2026-05-31T07:50:51Zhttps://riuma.uma.es/rest/oai/request

oai:riuma.uma.es:10630/304532026-02-03T12:17:35Zcom_10630_2254col_10630_37959

García-González, Francisco Aranda, Daniel Ávila-Ferrer, Francisco José Otero-Fernández-de-Molina, Juan Carlos Santoro, Fabrizio 2024-02-14T12:39:26Z 2024-02-14T12:39:26Z 2024 https://hdl.handle.net/10630/30453 SERS (Surface-Enhanced Raman Spectroscopy) has established itself as an important characterization technique, owing to both its characteristically high intensities and the large amount of information it is capable of yielding; however, this high sensibility also implies intrinsic complexity when it comes to extracting valuable information from the spectra. Electrochemical SERS (EC-SERS), in which the substrate is a nanostructured electrode for which the electrode potential (Vel) can be tuned, poses further challenge given the sensibility of SERS spectra of certain molecules to Vel. This is the case for Pyridine, the most emblematic SERS molecule, for which the interaction between Charge-Transfer (CT) states and Plasmons has been proven to play a crucial. In this work, we have performed full diabatizations for systems consisting of Pyridine attached to different silver clusters, giving the possibility to readily define CT states, whose energy is tunable by an applied external field E, a microscopic analogous to Vel. Nuclear wavepacket propagations on the coupled potential energy surfaces including both local excitations of the metal and CT states were performed to retrieve Resonance Raman spectra. Our results show that the population transfer from bright metal states to CT states plays a most pivotal role when it comes to the shape and absolute intensities of EC-SERS spectra of Pyridine. eng open access Espectroscopía Raman Diabatic Approach for SERS: From Quantum Dynamics to Spectra. conference output