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<dc:title>Water adsorption and dissociation on gold catalysts supported on anatase-TiO2(101)</dc:title>
<dc:creator>Valdés, Haydée</dc:creator>
<dc:creator>Molina Martín, Luis Miguel</dc:creator>
<dc:creator>Alonso Martín, Julio Alfonso</dc:creator>
<dc:subject>Density functional theory</dc:subject>
<dc:subject>Teoría del funcional de densidad</dc:subject>
<dc:subject>Gold catalysis</dc:subject>
<dc:subject>Catálisis del oro</dc:subject>
<dc:subject>Titanium dioxide (TiO2)</dc:subject>
<dc:subject>Dióxido de titanio (TiO2)</dc:subject>
<dc:subject>Water</dc:subject>
<dc:subject>Agua</dc:subject>
<dc:subject>Reaction intermediates</dc:subject>
<dc:subject>Intermedio de reacción</dc:subject>
<dc:description>Producción Científica</dc:description>
<dc:description>The presence of water can strongly a ect the reactivity of gold catalysts. For this&#xd;
reason, ab initio density functional simulations have been performed to study&#xd;
the adsorption and dissociation of water on the anatase-TiO2(101) surface, both&#xd;
clean and in the presence of a supported model gold nanocluster, Au4. When&#xd;
adsorbed not too close to the cluster, water is adsorbed and dissociated with&#xd;
roughly the same binding energies and dissociation barriers as in the catalystfree&#xd;
surface. If the molecule adsorbs at the Au/TiO2 perimeter interface, making&#xd;
contact with gold, we  nd a slight stabilization of molecular water, whereas&#xd;
dissociated water becomes slightly less stable. The preferential mechanism for&#xd;
water dissociation is found to be a splitting of the H-OH bond at the TiO2&#xd;
surface, with the gold cluster playing a minor role. Calculations of the relative&#xd;
stability of various water-related species show that the gold catalyst favours&#xd;
accumulation of excess hydroxyls around its perimeter.</dc:description>
<dc:description>Ministerio de Economía, Industria y Competitividad y Fondo Europeo de Desarrollo ( grants MAT 2011-22781  /  MAT 2014-54378-R )</dc:description>
<dc:description>Consejería de Educación, Junta de Castilla y León (grants VA050U14   /  VA021G18)</dc:description>
<dc:description>Junta de Castilla y León  (postdoctoral contract CIP13702)</dc:description>
<dc:date>2019-05-21T11:14:06Z</dc:date>
<dc:date>2019-05-21T11:14:06Z</dc:date>
<dc:date>2019</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Applied Surface Science, 2019, vol. 487, p. 244-252</dc:identifier>
<dc:identifier>0169-4332</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/36048</dc:identifier>
<dc:identifier>10.1016/j.apsusc.2019.04.249</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://www.sciencedirect.com/science/article/pii/S016943321931267X</dc:relation>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>© 2019 Elsevier</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Elsevier</dc:publisher>
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<europeana:provider>Hispana</europeana:provider>
<europeana:type>TEXT</europeana:type>
<europeana:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</europeana:rights>
<europeana:dataProvider>UVaDOC. Repositorio Documental de la Universidad de Valladolid</europeana:dataProvider>
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