Performance study of passive and active direct borohydride fuel cell employing a commercial Pd decorated Ni-Co/C anode catalyst

被引:38
作者
Zhiani, Mohammad [1 ]
Mohammadi, Ismaeil [1 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Esfahan 8415683111, Iran
关键词
Passive direct borohydride fuel cell; Electrochemical impedance spectroscopy; Pd decorated Ni-Co/C; Pt/C; SUPPORTED COBALT HYDROXIDE; ETHANOL OXIDATION REACTION; HYDROGEN STORAGE ALLOY; SODIUM-BOROHYDRIDE; ELECTROCATALYTIC ACTIVITY; OXYGEN REDUCTION; CATHODE; MEMBRANE; AU; ELECTRODES;
D O I
10.1016/j.fuel.2015.11.016
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In this study, a new Pd decorated Ni-Co/C anode catalyst with remarkably high performance was introduced for using in direct borohydride fuel cell (DBFC) and compared to conventional 10 wt.% Pt/C anode catalyst. The activity and poisoning tolerance of both catalysts were investigated by electrochemical techniques in half-cell. The results indicated that the Pd decorated Ni-Co/C had higher activity compared to the 10 wt.% Pt/C in borohydride oxidation reaction (BOR). However, its poisoning tolerance was lower than 10 wt.% Pt/C during 200 cycles. Passive DBFC results demonstrated that the cell performance and open circuit voltage (OCV) were improved by using the Pd decorated Ni-Co/C as an anode catalyst compared to commercial 10 wt.% Pt/C; 126 mW cm(-2) vs. 76 mW cm(-2) and 1010 mV vs. 892 mV respectively. Moreover, the maximum peak power density of 761 mW cm(-2) was obtained by Pd decorated Ni-Co/C anode catalyst in active DBFC which is comparable to generated power by H-2/O-2 proton exchange membrane fuel cell (PEMFC); 772 mW cm(-2) at the same conditions. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:517 / 525
页数:9
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