Atomic nickel cluster decorated defect-rich copper for enhanced C2 product selectivity in electrocatalytic CO2 reduction

This work describes a coordination enabled galvanic replacement method to decorate atomic Ni clusters on defect-rich Cu surface to provide the first Ni/Cu bimetallic system that significantly enhances the production of C2 products from electrocatalytic CO2 reduction. Specifically, with a surface Ni/Cu ratio of 0.82 %, a 7-fold increase in the selectivity for C2 products was found in comparison with pristine Cu. Density functional theory calculations reveal that the rate determining step for *CO formation changes from the formation of *COOH on copper to the chemisorption of CO2 on Ni decorated surfaces. An alteration of binding sites from Ni-Ni bridge for *CO2 and *COOH to Ni-Cu bridge for *CO is discovered and is proposed to favor the key C-C coupling step. The catalytic mechanism demonstrated in the Cu-Ni system points to the new directions for the development of advanced bimetallic electrocatalysts for producing multi-carbon materials from CO2 reduction.

Automated summary

This work introduces a coordination enabled galvanic replacement method to decorate atomic Ni clusters on defect-rich Cu surface, resulting in significant enhancement of C2 products production in electrocatalytic CO2 reduction. With a surface Ni/Cu ratio of 0.82 %, a 7-fold increase in selectivity for C2 products was observed compared to pristine Cu, attributed to the chemisorption of CO2 on Ni decorated surfaces changing the rate determining step for *CO formation. The catalytic mechanism demonstrated in the Cu-Ni system points to new directions for the development of advanced bimetallic electrocatalysts for producing multi-carbon materials from CO2 reduction.