Oxidation reactions on neutral cobalt oxideclusters: experimental and theoretical studies

Abstract

Reactions of neutral cobalt oxide clusters (Co(m)O(n), m = 3-9, n = 3-13) with CO, NO, C(2)H(2), and C(2)H(4) in a fast flow reactor are investigated by time of flight mass spectrometry employing 118 nm (10.5 eV) single photon ionization. Strong cluster size dependent behavior is observed for all the oxidation reactions; the Co(3)O(4) cluster has the highest reactivity for reactions with CO and NO. Cluster reactivity is also highly correlated with either one or more following factors: cluster size, Co(iii) concentration, the number of the cobalt atoms with high oxidation states, and the presence of an oxygen molecular moiety (an O-O bond) in the Co(m)O(n) clusters. The experimental cluster observations are in good agreement with condensed phase Co(3)O(4) behavior. Density functional theory calculations at the BPW91/TZVP level are carried out to explore the geometric and electronic structures of the Co(3)O(4) cluster, reaction intermediates, transition states, as well as reaction mechanisms. CO, NO, C(2)H(2), and C(2)H(4) are predicted to be adsorbed on the Co(ii) site, and react with one of the parallel bridge oxygen atoms between two Co(iii) atoms in the Co(3)O(4) cluster. Oxidation reactions with CO, NO, and C(2)H(2) on the Co(3)O(4) cluster are estimated as thermodynamically favorable and overall barrierless processes at room temperature. The oxidation reaction with C(2)H(4) is predicted to have a very small overall barrier (<0.23 eV). The oxygen bridge between two Co(iii) sites in the Co(3)O(4) cluster is responsible for the oxidation reactions with CO, NO, C(2)H(2), and C(2)H(4). Based on the gas phase experimental and theoretical cluster studies, a catalytic cycle for these oxidation reactions on a condensed phase cobalt oxide catalyst is proposed.