4.8 Review

Carbon-Based Materials for Electrochemical Reduction of CO2 to C2+ Oxygenates: Recent Progress and Remaining Challenges

Journal

ACS CATALYSIS
Volume 11, Issue 4, Pages 2076-2097

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c04714

Keywords

carbon dioxide; electrochemical reduction; C-C coupling; C2+ oxygenates; carbon-based materials

Funding

  1. National Natural Science Foundation of China [21936002]
  2. China Postdoctoral Science Foundation [2020M670757]
  3. Liaoning Revitalization Talents Program [XLYC1801003]
  4. Fundamental Research Funds for the Central Universities [DUT20TD205]

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This review summarizes recent progress in the formation of C2+ oxygenates from CO2 reduction on carbon-based materials, highlighting strategies for achieving C-C coupling, the relationship between intermediate adsorption energy and selectivity of oxygenate production, and mechanisms of C2+ oxygenate generation and active site fabrication on carbon-based materials. Challenges and opportunities for electrochemical conversion of CO2 into C2+ oxygenates were discussed.
Electrochemical reduction of CO2 to multicarbon (C2+) products is desirable because of the higher energy density and economic value of C2+ products and the significant scientific issue for coupling of multicarbons. However, efficient conversion of CO2 into C2+ products remains challenging because of the difficulty in C-C coupling. Recently, numerous papers have reported carbon-based materials for C2+ products production from CO2 electrochemical reduction. Because of the unique properties of carbon-based materials in C2+ production, carbon-based materials can be used as a potential alternative for the electrocatalytic conversion of CO2. This Review summarized recent progresses in the formation of C2+ oxygenates from CO2 reduction on carbon-based materials. In this Review, we highlighted the strategies available for achieving C-C coupling on carbon-based electrocatalysts and revealed the relationships between intermediate adsorption energy and the selectivity of oxygenate production from CO2 reduction. Moreover, we provided the understandings for fabricating active sites of CO2 reduction on carbon-based materials and related mechanisms of C2+ oxygenate generation. The remaining challenges and opportunities for the electrochemical conversion of CO2 into C2+ oxygenates were discussed.

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