氧化还原
钒
流动电池
化学
半反应
反应速率常数
电极
电子转移
反应速率
介电谱
反应级数
无机化学
动力学
电解质
电池(电)
电化学
光化学
催化作用
热力学
物理化学
有机化学
功率(物理)
量子力学
物理
作者
Holger Fink,Jochen Friedl,Ulrich Stimming
标识
DOI:10.1021/acs.jpcc.5b12098
摘要
Vanadium flow batteries are a promising system for stationary energy storage. One of their shortcomings is a low power density caused by slow kinetics of the redox reactions. To alleviate this drawback, many studies tried to catalyze the redox reactions. However, up to now, there is no consensus in the literature on which of the two half-cell reactions, the V2+/V3+ or the VO2+/VO2+reaction, features the slower electron transfer. The present study is the first showing that reaction rates for the half-cells are of the same order of magnitude with their respective rate constants depending on the composition of the electrode material. The surface functional groups hydroxyl, carbonyl, and carboxyl on carbon increase the wetted surface area, catalyze the V2+/V3+ redox reaction, but impede the VO2+/VO2+ redox reaction. This complex situation was unraveled by using a newly developed procedure based on electrochemical impedance spectroscopy. Reaction mechanisms based on these results are discussed.
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