Iron, Cobalt, and Nitrogen Tri-Doped Ordered Mesoporous Carbon as a Highly Efficient Electrocatalyst for Oxygen Reduction Reaction

被引:9
|
作者
Ran, Wu [1 ]
Dong, Jing [1 ]
Sun, Tingting [2 ]
Chen, Jianfeng [1 ]
Xu, Lianbin [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
来源
CHEMISTRYSELECT | 2019年 / 4卷 / 26期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Fe; Co; N-tri-doping; hard template; ordered mesoporous structure; oxygen reduction reaction; silica nanospheres; FACILE SYNTHESIS; FE; CO; NANOTUBES; NANOSTRUCTURES; NANOPARTICLES; PERFORMANCE; GRAPHENE; CATALYST; SITES;
D O I
10.1002/slct.201901641
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Many heteroatom-doped carbon materials have recently been fabricated to enhance the electrocatalytic oxygen reduction reaction (ORR) performance as promising alternatives to the scarce and high cost Pt-based catalysts. Herein, Fe, Co, N-tri-doped ordered mesoporous carbon materials (Fe-Co-N-OMCs) are synthesized by a facile templating technique using ordered close-packed silica nanospheres as a hard template and ferric chloride hexahydrate (FeCl3.6H(2)O), cobalt chloride hexahydrate (CoCl2.6H(2)O), dicyandiamide (DCDA), and sucrose as Fe, Co, N and C source, respectively. This method can be easily extended to synthesize a variety of doped carbon-based materials containing ordered mesopores. The results show that the bimetallic doping in this carbon-based materials is more favorable than single metal doping in catalyzing the ORR process. The best performing catalyst (Fe-Co-N-OMC (1:1)) exhibits comparable ORR activity with a half-wave potential of 0.83V vs. reversible hydrogen electrode (RHE) and superior stability to the commercial 20wt% Pt/C in alkaline medium. The enhanced ORR performance of Fe-Co-N-OMC (1:1) could be attributed to the tri-doping of Fe, Co and N into the carbon skeleton for catalytic reactions and the ordered mesoporous structure for facile mass transport and more exposed active sites.
引用
收藏
页码:7728 / 7733
页数:6
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