Guiding the Catalytic Properties of Copper for Electrochemical CO2 Reduction by Metal Atom Decoration

Tuning bimetallic effects is a promising strategy to guide catalytic properties. However, the nature of these effects can be difficult to assess and compare due to the convolution with other factors such as the catalyst surface structure and morphology and differences in testing environments. Here, we investigate the impact of atomic-scale bimetallic effects on the electrochemical CO2 reduction performance of Cu-based catalysts by leveraging a systematic approach that unifies protocols for materials synthesis and testing and enables accurate comparisons of intrinsic catalytic activity and selectivity. We used the same physical vapor deposition method to epitaxially grow Cu(100) films decorated with a small amount of noble or base metal atoms and a combination of experimental characterization and first-principles calculations to evaluate their physicochemical and catalytic properties. The results indicate that the metal atoms segregate to under-coordinated Cu sites during physical vapor deposition, suppressing CO reduction to oxygenates and hydrocarbons and promoting competing pathways to CO, formate, and hydrogen. Leveraging these insights, we rationalize bimetallic design principles to improve catalytic selectivity for CO2 reduction to CO, formate, oxygenates, or hydrocarbons. Our study provides one of the most extensive studies on Cu bimetallics for CO2 reduction, establishing a systematic approach that is broadly applicable to research in catalyst discovery.

Automated summary

The study investigates the impact of atomic-scale bimetallic effects on the electrochemical CO2 reduction performance of Cu-based catalysts. Utilizing a systematic approach that unifies protocols for materials synthesis and testing, accurate comparisons of intrinsic catalytic activity and selectivity were made. The results show that metal atoms segregate to under-coordinated Cu sites during physical vapor deposition, affecting the formation of oxygenates and hydrocarbons during CO reduction.