Oxidation of CO and NO on Composition-Selected Cerium Oxide Cluster Cations

Abstract

The collisional reactions of composition-selected cerium oxide cluster cations, CenOm(+) (n = 2-6; m ≤ 2n), with CO and NO have been investigated under single collision conditions using a tandem mass spectrometer. At near-thermal energy, oxidation of CO and NO is observed only for the stoichiometric clusters, CenO2n(+) (n = 3-5), and the cross sections for the NO oxidation are found to be larger than those for the CO oxidation. In addition, the collision-energy dependence of the reaction cross sections reveals that the CO oxidation has a small activation barrier, whereas the NO oxidation is a barrierless process. These experimental findings are supported by density functional theory calculations.