{"title":"Closing Electron Transfer Loop to Boost Electrocatalytic Urea Synthesis.","authors":"Ruping Miao,Xupeng Qin,Yujie Wang,Siqing Wang,Kaizhi Gu,Yangyang Zhou,Dawei Chen,Dafeng Yan,Wenqi Gao,Qinghua Liu,Chen Chen,Shuangyin Wang","doi":"10.1002/anie.202517450","DOIUrl":null,"url":null,"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 (C60) as a redox-active electron mediator during the electrochemical reduction process, we effectively inhibit the irreversible reduction deactivation of positively charged copper (Cuδ+) active sites. The electron-accepting fullerene form ions (C60 n-) that engage in a spontaneous chemical redox reaction with nitrate ions, producing nitrite ions and regenerating neutral C60 (C60 n- + NO3 - → C60 + NO2 -). 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.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"28 1","pages":"e202517450"},"PeriodicalIF":16.9000,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202517450","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
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 (C60) as a redox-active electron mediator during the electrochemical reduction process, we effectively inhibit the irreversible reduction deactivation of positively charged copper (Cuδ+) active sites. The electron-accepting fullerene form ions (C60 n-) that engage in a spontaneous chemical redox reaction with nitrate ions, producing nitrite ions and regenerating neutral C60 (C60 n- + NO3 - → C60 + NO2 -). 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.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.