4.0 Review

Heterogeneous Catalysis for CO2 Conversion into Chemicals and Fuels

Journal

TRANSACTIONS OF TIANJIN UNIVERSITY
Volume 28, Issue 4, Pages 245-264

Publisher

SPRINGERNATURE
DOI: 10.1007/s12209-022-00326-x

Keywords

CO2 conversion; CO2 hydrogenation; CO2 electroreduction; Chemicals; Fuels

Funding

  1. National Key R&D Program of China [2021YFA1501503]
  2. National Natural Science Foundation of China [22002155, 22125205, 92045302]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB17020200]
  4. CAS Youth Innovation Promotion [Y201938]
  5. Natural Science Foundation of Liaoning Province [2021-MS-022]
  6. High-Level Talents Innovation Project of Dalian City [2020RQ038]

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Catalytic conversion of CO2 into chemicals and fuels is a method to reduce carbon emissions and achieve carbon neutrality. This review summarizes the recent progress in this field and highlights studies on different conversion routes. The structure-performance correlations of catalytic materials have been revealed through spectroscopy and density functional theory calculations. Improving catalytic selectivity and stability is necessary in the future.
Catalytic conversion of CO2 into chemicals and fuels is a viable method to reduce carbon emissions and achieve carbon neutrality. Through thermal catalysis, electrocatalysis, and photo(electro)catalysis, CO2 can be converted into a wide range of valuable products, including CO, formic acid, methanol, methane, ethanol, acetic acid, propanol, light olefins, aromatics, and gasoline, as well as fine chemicals. In this mini-review, we summarize the recent progress in heterogeneous catalysis for CO2 conversion into chemicals and fuels and highlight some representative studies of different conversion routes. The structure-performance correlations of typical catalytic materials used for the CO2 conversion reactions have been revealed by combining advanced in situ/operando spectroscopy and microscopy characterizations and density functional theory calculations. Catalytic selectivity toward a single CO2 reduction product/fraction should be further improved at an industrially relevant CO2 conversion rate with considerable stability in the future.(GRAPHICS)

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