4.8 Article

Etching-directed nitrogen doping strategy to construct efficient defective sites in carbon for electrocatalytic oxygen reduction

期刊

JOURNAL OF POWER SOURCES
卷 549, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jpowsour.2022.232122

关键词

Coupling sites; Active sites; Metal-free carbon; Electrocatalysis; ORR catalysts

资金

  1. National Natural Science Foundation of China
  2. Natural Science Foundation of Hunan Province
  3. Hunan Provincial Science and Technology Plan Project
  4. Postgraduate Scientific Research Innovation Project of Hunan Province
  5. [51972345]
  6. [22278444]
  7. [2021JJ30790]
  8. [2018RS3008]
  9. [2021zzts0065]

向作者/读者索取更多资源

The construction of synergistic coupling sites of intrinsic carbon defects and N dopants is crucial for enhancing the catalytic activities of metal-free carbon-based materials in the oxygen reduction reaction. Researchers have developed an etching-directed nitrogen doping strategy to construct carbon defect/N dopant coupling sites, where nitrogen is doped directionally at the freshly created intrinsic carbon defects during the synthesis of N-doped carbon. The resulting N-doped carbon catalyst with such coupling sites exhibits remarkable ORR catalytic activity and excellent long-term durability.
Construction of synergistic coupling sites of intrinsic carbon defects and N dopants in N-doped carbon is of great significance to improve the catalytic activities of metal-free carbon-based materials toward oxygen reduction reaction (ORR). However, the carbon-defect construction and N doping by existing strategies are usually inde-pendent processes, resulting in a random arrangement of the intrinsic carbon defects and N-dopants (i.e., hardly forming the coupling sites) in the resultant carbon materials. Herein, an etching-directed nitrogen doping strategy for constructing carbon defect/N dopant coupling sites is developed, in which nitrogen is directionally doped at the freshly created intrinsic carbon defects during the synthesis of N-doped carbon. The as-prepared N -doped carbon catalyst enriched with such coupling sites renders a remarkable ORR catalytic activity with an ORR half-wave potential of 0.891 V vs. RHE and an excellent long-term durability (3% current loss after 15,000 s at 0.6 V vs. RHE). Experimental characterizations and theoretical calculations reveal the formation mechanism of the coupling sites as well as the origin of their high catalytic activities toward ORR. This etching-directed ni-trogen doping strategy shows great universality for the controllable construction of active sites in carbon-based materials derived from different precursors for electrochemical energy storage and conversion applications.

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