Mechanistic Insights into the Unique Role of Copper in CO2 Electroreduction Reactions

Abstract

Cu demonstrates a unique capability towards CO₂ electroreduction that can close the anthropogenic carbon cycle; however, its reaction mechanism remains elusive, owing to the obscurity of the solid-liquid interface on Cu surfaces where electrochemical reactions occur. Using a genetic algorithm method in addition to density functional theory, we explicitly identify the configuration of a water bilayer on Cu(2 1 1) and build electrochemical models. These enable us to reveal a mechanistic picture for CO₂ electroreduction, finding the key intermediates CCO* for the C₂ H₄ pathway and CH* for the CH₄ pathway, which rationalize a series of experimental observations. Furthermore, we find that the interplay between the Cu surfaces, carbon monomers, and water network (but not the binding of CO*) essentially determine the unique capability of Cu towards CO₂ electroreduction, proposing a new and effective descriptor for exploiting optimal catalysts.

Keywords: carbon dioxide; density functional theory; electroreduction; intermediates; solid-liquid interface.