Porous Fe, Co, and N-co-doped carbon nanofibers as high-efficiency oxygen reduction catalysts

被引:17
|
作者
Yu, Ke [1 ]
Shi, Peng-Hui [1 ,4 ]
Fan, Jin-Chen [1 ,2 ,3 ,4 ]
Min, Yu-Lin [1 ,4 ]
Xu, Qun-Jie [1 ,4 ]
机构
[1] Shanghai Univ Elect Power, Coll Environm & Chem Engn, Shanghai Key Lab Mat Protect & Adv Mat Elect Powe, Shanghai 200090, Peoples R China
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Biointerfaces Inst, Ann Arbor, MI 48109 USA
[4] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrospinning; Nanostructures; Oxygen reduction reaction; Zeolitic imidazolate framework; Electrocatalysts; METAL-ORGANIC FRAMEWORK; HIGH ELECTROCATALYTIC ACTIVITY; MESOPOROUS CARBON; ACTIVE-SITES; NITROGEN; NANOTUBES; GRAPHENE; NANOPARTICLES; NANOSHEETS; HYBRID;
D O I
10.1007/s11051-019-4678-z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxygen reduction reaction (ORR) is an important reaction in fuel cells. Designing electrocatalysts with outstanding performance is always the key to renewable-energy technologies for fuel cells. Herein, we demonstrate the Fe, Co, and N co-doped porous carbon nanofibers (FeCo/N-C CNFs) as a novel high-performance electrocatalyst for ORR. The synthesis method of this electrocatalysts material is very simple via high-temperature calcination pyrolysis of zinc, cobalt bimetallic zeolitic imidazolate framework (ZIF)-coated electrospun polyacrylonitrile fibers. In alkaline media, the FeCo/N-C CNFs shows a Pt-like ORR performance. The FeCo/N-C CNFs catalysts exhibit excellent performance with an onset potential of 0.99 V and a half-wave potential of 0.83 V in 0.1 M KOH solution, which is similar to those of 20 wt% Pt/C catalysts. Meanwhile, regarding long-term durability and methanol tolerance, the as-synthesized FeCo/N-C CNF catalysts also outperform commercial Pt/C. The unusual catalytic activity mainly from the improvement of electron transfer channels and catalytic sites arise from Fe, Co, and N doping in the porous structure carbon nanofibers.
引用
收藏
页数:11
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