Siyi Xu, Chao Miao, Jingui Zheng, Xun Pan, Ruochen Yang, Lina Li, Yi Zhou, Guohua Zhao
ABSTRACT Electrocatalytic CO 2 coupling with nitrate to synthesize acetamide provides a promising way for the co‐valorization of greenhouse gas and environmental pollutants. Aiming at generating acetamide via C─C─N bonding, a N‐coordinated copper‐cobalt diatomic catalytic sites is constructed to achieve CO 2 reduction to ketene intermediate and NO 3 − to ammonia, thereby facilitating the nucleophilic attack of *NH 2 on *CH 2 CO to form acetamide. Based on the enhanced mass transfer of CO 2 in flow cell, an acetamide yield of 67.7 mg L −1 and a FE of 15.1% are achieved over CuCo diatomic sites. In situ FT‐IR, Raman spectroscopy, in situ XAFS combined with DFT suggest that CuCo diatomic pairs induce CO 2 and NO 3 − to stabilize on the catalytic surface via a favorable bridge adsorption configuration. And the electronic structure optimization promoted by interatomic electron interactions reduces the energy barriers for C─C and C─N bonding. This work achieves C─C─N bonding with ordered C─C and C─N coupling via diatomic sites, providing a novel strategy for the sustainable synthesis of acetamide.