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The studies of performance of the Au electrode modified by Zn as the anode electrocatalyst of direct borohydride fuel cell
被引:50
作者:
He, Peiying
[1
]
Wang, Xianyou
[1
]
Fu, Pei
[1
]
Wang, Hong
[1
]
Yi, Lanhua
[1
]
机构:
[1] Xiangtan Univ, Key Lab Environm Friendly Chem & Applicat, Minist Educ, Sch Chem, Xiangtan 411105, Hunan, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Direct borohydride fuel cell;
Au(1-x)Znx bimetallic;
Anode electrocatalyst;
Stability;
Borohydride oxidation;
ELECTROCHEMICAL OXIDATION;
HYDROGEN EVOLUTION;
HOLLOW NANOSPHERES;
ALLOY;
ELECTROOXIDATION;
CATALYSTS;
PLATINUM;
AG;
NANOPARTICLES;
THIOUREA;
D O I:
10.1016/j.ijhydene.2011.04.128
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 carbon supported Au-base electrocatalysts (Au(1-x)Znx/C, 0 <= x < 1) modified by Zn were synthesized by reverse microemulsion method and employed as anode electrocatalysts of direct borohydride fuel cell (DBFC). The physical and electrochemical properties were investigated by energy dispersive X-ray (EDX), X-ray diffraction (XRD), transmission electron microscopy (TEM), cyclic voltammetry (CV), chronopotentiometry and fuel cell test. The results showed that the morphologies of Au(1-x)Znx nanoparticles all were uniformly spherical no matter what Zn content changed, and the average particle size of Au(1-x)Znx bimetallics varied from 3 to 6 nm. The electrochemical measurements revealed that the Au(1-x)Znx/C electrocatalysts showed no activity toward the NaBH4 hydrolysis reaction and obviously improved the catalytic activity of borohydride oxidation. Compared with Au/C anode electrocatalyst, the stability of DBFC using the Au0.65Zn0.35/C as anode electrocatalyst was apparently improved, and the maximum power density of 39.5 mW cm(-2) was obtained at 20 degrees C. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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页码:8857 / 8863
页数:7
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