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<dc:title>Steric and chemical effects on the hydrogen adsorption and dissociation on free and graphene–supported palladium clusters</dc:title>
<dc:creator>Granja del Río, Alejandra</dc:creator>
<dc:creator>Alonso Martín, Julio Alfonso</dc:creator>
<dc:creator>López Santodomingo, María José</dc:creator>
<dcterms:abstract>Palladium doping enhances the hydrogen storage capacity of nanoporous carbons. The purpose of this&#xd;
work is to asses the effect of the carbonaceous support on the adsorption of hydrogen on Pd clusters.&#xd;
Hydrogen adsorbs on Pd clusters following two channels: molecular adsorption and dissociative&#xd;
chemisorption. These two adsorption channels are investigated on free Pd clusters and Pd clusters supported&#xd;
on pristine and defective (with vacancies) graphene using the Density Functional Formalism. Pd6&#xd;
is taken as case study. Free Pd6 can adsorb twelve hydrogen molecules in the molecular form, a number&#xd;
higher than the nine and eight molecules that can be adsorbed on the cluster supported on pristine graphene&#xd;
and on a graphene vacancy, respectively. However the most stable adsorption channel is, in all&#xd;
cases, the dissociative chemisorption of hydrogen. As the cluster is being loaded with hydrogen, there&#xd;
is a competition between the two adsorption channels. Pd6 supported on a graphene vacancy is able to&#xd;
dissociate three hydrogen molecules, whereas the free cluster can dissociate up to seven molecules. In&#xd;
both cases, six additional molecules can be adsorbed in the molecular form. The higher saturation limit&#xd;
obtained for the free clusters is explained in terms of the steric and chemical effects of the supporting&#xd;
layer. These effects are of primarily importance to asses the role of the Pd dopant on the adsorption&#xd;
and storage of hydrogen on nanoporous carbons.</dcterms:abstract>
<dcterms:dateAccepted>2018-03-19T10:52:33Z</dcterms:dateAccepted>
<dcterms:available>2018-03-19T10:52:33Z</dcterms:available>
<dcterms:created>2018-03-19T10:52:33Z</dcterms:created>
<dcterms:issued>2017</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Computational and Theoretical Chemistry 1107, 23-29 (2017)</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/29144</dc:identifier>
<dc:identifier>10.1016/j.comptc.2016.11.029</dc:identifier>
<dc:identifier>23</dc:identifier>
<dc:identifier>1107</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
<dc:publisher>Elsevier</dc:publisher>
</qdc:qualifieddc></metadata></record></GetRecord></OAI-PMH>