Nitrogen-coordinated single-atom catalysts with manganese and cobalt sites for acidic oxygen reduction

被引:29
|
作者
Chao, Guojie [1 ]
Zhang, Yizhe [1 ]
Zhang, Longsheng [1 ]
Zong, Wei [2 ]
Zhang, Nan [1 ]
Xue, Tiantian [2 ]
Fan, Wei [2 ]
Liu, Tianxi [1 ]
Xie, Yi [3 ]
机构
[1] Jiangnan Univ, Int Joint Res Lab Nano Energy Composites, Key Lab Synthet & Biol Colloids, Minist Educ,Sch Chem & Mat Engn, Wuxi, Jiangsu, Peoples R China
[2] Donghua Univ, State Key Lab Modificat Chem Fibers & Polymer Mat, Coll Mat Sci & Engn, Shanghai, Peoples R China
[3] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
CATHODE CATALYSTS; MN; ELECTROCATALYSTS; PERFORMANCE; STABILITY; FE; NI; CO;
D O I
10.1039/d1ta08029f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing a low-cost, highly active and durable catalyst for acidic oxygen reduction reaction (ORR) is of significant importance for proton-exchange electrolyte membrane fuel cell. In this work, we report an efficient catalyst based on Mn, Co and N co-doped carbon (MnCo-N-C) for acidic ORR. Electron microscopy and X-ray absorption spectroscopy indicate that atomic CoNx and MnNx sites are dispersed in the carbon matrices of MnCo-N-C. Raman spectroscopy verifies that the doping of Mn into carbon matrices can enable a higher graphitization degree, which can improve the corrosion resistance and catalytic durability of the MnCo-N-C catalyst towards ORR in challenging acidic media. As a result, the MnCo-N-C catalyst exhibits significantly improved ORR durability with a higher current retention of 81% after 50 h of test compared with that (52%) of the Co-N-C catalyst. Moreover, the half-wave potential of the MnCo-N-C catalyst increases by 100 mV compared with that of the Co-N-C catalyst.
引用
收藏
页码:5930 / 5936
页数:7
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