Electrochemical Impedance Spectroscopy and Cyclic Voltammetry Methods for Monitoring SmCl3 Concentration in Molten Eutectic LiCl-KCl

Michael R. Shaltry, K. Allahar, D. Butt, M. Simpson, S. Phongikaroon
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引用次数: 5

Abstract

Molten salt solutions consisting of eutectic LiCl-KCl and concentrations of samarium chloride (0.5 to 3.0 wt%) at 500℃ were analyzed using both cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The CV technique gave the average diffusion coefficient for Sm3+ over the concentration range. Equipped with Sm3+ diffusion coefficient, the Randles-Sevcik equation predicted Sm3+ concentration values that agree with the given experimental values. From CV measurements; the anodic, cathodic, and half-peak potentials were identified and subsequently used as a parameter to acquire EIS spectra. A six-element Voigt model was used to model the EIS data in terms of resistance-time constant pairs. The lowest resistances were observed at the half-peak potential with the associated resistance-time constant pairs characterizing the reversible reaction between Sm3+ and Sm2+. By extrapolation, the Voigt model estimated the polarization resistance and established a polarization resistance-concentration relationship.
电化学阻抗谱和循环伏安法监测熔融共晶LiCl-KCl中SmCl3浓度
用循环伏安法(CV)和电化学阻抗谱法(EIS)分析了500℃下由共晶LiCl-KCl和氯化钐(0.5 ~ 3.0 wt%)组成的熔盐溶液。CV技术给出了Sm3+在浓度范围内的平均扩散系数。加入Sm3+扩散系数后,Randles-Sevcik方程预测的Sm3+浓度与实验值吻合。从CV测量;确定了阳极、阴极和半峰电位,并将其作为获取EIS光谱的参数。采用六元Voigt模型对EIS数据进行电阻-时间常数对的建模。在半峰电位处观察到最低的电阻,相关的电阻-时间常数对表征了Sm3+和Sm2+之间的可逆反应。通过外推,Voigt模型估算了极化电阻,建立了极化电阻-浓度关系。
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