Coverage-dependent activation of CO over Ni/Cu(100) single atom alloys (SAAs)

Single atom alloys (SAAs) often bring new chemistry in heterogeneous catalysis and well-defined structure for the study of structure-activity relationship (SAR). However, the existing pressure gap causes the reported SARs quite divergent. Herein, we have studied CO activation over Ni/Cu(100) SAAs in ultrahigh vacuum (UHV) and millibar range. While the Ni SAAs formed on Cu(100) significantly enhance the CO adsorption strength under UHV conditions, the CO treatment at elevated pressure leads to notable surface carbon and oxygen deposition through surface reaction. Density functional theory calculations revealed that either dissociation or disproportionation is thermodynamically forbidden for the coverage of CO less than 5/16 ML. However, these two reaction pathways can be opened at higher CO coverages due to the elevated energy state involving repulsion between adsorbed CO. This work uncovers the initial activation process of CO and demonstrates one typical cause for the pressure gap in surface science study as well.