Understanding Electrochemical CO 2 Reduction Selectivity of Cu Binary Alloys from Electronic Structure Descriptors

We investigate the electrochemical reduction of carbon dioxide (CO 2 RR) using Cu-M (M = Ni, Pd, Ag, Au, Zn, Cr) binary alloys. Through experimental and theoretical analysis, we explore the structural and electronic properties of these alloys and their impact on CO 2 RR product selectivity. Our findings reveal that the d-band center of Cu-M alloys serves as a crucial descriptor, influencing product distribution. As the d-band center increases, more CO is produced, while the formation of C 2 products (ethylene and ethanol) follows a volcano-like trend. We also observe a linear scaling relationship between the d-band center and ethylene/ethanol selectivity, providing opportunities for fine-tuning product selectivity. The observation is explained by theoretical calculations that suggest that the d-band center effectively changes the relative binding of *CCH vs *CHCHOH, thereby controlling product selectivity into ethylene vs ethanol formation. We also find that this d-band center dependence is what makes the *CCH vs *CHCHOH adsorption energy, when properly corrected for alloy composition-dependencies, the most reliable theoretically accessible descriptor for ethylene/ethanol selectivity, while the *O adsorption energy does not show a clear correlation with experimental results. This study enhances our understanding of CO 2 RR catalysis and offers guidelines for designing Cu-based alloy electrocatalysts with improved activity and selectivity for sustainable CO 2 conversion.