A density functional theory study of NO reduction promoted by Au4+ and Au4

摘要

Density functional theory (DFT) is used to study the NO reduction by H2 on Au4+ and Au4 clusters. The reaction mechanism is explored along two possible entrances: one involves the complexes of the clusters with H2 and the other is related to the complexes of the clusters with NO. In all cases, it is found that the catalytic cycle involves two sequential elementary steps: the rupture of the H-H bond in H2 and the formation of H2O and N2O molecule. The calculated results show that the reaction mediated by Au4+ is energetically most favorable compared to that promoted by Au4, indicating that the charge state of Au clusters plays an essential role for the catalyzed NO reduction. The present theoretical study rationalizes the early experimental findings well and enriches our understanding of the catalytic NO reduction by Au-based catalysts.