电化学
电解质
砷酸盐
阿累尼乌斯方程
阳极
化学
电极
动力学
分析化学(期刊)
热稳定性
钒
无机化学
材料科学
核化学
活化能
物理化学
砷
色谱法
量子力学
物理
有机化学
作者
D. Noel Buckley,Andrea Bourke,Daniela Oboroceanu,Nathan Quill,Catherine Lenihan,Maria Al-Hajji Safi,Mallory A. Miller,Robert F. Savinell,Jesse S. Wainright,Robert P. Lynch
出处
期刊:ECS transactions
[The Electrochemical Society]
日期:2020-09-08
卷期号:98 (9): 223-239
被引量:3
标识
DOI:10.1149/09809.0223ecst
摘要
The electrochemical kinetics of the V II -V III reaction on carbon electrodes is enhanced by anodic treatment and inhibited by cathodic treatment. In contrast, the kinetics of V IV -V V is inhibited by anodic treatment and enhanced by cathodic treatment. Rate constants are greater for V IV -V V than for V II -V III under comparable conditions. The observed effects are attributed to oxygen-containing species on the surface of carbon electrodes and it is likely that enhancement of both V II -V III and V IV -V V is due to the same (active) state of the electrode. Oxidation of this active state leads to inhibition of V IV -V V while reduction of the same active state leads to inhibition of V II -V III . Using our standard methodology, we investigated the thermal stability of VFB catholytes. We showed that the induction time for precipitation of V 2 O 5 decreases exponentially with increasing temperature or V V concentration but increases exponentially with increasing sulphate concentration. Arrhenius plots show two linear regimes, at 45–70°C and 30–45°C, respectively. We model this to estimate acceleration factors for testing of electrolyte stability over a range of test and use temperatures. Both arsenate and phosphate are effective additives for improving the thermal stability of VFB catholytes.
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