4.8 Review

From Solar Energy to Fuels: Recent Advances in Light-Driven C1 Chemistry

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 49, 页码 17528-17551

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201814313

关键词

C-1 chemistry; CO2 hydrogenation; Fischer-Tropsch synthesis; photocatalysis; solar fuels

资金

  1. National Key Projects for Fundamental Research and Development of China [2018YFB1502002, 2016YFB0600901, 2017YFA0206904, 2017YFA0206900]
  2. National Natural Science Foundation of China [51825205, U1662118, 51772305, 51572270, 21871279, 21802154]
  3. Beijing Natural Science Foundation [2191002, 2194089, 2182078]
  4. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB17000000]
  5. Beijing Municipal Science and Technology Project [Z181100005118007]
  6. Royal Society-Newton Advanced Fellowship [NA170422]
  7. K. C. Wong Education Foundation
  8. International Partnership Program of Chinese Academy of Sciences [GJHZ1819, GJHZ201974]
  9. China Scholarship Council
  10. University of Auckland Faculty Research Development Fund
  11. Energy Education Trust of New Zealand
  12. MacDiarmid Institute for Advanced Materials and Nanotechnology

向作者/读者索取更多资源

Catalytic C-1 chemistry based on the activation/conversion of synthesis gas (CO+H-2), methane, carbon dioxide, and methanol offers great potential for the sustainable development of hydrocarbon fuels to replace oil, coal, and natural gas. Traditional thermal catalytic processes used for C-1 transformations require high temperatures and pressures, thereby carrying a significant carbon footprint. In comparison, solar-driven C-1 catalysis offers a greener and more sustainable pathway for manufacturing fuels and other commodity chemicals, although conversion efficiencies are currently too low to justify industry investment. In this Review, we highlight recent advances and milestones in light-driven C-1 chemistry, including solar Fischer-Tropsch synthesis, the water-gas-shift reaction, CO2 hydrogenation, as well as methane and methanol conversion reactions. Particular emphasis is placed on the rational design of catalysts, structure-reactivity relationships, as well as reaction mechanisms. Strategies for scaling up solar-driven C-1 processes are also discussed.

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