4.8 Article

Intrinsic Carbon-Defect-Driven Electrocatalytic Reduction of Carbon Dioxide

期刊

ADVANCED MATERIALS
卷 31, 期 19, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201808276

关键词

active sites; carbon-based catalysts; CO2 reduction; electrocatalysis; intrinsic carbon defects

资金

  1. National Key Projects for Fundamental Research and Development of China [2018YFB1502002, 2017YFA0206904, 2017YFA0206900, 2016YFB0600901]
  2. National Natural Science Foundation of China [51825205, 51772305, 51572270, 21871279, U1662118]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB17000000]
  4. Beijing Natural Science Foundation [2191002, 2182078, 2194089]
  5. Beijing Municipal Science and Technology Project [Z181100005118007]
  6. Royal Society-Newton Advanced Fellowship [NA170422]
  7. K.C. Wong Education Foundation
  8. Youth Innovation Promotion Association of the Chinese Academy of Sciences
  9. University of Auckland Faculty Research Development Fund
  10. Energy Education Trust of New Zealand
  11. Ministry of Business Innovation and Employment (MBIE) Catalyst Fund [MAUX1609]
  12. International Partnership Program of Chinese Academy of Sciences [GJHZ1819]

向作者/读者索取更多资源

Heteroatom-doped carbon catalysts are currently attracting enormous attention due to their excellent performance for the electrocatalytic carbon dioxide reduction reaction (ECRR). However, the origin of the high catalytic activities of doped-carbon materials remains obscure with the role of intrinsic carbon defects in promoting the ECRR receiving little attention despite the abundance of carbon defects in all carbon-based catalytic materials. Herein, a positive correlation is reported between the ECRR performance of carbonbased catalysts and the content of intrinsic carbon defects contained within these catalysts. Further, it is demonstrated that defective porous carbon catalysts containing no active heteroatom dopants also show excellent catalytic performance for ECRR. C K-edge near edge X-ray absorption fine structure measurements and density functional theory calculations reveal that sp(2) defects (octagonal and pentagonal) rather than edge defects are key to the excellent ECRR activity of the defective porous carbon catalysts. This work thus makes an important contribution to the understanding of the origin of the ECRR activity of carbon-based catalysts, with heteroatom doping perhaps being less important than previously envisaged for achieving a high ECRR performance.

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