Electrocatalytic synthesis of C–N coupling compounds from CO2 and nitrogenous species

Author:

Zhang Zheng1ORCID,Li Danyang1,Tu Yunchuan2,Deng Jiao3,Bi Huiting1,Yao Yongchao4,Wang Yan4,Li Tingshuai4,Luo Yongsong5,Sun Shengjun5,Zheng Dongdong5,Carabineiro Sónia A. C.6ORCID,Chen Zhou7,Zhu Junjiang1,Sun Xuping45ORCID

Affiliation:

1. Hubei Key Laboratory of Biomass Fibers and Eco‐Dyeing & Finishing College of Chemistry and Chemical Engineering Wuhan Textile University Wuhan Hubei China

2. School of Chemistry and Chemical Engineering Chongqing University Chongqing China

3. i‐Lab Vacuum Interconnected Nanotech Workstation (Nano‐X) Suzhou Institute of Nano‐Tech and Nano‐Bionics Chinese Academy of Sciences Suzhou Jiangsu China

4. Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of China Chengdu Sichuan China

5. College of Chemistry Chemical Engineering and Materials Science Shandong Normal University Jinan Shandong China

6. LAQV‐REQUIMTE Department of Chemistry NOVA School of Science and Technology Universidade NOVA de Lisboa 2829‐516 Caparica Portugal

7. College of Materials Xiamen University Xiamen Fujian China

Abstract

AbstractThe electrocatalytic synthesis of C–N coupling compounds from CO2 and nitrogenous species not only offers an effective avenue to achieve carbon neutrality and reduce environmental pollution, but also establishes a route to synthesize valuable chemicals, such as urea, amide, and amine. This innovative approach expands the application range and product categories beyond simple carbonaceous species in electrocatalytic CO2 reduction, which is becoming a rapidly advancing field. This review summarizes the research progress in electrocatalytic urea synthesis, using N2, NO2, and NO3 as nitrogenous species, and explores emerging trends in the electrosynthesis of amide and amine from CO2 and nitrogen species. Additionally, the future opportunities in this field are highlighted, including electrosynthesis of amino acids and other compounds containing C–N bonds, anodic C–N coupling reactions beyond water oxidation, and the catalytic mechanism of corresponding reactions. This critical review also captures the insights aimed at accelerating the development of electrochemical C–N coupling reactions, confirming the superiority of this electrochemical method over the traditional techniques.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Wiley

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