Closing Electron Transfer Loop to Boost Electrocatalytic Urea Synthesis

R Ruping Miao (State Key Laboratory of Chemo and Biosensing College of Chemistry and Chemical Engineering International Joint Laboratory of Energy Electrochemistry Hunan University Changsha China) X Xupeng Qin (National Synchrotron Radiation Laboratory) Y Yujie Wang (Shenyang National Laboratory for Materials Science, Institute of Metal Research) S Siqing Wang (State Key Laboratory of Herbage Improvement and Grassland Agro-ecosystems, College of Ecology, Lanzhou University) K Kaizhi Gu (Institute for Advanced Study) Y Yangyang Zhou (State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Advanced Catalytic Engineering Research Center of the Ministry of Education) D Dawei Chen (State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Advanced Catalytic Engineering Research Center of the Ministry of Education) D Dafeng Yan (Hubei Key Laboratory for Precision Synthesis of Small Molecule Pharmaceuticals & Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, College of Chemistry and Chemical Engineering) W Wenqi Gao (State Key Laboratory of Chemo and Biosensing College of Chemistry and Chemical Engineering International Joint Lab of Energy Electrochemistry of the Ministry of Education Hunan University Changsha China) Q Qinghua Liu (National Synchrotron Radiation Laboratory) C Chen Chen S Shuangyin Wang (State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering)

Abstract

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.

Article Details

Volume / Issue Vol. 64, Issue 50
Published December 08, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

R

Ruping Miao

State Key Laboratory of Chemo and Biosensing College of Chemistry and Chemical Engineering International Joint Laboratory of Energy Electrochemistry Hunan University Changsha China

X

Xupeng Qin

National Synchrotron Radiation Laboratory

Y

Yujie Wang

Shenyang National Laboratory for Materials Science, Institute of Metal Research

S

Siqing Wang

State Key Laboratory of Herbage Improvement and Grassland Agro-ecosystems, College of Ecology, Lanzhou University

K

Kaizhi Gu

Institute for Advanced Study

Y

Yangyang Zhou

State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Advanced Catalytic Engineering Research Center of the Ministry of Education

D

Dawei Chen

State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Advanced Catalytic Engineering Research Center of the Ministry of Education

D

Dafeng Yan

Hubei Key Laboratory for Precision Synthesis of Small Molecule Pharmaceuticals & Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, College of Chemistry and Chemical Engineering

W

Wenqi Gao

State Key Laboratory of Chemo and Biosensing College of Chemistry and Chemical Engineering International Joint Lab of Energy Electrochemistry of the Ministry of Education Hunan University Changsha China

Q

Qinghua Liu

National Synchrotron Radiation Laboratory

C

Chen Chen

S

Shuangyin Wang

State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering