating a wide range of surface nanostructures, opening an alternative &#145;bottom&#45;up&#146; route to the traditional &#145;top&#45;down&#146; fabrication methods of the microelectronics industry now approaching their fundamental limits. This review summarises some recent efforts of our team to grow molecular arrays on metal, insulating or semiconductor surfaces. In a fundamental approach, two&#45;dimensional surface arrays of nanometre size have been obtained under ultrahigh vacuum by evaporation of molecules, functionalised to favour the intermolecular links rather than molecule&amp;&#45;substrate ones. Intermolecular links such as hydrogen bonds, covalent or coordination bonding were profitably used to create various molecular networks. Alternatively, we also investigated molecular self&#45;assembly from the solution whose architectures are mainly fixed by the molecule&#45;substrate adsorption forces. Molecular assemblies were characterised using Scanning Near&#45;Field Microscopies &#40;Scanning Tunnelling Microscopy, non&#45;contact&#45;Atomic Force Microscopy&#41;, whereas electronic and vibrational properties were investigated by surface spectroscopy such as Ultra&#45;Violet and X&#45;ray Photoelectron Spectroscopy, infrared or Surface&#45;Enhanced Raman Spectroscopy.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045337</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 325 - 354</dc:source>
<dc:creator>L. Porte; M. Abel; P. Amsalem; F. Bocquet; F.C. Bocquet; V. Chevallier; S. Clair; G. Delafosse; S. Desbief; V. Gadenne; L. Giovanelli; M. Koudia; Y. Ksari; C. Loppacher; A. Merlen; L. Nony; O. Ourdjini; L. Patrone; R. Pawlak; J. Romann; J&#45;C. Valmalette; J&#45;M. Themlin</dc:creator>
<dc:contributor>Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France. &#39; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Universit&#233; Sud Toulon&#45;Var, IM2NP, B&#226;timent R, BP 132, F&#45;83957 La Garde Cedex, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Institut Sup&#233;rieur de l&#146;Electronique et du Num&#233;rique, IM2NP, Maison des Technologies, Place Georges Pompidou, F&#45;83000 Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Institut Sup&#233;rieur de l&#146;Electronique et du Num&#233;rique, IM2NP, Maison des Technologies, Place Georges Pompidou, F&#45;83000 Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Institut Sup&#233;rieur de l&#146;Electronique et du Num&#233;rique, IM2NP, Maison des Technologies, Place Georges Pompidou, F&#45;83000 Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Universit&#233; Sud Toulon&#45;Var, IM2NP, B&#226;timent R, BP 132, F&#45;83957 La Garde Cedex, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Institut Sup&#233;rieur d&#39;Electronique et du Num&#233;rique, IM2NP, Maison des Technologies, Place Georges Pompidou, F&#45;83000 Toulon, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France. &#39; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Universit&#233; Sud Toulon&#45;Var, IM2NP, B&#226;timent R, BP 132, F&#45;83957 La Garde Cedex, France. &#39; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France; Universit&#233; Sud Toulon&#45;Var, IM2NP, B&#226;timent R, BP 132, F&#45;83957 La Garde Cedex, France. &#39; Aix Marseille&#45;Universit&#233;, IM2NP &#150; Institut Mat&#233;riaux Micro&#233;lectronique et Nanosciences de Provence, Campus de Saint&#45;J&#233;r&#244;me &#150; Case 142, 13397 Marseille Cedex 20, France; CNRS, IM2NP &#40;UMR 6242&#41;, Nanostructuration Team, Marseille&#45;Toulon, France</dc:contributor>
<dc:subject>self&#45;organised growth</dc:subject>
<dc:subject>single&#45;crystalline surfaces</dc:subject>
<dc:subject>SCOFs</dc:subject>
<dc:subject>surface covalent organic frameworks</dc:subject>
<dc:subject>surface chemistry</dc:subject>
<dc:subject>interface chemistry</dc:subject>
<dc:subject>molecular arrays</dc:subject>
<dc:subject>surface nanostructures</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>metal surfaces</dc:subject>
<dc:subject>insulating surfaces</dc:subject>
<dc:subject>semiconductor surfaces</dc:subject>
<dc:subject>molecular self&#45;assembly.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>325</prism:startingPage>
<prism:endingPage>354</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045341">
<title>Thermoelectricity and heat balance in a metal&#47;dot&#47;metal junction</title>
<link>http://www.inderscience.com/link.php?id=45341</link>
<description>In this paper, we report on numerical calculations of stationary thermoelectric responses in a metal&#47;dot&#47;metal junction. We derive the Landauer expressions for both the electric and the heat currents, and first discuss the question of heat balance. Secondly, we calculate the Peltier coefficient in the non&#45;linear response regime, and discuss its relation with the Seebeck coefficient, and finally the figure of merit ZT in the linear response. In all regimes, we show how the applied gate voltage is a key parameter to obtain the maximum thermoelectric efficiency through the nanodevice.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45341"><b>Thermoelectricity and heat balance in a metal&#47;dot&#47;metal junction</b></A><br />Adeline Cr&#233;pieux; Fabienne Michelini<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 355 - 367</i><br />In this paper, we report on numerical calculations of stationary thermoelectric responses in a metal&#47;dot&#47;metal junction. We derive the Landauer expressions for both the electric and the heat currents, and first discuss the question of heat balance. Secondly, we calculate the Peltier coefficient in the non&#45;linear response regime, and discuss its relation with the Seebeck coefficient, and finally the figure of merit ZT in the linear response. In all regimes, we show how the applied gate voltage is a key parameter to obtain the maximum thermoelectric efficiency through the nanodevice.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045341</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 355 - 367</dc:source>
<dc:creator>Adeline Cr&#233;pieux; Fabienne Michelini</dc:creator>
<dc:contributor>Centre de Physique Th&#233;orique, 163 avenue de Luminy, 13288 Marseille, France. &#39; Institut Mat&#233;riaux Micro&#233;lectronique Nanosciences de Provence, Avenue Escadrille Normandie Niemen, 13397 Marseille, France</dc:contributor>
<dc:subject>thermoelectric effect</dc:subject>
<dc:subject>heat current</dc:subject>
<dc:subject>quantum dots</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>thermoelectricity</dc:subject>
<dc:subject>heat balance</dc:subject>
<dc:subject>nanodevices</dc:subject>
<dc:subject>gate voltage.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>355</prism:startingPage>
<prism:endingPage>367</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045342">
<title>Low&#45;dimensional materials for thermoelectric applications</title>
<link>http://www.inderscience.com/link.php?id=45342</link>
<description>In recent years, increasing awareness and concern for energy resources and the environment have stimulated significant advances in materials and technologies for energy conversion. By using a principle called &#145;the Seebeck effect&#146; thermoelectric modules can convert heat energy to electricity. The efficiency of a thermoelectric material is given by the figure of merit ZT &#61; &#40;S&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;2&amp;lt;&#47;SUP&amp;gt;&#963;&#47;&#954;&#41; T, where S is the Seebeck coefficient, T is the temperature, and &#963; and &#954; are the electrical and thermal conductivities, respectively. An improvement in ZT can be achieved by increasing S&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt;&#62;&#963; or reducing &#954;. However, in three&#45;dimensional &#40;3D&#41; materials, S, &#62;&#963; and &#954; are interrelated. By contrast, when dimensionality of materials is lowered down to the nanometre scale, these parameters can be tuned to some extent independently from one another to some extent. This paper reports on some examples of low&#45;dimensional thermoelectric materials with enhanced properties. Various calculation methods used to predict these properties are also presented, and the added value of the calculations as a complement to experiments in the improvement of thermoelectric materials is particularly stressed.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45342"><b>Low&#45;dimensional materials for thermoelectric applications</b></A><br />Pascal Boulet; Marie&#45;Christine Record<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 368 - 376</i><br />In recent years, increasing awareness and concern for energy resources and the environment have stimulated significant advances in materials and technologies for energy conversion. By using a principle called &#145;the Seebeck effect&#146; thermoelectric modules can convert heat energy to electricity. The efficiency of a thermoelectric material is given by the figure of merit ZT &#61; &#40;S&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;2&amp;lt;&#47;SUP&amp;gt;&#963;&#47;&#954;&#41; T, where S is the Seebeck coefficient, T is the temperature, and &#963; and &#954; are the electrical and thermal conductivities, respectively. An improvement in ZT can be achieved by increasing S&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;1&amp;lt;&#47;SUP&amp;gt;&#62;&#963; or reducing &#954;. However, in three&#45;dimensional &#40;3D&#41; materials, S, &#62;&#963; and &#954; are interrelated. By contrast, when dimensionality of materials is lowered down to the nanometre scale, these parameters can be tuned to some extent independently from one another to some extent. This paper reports on some examples of low&#45;dimensional thermoelectric materials with enhanced properties. Various calculation methods used to predict these properties are also presented, and the added value of the calculations as a complement to experiments in the improvement of thermoelectric materials is particularly stressed.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045342</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 368 - 376</dc:source>
<dc:creator>Pascal Boulet; Marie&#45;Christine Record</dc:creator>
<dc:contributor>Laboratoire Chimie Provence &#150; UMR CNRS 6264, Universit&#233; de Provence, Aix&#45;Marseille I, II et III, Avenue Normandie Niemen, 13397 Marseille, Cedex 20, France. &#39; Institut Mat&#233;riaux Micro&#233;lectronique Nanosciences de Provence IM2NP &#150; UMR CNRS 6242, Universit&#233; Aix&#45;Marseille III &#150; Paul C&#233;zanne,  Avenue Normandie Niemen, 13397 Marseille Cedex 20, France</dc:contributor>
<dc:subject>thermoelectricity</dc:subject>
<dc:subject>nanomaterials</dc:subject>
<dc:subject>quantum wells</dc:subject>
<dc:subject>quantum wires</dc:subject>
<dc:subject>quantum dots</dc:subject>
<dc:subject>confinement effects</dc:subject>
<dc:subject>calculations</dc:subject>
<dc:subject>density&#45;functional theory</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>Seebeck effect.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>368</prism:startingPage>
<prism:endingPage>376</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045343">
<title>Iridium &#40;III&#41; complexes as promising emitters for solid&#45;state Light&#45;Emitting Electrochemical Cells &#40;LECs&#41;</title>
<link>http://www.inderscience.com/link.php?id=45343</link>
<description>Light&#45;emitting Electrochemical Cells &#40;LECs&#41; constitute one of the most recent generations of Organic Light&#45;Emitting Diodes &#40;OLEDs&#41;. The main difference between LECs and OLEDs is that LECs include mobile ions in the active layer. Ionic transition&#45;metal complexes and especially ionic iridium &#40;III&#41; complexes have recently attracted widespread attention as potential electroluminescent materials for LECs. Herein, we present an overview of LECs incorporating ionic iridium &#40;III&#41; complexes as phosphorescent emitters. Synthetic strategies developed to introduce iridium &#40;III&#41; complexes in the active layer are also reviewed. Despite the numerous intrinsic drawbacks still remaining, recent advances make iridium&#45;based LECs promising devices for future commercial and scientific applications.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45343"><b>Iridium &#40;III&#41; complexes as promising emitters for solid&#45;state Light&#45;Emitting Electrochemical Cells &#40;LECs&#41;</b></A><br />Fr&#233;d&#233;ric Dumur; Denis Bertin; Didier Gigmes<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 377 - 395</i><br />Light&#45;emitting Electrochemical Cells &#40;LECs&#41; constitute one of the most recent generations of Organic Light&#45;Emitting Diodes &#40;OLEDs&#41;. The main difference between LECs and OLEDs is that LECs include mobile ions in the active layer. Ionic transition&#45;metal complexes and especially ionic iridium &#40;III&#41; complexes have recently attracted widespread attention as potential electroluminescent materials for LECs. Herein, we present an overview of LECs incorporating ionic iridium &#40;III&#41; complexes as phosphorescent emitters. Synthetic strategies developed to introduce iridium &#40;III&#41; complexes in the active layer are also reviewed. Despite the numerous intrinsic drawbacks still remaining, recent advances make iridium&#45;based LECs promising devices for future commercial and scientific applications.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045343</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 377 - 395</dc:source>
<dc:creator>Fr&#233;d&#233;ric Dumur; Denis Bertin; Didier Gigmes</dc:creator>
<dc:contributor>Laboratoire Chimie Provence, UMR 6264 CNRS, Universit&#233;s d&#39;Aix&#45;Marseille I, II, III, Facult&#233; des Sciences de Saint J&#233;r&#244;me, Avenue Escadrille Normandie&#45;Niemen, Case 542, 13397 Marseille cedex 20, France. &#39; Laboratoire Chimie Provence, UMR 6264 CNRS, Universit&#233;s d&#39;Aix&#45;Marseille I, II, III, Facult&#233; des Sciences de Saint J&#233;r&#244;me, Avenue Escadrille Normandie&#45;Niemen, Case 542, 13397 Marseille cedex 20, France. &#39; Laboratoire Chimie Provence, UMR 6264 CNRS, Universit&#233;s d&#39;Aix&#45;Marseille I, II, III, Facult&#233; des Sciences de Saint J&#233;r&#244;me, Avenue Escadrille Normandie&#45;Niemen, Case 542, 13397 Marseille cedex 20, France</dc:contributor>
<dc:subject>ionic complexes</dc:subject>
<dc:subject>LECs</dc:subject>
<dc:subject>light&#45;emitting electrochemical cells</dc:subject>
<dc:subject>iridium complexes</dc:subject>
<dc:subject>emitters</dc:subject>
<dc:subject>organic light&#45;emitting diodes</dc:subject>
<dc:subject>OLEDs</dc:subject>
<dc:subject>electroluminescent materials</dc:subject>
<dc:subject>nanotechnology.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>377</prism:startingPage>
<prism:endingPage>395</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045344">
<title>Stress effects on solid&#45;state dewetting of nano&#45;thin films</title>
<link>http://www.inderscience.com/link.php?id=45344</link>
<description>In this paper, we present a brief survey of stress effects on dewetting. For this purpose, i&#41; we develop a simple thermodynamic model to illustrate stress effects; ii&#41; we study stress effects in strained&#45;Silicon&#45;On&#45;Insulator &#40;s&#45;SOI&#41; thin films by means of Low Energy Electron Microscopy, and Atomic Force Microscopy; iii&#41; we discuss some available data. In particular, we show that while for s&#45;SOI the strain only provides a relatively small contribution to the total driving force for dewetting, in some other cases stress can really dominate the driving force for the dewetting.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45344"><b>Stress effects on solid&#45;state dewetting of nano&#45;thin films</b></A><br />F. Cheynis; E. Bussmann; F. Leroy; T. Passanante; P. M&#252;ller<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 396 - 411</i><br />In this paper, we present a brief survey of stress effects on dewetting. For this purpose, i&#41; we develop a simple thermodynamic model to illustrate stress effects; ii&#41; we study stress effects in strained&#45;Silicon&#45;On&#45;Insulator &#40;s&#45;SOI&#41; thin films by means of Low Energy Electron Microscopy, and Atomic Force Microscopy; iii&#41; we discuss some available data. In particular, we show that while for s&#45;SOI the strain only provides a relatively small contribution to the total driving force for dewetting, in some other cases stress can really dominate the driving force for the dewetting.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045344</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 396 - 411</dc:source>
<dc:creator>F. Cheynis; E. Bussmann; F. Leroy; T. Passanante; P. M&#252;ller</dc:creator>
<dc:contributor>Centre Interdisciplinaire de Nanoscience de Marseille, CNRS UPR 3118, Associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288, Marseille cedex 9, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS UPR 3118, Associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288, Marseille cedex 9, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS UPR 3118, Associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288, Marseille cedex 9, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS UPR 3118, Associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288, Marseille cedex 9, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS UPR 3118, Associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288, Marseille cedex 9, France</dc:contributor>
<dc:subject>solid&#45;state dewetting</dc:subject>
<dc:subject>nanothin films</dc:subject>
<dc:subject>strain</dc:subject>
<dc:subject>stress</dc:subject>
<dc:subject>SOI</dc:subject>
<dc:subject>thin films</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>silicon&#45;on&#45;insulator.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>396</prism:startingPage>
<prism:endingPage>411</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045345">
<title>Fabrication and growth of GaN&#45;based micro and nanostructures</title>
<link>http://www.inderscience.com/link.php?id=45345</link>
<description>GaN is considered as the material of choice for electromechanical, electronic and optoelectronic applications in the visible&#47;UV regions of the electromagnetic spectrum. However, the lack of an adapted substrate results in a very large density of defects, in particular dislocations, stacking faults and cracks. Under these circumstances, the growth of nanostructures appears as an appealing means of circumventing the problem. In this paper, we describe the fabrication and characterisation of GaN&#45;based nanostructures &#150; cantilevers, microdiscs, photonic crystals, micro and nanowires &#150; grown by metallorganic vapour phase epitaxy &#40;MOVPE&#41; and molecular beam epitaxy &#40;MBE&#41; and fabricated either by a bottom&#45;up or a top&#45;down approach. The applications envisaged at CRHEA will be examined.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45345"><b>Fabrication and growth of GaN&#45;based micro and nanostructures</b></A><br />Blandine Alloing; Emmanuel Beraudo; Yvon Cordier; Fabrice Semond; Sylvain Sergent; Olivier Tottereau; P. Venn&#233;gu&#232;s; St&#233;phane V&#233;zian; Jes&#250;s Z&#250;&#241;iga&#45;P&#233;rez<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 412 - 427</i><br />GaN is considered as the material of choice for electromechanical, electronic and optoelectronic applications in the visible&#47;UV regions of the electromagnetic spectrum. However, the lack of an adapted substrate results in a very large density of defects, in particular dislocations, stacking faults and cracks. Under these circumstances, the growth of nanostructures appears as an appealing means of circumventing the problem. In this paper, we describe the fabrication and characterisation of GaN&#45;based nanostructures &#150; cantilevers, microdiscs, photonic crystals, micro and nanowires &#150; grown by metallorganic vapour phase epitaxy &#40;MOVPE&#41; and molecular beam epitaxy &#40;MBE&#41; and fabricated either by a bottom&#45;up or a top&#45;down approach. The applications envisaged at CRHEA will be examined.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045345</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 412 - 427</dc:source>
<dc:creator>Blandine Alloing; Emmanuel Beraudo; Yvon Cordier; Fabrice Semond; Sylvain Sergent; Olivier Tottereau; P. Venn&#233;gu&#232;s; St&#233;phane V&#233;zian; Jes&#250;s Z&#250;&#241;iga&#45;P&#233;rez</dc:creator>
<dc:contributor>Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France. &#39; Centre de Recherche sur l&#39;H&#233;t&#233;ro&#45;Epitaxie et ses Applications, Centre National de la Recherche Scientifique, Parc de Sophia Antipolis Rue B. Gregory 06560 Valbonne, France</dc:contributor>
<dc:subject>resonators</dc:subject>
<dc:subject>microwires</dc:subject>
<dc:subject>nanowires</dc:subject>
<dc:subject>microdiscs</dc:subject>
<dc:subject>photonic crystals</dc:subject>
<dc:subject>gallium nitride</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>nanostructures</dc:subject>
<dc:subject>cantilevers.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>412</prism:startingPage>
<prism:endingPage>427</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045346">
<title>Boosting the Curie temperature in carbon&#45;doped Mn5Ge3&#47;Ge heterostructures</title>
<link>http://www.inderscience.com/link.php?id=45346</link>
<description>We have combined structural and magnetic characterisations to investigate the effect of carbon incorporation in epitaxial Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x films grown on Ge&#40;111&#41; by Molecular Beam Epitaxy &#40;MBE&#41;. It is shown that up to a carbon content of saturation of &#126;0.6, most of carbon can be incorporated into the interstitial sites of the Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3 lattice. Such a process results in a linear increase in the Curie temperature &#40;T&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;C&#41; of the alloy, which can reach a value as high as &amp;sim;430 K. Above this carbon content, T&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;C is found to decrease. Structural characterisations reveal that Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x films are in perfect epitaxy when x &amp;sim;0.6 whereas cluster formation in the grown layers is detected above that threshold. The clusters can be attributed to manganese carbide &#40;MnC&#41; compounds, which are formed when the carbon content exceeds the saturation value of 0.6 by consuming previously deposited carbon. In addition, we also show that after post&#45;thermal annealing, the carbon&#45;doped Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x alloys remain magnetically and structurally stable up to a temperature as high as 1123 K. The obtained results are very promising for integrating Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x into ferromagnetic&#47;semiconductor heterostructures, the ultimate goal being the realisation of spintronics devices.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45346"><b>Boosting the Curie temperature in carbon&#45;doped Mn5Ge3&#47;Ge heterostructures</b></A><br />A. Spiesser; M&#45;T. Dau; L.A. Michez; M. Petit; C. Coudreau; A. Glachant; V. Le Thanh<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 428 - 438</i><br />We have combined structural and magnetic characterisations to investigate the effect of carbon incorporation in epitaxial Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x films grown on Ge&#40;111&#41; by Molecular Beam Epitaxy &#40;MBE&#41;. It is shown that up to a carbon content of saturation of &#126;0.6, most of carbon can be incorporated into the interstitial sites of the Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3 lattice. Such a process results in a linear increase in the Curie temperature &#40;T&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;C&#41; of the alloy, which can reach a value as high as &amp;sim;430 K. Above this carbon content, T&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;C is found to decrease. Structural characterisations reveal that Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x films are in perfect epitaxy when x &amp;sim;0.6 whereas cluster formation in the grown layers is detected above that threshold. The clusters can be attributed to manganese carbide &#40;MnC&#41; compounds, which are formed when the carbon content exceeds the saturation value of 0.6 by consuming previously deposited carbon. In addition, we also show that after post&#45;thermal annealing, the carbon&#45;doped Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x alloys remain magnetically and structurally stable up to a temperature as high as 1123 K. The obtained results are very promising for integrating Mn&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;5Ge&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3C&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;x into ferromagnetic&#47;semiconductor heterostructures, the ultimate goal being the realisation of spintronics devices.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045346</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 428 - 438</dc:source>
<dc:creator>A. Spiesser; M&#45;T. Dau; L.A. Michez; M. Petit; C. Coudreau; A. Glachant; V. Le Thanh</dc:creator>
<dc:contributor>Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, Case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, Case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, Case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, Case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, Case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, Case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, Case 913, F&#45;13288 Marseille cedex 09, France</dc:contributor>
<dc:subject>spintronics</dc:subject>
<dc:subject>manganese magnetic compounds</dc:subject>
<dc:subject>ferromagnetism</dc:subject>
<dc:subject>carbon doping</dc:subject>
<dc:subject>Curie temperature</dc:subject>
<dc:subject>thermal stability</dc:subject>
<dc:subject>germanium</dc:subject>
<dc:subject>semiconductors</dc:subject>
<dc:subject>nanotechnology.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>428</prism:startingPage>
<prism:endingPage>438</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045347">
<title>Nanotechnologies dedicated to nucleation control</title>
<link>http://www.inderscience.com/link.php?id=45347</link>
<description>This paper highlights the work of our group on the control and the observation of nucleation with techniques using nanotechnologies. This control is performed either by triggering nucleation in time with an external field or by localising it spatially in a microdroplet. Localisation in time using light irradiation induces nucleation by forming radicals; the use of electric field acts locally on the density of the solution. Localisation in space with a microfluidic device produces hundreds of nanovolume crystallisers where concentration and temperature are easily monitored. Thus, accurate statistical studies lead to the nucleation parameters &#40;metastable zone, nucleation rate and polymorphism&#41;. Lastly, confinement with a microdroplet generator permits to reach very high supersaturations in fL to pL volumes allowing nucleation of a single crystal per microdroplet. All these methods clearly enhance nucleation in the metastable zone. Finally, they use small quantities of products offering potentialities for the screening of crystallisation conditions and phases &#40;polymorphism&#41;.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45347"><b>Nanotechnologies dedicated to nucleation control</b></A><br />Nadine Candoni; Zoubida Hammadi; Romain Grossier; Manuel Ildefonso; Eve Revalor; Nathalie Fert&#233;; Tetsuo Okutsu; Roger Morin; St&#233;phane Veesler<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 439 - 459</i><br />This paper highlights the work of our group on the control and the observation of nucleation with techniques using nanotechnologies. This control is performed either by triggering nucleation in time with an external field or by localising it spatially in a microdroplet. Localisation in time using light irradiation induces nucleation by forming radicals; the use of electric field acts locally on the density of the solution. Localisation in space with a microfluidic device produces hundreds of nanovolume crystallisers where concentration and temperature are easily monitored. Thus, accurate statistical studies lead to the nucleation parameters &#40;metastable zone, nucleation rate and polymorphism&#41;. Lastly, confinement with a microdroplet generator permits to reach very high supersaturations in fL to pL volumes allowing nucleation of a single crystal per microdroplet. All these methods clearly enhance nucleation in the metastable zone. Finally, they use small quantities of products offering potentialities for the screening of crystallisation conditions and phases &#40;polymorphism&#41;.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045347</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 439 - 459</dc:source>
<dc:creator>Nadine Candoni; Zoubida Hammadi; Romain Grossier; Manuel Ildefonso; Eve Revalor; Nathalie Fert&#233;; Tetsuo Okutsu; Roger Morin; St&#233;phane Veesler</dc:creator>
<dc:contributor>Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France. &#39; Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France. &#39; Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France. &#39; Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France. &#39; Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France. &#39; Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France. &#39; Department of Chemistry and Chemical Biology, Gunma University, KIRYU 375&#45;8515, Japan. &#39; Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France. &#39; Centre Interdisciplinaire de Nanosciences de Marseille, CNRS, Aix&#45;Marseille Universit&#233;, CINAM&#45;UPR3118, Campus de Luminy, Case 913, 13288 Marseille Cedex, France</dc:contributor>
<dc:subject>nucleation control</dc:subject>
<dc:subject>confinement</dc:subject>
<dc:subject>external field</dc:subject>
<dc:subject>crystallisation</dc:subject>
<dc:subject>polymorphism</dc:subject>
<dc:subject>metastable zone</dc:subject>
<dc:subject>microfluidics</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>microdroplets.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>439</prism:startingPage>
<prism:endingPage>459</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045348">
<title>Feasibility of simultaneous surface topography and XRF mapping using Shear Force Microscopy</title>
<link>http://www.inderscience.com/link.php?id=45348</link>
<description>Marketed sources equipped with polycapillary optics allow now laboratory X&#45;Ray Fluorescence &#40;XRF&#41; analysis with 5&#45;10 &#181;m lateral resolution. To improve it, we had the idea to use a thin cylindrical X&#45;ray capillary fitted to the XRF detector. The combination with near&#45;field microscopy would then lead to a simultaneous record of both topography and XRF from a sample at &#181;m lateral resolution. For this purpose, we have built a home&#45;made Shear Force Microscope to carry out this experiment in the future.In a first step, we have validated the microscope, operating in SNOM configuration, using test sample consisting in ZnO clusters deposited on a Si&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3N&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;4 grating. Second, the feasibility of  XRF collection through a thin X&#45;ray cylindrical capillary on Co&#47;Ti sample is shown in this work. The results suggest that sub&#45;1 &#181;m in&#45;lab XRF analysis is possible, replacing the optical fibre of our SNOM apparatus by an X&#45;ray capillary. On the basis of modelling our results, we then further discuss the possibility to reach 100 nm XRF resolution, combined to surface topography, working in synchrotron environment.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45348"><b>Feasibility of simultaneous surface topography and XRF mapping using Shear Force Microscopy</b></A><br />M. Dehlinger; C. Dorczynski; C. Fauquet; F. Jandard; D. Tonneau; A. Bjeoumikhov; S. Bjeoumikhova; R. Gubzhokov; A. Erko; I. Zizak; D. Pailharey; S. Ferrero; B. Dahmani<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 460 - 470</i><br />Marketed sources equipped with polycapillary optics allow now laboratory X&#45;Ray Fluorescence &#40;XRF&#41; analysis with 5&#45;10 &#181;m lateral resolution. To improve it, we had the idea to use a thin cylindrical X&#45;ray capillary fitted to the XRF detector. The combination with near&#45;field microscopy would then lead to a simultaneous record of both topography and XRF from a sample at &#181;m lateral resolution. For this purpose, we have built a home&#45;made Shear Force Microscope to carry out this experiment in the future.In a first step, we have validated the microscope, operating in SNOM configuration, using test sample consisting in ZnO clusters deposited on a Si&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3N&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;4 grating. Second, the feasibility of  XRF collection through a thin X&#45;ray cylindrical capillary on Co&#47;Ti sample is shown in this work. The results suggest that sub&#45;1 &#181;m in&#45;lab XRF analysis is possible, replacing the optical fibre of our SNOM apparatus by an X&#45;ray capillary. On the basis of modelling our results, we then further discuss the possibility to reach 100 nm XRF resolution, combined to surface topography, working in synchrotron environment.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045348</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 460 - 470</dc:source>
<dc:creator>M. Dehlinger; C. Dorczynski; C. Fauquet; F. Jandard; D. Tonneau; A. Bjeoumikhov; S. Bjeoumikhova; R. Gubzhokov; A. Erko; I. Zizak; D. Pailharey; S. Ferrero; B. Dahmani</dc:creator>
<dc:contributor>CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus de Luminy &#150; Case 913&#45;13288, Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus de Luminy &#150; Case 913&#45;13288, Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus de Luminy &#150; Case 913&#45;13288, Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus de Luminy &#150; Case 913&#45;13288, Marseille, France. &#39; CINaM&#45;CNRS, Aix&#45;Marseille Universit&#233;, Campus de Luminy &#150; Case 913&#45;13288, Marseille, France. &#39; IFG GmbH, 29&#47;31, Rudower&#45;chaussee, 12489 Berlin, Germany. &#39; IFG GmbH, 29&#47;31, Rudower&#45;chaussee, 12489 Berlin, Germany. &#39; IFG GmbH, 29&#47;31, Rudower&#45;chaussee, 12489 Berlin, Germany. &#39; HZB&#45;BESSY, Institute Nanometre Optics and Technology, Albert Einstein Strasse,  15, 12489 Berlin, Germany. &#39; HZB&#45;BESSY, Institute Nanometre Optics and Technology, Albert Einstein Strasse,  15, 12489 Berlin, Germany. &#39; Cie AXESS TECH, 750 Chemin de Beaupr&#233;, 13760, Saint Cannat, France. &#39; Cie AXESS TECH, 750 Chemin de Beaupr&#233;, 13760, Saint Cannat, France. &#39; Cie LovaLite, 18 Rue A.Savary, 25000 Besan&#231;on, France</dc:contributor>
<dc:subject>x&#45;ray spectroscopy</dc:subject>
<dc:subject>characterisation tools</dc:subject>
<dc:subject>nanocharacterisation</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>surface topography</dc:subject>
<dc:subject>XRF mapping</dc:subject>
<dc:subject>ZnO clusters</dc:subject>
<dc:subject>zinc oxide</dc:subject>
<dc:subject>silicon nitride</dc:subject>
<dc:subject>x&#45;ray fluorescence</dc:subject>
<dc:subject>x&#45;ray capillary</dc:subject>
<dc:subject>modelling.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>460</prism:startingPage>
<prism:endingPage>470</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045349">
<title>Role of the active layer thickness on the sensitivity of WO3 gas sensors</title>
<link>http://www.inderscience.com/link.php?id=45349</link>
<description>Sensitive materials in gas sensors are often polycrystalline semiconducting oxides such as WO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3, SnO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2, CuO or ZnO. They are most often composed of nanometric grains. They can be deposited either as thin or thick films. The film thickness plays an important role in the response stability and sensitivity of sensors. It is now well accepted that the relationship between the surface and volume of the sensitive layer plays a major role in the efficiency of detection. Many experimental and theoretical works were reported in explaining the experimental sensitivity vs. thickness relationships reported for the gas sensors prepared by different fabrication techniques. In addition, significant changes can be expected by adding catalytic nanograins in small quantities on the surface of the sensitive layers. For example, cobalt nanograins deposited on the surface of WO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3 sensors produce an important change in the WO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3 conductance. Indeed, cobalt changes the conduction type of the sensors from n&#45; to p&#45;type. This paper describes the effect of reducing the size of the sensors and nanostructured sensitive materials on the sensor response.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45349"><b>Role of the active layer thickness on the sensitivity of WO3 gas sensors</b></A><br />K. Aguir; J. Gu&#233;rin; N. Mliki; M. Bendahan<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 471 - 479</i><br />Sensitive materials in gas sensors are often polycrystalline semiconducting oxides such as WO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3, SnO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;2, CuO or ZnO. They are most often composed of nanometric grains. They can be deposited either as thin or thick films. The film thickness plays an important role in the response stability and sensitivity of sensors. It is now well accepted that the relationship between the surface and volume of the sensitive layer plays a major role in the efficiency of detection. Many experimental and theoretical works were reported in explaining the experimental sensitivity vs. thickness relationships reported for the gas sensors prepared by different fabrication techniques. In addition, significant changes can be expected by adding catalytic nanograins in small quantities on the surface of the sensitive layers. For example, cobalt nanograins deposited on the surface of WO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3 sensors produce an important change in the WO&amp;lt;SUB align&#61;&#34;right&#34;&amp;gt;3 conductance. Indeed, cobalt changes the conduction type of the sensors from n&#45; to p&#45;type. This paper describes the effect of reducing the size of the sensors and nanostructured sensitive materials on the sensor response.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045349</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 471 - 479</dc:source>
<dc:creator>K. Aguir; J. Gu&#233;rin; N. Mliki; M. Bendahan</dc:creator>
<dc:contributor>IM2NP, CNRS 6242, Aix&#45;Marseille University, FST, S152, 13397 Marseille, France. &#39; IM2NP, CNRS 6242, Aix&#45;Marseille University, FST, S152, 13397 Marseille, France. &#39; LMOP, Faculty of Sciences, Tunis El Manar University, Tunis, Tunisia. &#39; IM2NP, CNRS 6242, Aix&#45;Marseille University, FST, S152, 13397 Marseille, France</dc:contributor>
<dc:subject>metallic oxide gas sensors</dc:subject>
<dc:subject>WO3</dc:subject>
<dc:subject>cobalt nanograins</dc:subject>
<dc:subject>selectivity</dc:subject>
<dc:subject>ozone</dc:subject>
<dc:subject>modelling</dc:subject>
<dc:subject>film thickness</dc:subject>
<dc:subject>tungsten trioxide</dc:subject>
<dc:subject>nanomaterials</dc:subject>
<dc:subject>nanotechnology.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>471</prism:startingPage>
<prism:endingPage>479</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045350">
<title>Erbium&#45;doped nanoparticles in silica&#45;based optical fibres</title>
<link>http://www.inderscience.com/link.php?id=45350</link>
<description>Developing of new rare&#45;earth &#40;RE&#41;&#45;doped optical fibres for power amplifiers and lasers requires continuous improvements in the fibre spectroscopic properties &#40;like shape and width of the gain curve, optical quantum efficiency, resistance to spectral hole burning and photodarkening...&#41;. Silica glass as a host material for fibres has proved to be very attractive. However, some potential applications of RE&#45;doped fibres suffer from limitations in terms of spectroscopic properties resulting from clustering or inappropriate local environment when doped into silica. To this aim, we present a new route to modify some spectroscopic properties of RE ions in silica&#45;based fibres based on the incorporation of erbium ions in amorphous dielectric nanoparticles, grown in&#45;situ in fibre preforms. By adding alkaline earth elements, in low concentration into silica, one can obtain a glass with an immiscibility gap. Then, phase separation occurs under an appropriate heat treatment. We investigated the role of three alkaline&#45;earth elements&#58; magnesium, calcium and strontium. We present the achieved stabilisation of nanometric erbium&#45;doped dielectric nanoparticles within the core of silica fibres. We present the nanoparticle dimensional characterisation in fibre samples. We also show the spectroscopic characterisation of erbium in preform and fibre samples with different compositions. This new route could have important potentials in improving RE&#45;doped fibre amplifiers and laser sources.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45350"><b>Erbium&#45;doped nanoparticles in silica&#45;based optical fibres</b></A><br />Wilfried Blanc; Val&#233;rie Mauroy; Bernard Dussardier<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 480 - 487</i><br />Developing of new rare&#45;earth &#40;RE&#41;&#45;doped optical fibres for power amplifiers and lasers requires continuous improvements in the fibre spectroscopic properties &#40;like shape and width of the gain curve, optical quantum efficiency, resistance to spectral hole burning and photodarkening...&#41;. Silica glass as a host material for fibres has proved to be very attractive. However, some potential applications of RE&#45;doped fibres suffer from limitations in terms of spectroscopic properties resulting from clustering or inappropriate local environment when doped into silica. To this aim, we present a new route to modify some spectroscopic properties of RE ions in silica&#45;based fibres based on the incorporation of erbium ions in amorphous dielectric nanoparticles, grown in&#45;situ in fibre preforms. By adding alkaline earth elements, in low concentration into silica, one can obtain a glass with an immiscibility gap. Then, phase separation occurs under an appropriate heat treatment. We investigated the role of three alkaline&#45;earth elements&#58; magnesium, calcium and strontium. We present the achieved stabilisation of nanometric erbium&#45;doped dielectric nanoparticles within the core of silica fibres. We present the nanoparticle dimensional characterisation in fibre samples. We also show the spectroscopic characterisation of erbium in preform and fibre samples with different compositions. This new route could have important potentials in improving RE&#45;doped fibre amplifiers and laser sources.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045350</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 480 - 487</dc:source>
<dc:creator>Wilfried Blanc; Val&#233;rie Mauroy; Bernard Dussardier</dc:creator>
<dc:contributor>LPMC, Universit&#233; de Nice&#45;Sophia Antipolis, CNRS UMR6622, Parc Valrose, 06108 Nice cedex, France. &#39; LPMC, Universit&#233; de Nice&#45;Sophia Antipolis, CNRS UMR6622, Parc Valrose, 06108 Nice cedex, France. &#39; LPMC, Universit&#233; de Nice&#45;Sophia Antipolis, CNRS UMR6622, Parc Valrose, 06108 Nice cedex, France</dc:contributor>
<dc:subject>optical fibres</dc:subject>
<dc:subject>erbium</dc:subject>
<dc:subject>spectroscopy</dc:subject>
<dc:subject>nanoparticles</dc:subject>
<dc:subject>phase separation</dc:subject>
<dc:subject>silica glass</dc:subject>
<dc:subject>alkaline&#45;earth elements</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>rare earth elements</dc:subject>
<dc:subject>power amplifiers</dc:subject>
<dc:subject>lasers</dc:subject>
<dc:subject>magnesium</dc:subject>
<dc:subject>calcium</dc:subject>
<dc:subject>strontium.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>480</prism:startingPage>
<prism:endingPage>487</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045353">
<title>Near field optical microscopy&#58; a brief review</title>
<link>http://www.inderscience.com/link.php?id=45353</link>
<description>Near Field Optical Microscopy &#40;NSOM&#41; has evolved into a mature member of the family of scanning probe microscopy. In this article, we briefly go over the principle of NSOM, its breakthroughs and setbacks. We will describe some of the most commonly used NSOM modalities and conclude with the recent advances based on optical nanoantennas. We will then highlight the potential of this high&#45;resolution optical microscopy for chemical and biological applications as well as for materials sciences.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45353"><b>Near field optical microscopy&#58; a brief review</b></A><br />A.L. Lereu; A. Passian; Ph. Dumas<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 488 - 501</i><br />Near Field Optical Microscopy &#40;NSOM&#41; has evolved into a mature member of the family of scanning probe microscopy. In this article, we briefly go over the principle of NSOM, its breakthroughs and setbacks. We will describe some of the most commonly used NSOM modalities and conclude with the recent advances based on optical nanoantennas. We will then highlight the potential of this high&#45;resolution optical microscopy for chemical and biological applications as well as for materials sciences.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045353</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 488 - 501</dc:source>
<dc:creator>A.L. Lereu; A. Passian; Ph. Dumas</dc:creator>
<dc:contributor>CINaM CNRS &#150; Campus de Luminy, 13288 Marseille, France. &#39; Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA; Department of Physics, University of Tennessee, Knoxville TN 37996&#45;1200, USA. &#39; CINaM CNRS &#150; Campus de Luminy, 13288 Marseille, France</dc:contributor>
<dc:subject>near field optical microscopy</dc:subject>
<dc:subject>optical nanoantennas</dc:subject>
<dc:subject>plasmons</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>scanning probe microscopy.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>488</prism:startingPage>
<prism:endingPage>501</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045352">
<title>Nanodrug potential in cancer therapy&#58; efficacy&#47;toxicity studies in cancer cells</title>
<link>http://www.inderscience.com/link.php?id=45352</link>
<description>The interest of nanotechnology to find a more effective approach for drug delivery is growing fast. Nanoparticles as drug vehicles potentially improve the pharmacokinetic and pharmacodynamic properties of various types of drugs, and provide a tool to visualise molecules and tumour target cells that otherwise cannot be detected through conventional imaging. However, there are many aspects of nanoparticle formulation, characterisation and their effect on delivery of drugs and therapeutics that remain to be explored. This review summarises the main characteristics of nanoparticles for drug delivery in cancer treatment, and describes an experimental approach for evaluating efficacy and toxicity of nanocarriers in cancer cells.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45352"><b>Nanodrug potential in cancer therapy&#58; efficacy&#47;toxicity studies in cancer cells</b></A><br />Alessandra Pagano; St&#233;phane Honor&#233;; Marie&#45;Anne Est&#232;ve; Diane Braguer<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 502 - 516</i><br />The interest of nanotechnology to find a more effective approach for drug delivery is growing fast. Nanoparticles as drug vehicles potentially improve the pharmacokinetic and pharmacodynamic properties of various types of drugs, and provide a tool to visualise molecules and tumour target cells that otherwise cannot be detected through conventional imaging. However, there are many aspects of nanoparticle formulation, characterisation and their effect on delivery of drugs and therapeutics that remain to be explored. This review summarises the main characteristics of nanoparticles for drug delivery in cancer treatment, and describes an experimental approach for evaluating efficacy and toxicity of nanocarriers in cancer cells.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045352</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 502 - 516</dc:source>
<dc:creator>Alessandra Pagano; St&#233;phane Honor&#233;; Marie&#45;Anne Est&#232;ve; Diane Braguer</dc:creator>
<dc:contributor>Aix&#45;Marseille Univ, CRO2, 13385 Marseille, France; INSERM UMR911, 13385 Marseille, France. &#39; Aix&#45;Marseille Univ, CRO2, 13385 Marseille, France; INSERM UMR911, 13385 Marseille, France; Assistance Publique&#45;H&#244;pitaux de Marseille, 13385 Marseille, France. &#39; Aix&#45;Marseille Univ, CRO2, 13385 Marseille, France; INSERM UMR911, 13385 Marseille, France; Assistance Publique&#45;H&#244;pitaux de Marseille, 13385 Marseille, France. &#39; Aix&#45;Marseille Univ, CRO2, 13385 Marseille, France; INSERM UMR911, 13385 Marseille, France; Assistance Publique&#45;H&#244;pitaux de Marseille, 13385 Marseille, France</dc:contributor>
<dc:subject>nanodrugs</dc:subject>
<dc:subject>nanocarriers</dc:subject>
<dc:subject>nanotoxicology</dc:subject>
<dc:subject>drug delivery</dc:subject>
<dc:subject>cancer treatment</dc:subject>
<dc:subject>tumour cells</dc:subject>
<dc:subject>nanomedicine</dc:subject>
<dc:subject>nanodiamond</dc:subject>
<dc:subject>microtubule</dc:subject>
<dc:subject>paclitaxel</dc:subject>
<dc:subject>cancer cells</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>nanoparticles</dc:subject>
<dc:subject>therapeutics.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>502</prism:startingPage>
<prism:endingPage>516</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045351">
<title>Plastic neuronal probes for implantation in cortical and subcortical areas of the rat brain</title>
<link>http://www.inderscience.com/link.php?id=45351</link>
<description>We discuss the fabrication of flexible implantable probes for recording neuronal activity in the rat brain. We fabricated such probes bearing 12 platinum electrodes, using polyimide as a substrate and SU&#45;8 as an insulation layer. The fabrication process was simplified through the use of laser ablation to define the probe outline. The probes showed not only good mechanical flexibility but also the required stiffness for implantation. Histology results and electrical recordings of neuronal activity lend support to the idea that the combination of polyimide and SU&#45;8 represents a good choice of materials for the fabrication of implantable neuronal probes.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45351"><b>Plastic neuronal probes for implantation in cortical and subcortical areas of the rat brain</b></A><br />Esma Ismailova; Thomas Doublet; Dion Khodagholy; Pascale Quilichini; Antoine Ghestem; Sang Yoon Yang; Christophe Bernard; George G. Malliaras<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 517 - 528</i><br />We discuss the fabrication of flexible implantable probes for recording neuronal activity in the rat brain. We fabricated such probes bearing 12 platinum electrodes, using polyimide as a substrate and SU&#45;8 as an insulation layer. The fabrication process was simplified through the use of laser ablation to define the probe outline. The probes showed not only good mechanical flexibility but also the required stiffness for implantation. Histology results and electrical recordings of neuronal activity lend support to the idea that the combination of polyimide and SU&#45;8 represents a good choice of materials for the fabrication of implantable neuronal probes.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045351</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 517 - 528</dc:source>
<dc:creator>Esma Ismailova; Thomas Doublet; Dion Khodagholy; Pascale Quilichini; Antoine Ghestem; Sang Yoon Yang; Christophe Bernard; George G. Malliaras</dc:creator>
<dc:contributor>Centre Micro&#233;lectronique de Provence, Department of Bioelectronics, Ecole Nationale Sup&#233;rieure des Mines de Saint Etienne, 880 route de Mimet, 13541 Gardanne, France. &#39; INSERM U 751, Universit&#233; de la M&#233;diterran&#233;e, Facult&#233; de M&#233;decine La Timone, 27 Bd. Jean Moulin, 13385 Marseille Cedex 05, France; Microvitae Technologies, P&#244;le d&#146;Activit&#233; Y. Morandat, 1480 rue d&#146;Arm&#233;nie, 13120 Gardanne, France. &#39; Centre Micro&#233;lectronique de Provence, Department of Bioelectronics, Ecole Nationale Sup&#233;rieure des Mines de Saint Etienne, 880 Route de Mimet, 13541 Gardanne, France. &#39; INSERM U 751, Universit&#233; de la M&#233;diterran&#233;e, Facult&#233; de M&#233;decine La Timone, 27 Bd. Jean Moulin, 13385 Marseille Cedex 05, France. &#39; INSERM U 751, Universit&#233; de la M&#233;diterran&#233;e, Facult&#233; de M&#233;decine La Timone, 27 Bd. Jean Moulin, 13385 Marseille Cedex 05, France. &#39; Department of Materials Science and Engineering, Cornell University, Ithaca, NY 14853&#45;1501, USA. &#39; INSERM U 751, Universit&#233; de la M&#233;diterran&#233;e, Facult&#233; de M&#233;decine La Timone, 27 Bd. Jean Moulin, 13385 Marseille Cedex 05, France. &#39; Centre Micro&#233;lectronique de Provence, Department of Bioelectronics, Ecole Nationale Sup&#233;rieure des Mines de Saint Etienne, 880 Route de Mimet, 13541 Gardanne, France</dc:contributor>
<dc:subject>bioelectronics</dc:subject>
<dc:subject>implantable electrodes</dc:subject>
<dc:subject>hippocampus</dc:subject>
<dc:subject>cortex</dc:subject>
<dc:subject>in vivo recordings</dc:subject>
<dc:subject>flexible microarrays</dc:subject>
<dc:subject>plastic probes</dc:subject>
<dc:subject>neuronal probes</dc:subject>
<dc:subject>rat brains</dc:subject>
<dc:subject>flexible probes</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>laser ablation</dc:subject>
<dc:subject>polyimide.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>517</prism:startingPage>
<prism:endingPage>528</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045340">
<title>Microfluidic tools to investigate pathologies in the blood microcirculation</title>
<link>http://www.inderscience.com/link.php?id=45340</link>
<description>We show how microfluidics technology can be used to fabricate simple and innovative biomimetic tools to shed new light on physiopathological events occurring in the blood microcirculation. Examples of applications are given in the context of the acute respiratory distress syndrome &#40;ARDS&#41;, an inflammatory disease of the lung triggered by a massive arrest of white blood cells in the lung microvasculature. The main challenge consists in building relevant micro&#45;devices to reproduce key biological characteristics of blood capillaries. We present a series of tools that permit us to decouple the role of the multiple parameters involved in complex biological events. Straight narrow channels with non&#45;adherent walls are used to characterise the passage of a cell in 4 m wide constrictions in the absence of adhesion, whereas channels covered by endothelial cells allow a quantitative measurement of cell adhesion in the absence of mechanical constraints. We show that incubation of white blood cells in sera of ARDS patients increases their stiffness, confirming the role of stiffness on the abnormal sequestration of white blood cells, whereas we could not bring to light a significant adhesion increase. The multiple branches and constrictions of the blood microvasculature network are mimicked here by series of interconnected crenelled constrictions with different symmetries. In symmetric crenels, cells adopt a stable deformed shape after a few constrictions and travel fast through successive constrictions with a constant orientation. In asymmetric channels, cell orientation and trajectory are perturbed between two constrictions. Unfavourable orientations upon entry can yield temporary or even definitive arrests with the stiffest cells. Finally, we present a new artificial micro&#45;vessel with porous walls to mimic the porosity of real blood vessels. This new tool is useful to observe directly under a microscope the late stages of inflammation in the microvasculature such as immune cells transmigration, or the infection of a micro&#45;vessel by pathogenic bacteria.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45340"><b>Microfluidic tools to investigate pathologies in the blood microcirculation</b></A><br />Pascal Preira; Thomas Leoni; Marie&#45;Pierre Valignat; Annemarie Lellouch; Philippe Robert; Jean&#45;Marie Forel; Laurent Papazian; Guillaume Dumenil; Pierre Bongrand; Olivier Th&#233;odoly<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 529 - 547</i><br />We show how microfluidics technology can be used to fabricate simple and innovative biomimetic tools to shed new light on physiopathological events occurring in the blood microcirculation. Examples of applications are given in the context of the acute respiratory distress syndrome &#40;ARDS&#41;, an inflammatory disease of the lung triggered by a massive arrest of white blood cells in the lung microvasculature. The main challenge consists in building relevant micro&#45;devices to reproduce key biological characteristics of blood capillaries. We present a series of tools that permit us to decouple the role of the multiple parameters involved in complex biological events. Straight narrow channels with non&#45;adherent walls are used to characterise the passage of a cell in 4 m wide constrictions in the absence of adhesion, whereas channels covered by endothelial cells allow a quantitative measurement of cell adhesion in the absence of mechanical constraints. We show that incubation of white blood cells in sera of ARDS patients increases their stiffness, confirming the role of stiffness on the abnormal sequestration of white blood cells, whereas we could not bring to light a significant adhesion increase. The multiple branches and constrictions of the blood microvasculature network are mimicked here by series of interconnected crenelled constrictions with different symmetries. In symmetric crenels, cells adopt a stable deformed shape after a few constrictions and travel fast through successive constrictions with a constant orientation. In asymmetric channels, cell orientation and trajectory are perturbed between two constrictions. Unfavourable orientations upon entry can yield temporary or even definitive arrests with the stiffest cells. Finally, we present a new artificial micro&#45;vessel with porous walls to mimic the porosity of real blood vessels. This new tool is useful to observe directly under a microscope the late stages of inflammation in the microvasculature such as immune cells transmigration, or the infection of a micro&#45;vessel by pathogenic bacteria.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045340</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 529 - 547</dc:source>
<dc:creator>Pascal Preira; Thomas Leoni; Marie&#45;Pierre Valignat; Annemarie Lellouch; Philippe Robert; Jean&#45;Marie Forel; Laurent Papazian; Guillaume Dumenil; Pierre Bongrand; Olivier Th&#233;odoly</dc:creator>
<dc:contributor>Universit&#233; de la M&#233;diterran&#233;e, Adhesion &#38; Inflammation, INSERM U600&#45;CNRS UMR6212, Case 937, 163 Avenue de Luminy, F&#45;13009 Marseille, France. &#39; Universit&#233; de la M&#233;diterran&#233;e, Adhesion &#38; Inflammation, INSERM U600&#45;CNRS UMR6212, Case 937, 163 Avenue de Luminy, F&#45;13009 Marseille, France. &#39; Universit&#233; de la M&#233;diterran&#233;e, Adhesion &#38; Inflammation, INSERM U600&#45;CNRS UMR6212, Case 937, 163 Avenue de Luminy, F&#45;13009 Marseille, France. &#39; Universit&#233; de la M&#233;diterran&#233;e, Adhesion &#38; Inflammation, INSERM U600&#45;CNRS UMR6212, Case 937, 163 Avenue de Luminy, F&#45;13009 Marseille, France. &#39; Universit&#233; de la M&#233;diterran&#233;e, Adhesion &#38; Inflammation, INSERM U600&#45;CNRS UMR6212, Case 937, 163 Avenue de Luminy, F&#45;13009 Marseille, France. &#39; Unit&#233; de Recherche sur les Maladies Infectieuses et Tropicales Emergentes &#40;URMITE&#41; UMR6236, CNRS&#47;Universit&#233; Aix&#45;Marseille 2, H&#244;pital Nord, Chemin des Bourrely, 13015 Marseille Cedex 20, France. &#39; Unit&#233; de Recherche sur les Maladies Infectieuses et Tropicales Emergentes &#40;URMITE&#41; UMR6236, CNRS&#47;Universit&#233; Aix&#45;Marseille 2, H&#244;pital Nord, Chemin des Bourrely, 13015 Marseille Cedex 20, France. &#39; Universit&#233; Paris Descartes, Facult&#233; de M&#233;decine Paris Descartes, Paris F&#45;75006, France; PARCC, Centre de Recherche Cardiovasculaire &#225; l&#146;HEGP, Inserm U970, 56 rue Leblanc, 75015 Paris, France. &#39; Universit&#233; de la M&#233;diterran&#233;e, Adhesion &#38; Inflammation, INSERM U600&#45;CNRS UMR6212, Case 937, 163 Avenue de Luminy, F&#45;13009 Marseille, France. &#39; Universit&#233; de la M&#233;diterran&#233;e, Adhesion &#38; Inflammation, INSERM U600&#45;CNRS UMR6212, Case 937, 163 Avenue de Luminy, F&#45;13009 Marseille, France</dc:contributor>
<dc:subject>microfluidics</dc:subject>
<dc:subject>lung microvasculature</dc:subject>
<dc:subject>cell mechanics</dc:subject>
<dc:subject>cell adhesion</dc:subject>
<dc:subject>cell migration</dc:subject>
<dc:subject>cell transmigration</dc:subject>
<dc:subject>acute respiratory distress syndrome</dc:subject>
<dc:subject>ARDS</dc:subject>
<dc:subject>meningitis</dc:subject>
<dc:subject>blood microcirculation</dc:subject>
<dc:subject>blood circulation</dc:subject>
<dc:subject>biomimetics</dc:subject>
<dc:subject>inflammation</dc:subject>
<dc:subject>inflammatory diseases</dc:subject>
<dc:subject>lung disease</dc:subject>
<dc:subject>white blood cells</dc:subject>
<dc:subject>blood capillaries.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>529</prism:startingPage>
<prism:endingPage>547</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045339">
<title>Advanced microscopy techniques for biological imaging</title>
<link>http://www.inderscience.com/link.php?id=45339</link>
<description>We show that using phase and polarisation information in optical microscopy can provide new insights into biomolecular processes for biological functional imaging. Quantitative phase imaging is demonstrated in living cells with promising capabilities in terms of cells composition and morphology studies. Polarisation&#45;resolved non&#45;linear optical microscopy is described in tissues and lipid membranes with emphasis on the specific properties of two&#45;photon excited fluorescence, Second Harmonic Generation and Coherent Anti&#45;Stokes Raman Imaging. These techniques, based on far field microscopy, provide new information at the molecular scale, complementary to more traditional fluorescence microscopy techniques.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45339"><b>Advanced microscopy techniques for biological imaging</b></A><br />Serge Monneret; Sophie Brasselet<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 548 - 566</i><br />We show that using phase and polarisation information in optical microscopy can provide new insights into biomolecular processes for biological functional imaging. Quantitative phase imaging is demonstrated in living cells with promising capabilities in terms of cells composition and morphology studies. Polarisation&#45;resolved non&#45;linear optical microscopy is described in tissues and lipid membranes with emphasis on the specific properties of two&#45;photon excited fluorescence, Second Harmonic Generation and Coherent Anti&#45;Stokes Raman Imaging. These techniques, based on far field microscopy, provide new information at the molecular scale, complementary to more traditional fluorescence microscopy techniques.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045339</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 548 - 566</dc:source>
<dc:creator>Serge Monneret; Sophie Brasselet</dc:creator>
<dc:contributor>Aix&#45;Marseille Universit&#233;, CNRS, Institut Fresnel, Campus de Saint&#45;J&#233;r&#244;me, 13013 Marseille, France. &#39; Aix&#45;Marseille Universit&#233;, CNRS, Institut Fresnel, Campus de Saint&#45;J&#233;r&#244;me, 13013 Marseille, France</dc:contributor>
<dc:subject>quantitative phase microscopy</dc:subject>
<dc:subject>wavefront sensing</dc:subject>
<dc:subject>nonlinear microscopy</dc:subject>
<dc:subject>polarisation</dc:subject>
<dc:subject>biological imaging</dc:subject>
<dc:subject>biomolecular processes</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>tissues</dc:subject>
<dc:subject>lipid membranes.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>548</prism:startingPage>
<prism:endingPage>566</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045338">
<title>Regular arrays of palladium and palladium&#45;gold clusters supported on ultrathin alumina films&#58; stability under oxygen</title>
<link>http://www.inderscience.com/link.php?id=45338</link>
<description>Grazing Incidence Small Angle X&#45;ray Scattering &#40;GISAXS&#41; studies were conducted to determine the effect of oxygen on regular arrays of mono &#40;Pd&#41;&#45;  and bimetallic &#40;Pd&#45;Au&#41; clusters. Unlike bimetallic Pd&#45;Au particles, pure palladium clusters are not stable at a partial oxygen pressure of 10&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;6&amp;lt;&#47;SUP&amp;gt;  mbar. A comparison of the experimental data with Fourier transforms of known distributions reveals that Pd clusters move and that their aspect ratio increases. These results are explained by the adsorption of oxygen that changes the equilibrium shape of the Pd particles and reduces the adhesion energy. In the case of bimetallic Pd&#45;Au clusters, the presence of Au on the surface of the particle prevents adsorption of oxygen.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45338"><b>Regular arrays of palladium and palladium&#45;gold clusters supported on ultrathin alumina films&#58; stability under oxygen</b></A><br />Georges Sitja; Maxence Marsault; Fr&#233;d&#233;ric Leroy; S&#233;verine Le Moal; Claude R. Henry<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 567 - 575</i><br />Grazing Incidence Small Angle X&#45;ray Scattering &#40;GISAXS&#41; studies were conducted to determine the effect of oxygen on regular arrays of mono &#40;Pd&#41;&#45;  and bimetallic &#40;Pd&#45;Au&#41; clusters. Unlike bimetallic Pd&#45;Au particles, pure palladium clusters are not stable at a partial oxygen pressure of 10&amp;lt;SUP align&#61;&#34;right&#34;&amp;gt;&amp;minus;6&amp;lt;&#47;SUP&amp;gt;  mbar. A comparison of the experimental data with Fourier transforms of known distributions reveals that Pd clusters move and that their aspect ratio increases. These results are explained by the adsorption of oxygen that changes the equilibrium shape of the Pd particles and reduces the adhesion energy. In the case of bimetallic Pd&#45;Au clusters, the presence of Au on the surface of the particle prevents adsorption of oxygen.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045338</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 567 - 575</dc:source>
<dc:creator>Georges Sitja; Maxence Marsault; Fr&#233;d&#233;ric Leroy; S&#233;verine Le Moal; Claude R. Henry</dc:creator>
<dc:contributor>Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288 Marseille cedex 09, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille, CNRS &#150; UPR 3118, associated to Aix&#45;Marseille Universit&#233;, Campus de Luminy, case 913, F&#45;13288 Marseille cedex 09, France</dc:contributor>
<dc:subject>model catalysts</dc:subject>
<dc:subject>nanostructured alumina</dc:subject>
<dc:subject>particles arrays</dc:subject>
<dc:subject>palladium clusters</dc:subject>
<dc:subject>gold</dc:subject>
<dc:subject>oxygen adsorption</dc:subject>
<dc:subject>GISAXS</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>bimetallic clusters.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>567</prism:startingPage>
<prism:endingPage>575</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045335">
<title>Structure and properties of nanoscale materials&#58; theory and atomistic computer simulation</title>
<link>http://www.inderscience.com/link.php?id=45335</link>
<description>We present a review of a few research topics developed within the &#34;Theory and Atomistic Computer Simulation&#34; Department at CINaM. The bottom line of the scientific activity is to use up&#45;to&#45;date theoretical and computer simulation techniques to address physics and materials science problems, often at the nanometric scale, in close contact with experimental groups. It ranges from the study of the structure and properties of molecular systems for organic electronics to metallic clusters and alloys, magnetic oxides, nuclear fuels and carbon&#45;based nanostructures. These studies are motivated by fundamental research questions as well as more applied goals including environmental and energy issues, or information technologies. This broad spectrum of activities requires a large range of techniques, from theory and ab initio calculations to semi&#45;empirical models incorporated in Monte Carlo or molecular dynamics simulations.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45335"><b>Structure and properties of nanoscale materials&#58; theory and atomistic computer simulation</b></A><br />C. Bichara; P. Marsal; C. Mottet; R. Pellenq; F. Ribeiro; A. Sa&#250;l; G. Tr&#233;glia; H.&#45;Ch. Weissker<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 576 - 604</i><br />We present a review of a few research topics developed within the &#34;Theory and Atomistic Computer Simulation&#34; Department at CINaM. The bottom line of the scientific activity is to use up&#45;to&#45;date theoretical and computer simulation techniques to address physics and materials science problems, often at the nanometric scale, in close contact with experimental groups. It ranges from the study of the structure and properties of molecular systems for organic electronics to metallic clusters and alloys, magnetic oxides, nuclear fuels and carbon&#45;based nanostructures. These studies are motivated by fundamental research questions as well as more applied goals including environmental and energy issues, or information technologies. This broad spectrum of activities requires a large range of techniques, from theory and ab initio calculations to semi&#45;empirical models incorporated in Monte Carlo or molecular dynamics simulations.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045335</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 576 - 604</dc:source>
<dc:creator>C. Bichara; P. Marsal; C. Mottet; R. Pellenq; F. Ribeiro; A. Sa&#250;l; G. Tr&#233;glia; H.&#45;Ch. Weissker</dc:creator>
<dc:contributor>Centre Interdisciplinaire de Nanoscience de Marseille &#40;CINaM&#41; &#150; CNRS and Aix&#45;Marseille University, Campus de Luminy &#150; Case 913 &#150; 13288 &#150; Marseille CEDEX, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille &#40;CINaM&#41; &#150; CNRS and Aix&#45;Marseille University, Campus de Luminy &#150; Case 913 &#150; 13288 &#150; Marseille CEDEX, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille &#40;CINaM&#41; &#150; CNRS and Aix&#45;Marseille University, Campus de Luminy &#150; Case 913 &#150; 13288 &#150; Marseille CEDEX, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille &#40;CINaM&#41; &#150; CNRS and Aix&#45;Marseille University, Campus de Luminy &#150; Case 913 &#150; 13288 &#150; Marseille CEDEX, France; Department of Civil and Environmental Engineering, MIT, 77 Massachusetts Avenue, 02139, Cambridge, MA, USA. &#39; Institut de Radioprotection et Suret&#233; Nucl&#233;aire &#40;IRSN&#41;, DPAM, SEMCA, LEC, CE Cadarache, BP 13, 13115 Saint Paul&#45;lez&#45;Durance, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille &#40;CINaM&#41; &#150; CNRS; Aix&#45;Marseille University, Campus de Luminy &#150; Case 913 &#150; 13288 &#150; Marseille CEDEX, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille &#40;CINaM&#41; &#150; CNRS; Aix&#45;Marseille University, Campus de Luminy &#150; Case 913 &#150; 13288 &#150; Marseille CEDEX, France. &#39; Centre Interdisciplinaire de Nanoscience de Marseille &#40;CINaM&#41; &#150; CNRS; Aix&#45;Marseille University, Campus de Luminy &#150; Case 913 &#150; 13288 &#150; Marseille CEDEX, France; European Theoretical Spectroscopy Facility, Spain</dc:contributor>
<dc:subject>atomic structure</dc:subject>
<dc:subject>electronic structure</dc:subject>
<dc:subject>ab&#45;initio calculations</dc:subject>
<dc:subject>Monte Carlo simulation</dc:subject>
<dc:subject>nanoscale materials</dc:subject>
<dc:subject>molecular dynamics</dc:subject>
<dc:subject>nanomaterials</dc:subject>
<dc:subject>nanotechnolgy</dc:subject>
<dc:subject>modelling</dc:subject>
<dc:subject>organic electronics</dc:subject>
<dc:subject>metallic clusters</dc:subject>
<dc:subject>alloys</dc:subject>
<dc:subject>magnetic oxides</dc:subject>
<dc:subject>nuclear fuels</dc:subject>
<dc:subject>carbon&#45;based nanostructures.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>576</prism:startingPage>
<prism:endingPage>604</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045334">
<title>Indigo&#47;sepiolite nanohybrids&#58; stability of natural pigments inspired by Maya blue</title>
<link>http://www.inderscience.com/link.php?id=45334</link>
<description>Maya blue is formed from insertion of indigo into palygorskite and sepiolite. Sepiolite and palygorskite are porous fibrous clays. Controlling the insertion, location and organisation of organic molecules in the cavities of nanotubes associated with the release or stability of these molecules is a crucial challenge in the evolution towards unusual properties in nanotechnologies. We validate simple FTIR analyses able to determine the location of indigo in or outside the pores of the fibres. Then, we compare the stability of indigo&#47;palygorskite and indigo&#47;sepiolite systems obtained from similar formulations. The heating treatment is stopped when all indigo is complexed with the clay. We show that in these conditions indigo&#47;palygorskite is more stable than indigo&#47;sepiolite. The formation of stable pigment is more complicated for indigo&#45;sepiolite than for indigo&#45;palygorskite.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45334"><b>Indigo&#47;sepiolite nanohybrids&#58; stability of natural pigments inspired by Maya blue</b></A><br />Fran&#231;oise Giulieri; Sonia Ovarlez; Anne&#45;Marie Chaze<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 605 - 617</i><br />Maya blue is formed from insertion of indigo into palygorskite and sepiolite. Sepiolite and palygorskite are porous fibrous clays. Controlling the insertion, location and organisation of organic molecules in the cavities of nanotubes associated with the release or stability of these molecules is a crucial challenge in the evolution towards unusual properties in nanotechnologies. We validate simple FTIR analyses able to determine the location of indigo in or outside the pores of the fibres. Then, we compare the stability of indigo&#47;palygorskite and indigo&#47;sepiolite systems obtained from similar formulations. The heating treatment is stopped when all indigo is complexed with the clay. We show that in these conditions indigo&#47;palygorskite is more stable than indigo&#47;sepiolite. The formation of stable pigment is more complicated for indigo&#45;sepiolite than for indigo&#45;palygorskite.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045334</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 605 - 617</dc:source>
<dc:creator>Fran&#231;oise Giulieri; Sonia Ovarlez; Anne&#45;Marie Chaze</dc:creator>
<dc:contributor>Laboratoire Chimie des Mat&#233;riaux Organiques et M&#233;talliques, Universit&#233; Nice&#45;Sophia Antipolis, Parc Valrose, 06108 Nice cedex 2, France. &#39; Laboratoire Chimie des Mat&#233;riaux Organiques et M&#233;talliques, Universit&#233; Nice&#45;Sophia Antipolis, Parc Valrose, 06108 Nice cedex 2, France. &#39; Laboratoire Chimie des Mat&#233;riaux Organiques et M&#233;talliques, Universit&#233; Nice&#45;Sophia Antipolis, Parc Valrose, 06108 Nice cedex 2, France</dc:contributor>
<dc:subject>nanohybrids</dc:subject>
<dc:subject>indigo</dc:subject>
<dc:subject>sepiolite</dc:subject>
<dc:subject>palygorskite</dc:subject>
<dc:subject>nanopigments</dc:subject>
<dc:subject>porous clays</dc:subject>
<dc:subject>fibrous clays</dc:subject>
<dc:subject>natural pigments</dc:subject>
<dc:subject>Maya blue</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>organic molecules</dc:subject>
<dc:subject>nanotubes.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>605</prism:startingPage>
<prism:endingPage>617</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJNT.2012.045332">
<title>Morphology and reactivity of aluminium nanocrystalline powders</title>
<link>http://www.inderscience.com/link.php?id=45332</link>
<description>Aluminium powders obtained by mechanical milling are characterised in terms of morphology, nanostructure and thermal properties. Platelets like particles with a thickness in the micrometre range are obtained. It is shown that these platelets are constituted of many nanocrystallites whose size governs the melting behaviour of the powders. Their reactivity towards oxygen is compared with that of spherical particles. Samples obtained by mechanical milling start to be oxidised at a higher temperature the amount of oxidised material is higher than that in the case of spherical particles having the same surface area. Both the thermal behaviour and the reactivity could be explained by the presence of alumina at the grain boundaries. This work shows that the milling process appears as a good alternative to gas condensation methods or wire electro&#45;explosion processes to prepare highly reactive particles.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=45332"><b>Morphology and reactivity of aluminium nanocrystalline powders</b></A><br />B&#233;rang&#232;re Andr&#233;; Marie&#45;Vanessa Coulet; Myriam Dumont; Jacques Rogez; Vasile Heresanu; Benoit Rufino; Renaud Bouchet; Renaud Denoyel<br /><i>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 618 - 629</i><br />Aluminium powders obtained by mechanical milling are characterised in terms of morphology, nanostructure and thermal properties. Platelets like particles with a thickness in the micrometre range are obtained. It is shown that these platelets are constituted of many nanocrystallites whose size governs the melting behaviour of the powders. Their reactivity towards oxygen is compared with that of spherical particles. Samples obtained by mechanical milling start to be oxidised at a higher temperature the amount of oxidised material is higher than that in the case of spherical particles having the same surface area. Both the thermal behaviour and the reactivity could be explained by the presence of alumina at the grain boundaries. This work shows that the milling process appears as a good alternative to gas condensation methods or wire electro&#45;explosion processes to prepare highly reactive particles.</p>]]></content:encoded>
<dc:identifier>10.1504/IJNT.2012.045332</dc:identifier>
<dc:source>International Journal of Nanotechnology, Vol. 9, No. 3/4/5/6/7 (2012) pp. 618 - 629</dc:source>
<dc:creator>B&#233;rang&#232;re Andr&#233;; Marie&#45;Vanessa Coulet; Myriam Dumont; Jacques Rogez; Vasile Heresanu; Benoit Rufino; Renaud Bouchet; Renaud Denoyel</dc:creator>
<dc:contributor>IM2NP &#150; UMR 6242 CNRS &#150; Aix Marseille Universit&#233;, Campus de Saint J&#233;r&#244;me &#150; Case 251, 13397 Marseille Cedex 20, France. &#39; IM2NP &#150; UMR 6242 CNRS &#150; Aix Marseille Universit&#233;, Campus de Saint J&#233;r&#244;me &#150; Case 251, 13397 Marseille Cedex 20, France. &#39; IM2NP &#150; UMR 6242 CNRS &#150; Aix Marseille Universit&#233;, Campus de Saint J&#233;r&#244;me &#150; Case 251, 13397 Marseille Cedex 20, France. &#39; IM2NP &#150; UMR 6242 CNRS &#150; Aix Marseille Universit&#233;, Campus de Saint J&#233;r&#244;me &#150; Case 251, 13397 Marseille Cedex 20, France. &#39; CINaM &#150; UPR 3118 &#150; CNRS, Campus de Luminy &#150; Case 913, 13288 Marseille Cedex 9, France. &#39; LCP &#150; UMR 6264 CNRS &#150; Aix Marseille Universit&#233;, Campus de Saint J&#233;r&#244;me, Bat. MADIREL, 13397 Marseille Cedex 20, France. &#39; LCP &#150; UMR 6264 CNRS &#150; Aix Marseille Universit&#233;, Campus de Saint J&#233;r&#244;me, Bat. MADIREL, 13397 Marseille Cedex 20, France. &#39; LCP &#150; UMR 6264 CNRS &#150; Aix Marseille Universit&#233;, Campus de Saint J&#233;r&#244;me, Bat. MADIREL, 13397 Marseille Cedex 20, France</dc:contributor>
<dc:subject>aluminium nanopowders</dc:subject>
<dc:subject>mechanical milling</dc:subject>
<dc:subject>reactivity</dc:subject>
<dc:subject>nanocrystalline powders</dc:subject>
<dc:subject>nanotechnology</dc:subject>
<dc:subject>morphology</dc:subject>
<dc:subject>nanostructure</dc:subject>
<dc:subject>thermal properties</dc:subject>
<dc:subject>platelets.</dc:subject>
<dc:date>2012-02-06T23:20:50-05:00</dc:date>
<prism:volume>9</prism:volume>
<prism:number>3/4/5/6/7</prism:number>
<prism:startingPage>618</prism:startingPage>
<prism:endingPage>629</prism:endingPage>
<prism:publicationDate>2012-02-06T23:20:50-05:00</prism:publicationDate>
</item>
</rdf:RDF>

