期刊
JOURNAL OF ENERGY CHEMISTRY
卷 56, 期 -, 页码 470-485出版社
ELSEVIER
DOI: 10.1016/j.jechem.2020.08.030
关键词
Electrocatalysis; Oxygen reduction reaction; Metal-nitrogen/carbon; Fuel cell
资金
- National Natural Science Foundation of China [21421001, 21573115, 21875118]
- Natural Science Foundation of Tianjin [19JCZDJC37700]
The importance of accelerating the sluggish oxygen reduction reaction (ORR) process at the cathode with earth-abundant metal-based catalysts for the commercialization of low-temperature polymer electrolyte membrane fuel cells is discussed. Transition metal-nitrogen-carbon (M-N/C) catalysts are considered as the most promising non-precious metal catalysts for ORR, due to their high catalytic activity, long-term stability, and low cost. Different M-N/C catalysts classified by precursors and strategies for design and optimization are highlighted, along with the challenges and possible opportunities for future development of high-performance ORR catalysts.
It is of vital importance to accelerate the sluggish oxygen reduction reaction (ORR) process at the cathode with earth-abundant metal-based catalysts for the commercialization of low-temperature polymer electrolyte membrane fuel cells. In consideration of high catalytic activity, long-term stability and low cost of potential ORR electrocatalysts, transition metal species have attracted much interest and transition metal-nitrogen-carbon (M-N/C, M = Fe, Co, Ni, Mn, etc.) catalysts have been widely considered as the most promising non-precious metal catalysts for ORR. Herein, the fundamental understanding of ORR catalytic mechanism and the identification of active centers are briefly introduced, and then different M-N/C catalysts classified by precursors with the strategies for design and optimization are highlighted. The challenges and possible opportunity for future development of high-performance ORR catalysts are finally proposed. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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