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dc.contributor.authorAranda, Daniel
dc.contributor.authorValdivia, Samuel
dc.contributor.authorAvila, Francisco J.
dc.contributor.authorSoto-Martin, Juan 
dc.contributor.authorLópez-Tocón, Isabel 
dc.contributor.authorOtero-Fernandezde-Molina, Juan Carlos 
dc.date.accessioned2019-07-25T10:35:46Z
dc.date.available2019-07-25T10:35:46Z
dc.date.created2019
dc.date.issued2019-07-25
dc.identifier.urihttps://hdl.handle.net/10630/18147
dc.description.abstractThe electromagnetic/plasmonic (SERS-PL) and the chemical (usually involving resonant photoinduced metal-adsorbate (M-A) charge transfer processes (SERS-CT:M-A+hn-->M+-A-)) mechanisms are recognized as the two main contributions to the enhancement of a particular band in a SERS record. The key problem is to know which mechanism dominates the spectrum and to apply the corresponding selection rules. Many spectra have been analyzed according to the so-called “SERS propensity rules” of the PL mechanism. In this way, it would be possible to get information about the perpendicular/parallel orientation of the adsorbate on the nanoparticle if in-plane/out-of-plane vibrations of planar aromatic molecules show relative enhancement. The SERS of pyridazine (Pdz) on a silver electrode (Figure 1) is a very special case where the relative intensities are tuned by the electrode potential. Three different types of spectra are recorded showing no selective intensification (0 V) or in-plane (-0.5 V) and out-of-plane (-0.75 V) enhancements. The relative activity of both in-plane (8a and 19b modes) and out-of-plane (16b mode) vibrations can be explained under the same resonant SERS-CT chemical mechanism due to Franck-Condon factors related to differences between the equilibrium geometries (A1 vibrations, DQ≠0) and gradients (B1 vibrations, Dn≠0 and DQ≠0), respectively, of the potential energy surfaces of the involved ground and photoinduced CT electronic states. Therefore, it is not necessary to resort to any change in the orientation of the adsorbate, which is the standard explanation based on the propensity rules of the SERS-PL mechanism. This conclusion is supported on the basis of electronic structure calculations of the properties of Ag2-Pdz clusters in the ground (S0;A1) and excited states with CT characteristics (CT0;A2 and CT1;B1).en_US
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Tech.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.otherSERS,en_US
dc.subject.otherselection rulesen_US
dc.subject.othercharge transferen_US
dc.subject.otherelectrochemistryen_US
dc.subject.otherchemical mechanismen_US
dc.titleSelection rules of surface-enhanced Raman scattering: the role of the out-of-plane vibrationsen_US
dc.typeinfo:eu-repo/semantics/conferenceObjecten_US
dc.centroFacultad de Cienciasen_US
dc.relation.eventtitle10th International Conference on Advanced Vibrational Spectroscopy (ICAVS10)en_US
dc.relation.eventplaceNueva Zelanda (Australia)en_US
dc.relation.eventdate07-07-2019en_US
dc.rights.ccAttribution-NonCommercial-NoDerivatives 4.0 Internacional*


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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