Mechanistic interpretation of CO oxidation turnover rates on supported Au clusters

0021-9517/$ see front matter Published by Elsevier doi:10.1016/j.jcat.2011.09.015 ⇑ Corresponding author. Fax: +1 510 642 4778. E-mail address: [email protected] (E. Iglesia). 1 Present address: Institute of Catalysis and Petroche 28049 Madrid, Spain. 2 Present address: Chevron Corporation, Richmond, Kinetic and isotopic data are used to interpret the mechanistic role of gaseous H2O molecules and of nonreducible (Al2O3) and reducible (TiO2, Fe2O3) supports on CO oxidation turnovers catalyzed by small Au clusters (<5 nm). H2O acts as a co-catalyst essential for O2 activation and for catalyst stability in CO oxidation at near-ambient temperatures, but also inhibits rates via competitive adsorption at higher H2O pressures. The effects of CO, O2, and H2O pressures on CO oxidation turnover rates, the absence of O2/ O2 and O2/H2 O exchange, and the small H2O/D2O kinetic isotope effects are consistent with quasi-equilibrated molecular adsorption of CO, O2, and H2O on Au clusters with the kinetic relevance of H2O-mediated O2 activation via the formation of hydroperoxy intermediates ( OOH), which account for the remarkable reactivity and H2O effects on Au clusters. These elementary steps proceed on Au clusters without detectable requirements for support interface sites, which are no longer required when H2O is present and mediates O2 activation steps. Rate enhancements by H2O were also observed for CO oxidation on Pt clusters (1.3 nm), which is also limited by O2 activation steps, suggesting H2O-aided O2 activation and OOH species in oxidations involving kinetically-relevant O2 activation. These intermediates have also been proposed to account for the ability of O2/H2O mixtures to act as reactants in alkene epoxidation on Au-based catalysts. Published by Elsevier Inc.