Single atom alloy clusters Agn-1X- (X = Cu, Au; n=7-20) reacting with O2: Symmetry-adapted orbital model

Single atom alloy AgCu catalysts have attracted great attention, since doping the single Cu atom introduces narrow free-atom-like Cu 3d states in the electronic structure. These peculiar electronic states can reduce the activation energies in some reactions and offer valuable guidelines for improving catalytic performance. However, the geometric tuning effect of single Cu atoms in Ag catalysts and the structure-activity relationship of AgCu catalysts remain unclear. Here, we prepared well-resolved pristine Ag-n(-) as well as single atom alloy Agn-1Cu- and Agn-1Au- (n = 7-20) clusters and investigated their reactivity with O-2. We found that replacing an Ag atom in Ag-n(-) (n = 15-18) with a Cu atom significantly increases the reactivity with O-2, while replacement of an Ag with an Au atom has negligible effects. The adsorption of O-2 on Ag-n(-) or Agn-1Cu- clusters follows the single electron transfer mechanism, in which the cluster activity is dependent on two descriptors, the energy level of alpha-HOMO (strong correlation) and the alpha-HOMO-LUMO gap (weak correlation). Our calculation demonstrated that the cluster arrangements caused by single Cu atom alloying would affect the above activity descriptors and, therefore, regulates clusters' chemical activity. In addition, the observed reactivity of clusters in the representative sizes with n = 17-19 can also be interpreted using the symmetry-adapted orbital model. Our work provides meaningful information to understand the chemical activities of related single-atom-alloy catalysts.

Automated summary

Single atom alloy AgCu catalysts, with narrow free-atom-like Cu 3d states in the electronic structure, have attracted much attention for their potential in reducing activation energies and improving catalytic performance. However, the geometric tuning effect of single Cu atoms in Ag catalysts and the structure-activity relationship of AgCu catalysts still need to be explored.