Theory of Raman scattering by molecules adsorbed at electrode surfaces. Model calculations for resonance Raman scattering by an adsorbed diatomic

Frederick W. King, George C Schatz

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Model calculations of the resonant Raman cross section of a homonuclear diatomic adsorbate on a metallic electrode surface are performed. If the excited intermediate electronic state is weakly dipole coupled to the electronic ground state (relative to some other excited electronic states), electric field induced intensity borrowing is found to be very large for the adsorbate. The important excited state involved is that describing charge transfer from adsorbate to the metallic substrate. We have also carried out a simplified calculation of the vibrational Franck-Condon factors for the adsorbate. Combining electronic with vibrational enhancement factors, we find that there may be an overall intensity enhancement for the adsorbate of 104-108 depending on the electric field strength.

Original languageEnglish
Pages (from-to)245-256
Number of pages12
JournalChemical Physics
Volume38
Issue number2
DOIs
Publication statusPublished - Apr 15 1979

Fingerprint

resonance scattering
Adsorbates
Raman scattering
Raman spectra
Electrodes
Molecules
electrodes
electronics
Electronic states
molecules
Electric fields
augmentation
electric field strength
Excited states
Ground state
charge transfer
Charge transfer
dipoles
ground state
electric fields

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Spectroscopy
  • Atomic and Molecular Physics, and Optics

Cite this

Theory of Raman scattering by molecules adsorbed at electrode surfaces. Model calculations for resonance Raman scattering by an adsorbed diatomic. / King, Frederick W.; Schatz, George C.

In: Chemical Physics, Vol. 38, No. 2, 15.04.1979, p. 245-256.

Research output: Contribution to journalArticle

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