The catalytic effect of bismuth for VO2+/VO2+ and V3+/V2+ redox couples in vanadium flow batteries

被引:62
作者
Yang, Xiaofei [1 ,2 ]
Liu, Tao [1 ]
Xu, Chi [1 ,2 ]
Zhang, Hongzhang [1 ,3 ]
Li, Xianfeng [1 ,3 ]
Zhang, Huamin [1 ,3 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Div Energy Storage, Dalian 116023, Liaoning, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[3] Collaborat Innovat Ctr Chem Energy Mat iChEM, Dalian 116023, Liaoning, Peoples R China
关键词
Vanadium flow battery; Bismuth; Catalysis; Electrochemical activity; Energy efficiency; GRAPHITE ELECTRODE MATERIALS; POSITIVE ELECTRODE; CARBON PAPER; FELT; PERFORMANCE; CELL;
D O I
10.1016/j.jechem.2016.09.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The effect of bismuth (Bi) for both VO2+/VO2+ and V3+/V2+ redox couples in vanadium flow batteries (VFBs) has been investigated by directly introducing Bi on the surface of carbon felt (CF). The results show that Bi has no catalytic effect for VO2+/VO2(+) redox couple. During the first charge process, Bi is oxidized to Bi3+ (never return back to Bi metal in the subsequent cycles) due to the low standard redox potential of 0.308 V (vs. SHE) for Bi3+/Bi redox couple compared with VO2+/VO2+ redox couple and Bi3+ exhibit no (or neglectable) electro-catalytic activity. Additionally, the relationship between Bi loading and electrochemical activity for V3+/V2+ redox couple was studied in detail. 2 wt% Bi-modified carbon felt (2%-BiCF) exhibits the highest electrochemical activity. Using it as negative electrode, a high energy efficiency (EE) of 79.0% can be achieved at a high current density of 160 mA/cm(2), which is 5.5% higher than the pristine one. Moreover, the electrolyte utilization ratio is also increased by more than 30%. Even the cell operated at 140 mA/cm(2) for over 300 cycles, the EE can reach 80.9% without obvious fluctuation and attenuation, suggesting excellent catalytic activity and electrochemical stability in VFBs. (C) 2016 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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