A self-sponsored doping approach for controllable synthesis of S and N co-doped trimodal-porous structured graphitic carbon electrocatalysts

被引:192
作者
Li, Yibing [1 ]
Zhang, Haimin [1 ]
Wang, Yun [1 ]
Liu, Porun [1 ]
Yang, Huagui [1 ]
Yao, Xiangdong [1 ]
Wang, Dan [1 ,3 ]
Tang, Zhiyong [1 ]
Zhao, Huijun [1 ,2 ]
机构
[1] Griffith Univ, Ctr Clean Environm & Energy, Nathan, Qld 4222, Australia
[2] Chinese Acad Sci, Inst Solid State Phys, Ctr Environm & Energy Nanomat, Hefei 230031, Peoples R China
[3] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
关键词
OXYGEN-REDUCTION REACTION; METAL-FREE ELECTROCATALYSTS; ELECTROLYTE FUEL-CELLS; GRAPHENE OXIDE; O-2; REDUCTION; NITROGEN; NANOTUBES; CATALYSTS; SULFUR; BORON;
D O I
10.1039/c4ee01779j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile self-sponsored doping approach is developed to synthesize S and N co-doped trimodal-porous structured graphitic carbon network electrocatalysts. It utilizes a sole precursor (1-allyl-2-thiourea) to realize a precisely controlled co-doping of S and N during a concurrent graphitic carbon growth process by simple control of the pyrolysis temperature. The results reveal that the doping effect is heavily dependent on the doping density and a maximal catalytic activity could only be achieved with an optimal doping level. The presence of a macro-pore structure in the trimodal-porous network enhances the mass transport, enabling the full utilization of large surface areas created by micro- and meso-pores. The resultant electrocatalyst possesses high ORR catalytic activity with excellent durability and high resistance to the inhibition effect of fuel molecules. The findings of this work would be valuable for design and fabrication of high performance carbon-based electrocatalysts.
引用
收藏
页码:3720 / 3726
页数:7
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