4.8 Article

N, P-Codoped Graphene Dots Supported on N-Doped 3D Graphene as Metal-Free Catalysts for Oxygen Reduction

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 26, 页码 30512-30523

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c03141

关键词

graphene dots; 3D graphene; nitrogen-doped; phosphorus-doped; heteroatom doping; oxygen reduction reaction (ORR)

资金

  1. Youth Science and Technology Talent Growth Program of Guizhou Provincial Education Department [Qianjiao-heKY[2021]295]
  2. National Natural Science Foundation of China [22005072, 51971029]
  3. Natural Sciences and Engineering Research Council of Canada (NSERC)
  4. Fonds de la Recherche du Quebec sur la Nature et les Technologies (FRQNT)
  5. Centre Quebecois sur les Materiaux Fonctionnels (CQMF)
  6. Canada Research Chair program
  7. ECS-Toyota Young Investigator Fellowship
  8. CSC scholarship
  9. NSFC-BRICS STI Framework Program [51861145309]
  10. National ST Major Project [2018ZX10301201]

向作者/读者索取更多资源

Nitrogen and phosphorus-codoped graphene dots supported on nitrogen-doped three-dimensional graphene were synthesized by freezing-annealing process, serving as a metal-free catalyst for oxygen reduction reaction. The catalyst exhibited excellent ORR activity, higher tolerance to methanol, and better stability compared to commercial Pt/C, indicating the potential for various applications.
Nitrogen and phosphorus-codoped graphene dots supported on nitrogen-doped three-dimensional graphene (N, P-GDs/N-3DG) have been synthesized by a facile freeze-annealing process. On the surface of the 3D interconnected porous structure, the N, P-GDs are uniformly dispersed. The as-prepared N, P-GDs/N-3DG material served as a metal-free catalyst for oxygen reduction reaction (ORR) in an alkaline medium and evaluated by a rotating ring-disk electrode. The N, P-GDs/N-3DG catalyst exhibits excellent ORR activity, which is comparable to that of the commercial Pt/C catalyst. Furthermore, it exhibits a higher tolerance to methanol and better stability than the Pt/C. This enhanced electrochemical catalytic performance can be ascribed to the presence of abundant functional groups and edge defects. This study indicates that P-N bonded structures play a vital role as the active sites in ORR.

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