Highly-defective Fe-N-C catalysts towards pH-Universal oxygen reduction reaction

被引:133
|
作者
Wei, Xiaoqian [1 ]
Luo, Xin [1 ]
Wang, Hengjia [1 ]
Gu, Wenling [1 ]
Cai, Weiwei [2 ]
Lin, Yuehe [3 ]
Zhu, Chengzhou [1 ]
机构
[1] Cent China Normal Univ, Coll Chem, Int Joint Res Ctr Intelligent Biosensing Technol, Key Lab Pesticide & Chem Biol,Minist Educ, Wuhan 430079, Peoples R China
[2] China Univ Geosci, Fac Mat Sci & Chem, Sustainable Energy Lab, Wuhan 430074, Peoples R China
[3] Washington State Univ, Sch Mech & Mat Engn, Pullman, WA 99164 USA
关键词
Nonprecious metal catalysts; Fe-N-C catalysts; Defect engineerings; Etching; Oxygen reduction reaction; METAL-FREE ELECTROCATALYSTS; POROUS CARBON NANOSHEETS; EFFICIENT ELECTROCATALYST; GRAPHENE NANORIBBONS; ACTIVE-SITES; PERFORMANCE; IRON; NANOPARTICLES; EVOLUTION; ELECTRODE;
D O I
10.1016/j.apcatb.2019.118347
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
The defect engineering of nonprecious metal catalysts (NPMCs) is of significance to advance the oxygen reduction reaction (ORR) catalysts for the application of electrochemical energy devices. Herein, a facile H2O2 etching strategy is proposed to design Fe and N co-doped carbon catalysts (Fe-N-C/H2O2). Thanks to the etching of C, the defective carbon (DC) is endowed with robust anchoring ability, which is conducive to the modulation of active sites and microstructures, and further improvement of their ORR performances. Due to the supporting effect, the effective 3D nanostructures can be constructed. Integrated with the composition and morphology features, the resultant Fe-N-C/H2O2 achieves remarkable ORR performance with onset potential of 0.93 V and super stability with a subtle negative shift of 13.1 mV after 20 000 cycles in 0.1 M HClO4. Meanwhile, superior ORR performances are also revealed in alkaline and neutral electrolytes. This work provides an effective strategy for the design of advanced electrocatalysts towards fuel cells.
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页数:7
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