流动电池
极化(电化学)
电子转移
钒
化学
反应机理
反应级数
动能
电极
化学反应
无机化学
电化学
动力学
分析化学(期刊)
氧化还原
物理化学
催化作用
电解质
反应速率常数
物理
有机化学
量子力学
作者
Minghua Jing,Dawei Fang,Xinzhuang Fan,Jianguo Liu,Chuanwei Yan
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2020-12-01
卷期号:167 (16): 160539-160539
被引量:5
标识
DOI:10.1149/1945-7111/abd36d
摘要
The oxidation and reduction reaction mechanisms of the VO 2 + /VO 2+ redox couple have been studied to better understand the electrode reaction processes and further optimize the battery performance of vanadium flow battery (VFB) in our previous work. However, it is found that the negative electrode process of VFB plays a more important role in the improvement of the overall battery performance as research continues. Hence, the reduction reaction mechanism of V 3+ in acidic solutions has been investigated systematacially in this work. Potentiodynamic polarization combined with rotating disk electrode have been applied to calculate the reaction orders ( m ) and the electron transfer number ( n ) of the reduction reaction of V 3+ . The results of this work demonstrated that the reduction reaction of V 3+ is a single electron transfer step and H + keeps out of the electrochemical reaction. Furthermore, the kinetic equation for the reduction reaction of V 3+ has been established, and the theoretic polarization curve based on the established kinetic equation is well consistent with the experimental result, indicating an accurate prediction of the polarization behavior in V 3+ acidic solutions.
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