FeS as a promising cathode catalyst for direct borohydride fuel cells

被引:10
|
作者
Lin, Longxia [1 ]
Qin, Haiying [1 ]
Jia, Junkang [1 ]
Ji, Zhenguo [1 ]
Chi, Hongzhong [1 ]
Ni, Hualiang [1 ]
Wang, Juan [2 ]
He, Yan [2 ]
Liu, Jiabin [3 ]
机构
[1] Hangzhou Dianzi Univ, Coll Mat & Environm Engn, Hangzhou 310018, Zhejiang, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201800, Peoples R China
[3] Zhejiang Univ, Sch Mat Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Electrocatalyst; Direct borohydride fuel cell; Oxygen reduction reaction; OXYGEN REDUCTION REACTION; ELECTROCATALYTIC ACTIVITY; SODIUM-BOROHYDRIDE; EFFICIENT CATALYST; ALKALINE MEDIA; GRAPHENE; SULFUR; PHTHALOCYANINE; NANOPARTICLES;
D O I
10.1016/j.jallcom.2018.07.269
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 sluggish oxygen reduction reaction (ORR) in cathode is the bottleneck of polymer electrolyte membrane fuel cell. Discovery of ORR catalysts with high activity and low cost is the key solution for the cell development. In this work, we synthesized a novel polypyrrole modified carbon supported FeS (FeS-PPy-BP) through two-step reaction and used it as cathode catalyst in direct borohydride fuel cell (DBFC). The catalyst had an onset ORR potential of 0.89 V (vs. reversible hydrogen electrode (RHE)), little lower than the onset potential of commercial Pt/C. The ORR on the FeS-PPy-BP was mainly through 4-electron process with a low yield of H2O2 (below 5%). The FeS-PPy-BP exhibited a good catalytic stability. The half-wave potential shift of the FeS-PPy-BP after 5000 cycles was 31 mV while that of the Pt/C was 42 mV. The DBFCs using the FeS-PPy-BP as cathode catalyst achieved a maximum power density of 140.5 and 78.8 mW cm(-2) at 60 and 30 degrees C, respectively. The outstanding electrochemical properties and the cell performances strongly support the FeS-PPy-BP as a promising cathode catalyst for DBFC. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 140
页数:5
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