电解液浓度对锌-离子电池活性材料六氰基铁酸铜电化学行为的影响

Sangyup Lee, Paul Maldonado Nogales, S. Jeong
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摘要

本研究探讨了电解质浓度对六氰合铁酸铜(CuHCF)电化学行为的影响,CuHCF 是一种很有前途的锌离子水溶液电池电极活性材料。研究人员采用循环伏安法、充放电测量法和 X 射线衍射分析法评估了不同电解质浓度下 CuHCF 电极的电化学反应和结构完整性。结果表明,电解质浓度对 CuHCF 电极的电化学性能有显著影响。具体来说,当电解质浓度从 1.0 摩尔 dm-3 增加到 2.0 摩尔 dm-3 时,充放电容量最初会增加,随后会降低。容量下降的原因是在 0.0-0.3 V 的低电位区域发生了电极/电解质界面反应,同时 CuHCF 活性材料的结构也发生了变化。值得注意的是,这些发现强调了 CuHCF 电极的电化学性能与锌离子的水合结构以及电解质溶液的 pH 值之间的密切联系。因此,优化电解质成分对于提高采用 CuHCF 电极的锌离子水电池的性能具有巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of Electrolyte Concentration on the Electrochemical Behavior of Copper Hexacyanoferrate as an Active Material for Zinc-Ion Batteries
This study investigates the impact of electrolyte concentration on the electrochemical behavior of copper hexacyanoferrate (CuHCF), a promising active material for aqueous zinc-ion battery electrodes. Cyclic voltammetry, charge-discharge measurements, and X-ray diffraction analysis were employed to assess the electrochemical reactions and structural integrity of the CuHCF electrode under varying electrolyte concentrations. The results revealed a significant influence of electrolyte concentration on the electrochemical performance of the CuHCF electrode. Specifically, the charge-discharge capacity exhibited an initial increase as the electrolyte concentration increased from 1.0 to 2.0 mol dm‒3, followed by a subsequent decrease. This decrease in capacity was attributed to the occurrence of an electrode/electrolyte interfacial reaction in the low-potential region of 0.0–0.3 V, coupled with structural changes in the CuHCF active material. Notably, these findings underscore the strong correlation between the electrochemical performance of the CuHCF electrode and the hydration structure of zinc ions, as well as the pH of the electrolyte solution. Thus, optimizing the electrolyte composition holds significant potential for enhancing the performance of aqueous zinc-ion batteries employing CuHCF electrodes.
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