Boosting the Proton‐coupled Electron Transfer via Fe−P Atomic Pair for Enhanced Electrochemical CO₂ Reduction

Abstract

Single-atom catalysts exhibit superior CO₂ -to-CO catalytic activity, but poor kinetics of proton-coupled electron transfer (PCET) steps still limit the overall performance toward the industrial scale. Here, we constructed a Fe-P atom paired catalyst onto nitrogen doped graphitic layer (Fe₁ /PNG) to accelerate PCET step. Fe₁ /PNG delivers an industrial CO current of 1 A with FE_CO over 90 % at 2.5 V in a membrane-electrode assembly, overperforming the CO current of Fe₁ /NG by more than 300 %. We also decrypted the synergistic effects of the P atom in the Fe-P atom pair using operando techniques and density functional theory, revealing that the P atom provides additional adsorption sites for accelerating water dissociation, boosting the hydrogenation of CO₂ , and enhancing the activity of CO₂ reduction. This atom-pair catalytic strategy can modulate multiple reactants and intermediates to break through the inherent limitations of single-atom catalysts.