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<title>Nature Materials</title>
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<item rdf:about="http://dx.doi.org/10.1038/nmat2332">
<title>Highly conductive &#8764;40-nm-long molecular wires&#160;assembled by stepwise incorporation of&#160;metal&#160;centres</title>
<link>http://dx.doi.org/10.1038/nmat2332</link>
<description>A long-standing problem with molecular wires is their poor transport properties. Highly conductive and very long wires have now been synthesized by incorporating metal centres into rigid molecular backbones, which shows promise for their use in electronic devices.</description>
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<p>
<b>Highly conductive &#8764;40-nm-long molecular wires&#160;assembled by stepwise incorporation of&#160;metal&#160;centres</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2332">doi:10.1038/nmat2332</a>
</p>
<p>Authors: Nunzio Tuccitto, Violetta Ferri, Marco Cavazzini, Silvio Quici, Genady Zhavnerko, Antonino Licciardello
&amp; Maria Anita Rampi</p>
<p>One of the main goals of molecular electronics is to achieve electronic functions from devices consisting of tailored organic molecules connecting two metal electrodes. The fabrication of nanometre-scale spaced electrodes still results in expensive, and often scarcely reproducible, devices. On the other hand, the &#8216;conductance&#8217; of long organic molecules&#8212;generally dominated by the tunnelling mechanism&#8212;is very poor. Here, we show that by incorporating a large number of metal centres into rigid molecular backbones we can obtain very long (up to 40&#8201;nm) and highly &#8216;conductive&#8217; molecular wires. The metal-centre molecular wires are assembled in situ on metal surfaces via a sequential stepwise coordination of metal ions by terpyridine-based ligands. They form highly ordered molecular films of elevated mechanical robustness. The electrical properties, characterized by a junction based on Hg electrodes, indicate that the &#8216;conductance&#8217; of these metal-centre molecular wires does not decrease significantly even for very long molecular wires, and depends on the nature of the incorporated redox centre. The outstanding electrical and mechanical characteristics of these easy-to-assemble molecular systems open the door to a new generation of molecular wires, able to bridge large-gap electrodes, and to form robust films for organic electronics.</p>
]]></content:encoded>
<dc:title>Highly conductive &#8764;40-nm-long molecular wires&#160;assembled by stepwise incorporation of&#160;metal&#160;centres</dc:title>
<dc:creator>Nunzio Tuccitto</dc:creator>
<dc:creator>Violetta Ferri</dc:creator>
<dc:creator>Marco Cavazzini</dc:creator>
<dc:creator>Silvio Quici</dc:creator>
<dc:creator>Genady Zhavnerko</dc:creator>
<dc:creator>Antonino Licciardello</dc:creator>
<dc:creator>Maria Anita Rampi</dc:creator>
<dc:identifier>doi:10.1038/nmat2332</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-16</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-16</prism:publicationDate>
<prism:section>Letter</prism:section>
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<item rdf:about="http://dx.doi.org/10.1038/nmat2330">
<title>A map for phase-change materials</title>
<link>http://dx.doi.org/10.1038/nmat2330</link>
<description>Phase-change materials are widely used as non-volatile memories, for example in optical data storage, but the search for improved phase-change materials has proved difficult. Based on a fundamental understanding of their bonding characteristics, a systematic prediction of phase-change properties has now become possible.</description>
<content:encoded><![CDATA[

<p>
<b>A map for phase-change materials</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2330">doi:10.1038/nmat2330</a>
</p>
<p>Authors: Dominic Lencer, Martin Salinga, Blazej Grabowski, Tilmann Hickel, J&#246;rg Neugebauer
&amp; Matthias Wuttig</p>
]]></content:encoded>
<dc:title>A map for phase-change materials</dc:title>
<dc:creator>Dominic Lencer</dc:creator>
<dc:creator>Martin Salinga</dc:creator>
<dc:creator>Blazej Grabowski</dc:creator>
<dc:creator>Tilmann Hickel</dc:creator>
<dc:creator>J&#246;rg Neugebauer</dc:creator>
<dc:creator>Matthias Wuttig</dc:creator>
<dc:identifier>doi:10.1038/nmat2330</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-16</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-16</prism:publicationDate>
<prism:section>Article</prism:section>
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<item rdf:about="http://dx.doi.org/10.1038/nmat2331">
<title>Electronic two-terminal bistable graphitic memories</title>
<link>http://dx.doi.org/10.1038/nmat2331</link>
<description>Carbon-based structures are being intensively investigated for their use in electronic devices. A pronounced non-volatile switching is now observed in two-terminal devices made from graphitic sheets. The highly reliable switching mechanism is explained by the local breaking and rejoining of atomic bonds in the sheets.</description>
<content:encoded><![CDATA[

<p>
<b>Electronic two-terminal bistable graphitic memories</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2331">doi:10.1038/nmat2331</a>
</p>
<p>Authors: Yubao Li, Alexander Sinitskii
&amp; James M. Tour</p>
]]></content:encoded>
<dc:title>Electronic two-terminal bistable graphitic memories</dc:title>
<dc:creator>Yubao Li</dc:creator>
<dc:creator>Alexander Sinitskii</dc:creator>
<dc:creator>James M. Tour</dc:creator>
<dc:identifier>doi:10.1038/nmat2331</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-16</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-16</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2318">
<title>From Mott state to superconductivity in&#160;1T-TaS2</title>
<link>http://dx.doi.org/10.1038/nmat2318</link>
<description>Superconductivity is a complex and fascinating phenomenon, made more so by its coexistence with other collective electronic states. A study of the layered compound 1T-TaS2 under pressure enables the various states of the material to be investigated and compared with other commonly studied layered superconductors.</description>
<content:encoded><![CDATA[

<p>
<b>From Mott state to superconductivity in&#160;1T-TaS2</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2318">doi:10.1038/nmat2318</a>
</p>
<p>Authors: B. Sipos, A. F. Kusmartseva, A. Akrap, H. Berger, L. Forr&#243;
&amp; E. Tuti&#353;</p>
]]></content:encoded>
<dc:title>From Mott state to superconductivity in&#160;1T-TaS2</dc:title>
<dc:creator>B. Sipos</dc:creator>
<dc:creator>A. F. Kusmartseva</dc:creator>
<dc:creator>A. Akrap</dc:creator>
<dc:creator>H. Berger</dc:creator>
<dc:creator>L. Forr&#243;</dc:creator>
<dc:creator>E. Tuti&#353;</dc:creator>
<dc:identifier>doi:10.1038/nmat2318</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-09</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-09</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2317">
<title>A metal-free polymeric photocatalyst for hydrogen production from water under visible&#160;light</title>
<link>http://dx.doi.org/10.1038/nmat2317</link>
<description>Hydrogen generated from splitting water using a catalyst and solar energy is an ideal energy source. A polymeric carbon nitride photocatalyst that is thermally and chemically stable is now shown to produce hydrogen from water even in the absence of noble metal catalysts.</description>
<content:encoded><![CDATA[

<p>
<b>A metal-free polymeric photocatalyst for hydrogen production from water under visible&#160;light</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2317">doi:10.1038/nmat2317</a>
</p>
<p>Authors: Xinchen Wang, Kazuhiko Maeda, Arne Thomas, Kazuhiro Takanabe, Gang Xin, Johan M. Carlsson, Kazunari Domen
&amp; Markus Antonietti</p>
]]></content:encoded>
<dc:title>A metal-free polymeric photocatalyst for hydrogen production from water under visible&#160;light</dc:title>
<dc:creator>Xinchen Wang</dc:creator>
<dc:creator>Kazuhiko Maeda</dc:creator>
<dc:creator>Arne Thomas</dc:creator>
<dc:creator>Kazuhiro Takanabe</dc:creator>
<dc:creator>Gang Xin</dc:creator>
<dc:creator>Johan M. Carlsson</dc:creator>
<dc:creator>Kazunari Domen</dc:creator>
<dc:creator>Markus Antonietti</dc:creator>
<dc:identifier>doi:10.1038/nmat2317</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-09</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-09</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2319">
<title>Single-molecule nanocatalysis reveals heterogeneous reaction pathways and catalytic&#160;dynamics</title>
<link>http://dx.doi.org/10.1038/nmat2319</link>
<description>Nanomaterials are effective catalysts for many chemical reactions, however, their catalytic properties are most often determined by ensembles of nanoparticles, and so far only averaged results have been measured. Now, the heterogeneous reactivity and the surface structure dynamics of individual gold nanoparticles are revealed by monitoring single fluorogenic reactions.</description>
<content:encoded><![CDATA[

<p>
<b>Single-molecule nanocatalysis reveals heterogeneous reaction pathways and catalytic&#160;dynamics</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2319">doi:10.1038/nmat2319</a>
</p>
<p>Authors: Weilin Xu, Jason S. Kong, Yun-Ting E. Yeh
&amp; Peng Chen</p>
]]></content:encoded>
<dc:title>Single-molecule nanocatalysis reveals heterogeneous reaction pathways and catalytic&#160;dynamics</dc:title>
<dc:creator>Weilin Xu</dc:creator>
<dc:creator>Jason S. Kong</dc:creator>
<dc:creator>Yun-Ting E. Yeh</dc:creator>
<dc:creator>Peng Chen</dc:creator>
<dc:identifier>doi:10.1038/nmat2319</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-09</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-09</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2316">
<title>Accordion-like honeycombs for tissue engineering of cardiac anisotropy</title>
<link>http://dx.doi.org/10.1038/nmat2316</link>
<description>Construction of tissue-engineering scaffolds that mimic cardiac anisotropy is a challenge. Now, accordion-like honeycomb scaffolds have been created that can form tissue grafts with preferentially aligned heart cells, and with mechanical properties that closely resemble the anisotropy of native myocardium.</description>
<content:encoded><![CDATA[

<p>
<b>Accordion-like honeycombs for tissue engineering of cardiac anisotropy</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2316">doi:10.1038/nmat2316</a>
</p>
<p>Authors: George C. Engelmayr, Mingyu Cheng, Christopher J. Bettinger, Jeffrey T. Borenstein, Robert Langer
&amp; Lisa E. Freed</p>
]]></content:encoded>
<dc:title>Accordion-like honeycombs for tissue engineering of cardiac anisotropy</dc:title>
<dc:creator>George C. Engelmayr</dc:creator>
<dc:creator>Mingyu Cheng</dc:creator>
<dc:creator>Christopher J. Bettinger</dc:creator>
<dc:creator>Jeffrey T. Borenstein</dc:creator>
<dc:creator>Robert Langer</dc:creator>
<dc:creator>Lisa E. Freed</dc:creator>
<dc:identifier>doi:10.1038/nmat2316</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-02</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-02</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2301">
<title>Insight into silicate-glass corrosion mechanisms</title>
<link>http://dx.doi.org/10.1038/nmat2301</link>
<description>Understanding the corrosion mechanism of aqueous silicate glass is crucial for the long-term durability of nuclear waste glasses. This mechanism is generally thought to be associated with chemical affinity, but it is now demonstrated that morphological transformations also have an important role in the leaching kinetics of these glasses.</description>
<content:encoded><![CDATA[

<p>
<b>Insight into silicate-glass corrosion mechanisms</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2301">doi:10.1038/nmat2301</a>
</p>
<p>Authors: C&#233;line Cailleteau, Fr&#233;d&#233;ric Angeli, Fran&#231;ois Devreux, St&#233;phane Gin, Jacques Jestin, Patrick Jollivet
&amp; Olivier Spalla</p>
]]></content:encoded>
<dc:title>Insight into silicate-glass corrosion mechanisms</dc:title>
<dc:creator>C&#233;line Cailleteau</dc:creator>
<dc:creator>Fr&#233;d&#233;ric Angeli</dc:creator>
<dc:creator>Fran&#231;ois Devreux</dc:creator>
<dc:creator>St&#233;phane Gin</dc:creator>
<dc:creator>Jacques Jestin</dc:creator>
<dc:creator>Patrick Jollivet</dc:creator>
<dc:creator>Olivier Spalla</dc:creator>
<dc:identifier>doi:10.1038/nmat2301</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-10-26</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-10-26</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2302">
<title>Hierarchical nanofabrication&#160;of&#160;microporous crystals with ordered mesoporosity</title>
<link>http://dx.doi.org/10.1038/nmat2302</link>
<description>Zeolite nanocrystals with three-dimensionally ordered mesoporous structures are important for designing molecularly accessible and selective catalysts. With a single zeolite synthesis procedure, uniform nanocrystals and crystal zeolites with ordered imprinted mesoporosity can now be obtained.</description>
<content:encoded><![CDATA[

<p>
<b>Hierarchical nanofabrication&#160;of&#160;microporous crystals with ordered mesoporosity</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2302">doi:10.1038/nmat2302</a>
</p>
<p>Authors: Wei Fan, Mark A. Snyder, Sandeep Kumar, Pyung-Soo Lee, Won Cheol Yoo, Alon V. McCormick, R. Lee Penn, Andreas Stein
&amp; Michael Tsapatsis</p>
]]></content:encoded>
<dc:title>Hierarchical nanofabrication&#160;of&#160;microporous crystals with ordered mesoporosity</dc:title>
<dc:creator>Wei Fan</dc:creator>
<dc:creator>Mark A. Snyder</dc:creator>
<dc:creator>Sandeep Kumar</dc:creator>
<dc:creator>Pyung-Soo Lee</dc:creator>
<dc:creator>Won Cheol Yoo</dc:creator>
<dc:creator>Alon V. McCormick</dc:creator>
<dc:creator>R. Lee Penn</dc:creator>
<dc:creator>Andreas Stein</dc:creator>
<dc:creator>Michael Tsapatsis</dc:creator>
<dc:identifier>doi:10.1038/nmat2302</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-10-26</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-10-26</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2292">
<title>Unexpected power-law stress relaxation of entangled ring polymers</title>
<link>http://dx.doi.org/10.1038/nmat2292</link>
<description>How do entangled polymer rings relax? Linear polymers can ease their stress because their chains have ends, but cyclic polymers do not. Even trace amounts of linear chains dominate the mechanical properties if present as impurities. Investigation of carefully purified ring polymers reveals they exhibit self-similar dynamics and a power-law stress relaxation.</description>
<content:encoded><![CDATA[

<p>
<b>Unexpected power-law stress relaxation of entangled ring polymers</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2292">doi:10.1038/nmat2292</a>
</p>
<p>Authors: M. Kapnistos, M. Lang, D. Vlassopoulos, W. Pyckhout-Hintzen, D. Richter, D. Cho, T. Chang
&amp; M. Rubinstein</p>
]]></content:encoded>
<dc:title>Unexpected power-law stress relaxation of entangled ring polymers</dc:title>
<dc:creator>M. Kapnistos</dc:creator>
<dc:creator>M. Lang</dc:creator>
<dc:creator>D. Vlassopoulos</dc:creator>
<dc:creator>W. Pyckhout-Hintzen</dc:creator>
<dc:creator>D. Richter</dc:creator>
<dc:creator>D. Cho</dc:creator>
<dc:creator>T. Chang</dc:creator>
<dc:creator>M. Rubinstein</dc:creator>
<dc:identifier>doi:10.1038/nmat2292</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-10-26</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-10-26</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2315">
<title>Structural and magnetic phase diagram of CeFeAsO1&#8722; xFx and its relation to high-temperature superconductivity</title>
<link>http://dx.doi.org/10.1038/nmat2315</link>
<description>According to a neutron-scattering study of the structural and magnetic properties of the pnictide CeFeAsO1&#8722;xFx, the phase diagram of this material shows considerable similarities with the high-Tc cuprate superconductors. These results are an important addition to the effort to find out where superconductivity in these iron&#8211;arsenic alloys arises.</description>
<content:encoded><![CDATA[

<p>
<b>Structural and magnetic phase diagram of CeFeAsO1&#8722; xFx and its relation to high-temperature superconductivity</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2315">doi:10.1038/nmat2315</a>
</p>
<p>Authors: Jun Zhao, Q. Huang, Clarina de la Cruz, Shiliang Li, J. W. Lynn, Y. Chen, M. A. Green, G. F. Chen, G. Li, Z. Li, J. L. Luo, N. L. Wang
&amp; Pengcheng Dai</p>
]]></content:encoded>
<dc:title>Structural and magnetic phase diagram of CeFeAsO1&#8722; xFx and its relation to high-temperature superconductivity</dc:title>
<dc:creator>Jun Zhao</dc:creator>
<dc:creator>Q. Huang</dc:creator>
<dc:creator>Clarina de la Cruz</dc:creator>
<dc:creator>Shiliang Li</dc:creator>
<dc:creator>J. W. Lynn</dc:creator>
<dc:creator>Y. Chen</dc:creator>
<dc:creator>M. A. Green</dc:creator>
<dc:creator>G. F. Chen</dc:creator>
<dc:creator>G. Li</dc:creator>
<dc:creator>Z. Li</dc:creator>
<dc:creator>J. L. Luo</dc:creator>
<dc:creator>N. L. Wang</dc:creator>
<dc:creator>Pengcheng Dai</dc:creator>
<dc:identifier>doi:10.1038/nmat2315</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-10-26</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-10-26</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2295">
<title>Ultrahigh stress and strain in hierarchically structured hollow nanoparticles</title>
<link>http://dx.doi.org/10.1038/nmat2295</link>
<description>Nanocrystalline materials usually exhibit high strength and their deformation caused by stress is limited. Nanocrystalline CdS with spherical and hierarchical shell geometry is shown not only to withstand extreme stresses, but also to deform considerably before failure.</description>
<content:encoded><![CDATA[

<p>
<b>Ultrahigh stress and strain in hierarchically structured hollow nanoparticles</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2295">doi:10.1038/nmat2295</a>
</p>
<p>Authors: Z. W. Shan, G. Adesso, A. Cabot, M. P. Sherburne, S. A. Syed Asif, O. L. Warren, D. C. Chrzan, A. M. Minor
&amp; A. P. Alivisatos</p>
]]></content:encoded>
<dc:title>Ultrahigh stress and strain in hierarchically structured hollow nanoparticles</dc:title>
<dc:creator>Z. W. Shan</dc:creator>
<dc:creator>G. Adesso</dc:creator>
<dc:creator>A. Cabot</dc:creator>
<dc:creator>M. P. Sherburne</dc:creator>
<dc:creator>S. A. Syed Asif</dc:creator>
<dc:creator>O. L. Warren</dc:creator>
<dc:creator>D. C. Chrzan</dc:creator>
<dc:creator>A. M. Minor</dc:creator>
<dc:creator>A. P. Alivisatos</dc:creator>
<dc:identifier>doi:10.1038/nmat2295</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-10-19</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-10-19</prism:publicationDate>
<prism:section>Article</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nmat2337">
<title>Let the Sun shine</title>
<link>http://dx.doi.org/10.1038/nmat2337</link>
<description/>
<content:encoded><![CDATA[

<p>
<b>Let the Sun shine</b>
</p>
<p>Nature Materials. <a href="http://dx.doi.org/10.1038/nmat2337">doi:10.1038/nmat2337</a>
</p>
]]></content:encoded>
<dc:title>Let the Sun shine</dc:title>
<dc:identifier>doi:10.1038/nmat2337</dc:identifier>
<dc:source>Nature Materials</dc:source>
<dc:date>2008-11-04</dc:date>
<prism:publicationName>Nature Materials</prism:publicationName>
<prism:publicationDate>2008-11-04</prism:publicationDate>
<prism:section>Erratum</prism:section>
</item>
</rdf:RDF>
