4.6 Article Proceedings Paper

A CO2 adsorption dominated carbon defect-based electrocatalyst for efficient carbon dioxide reduction

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 8, Issue 3, Pages 1205-1211

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ta11473d

Keywords

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Funding

  1. National MCF Energy RD Program [2018YFE0306105]
  2. National Natural Science Foundation of China [51725204, 51972216, 21471106, 21771132, 21571139, 21871209]
  3. Collaborative Innovation Center of Suzhou Nano Science Technology
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  5. Key-Area Research and Development Program of Guangdong Province [2019B010933001]
  6. 111 Project
  7. Natural Science Foundation of Tianjin [17JCQNJC05900]
  8. Natural Science Foundation of Jiangsu Province [BK20190041, BK20190828]
  9. Special Program of Talents Development for Excellent Youth Scholars in Tianjin [TJTZJH-QNBJRC-2-3]

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Controlling interface gas adsorption properties of carbon materials is a prerequisite for exploiting efficient metal-free electrocatalysts but it is usually ignored. Herein, we fabricate a hierarchical porous carbon electrocatalyst with defect (DHPC) by carbon thermal reaction, which shows good CO2RR selectivity and stability. The experimental results indicated that the carbon defect might be the active center for efficient CO2RR performance because it can serve as a Lewis base center and provide an appropriate CO2-chemisorption energy. Moreover, X-ray absorption spectroscopy (XAS) results demonstrated that the carbon defect can induce a reversible carbon-carbon interface with CO2 gas molecule, which would be further strengthened under an applied bias. Besides, the (CO2)-C-13 isotope labelling experiment and density functional theory calculations further confirmed that the high CO2RR performance of DHPC comes from its intrinsic defect sites. This study not only provides a new avenue and concept to design CO2RR electrocatalysts but also, to some extent, indicates a possible catalytic mechanism for carbon defect-based electrocatalysts.

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