Isotopic effects observed m the mfrared spectra of CO adsorbed on the Cu(ll1) surface are shown to be compatible with a dlpolecouphng model which relates frequency shifts to the accompanying changes III infrared band mtenslty.
Coverage-dependent Bond Length of Chlorine Adsorbed on Cu{111}
โ Scribed by Way, W. K.; Pike, A. C.; Rosencrance, S. W.; Braun, R. M.; Winograd, N.
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 515 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0142-2421
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โฆ Synopsis
The adsorption of CI, on Cu{lll} at 300 K has been studied using shadow-cone-enhanced secondary ion mass spectrometry (SIMS). The system has been investigated for chlorine coverages ranging from 0.08 to 0.33 monolayer (ML), including the Cu{lll}-(J3 x J3)R3O0-CI surface. The secondary Cu* ion intensity has been measured as a function of the incidence angle of the primary ion beam. The enhanced intensity features in the spectra are compared with results from a two-body interaction calculation that uses the Moliere approximation to the ThomasFermi potential. A chlorine-copper interlayer spacing of 1.87 f 0.04 is measured between the coverages of 0.17 and 0.33 ML. This value corresponds to a chlorinoe-copper bond length of 2.38 f 0.04 A. At 0.08 ML, the chlorine-copper bond length is expanded to 2.48 f 0.04 A. These results suggest that the chlorine-copper bond is more ionic in the low coverage limit.
๐ SIMILAR VOLUMES
The temperature dependence of the rate constant and the effective diffusion coefficient of incorporation of lead atoms from an underpotential monolayer adsorbate on Ag(ll1) into the silver crystal lattice at low and high coverages is investigated. The transfer activation energy in both cases and the