Size-dependent catalytic activity for CO oxidation over sub-nano-Au clusters.

Abstract

Gold (Au) nanocatalysts present outstanding activity for many reactions and have long attracted much attention, but the size effect of sub-nano-clusters on catalytic activity lacks systematic research. Using CO oxidation as a probe reaction, the size-dependent catalytic capability of sub-nano-Au clusters was explored. The global-minimum (GM) structures of AuN (N = 2-300, <2.5 nm) were obtained utilizing revised particle swarm optimization (RPSO) combined with density functional theory (DFT) calculations and the Gupta empirical potential. Geometric structural descriptors built a bridge among geometric features, adsorption energy, and the CO oxidation rate of each site of any given sub-nano-Au clusters, making it possible for high-throughput evaluation of the adsorption energy and catalytic activity of the whole sub-nano-Au cluster. The activity per unit mass of sub-nano-Au clusters shows a volcano-shaped relationship with the cluster size, where the sub-nano-Au clusters with a 0.75 nm diameter possess the highest CO2 formation rate per unit mass. The Edge and Kink sites have a higher turnover frequency (approximately 106) than the Face sites (approximately 102), which contribute the most to CO2 formation. The weak adsorption of CO and O2 was found to be a crucial factor determining the inferior activity of the Face site to the Kink and Edge sites. The adsorption process rather than the surface reaction step becomes the rate-determining step on the Face site, attributed to the decreased activity per unit mass of sub-nano-Au clusters. This work provides an in-depth mechanistic understanding of size-dependent catalytic activity for Au clusters at the sub-nano level.