Fe-N co-decorated hierarchically porous graphene as a highly efficient electrocatalyst for the oxygen reduction reaction

被引:15
|
作者
Cao, Jianyu [1 ]
Jia, Xiaodi [1 ]
Guo, Mengwei [1 ]
Du, Yingying [1 ]
Xu, Juan [1 ]
Chen, Zhidong [1 ,2 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Changzhou Univ, Jiangsu Collaborat Innovat Ctr Photovolta Sci & E, Sch Mat Sci & Engn, Jiangsu Key Lab Mat Surface Sci & Technol, Changzhou 213164, Peoples R China
来源
SUSTAINABLE ENERGY & FUELS | 2018年 / 2卷 / 01期
基金
中国国家自然科学基金;
关键词
METAL-FREE ELECTROCATALYSTS; CARBON NANOTUBES; FUEL-CELL; IRON; CATALYST; PERFORMANCE; SUPPORT; HYBRID; SITES;
D O I
10.1039/c7se00458c
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
Fe-N co-decorated hierarchically porous graphene (FeN/G) was prepared by a facile one-step pyrolysis method. In the pyrolysis synthesis process, dicyandiamide was introduced as a nitrogen precursor and sacrificial templating agent, together with ferric nitrate utilized as an iron precursor, to aid in the formation of graphene nanosheets and their self-assembly into an interconnected porous framework. Consequently, the resultant FeN/G framework shows a relatively large specific surface area (401.1 m(2) g(-1)), hierarchically porous structure and abundant meso-/macropores. Such highly desired FeNC structures not only possess sufficient catalytically active sites for the oxygen reduction reaction (ORR) but also guarantee fast transfer of reactants and ions, which provides excellent catalytic activity with positive onset and half-wave potentials, large kinetic-limiting current density, and remarkable durability that is obviously better than the commercial Pt/C in alkaline medium.
引用
收藏
页码:169 / 174
页数:6
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