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Nitrogen doped mesoporous carbon derived from copolymer and supporting cobalt oxide for oxygen reduction reaction in alkaline media  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Nitrogen doped mesoporous carbon derived from copolymer and supporting cobalt oxide for oxygen reduction reaction in alkaline media

作者:Huang, Haojun[1];Wang, Qing[1];Wei, Qinglian[1];Huang, YongMin[1,2]

机构:[1]E China Univ Sci & Technol, Key Lab Specially Funct Polymer Mat & Related Tec, Dept Chem, Minist Educ, Shanghai 200237, Peoples R China;[2]Shanghai Inst Space Prop, Shanghai Engn Res Ctr Space Engine, Shanghai 201112, Peoples R China

年份:2015

卷号:40

期号:18

起止页码:6072

外文期刊名:INTERNATIONAL JOURNAL OF HYDROGEN ENERGY

收录:;EI(收录号:20151400716268);WOS:【SCI-EXPANDED(收录号:WOS:000354154300008)】;

基金:Financial support for this work was provided by the National Natural Science Foundation of China (No. 21476071), Shanghai Leading Academic Discipline Project (B502) and the Shanghai Engineering Research Center of Space Engine (Grant No. 13DZ2250600).

语种:英文

外文关键词:Mesoporous carbon; Nitrogen doped; Non-precious metal catalysts; Oxygen reduction reaction

摘要:The nitrogen doped mesoporous carbon (NMC) derived from pyrrole-co-furfural copolymer has been successfully developed by using an SBA-15 template. The as-prepared NMCs possess well-defined mesoporous structures with a narrow pore size distribution, high porosity and large surface area (up to similar to 1812 m(2) g(-1)). Using NMC as the supports, a hybrid catalyst of CoO nanoparticles loaded on NMCs (CoNMC) were prepared for the electrocatalytic oxygen reduction reaction (ORR) in alkaline media. The optimized CoNMC catalyst exhibits efficient catalytic activity with a four-electron reaction pathway and superior stability to the commercial Pt/C electrocatalyst. Furthermore, the high catalytic activity of CoNMC catalysts are mainly attributed to the high surface area and the synergetic effect between the N-doped carbon supports and cobalt oxides. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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