Electrochemical conversion of CO2 via C−X bond formation: recent progress and perspective

电化学 透视图(图形) 材料科学 债券 纳米技术 化学 电极 物理化学 计算机科学 业务 财务 人工智能
作者
Shuaiqiang Jia,Mengke Dong,Qinggong Zhu,Xinchen Kang,Haihong Wu,Buxing Han
出处
期刊:Chemical synthesis [OAE Publishing Inc.]
卷期号:4 (4) 被引量:19
标识
DOI:10.20517/cs.2024.32
摘要

With the depletion of traditional energy sources and growing environmental concerns, it is becoming increasingly urgent to develop green, low-emission renewable energy technologies to replace fossil fuel-driven methods that emit carbon dioxide (CO2). Currently, the electrochemical production of high-value-added chemicals and fuels from CO2 has aroused great interest from scientists. However, to make full use of CO2 for the preparation of chemicals, it is necessary to expand the range of electrosynthesis methods, in particular by expanding reaction pathways through the reaction of CO2 with different substrates. In general, CO2 can form new covalent bonds with substrate molecules through the formation of C−X bonds, including C−H, C−C, C−N, C−O, and C−S bonds, which would expand the range of possible products by diversifying the reaction pathway. In this review, we focus on the research progress in electrochemical conversion of CO2 through C−X bond formation. We start by examining fundamentals of the reactions and summarizing the reaction modes. Next, we discuss the electrosynthesis of C−X bonds (C−H, C−C, C−N, C−O, C−S) using CO2 and different substrate molecules. Finally, (i) strategies for the design and activity optimization of catalyst materials and (ii) the future development of forming five types of bonds from CO2 and small molecules are discussed, along with an outlook on their future research prospects.
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