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dc.contributor.authorCenteno, Silvia 
dc.contributor.authorRuano, Cristina
dc.contributor.authorRomán-Pérez, Jéssica
dc.contributor.authorLópez-Tocón, Isabel 
dc.contributor.authorSoto-Martin, Juan 
dc.contributor.authorOtero-Fernandezde-Molina, Juan Carlos 
dc.date.accessioned2013-10-29T12:52:31Z
dc.date.available2013-10-29T12:52:31Z
dc.date.issued2013-10-29
dc.identifier.urihttp://hdl.handle.net/10630/6183
dc.descriptionResumen de conferencia presentada en el congreso ICP2013 en Lovaina (Bélgica) en julio de 2013es_ES
dc.description.abstractThis work deals with the unexplained efficiency of the electrode potential (EV) in tuning the energy of Charge Transfer (ECT) electronic states of hybrid systems formed by molecules and metal nanostructures. Huge energy gains (G) of up to 5 eV/V observed in electrochemical SERS experiences have been tentatively explained by a local increase of the electric potential at specific adsorption sites.[1] This gain, which is in conflict with the classical picture of the metal-adsorbate CT mechanism (G=1), can be quite relevant since it means that a relatively small change in the applied voltage can produce a large shift in the CT states, and consequently, it can greatly modify the resonant conditions in a SERS experiment. [2] Supported on electronic structure calculations of metal-molecule nanoclusters, we are able to elucidate that this “anomalous” gain is mainly due to two different contributions, firstly, the sensitivity of the CT electronic states of each particular metal-molecule system on the effective charge excess of the metal, and, secondly, to an enhanced electric capacitance of the metallic nanocluster with respect to the macroscopic values. We associate this last contribution with the so-called “edge effect” that causes inhomogeneities in the density charge at local sites of the metallic surface which could correspond to the very popular "hot spots" between the SERS community. [1] L. Cui, D-Y Wu, A. Wang, B. Ren, Z-Q Tian, J. Phys. Chem. C, 2010, 114, 16588-16595. [2] A. Otto, Surface Science, 1984, 138, 319-338es_ES
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional de Andalucía Tech.es_ES
dc.language.isoenges_ES
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEspectroscopía Ramanes_ES
dc.subjectNanopartículases_ES
dc.subject.otherSurface-enhanced Raman spectroscopyes_ES
dc.subject.otherMetallic nanoparticleses_ES
dc.subject.otherPhotoinduced charge transfer processeses_ES
dc.titleSurface-enhanced photoinduced charge transfer processes in metal-molecule nanoclusterses_ES
dc.typeinfo:eu-repo/semantics/conferenceObjectes_ES
dc.centroFacultad de Cienciases_ES
dc.relation.eventtitleInternational Conference on Photochemistry ICP2013es_ES
dc.relation.eventplaceLovaina, Bélgicaes_ES
dc.relation.eventdate21-07-13es_ES


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