Aspects of the adsorption of chloride on silver revealed through surface enhanced Raman scattering

作者: D. Roy , T.E. Furtak

DOI: 10.1016/0022-0728(87)80109-2

关键词:

摘要: Abstract The surface coverage of halide ions on Ag is found to be the most dominant factor determining potential dependence Cl-Ag Raman intensity and mode energy. observed signals are predominantly associated with active sites which stabilized by coadsorbed ions. identified as intrinsically resonant clusters. resonance in clusters gives rise short-range enhancement scattering this situation. We compare our experiments other recently results point out why uncorrected magnitude not a simple measure adsorbed chloride.

参考文章(52)
Micheal J. Weaver, Joseph T. Hupp, Felix Barz, Joseph G. Gordon, Michael R. Philpott, Surface-Enhanced Raman Spectroscopy of Electrochemically Characterized Interfaces. Relations between Raman Scattering Intensity and Surface Coverage for Simple Anionic Adsorbates. Journal of Electroanalytical Chemistry. ,vol. 160, pp. 321- 333 ,(1984) , 10.1016/S0022-0728(84)80135-7
Roger C. Baetzold, Calculated Properties of Metal Aggregates. II. Silver and Palladium The Journal of Chemical Physics. ,vol. 55, pp. 4363- 4370 ,(1971) , 10.1063/1.1676761
T.E. Furtak, D. Roy, The short-range mechanism of surface enhanced raman scattering Surface Science. ,vol. 158, pp. 126- 146 ,(1985) , 10.1016/0167-2584(85)90009-X
T. E. Furtak, D. Roy, Nature of the active site in surface-enhanced Raman scattering Physical Review Letters. ,vol. 50, pp. 1301- 1304 ,(1983) , 10.1103/PHYSREVLETT.50.1301