Advances in Catalysts for Urea Electrosynthesis Utilizing CO2 and Nitrogenous Materials: A Mechanistic Perspective

Author:

Zhang Mengfei1,Feng Tianjian1,Che Xuanming1,Wang Yuhan1,Wang Pengxian1ORCID,Chai Mao2,Yuan Menglei3ORCID

Affiliation:

1. Queen Mary University of London Engineering School, Northwestern Polytechnical University, Xi’an 710129, China

2. Guoneng Shanxi Hequ Power Generation Co., Ltd., Xinzhou 036500, China

3. State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi’an 710072, China

Abstract

Electrocatalytic urea synthesis from CO2 and nitrogenous substances represents an essential advance for the chemical industry, enabling the efficient utilization of resources and promoting sustainable development. However, the development of electrocatalytic urea synthesis has been severely limited by weak chemisorption, poor activation and difficulties in C–N coupling reactions. In this review, catalysts and corresponding reaction mechanisms in the emerging fields of bimetallic catalysts, MXenes, frustrated Lewis acid–base pairs and heterostructures are summarized in terms of the two central mechanisms of molecule–catalyst interactions as well as chemical bond cleavage and directional coupling, which provide new perspectives for improving the efficiency of electrocatalytic synthesis of urea. This review provides valuable insights to elucidate potential electrocatalytic mechanisms.

Funder

Qin Chuangyuan Cites High-level Innovation and Entrepreneurship Talent Programs

Fundamental Research Funds for the Central Universities

Anhui Province International Research Center on Advanced Building Materials

Publisher

MDPI AG

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