电容感应
线性扫描伏安法
电容器
扫频响应分析
电极
电容
电化学
循环伏安法
扩散
材料科学
电解质
航程(航空)
分析化学(期刊)
水平扫描速率
伏安法
阶跃势薛定谔方程的解
电气工程
化学
热力学
电压
工程类
色谱法
复合材料
物理
物理化学
作者
Marveh Forghani,Scott W. Donne
摘要
Several electrochemical methods have been developed to determine the contribution of different charge storage mechanisms, such as via the electrical double layer and diffusion-limited processes, to electrochemical capacitor behavior. This includes using cyclic voltammetry (CV) data at different sweep rates to obtain the relationship between voltammetric current and sweep rate, and also the relationship between voltammetric charge and sweep rate. Step potential electrochemical spectroscopy (SPECS) also has been used to effectively differentiate between different charge storage mechanisms. Herein we compare these three methods experimentally and also discuss their advantages and limitations toward differentiating between different charge storage mechanisms. These methods have been applied to electrolytic manganese dioxide (EMD) in 0.5 M K2SO4 between 0.0–0.8 V (vs SCE). It was found that in all cases, the specific capacitance was decreased by increasing the sweep rate. The capacitance-sweep rate dependence was only found to be accurate in a short range of low sweep rates. Overall there was good agreement between the SPECS and current-sweep rate dependence models over the full range of sweep rates. However, the SPECS method provided more precise information about the kinetic behavior of the electrochemical cell through a full range of sweep rates.
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