AVS 62nd International Symposium & Exhibition | |
Surface Science | Wednesday Sessions |
Session SS+AS+EN-WeA |
Session: | Metals, Alloys & Oxides: Reactivity and Catalysis |
Presenter: | Felicia Lucci, Tufts University Department of Chemistry |
Authors: | F.R. Lucci, Tufts University Department of Chemistry E.C.H. Sykes, Tufts University Department of Chemistry |
Correspondent: | Click to Email |
Pd-Au alloys are known to catalyze a wide range of hydrogenation and oxidation reactions; however, the size of Pd ensembles in Au required for small molecule activation is not well understood. On the atomic scale, we investigate size effects of Pd atoms in Au for the catalytic activation of H2 and O2. We show that isolated Pd atoms are capable of catalyzing the dissociative adsorption of H2, a process which was previously thought to require contiguous Pd sites. H spillover from active Pd sites to the Au surface can be induced the adsorption of CO. Conversely, single Pd atoms are not capable of O2 dissociation. Small Pd clusters on Au enable O2 activation and adsorption at Pd-Au interface sites. Since weakly bound H and O atoms are capable of enhancing reaction selectivity on Au substrates, this Pd-Au system serves as an ideal model system with which to probe selective hydrogenation and oxidation reactions at both single and ensemble active sites.