4.4 Article

A Nitrogen, Sulfur co-Doped Porphyrin-based Covalent Organic Framework as an Efficient Catalyst for Oxygen Reduction

Journal

CHEMICAL RESEARCH IN CHINESE UNIVERSITIES
Volume 38, Issue 1, Pages 167-172

Publisher

HIGHER EDUCATION PRESS
DOI: 10.1007/s40242-021-1374-1

Keywords

Covalent organic framework(COF); Oxygen reduction reaction; co-Doped material

Funding

  1. National Natural Science Foundation of China [22025504, 21621001, 21390394]
  2. 111 Project of China [BP0719036, B17020]
  3. China Postdoctoral Science Foundation [2020TQ0118, 2020M681034]
  4. Program for JLU Science and Technology Innovative Research Team, China

Ask authors/readers for more resources

ORR is crucial for energy conversion systems, and the development of cheap, durable and highly-active catalysts is urgently needed. This study introduces a metal-free nitrogen and sulfur co-doped porphyrin-based COF as an efficient ORR catalyst, showcasing improved activity and synergistic effects compared to single-atom doping. Reasonable design of stable metal-free COFs with high electrochemical activity can promote their wide applications.
Oxygen reduction reaction(ORR) is a significant reaction for energy conversion systems(such as fuel cells, metal-air batteries, etc.). It is an urgent need to develop cheap, durable and highly-active catalysts for efficient ORR. Hence, we report a metal-free nitrogen and sulfur co-doped porphyrin-based covalent organic framework(COF) as a high-efficiency ORR catalyst[the onset potential(E-o) is 0.79 V and the half-wave potential(E-1/2) is 0.70 V]. The double doping of N and S atoms causes uneven charge distribution around carbon atoms, which can act as catalytic active centers, improving ORR activity. Compared with single-atom doping, double atoms doping exhibits a higher activity due to the synergistic effect between different elements. These results demonstrate that reasonable design of stable metal-free COFs with a high electrochemical activity can promote their wide applications.

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