RARE-GAS THERMAL-DESORPTION FROM FLAT AND STEPPED PLATINUM SURFACES -LATERAL INTERACTIONS AND THE INFLUENCE OF DIMENSIONALITY

Citation
W. Widdra et al., RARE-GAS THERMAL-DESORPTION FROM FLAT AND STEPPED PLATINUM SURFACES -LATERAL INTERACTIONS AND THE INFLUENCE OF DIMENSIONALITY, Physical review. B, Condensed matter, 57(7), 1998, pp. 4111-4126
Citations number
50
Categorie Soggetti
Physics, Condensed Matter
ISSN journal
01631829
Volume
57
Issue
7
Year of publication
1998
Pages
4111 - 4126
Database
ISI
SICI code
0163-1829(1998)57:7<4111:RTFFAS>2.0.ZU;2-F
Abstract
High-resolution thermal-desorption data are presented for xenon desorp tion from flat Pt(111) and stepped Pt(997) surfaces. Analysis of the e xperimental data and comparison with detailed lattice-gas models which are able to describe different adsorption sites on the stepped surfac e reveal similar xenon single-particle binding energies of 253 meV and 264 meV on Pt(111) and on the terraces of a Pt(997) surface, respecti vely. The extracted corresponding lateral interactions are attractive and again of similar value (pairwise attraction of 11 meV). However, f or terrace desorption different kinetics are observed: On the flat (11 1) surface desorption is zero order over a wide range of coverage, due to equilibrium between adsorbate condensate and two-dimensional gas, whereas on the stepped surface terrace desorption is near first order. We interpret the changed desorption kinetics as a consequence of the finite size of the (111) terraces in one direction on the stepped surf ace, i.e., as an influence of dimensionality on adlayer statistics. On the basis of the lattice-gas model we demonstrate the influence of di fferent terrace widths. For adsorption on Pt(997) we find complete xen on step decoration before terrace adsorption starts with a binding ene rgy of about 400 meV and a pairwise repulsion of about 16 meV. Complet ion of the step decoration is accompanied by a work function change of 0.47 eV which might explain the observed repulsion as due to dipole-d ipole interaction along the steps. [S0163-1829(98)03407-9].