Abstract

Harmonic oscillator models are used to explain recent experimental data on infrared absorption by CO molecules adsorbed on two stepped platinum surfaces. These data reveal only a lower frequency band at low coverage and only a higher frequency band at high coverage. Both bands exist over a range of intermediate coverages. The data are explained by a coupled-dipole model which includes the effects of electronic polarizability, the tilted orientation of CO molecules at step sites, and the electric field enhancement at step sites. The lower-frequency band is associated with CO molecules adsorbed on step sites and the higher-frequency band is associated with two-dimensional islands consisting of both step and terrace CO. The model explains the observed variation of frequency and intensity with coverage for CO adsorption on Pt(533) and Pt(432) surfaces. The model calculations indicate that the wavenumber for a single, linearly bonded CO molecule is about 9 cm −1 higher on a terrace site than on a step site.

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