Mechanistic study of the competition between carbon dioxide reduction and hydrogen evolution reaction and selectivity tuning via loading single-atom catalysts on graphitic carbon nitride

Abstract

In the context of catalytic CO₂ reduction (CO₂RR), the interference of the inherent hydrogen evolution reaction (HER) and the possible selectivity towards CO have posed a significant challenge to the generation of formic acid. To address this hurdle, in this work, we have investigated the impact of different single-atom metal catalysts on tuning selectivity by employing density functional theory (DFT) calculations to scrutinize the reaction pathways. Single-atom catalysts supported on carbon-based systems have proven to be pivotal in altering both the activity and selectivity of the CO₂RR. In this study, a series of single-atom-metal-loaded g-C₃N₄ monolayers (MCN, M = Ni, Cu, Zn, Ga, Cd, In, Sn, Pb, Ag, Au, Bi, Pd and Pt) were systematically examined. Through detailed DFT calculations, we explored their influence on reaction selectivity between the *COOH and *OCHO intermediates. Notably, NiCN favors the reaction via the *OCHO route, with a significantly lower rate-determining potential of 0.36 eV, which is approximately 73.5% lower than that of the CN system (1.36 eV). Most importantly, the Ni single-atom catalyst with lower coordination significantly enhances CO₂ adsorption, promoting CO₂RR over HER. Overall, this study, guided by DFT calculations, provides a theoretical prediction of how the selection of single-atom metal catalysts can effectively modulate the reaction pathway, thereby offering a potential solution for achieving high product selectivity in CO₂RR.