Mechanistic insights into the oxidation of catalytically relevant AgCu near‐surface alloy interfaces

Abstract

AbstractRecent heterogeneous catalysis studies have demonstrated that synergy between Ag and Cu can lead to more selective partial oxidation chemistries. We performed a series of scanning tunneling microscope experiments to gain a better understanding of the AgCu system under oxidative conditions. These experiments were carried out by exposing sub‐monolayer coverages of Ag on Cu(111), in the form of a near‐surface alloy (NSA), to range of oxygen exposures and temperatures. This enabled us to study the initial stages of oxidation of well‐defined Ag/Cu interfaces with atomic resolution and thereby understand the dynamic response of the AgCu NSA to oxygen environments. At low oxygen exposures, oxidation was observed on exposed Cu terraces and at the interface between the AgCu NSA and Cu(111). Higher oxygen exposure led to the segregation of Cu atoms up through the Ag layer and the appearance of surface adsorbed oxygen. Significant phase segregation of Cu was then observed at higher oxygen exposures at elevated temperatures, evidenced by the formation of Cu oxide patches within and on the top of the Ag layer. These results provide a more detailed picture of how AgCu NSAs interact with, and restructure in response to, oxygen.