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                  <mods:namePart>Aranda, Daniel</mods:namePart>
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                  <mods:namePart>García-González, Francisco</mods:namePart>
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                  <mods:namePart>Ávila-Ferrer, Francisco José</mods:namePart>
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                  <mods:namePart>López-Tocón, Isabel</mods:namePart>
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                  <mods:namePart>Soto-Martín, Juan</mods:namePart>
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                  <mods:namePart>Otero-Fernández-de-Molina, Juan Carlos</mods:namePart>
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               <mods:identifier type="citation">J. Chem. Theory Comput. 2022, 18, 11, 6802–6815</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/10630/28327</mods:identifier>
               <mods:identifier type="doi">10.1021/acs.jctc.2c00633</mods:identifier>
               <mods:abstract>We present a computational approach for electrochemical Surface-Enhanced Raman Scattering&#xd;
(EC-SERS). The surface excess of charge induced by the electrode potential (Vel) was introduced&#xd;
by applying an external electric  eld to a set of clusters [Agn]q with (n,q) of (19, 1) or (20,0) on&#xd;
which a molecule adsorbs. Using DFT/TD-DFT calculations, these metal-molecule complexes were&#xd;
classi ed by the adsorbate partial charge, and the main Vel-dependent properties were simultaneously&#xd;
studied with the aid of vibronic resonance Raman computations. Namely, changes on the vibrational&#xd;
wavenumbers, relative intensities and enhancement factors for all SERS mechanisms: chemical or&#xd;
nonresonant, and resonance Raman with bright states of the adsorbate, charge-transfer states and&#xd;
plasmon-like excitations on the metal cluster. We selected two molecules to test our model, pyridine,&#xd;
for which Vel has a remarkable e ect, and 9,10-bis((E)-2-(pyridin-4-yl)vinyl)anthracene, which is almost&#xd;
insensitive to the applied bias. The results nicely reproduced most of the experimental observations,&#xd;
while the limitations of our approach were critically evaluated. We detected that accounting explicitly&#xd;
for the surface charges is key for EC-SERS models and that the highest calculated enhancement factors,&#xd;
up to 107-108, are obtained by interstate coupling of bright local excitations of the metal cluster and</mods:abstract>
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               <mods:subject>
                  <mods:topic>Espectroscopía Raman</mods:topic>
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               <mods:titleInfo>
                  <mods:title>A computational approach for electrochemical SERS.Key role of the surface charges and synergy between EM and CT mechanisms.</mods:title>
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