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

  • Shuaiqiang Jia
  • , Mengke Dong
  • , Qinggong Zhu*
  • , Xinchen Kang
  • , Haihong Wu*
  • , Buxing Han*
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

17 Scopus citations

Abstract

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.

Original languageEnglish
Article number60
JournalChemical Synthesis
Volume4
Issue number4
DOIs
StatePublished - Dec 2024

Keywords

  • Carbon dioxide
  • C−X bonds
  • electrosynthesis
  • high-value-added chemicals
  • new covalent bonds

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