Direct hydrazine borane fuel cells using non-noble carbon-supported polypyrrole cobalt hydroxide as an anode catalyst

被引:6
|
作者
Zhang, Yang [1 ]
Zhu, Gang [2 ]
Chen, Zhenying [3 ]
Liu, Yingying [1 ]
Ye, Donghao [2 ]
Wang, Ao [2 ]
Jiang, Wenxing [1 ]
Deng, Chengwei [4 ]
Zhuang, Xiaodong [3 ]
Zhang, Junliang [1 ]
Ke, Changchun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Inst Fuel Cells, Sch Mech Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Wuhan Inst Marine Elect Prop, Wuhan 430064, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Meso Entropy Matter Lab, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[4] Shanghai Inst Space Power Sources, State Key Lab Space Power Sources Technol, Shanghai 200245, Peoples R China
基金
中国国家自然科学基金;
关键词
AMMONIA-BORANE; PERFORMANCE; LAYER; NANOPARTICLES; BOROHYDRIDE; EFFICIENT; PLATINUM; ELECTROOXIDATION; CROSSOVER; GDL;
D O I
10.1039/d3se00329a
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
A novel proof-of-concept direct liquid fuel cell (DLFC) feeding on hydrazine borane (N2H4BH3, HB) is developed. Non-noble carbon-supported polypyrrole cobalt hydroxide (C-PPY-Co(OH)(2)) was used as an anode catalyst, which catalyzed HB electro-oxidation reactions to achieve an electron transfer number of 7.63 e(-). The energy density of HB is 9947 W h kg(-1), exceeding that of traditional liquid fuels for DLFCs. The open circuit voltage of the fuel cell is 1.201 V, higher than that of direct methanol fuel cells (DMFCs) and direct hydrazine fuel cells (DHFCs). The fuel cell obtains a peak power density of 60 mW cm(-2), and the crossover current density of fuel is significantly lower than that of existing DLFCs. The electro-oxidation kinetics of HB on a Ni foam electrode is faster than that of a carbon paper. In addition, the mass transport resistance of the Ni foam electrode is 54 s cm(-1), much lower than that of the carbon paper electrode (231 s cm(-1)).
引用
收藏
页码:2594 / 2600
页数:7
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