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Charge transfer at the nanoscale and the role of the out-of-plane vibrations in the selection rules of surface-enhanced Raman scattering

Abstract

Surface-enhanced Raman spectra (SERS) of pyridazine shows the selective enhancement of the bands recorded at about 1570, 1450 and 380 cm-1, which are assigned to two different types of vibrations. The two first ones correspond to in-plane 8a;νring and 19b;δ(CH) totally symmetric A1 modes, respectively, while the last band is assigned to the out-of-plane 16b;τring;B1 vibration. The selective enhancement has been analyzed on the basis of a resonant Raman process involving photoexcited metal(M)-to-molecule(A) charge transfer (CT: M-A+hν→M+-A-) states of the metal-adsorbate surface complex, which have been also related to the doublet electronic states of the corresponding radical anion of the adsorbate (A-). According to selection rules of the electromagnetic/plasmonic SERS enhancement mechanism, the simultaneous enhancement of in-plane and out-of-plane modes could be attributed to different orientations of the adsorbate (perpendicular and parallel, respectively, or tilted) with respect to the metallic surface. The calculated resonance Raman-CT spectra (SERS-CT) and the vibrational wavenumbers of isolated pyridazine and of pyridazine-Ag2 complex obtained from electronic structure calculations, point out a single type of molecules adsorbed with perpendicular orientation. The relative SERS enhancements of both in-plane and out-of-plane modes are due to Franck-Condon factors related to differences between the equilibrium geometries (A1 vibrations, ΔQ≠0) and gradients (B1 vibrations, Δν≠0 and ΔQ≠0), respectively, of the potential energy surfaces of the involved ground and photoinduced CT electronic states. Therefore, the selective enhancement of the SERS bands of pyridazine is controlled by a general metal-to-molecule resonant CT mechanism. This conclusion supports the usefulness of SERS on studying the subtle electronic structure of charged interfaces as well as key processes such as electron transfer at the nanoscale.

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Publication details

The article was received on 05 Sep 2018, accepted on 07 Nov 2018 and first published on 07 Nov 2018


Article type: Paper
DOI: 10.1039/C8CP05623D
Citation: Phys. Chem. Chem. Phys., 2018, Accepted Manuscript
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    Charge transfer at the nanoscale and the role of the out-of-plane vibrations in the selection rules of surface-enhanced Raman scattering

    D. Aranda Ruiz, S. Valdivia Mantas, F. J. Avila, J. Soto, J. C. Otero and I. López Tocón, Phys. Chem. Chem. Phys., 2018, Accepted Manuscript , DOI: 10.1039/C8CP05623D

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