Carbonized tubular polypyrrole with a high activity for the Br2/Br- redox reaction in zinc-bromine flow batteries

被引:60
作者
Wu, M. C. [1 ,2 ]
Zhao, T. S. [1 ,2 ]
Zhang, R. H. [1 ,2 ]
Wei, L. [1 ,2 ]
Jiang, H. R. [1 ,2 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, HKUST Energy Inst, Kowloon, Hong Kong, Peoples R China
关键词
Zinc-bromine flow battery; Br-2/Br- redox reaction; Carbonized tubular polypyrrole; Energy storage; NITROGEN-DOPED CARBON; OXYGEN REDUCTION REACTION; GRAPHITE FELT ELECTRODES; RESEARCH-AND-DEVELOPMENT; HIGH-ENERGY-DENSITY; MESOPOROUS CARBON; ALL-VANADIUM; ELECTROCATALYTIC PERFORMANCE; POSITIVE ELECTROLYTE; LI-O-2; BATTERIES;
D O I
10.1016/j.electacta.2018.07.192
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Zinc-bromine flow batteries have been regarded as one of the most promising technologies for largescale energy storage. However, the widespread application of this technology is still hindered by its low power density, primarily resulting from a large polarization in the Br-2/Br- electrode. In this work, carbonized tubular polypyrrole with abundant nitrogen- and oxygen-containing functional groups is synthesized and, for the first time, applied to a zinc-bromine flow battery as a positive electrode material. Experimental results unravel that carbonized tubular polypyrrole exhibits a high activity toward the Br-2/Br- redox reaction, and enables the zinc-bromine flow battery to be operated at a current density of 80 mA cm(-2) with a high energy efficiency of 76.0%. In contrast, the battery with the pristine graphite felt electrode can only output an energy efficiency of 69.4% at the same current density. In addition, no degradation is observed for the zinc-bromine flow battery equipped with carbonized tubular polypyrrole for 100 cycles. These superior results suggest that carbonized tubular polypyrrole is a promising positive electrode material for zinc-bromine flow batteries. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:569 / 576
页数:8
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