Nonbonding Metal–Metal Interaction in Metal–Nitrogen–Carbon Single-Atom Catalysts Boosts CO Electroreduction

Metal-nitrogen-carbon single-atom catalysts (SACs) have recently emerged as selective electrocatalysts for the reduction of CO₂ to CO, but their ability to further electroreduce CO is poor. Here, based on constant-potential density functional theory simulations, we predict that Co-N-M (M = Fe, Co) SACs with nonbonding metallic centers bridged by a common nitrogen atom can catalyze four-electron reduction of CO to methanol at an ultralow overpotential of 220-310 mV. We show that the metal atoms in the SACs are terminated by H species which prevent the formation of σ bonding between CO and the metal atoms. Thanks to the nonbonding electrostatic repulsion between Co and its adjacent M atom, the Co d_xz band is broadened and shifted toward the Fermi level, leading to enhanced d_xz - 2π* interaction that gives rise to stable CO adsorption and promotes its active and selective reduction. This work offers an alternative strategy to tackle the challenge of CO electroreduction on SACs and highlights the role of nonbonding metal-metal interactions in modulating adsorption properties of SACs.