流动电池
介电谱
循环伏安法
钒
氧化还原
电解质
电极
化学
电化学
分析化学(期刊)
参比电极
电阻抗
无机化学
材料科学
电气工程
物理化学
色谱法
工程类
作者
Anand Kumar Tripathi,Debittree Choudhury,Miji E. Joy,Manoj Neergat
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2022-05-01
卷期号:169 (5): 050513-050513
被引量:5
标识
DOI:10.1149/1945-7111/ac6aeb
摘要
The kinetics of redox reactions relevant to vanadium redox flow battery (VRFB) is investigated using voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in a three-electrode configuration and in a VRFB setup (two-electrode configuration). Impedance spectra are recorded in the VRFB setup with equimolar concentration of V 5+ /V 4+ and V 3+ /V 2+ solutions as positive and negative electrolytes, respectively (full-cell; asymmetric feed system); with an equimolar V 5+ /V 4+ electrolyte on both sides (symmetric feed system 1); and also with V 3+ /V 2+ electrolyte on both sides (symmetric feed system 2). Impedance of the full-cell VRFB (recorded with asymmetric feed system) is comparable to the sum of the half of the impedance of symmetric feed systems (of V 5+ /V 4+ and V 3+ /V 2+ electrolytes) at open circuit potential (OCP). Impedance and voltammograms recorded in the three-electrode configuration using Vulcan XC-72 modified rotating disk electrode, and the impedance recorded in the two-electrode full-cell configuration unequivocally confirms that the V 5+ /V 4+ redox reaction limits the VRFB performance. The optimal performance of the VRFB with the in situ treated carbon felt compressed to 47% is ∼389 and ∼336 mW cm −2 with 5 and 25 cm 2 cell area, respectively.
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