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Electrochemical Reduction of CO2 to CO over Transition Metal/N-Doped Carbon Catalysts: The Active Sites and Reaction Mechanism

  • Shuyu Liang
  • , Liang Huang
  • , Yanshan Gao
  • , Qiang Wang*
  • , Bin Liu*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

184 Downloads (CityUHK Scholars)

Abstract

Electrochemical CO2 reduction to value-added chemicals/fuels provides a promising way to mitigate CO2 emission and alleviate energy shortage. CO2-to-CO conversion involves only two-electron/proton transfer and thus is kinetically fast. Among the various developed CO2-to-CO reduction electrocatalysts, transition metal/N-doped carbon (M-N-C) catalysts are attractive due to their low cost and high activity. In this work, recent progress on the development of M-N-C catalysts for electrochemical CO2-to-CO conversion is reviewed in detail. The regulation of the active sites in M-N-C catalysts and their related adjustable electrocatalytic CO2 reduction performance is discussed. A visual performance comparison of M-N-C catalysts for CO2 reduction reaction (CO2RR) reported over the recent years is given, which suggests that Ni and Fe-N-C catalysts are the most promising candidates for large-scale reduction of CO2 to produce CO. Finally, outlooks and challenges are proposed for future research of CO2-to-CO conversion. © 2021 The Authors. Advanced Science published by Wiley-VCH GmbH
Original languageEnglish
Article number2102886
JournalAdvanced Science
Volume8
Issue number24
Online published31 Oct 2021
DOIs
Publication statusPublished - 22 Dec 2021
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 13 - Climate Action
    SDG 13 Climate Action

Research Keywords

  • carbon monoxide
  • carbon-based materials
  • CO2 reduction
  • single-atom catalysts

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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