Closing Electron Transfer Loop to Boost Electrocatalytic Urea Synthesis

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<sub>60</sub>) as a redox-active electron mediator during the electrochemical reduction process, we effectively inhibit the irreversible reduction deactivation of positively charged copper (Cu<sup>δ+</sup>) active sites. The electron-accepting fullerene form ions (C<sub>60</sub> <sup>n-</sup>) that engage in a spontaneous chemical redox reaction with nitrate ions, producing nitrite ions and regenerating neutral C<sub>60</sub> (C<sub>60</sub> <sup>n-</sup> + NO<sub>3</sub> <sup>-</sup> → C<sub>60</sub> + NO<sub>2</sub> <sup>-</sup>). 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<sup>-1</sup> g<sup>-1</sup>, 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.

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Journal
Angewandte Chemie International Edition
Published
2025-10-20
DOI
https://doi.org/10.1002/anie.202517450
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
0.00

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article

Closing Electron Transfer Loop to Boost Electrocatalytic Urea Synthesis

Ruping Miao, Dafeng Yan, Yangyang Zhou, Xupeng Qin et al.
Angewandte Chemie International Edition
Ammonia Synthesis and Nitrogen Reduction
article

Closing Electron Transfer Loop to Boost Electrocatalytic Urea Synthesis

Ruping Miao, Dafeng Yan, Yangyang Zhou, Xupeng Qin, Kaizhi Gu, Dawei Chen, Yujie Wang, Chen Chen, Qinghua Liu, Siqing Wang, Wenqi Gao
article en

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<sub>60</sub>) as a redox-active electron mediator during the electrochemical reduction process, we effectively inhibit the irreversible reduction deactivation of positively charged copper (Cu<sup>δ+</sup>) active sites. The electron-accepting fullerene form ions (C<sub>60</sub> <sup>n-</sup>) that engage in a spontaneous chemical redox reaction with nitrate ions, producing nitrite ions and regenerating neutral C<sub>60</sub> (C<sub>60</sub> <sup>n-</sup> + NO<sub>3</sub> <sup>-</sup> → C<sub>60</sub> + NO<sub>2</sub> <sup>-</sup>). 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<sup>-1</sup> g<sup>-1</sup>, 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.

Angewandte Chemie International EditionVol. 64(50)
University of Science and Technology of China (CN), Central South University (CN), Ministry of Education (SA), Institute for Advanced Study (DE), National Synchrotron Radiation Laboratory (CN), Chemical Synthesis Lab (SG), Hubei University (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Natural Science Foundation of Hubei Province
Openalex Percentile: Top 82%
Ammonia Synthesis and Nitrogen Reduction
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