Lattice oxygen self-spillover on reducible oxide supported metal cluster: the water–gas shift reaction on Cu/CeO<sub>2</sub> catalyst
Yaqiong Su, Guang‐Jie Xia, Yanyang Qin, Shujiang Ding, Yang‐Gang Wang
Abstract
molecular dynamics simulations, we have identified an unprecedented spillover of the surface lattice oxygen from the ceria support to the Cu cluster, which is rarely considered previously but may widely exist in oxide supported metal catalysts under realistic conditions. The oxygen spillover causes a highly energetic preference of the monolayered configuration of the supported Cu nanocluster, compared to multilayered configurations. Due to the strong metal-oxide interaction, after the O spillover the monolayered cluster is highly oxidized by transferring electrons to the Ce 4f orbitals. The water-gas-shift reaction is further found to more favorably take place on the supported copper monolayer than the copper-ceria periphery, where the on-site oxygen and the adjacent oxidized Cu sites account for the catalytically active sites, synergistically facilitating the water dissociation and the carboxyl formation. The present work provides mechanistic insights into the strong metal-support interaction and its role in catalytic reactions, which may pave a way towards the rational design of metal-oxide catalysts with promising stability, dispersion and catalytic activity.