| pubmed-article:18825289 | pubmed:abstractText | As catalysis research strives toward designing structurally and functionally well-defined catalytic centers containing as few active metal atoms as possible, the importance of understanding the reactivity of small metal clusters, and in particular of systematic comparisons of reaction types and cluster sizes, has grown concomitantly. Here we report density functional theory calculations (GGA-PW91) that probe the relationship between particle size, intermediate structures, and energetics of CO and NO oxidation by molecular and atomic oxygen on Pt(x) clusters (x = 1-5 and 10). The preferred structures, charge distributions, vibrational spectra, and energetics are systematically examined for oxygen (O(2), 2O, and O), CO, CO(2), NO, and NO(2), for CO/NO co-adsorbed with O(2), 2O, and O, and for CO(2)/NO(2) co-adsorbed with O. The binding energies of oxygen, CO, NO, and of the oxidation products CO(2) and NO(2) are all markedly enhanced on Pt(x) compared to Pt(111), and they trend toward the Pt(111) levels as cluster size increases. Because of the strong interaction of both the reactants and products with the Pt(x) clusters, deep energy sinks develop on the potential energy surfaces of the respective oxidation processes, indicating worse reaction energetics than on Pt(111). Thus the smallest Pt clusters are less effective for catalyzing CO and NO oxidation in their original state than bulk Pt. Our results further suggests that oxidation by molecular O(2) is thermodynamically more favourable than by atomic O on Pt(x). Conditions and applications in which the Pt(x) clusters may be effective catalysts are discussed. | lld:pubmed |
