PPy enhanced Fe, W Co-doped Co3O4 free-standing electrode for highly-efficient oxygen evolution reaction

被引:6
|
作者
Hu, Qingzhao [1 ]
Liu, Yan [1 ]
Ma, Longtao [2 ]
Zhang, Xuming [1 ]
Huang, Haitao [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Appl Phys, Kowloon 999077, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Dept Mat Sci & Engn, Kowloon 999077, Hong Kong, Peoples R China
关键词
Oxygen evolution reaction; Free-standing electrode; Electrodeposition; PPy; REDUCTION REACTION; CATALYTIC-ACTIVITY; HIGH-PERFORMANCE; NANOPARTICLES; ELECTROCATALYST; NANOCOMPOSITES; NANOSHEETS; MECHANISM; COOOH; FILMS;
D O I
10.1007/s10800-018-1211-5
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical catalysts for the oxygen evolution reaction (OER) play a key role in highly-efficient water splitting and many other important energy conversion applications. Transition metal oxides are promising OER catalysts. In this work, Fe, W co-doped Co3O4 was grown on carbon fiber cloth (FeWCo3O4/CFC) and polypyrrole (PPy)/carbon fiber cloth (FeWCo3O4/PPy/CFC) through a simple anodic electrodeposition method. The FeWCo3O4/CFC free-standing electrode reached an electrocatalytic current density of 30.7mAcm(-2) at 400mV overpotential with a Tafel slope of 177mVdec(-1). The PPy can serve as conductive binder and improve the contact between FeWCo3O4 and substrate. The resulting FeWCo3O4/PPy/CFC free-standing electrode reached an electrocatalytic current density of 36.2mAcm(-2) at 400mV overpotential with a Tafel slope of 163mVdec(-1). The FeWCo3O4/PPy/CFC free-standing electrode shows low electric resistance and is able to catalyze OER at 10mAcm(-2) for 12h without obvious decay under the optimized electrodeposition conditions. This study provides new insight for design and synthesis of highly-efficient OER catalyst. [GRAPHICS]
引用
收藏
页码:1189 / 1195
页数:7
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