A Cheap Polypyrrole-Derived Fe-N-C Electrocatalyst with Ultrahigh Oxygen Reduction Activity in Alkaline Electrolyte

被引:2
|
作者
Liu, Yao [1 ]
Liu, Xiaojing [2 ]
Liu, Junli [1 ]
Guo, Chaozhong [1 ]
Li, Yanrong [3 ]
Zhang, Jin [3 ]
Li, Zhongbin [1 ]
机构
[1] Chongqing Univ Arts & Sci, Engn Res Ctr New Energy Storage Devices & Applica, Sch Mat & Chem Engn, Res Inst New Mat Technol, Chongqing 402160, Peoples R China
[2] Ningbo Univ, Fac Mat Sci & Chem Engn, Ningbo Key Lab Specialty Polymers, Ningbo 315211, Zhejiang, Peoples R China
[3] Chongqing Univ Technol, Coll Mat Sci & Engn, Chongqing 400054, Peoples R China
来源
关键词
Porous carbon; Oxygen reduction; Electrocatalyst; Molecular sieve; CATALYSTS; CARBON; PERFORMANCE; CATHODE; OXIDE; NANOPARTICLES; GRAPHENE; IONS; SITE;
D O I
10.20964/2019.06.76
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Ternary Fe-N-C catalysts are regarded as the most promising candidates for low-cost alternatives to the Pt-based materials for catalyzing the oxygen reduction reaction (ORR). In this paper, the Fe and N co-doped carbon catalyst (Fe-Py@K-800) with the unique foam-like 3D structure has been fabricated by using the molecular sieve as a new solid-state template. The results of physical characterization indicate that Fe atoms are coordinated with nitrogen atoms to form the Fe-N ORR-active structure. In contrast with the commercial Pt/C catalyst, the Fe-Py@K-800 displays a comparable ORR electrocatalytic activity with an onset potential of similar to 1.1 V and a half-wave potential of similar to 0.88 V (vs. RHE), however, the long-term stability of Fe-Py@K-800 is obviously better. These results show that iron-organic coordination in the pyrrole ring will play a role in the generation of nitrogen-rich active sites, which facilitates the enhancement of ORR activity in alkaline electrolyte.
引用
收藏
页码:5820 / 5830
页数:11
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