Ruping Miao, Xupeng Qin, Yujie Wang, Siqing Wang, Siqing Wang, Kaizhi Gu, Yangyang Zhou, Dawei Chen, Dafeng Yan, Wenqi Gao, Qinghua Liu, Chen Chen, Shuangyin Wang, Shuangyin Wang
Abstract The electrocatalytic C─N coupling of carbon dioxide and nitrate presents a promising approach for environmentally friendly urea synthesis. In this work, we propose a strategy to boost efficient and durable urea synthesis by coupling the electrochemical and chemical steps. Utilizing fullerene (C 60 ) as a redox‐active electron mediator during the electrochemical reduction process, we effectively inhibit the irreversible reduction deactivation of positively charged copper (Cu δ+ ) active sites. The electron‐accepting fullerene form ions (C 60 n– ) that engage in a spontaneous chemical redox reaction with nitrate ions, producing nitrite ions and regenerating neutral C 60 (C 60 n– + NO 3 – → C 60 + NO 2 – ). This recycling mechanism closes the electron transfer loop while optimizing the overall reaction pathway. The urea yield rate is dramatically increased to 385.9 mmol h −1 g −1 , accompanied by long‐term durability. Our findings provide a valuable framework for designing highly efficient electrocatalyst for coupling reactions, advancing the field of sustainable urea synthesis.