使用 "盐包水型 "电解质的新型对称铅基电池

Xinping Duan, Mingqiang Li, Lixiang Wang, Jingwen Li, Shuailiang Xu, Haochen Weng
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引用次数: 0

摘要

铅酸电池被广泛应用于大中型储能系统,但由于其在实际应用中存在比容量低、硫化不可逆等缺点,其在新兴技术中的应用一直受到限制。我们尝试将 "盐包水 "电解质应用于新型对称铅基电池,并探索了多种活性材料基底,结果表明石墨箔集流电池的性能最佳。高浓度的盐中水电解质可拓宽电化学稳定性窗口,从而使这些电池表现出卓越的放电性能,在放电电流密度为 0.1 A g-1 时,可逆比容量为 167 mAh g-1,活性材料利用率提高到理论容量的 69.6%。此外,电池在 800 次循环后仍能保持 152 mAh g-1 的放电容量,容量保持率高达 91%,优于大多数预先报告的数值。利用拉曼光谱、X 射线衍射、X 射线光电子能谱、扫描电子显微镜和透射电子显微镜分析了正极的充电和放电机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A new symmetrical lead-based battery using a “water-in-salt” electrolyte

A new symmetrical lead-based battery using a “water-in-salt” electrolyte

Lead–acid batteries are widely used in medium and large energy storage systems, but their application in emerging technologies has been limited by shortcomings in practical applications, such as low specific capacity and irreversible sulfation. We tried to apply “water-in-salt” electrolytes to novel symmetric lead-based batteries, exploring a variety of active material substrates to show that graphite foil current collector batteries perform best. An elevated concentration of water-in-salt electrolyte can broaden the electrochemical stability window, which enables these batteries to show excellent discharge performance, with a reversible specific capacity of 167 mAh g−1 at a discharge current density of 0.1 A g−1, increasing the active material utilization to 69.6% of theoretical capacity. In addition, the batteries maintained a discharge capacity of 152 mAh g−1 after 800 cycles, with a capacity retention rate of 91%, which is better than most pre-reported values. The charging and discharging mechanisms of the positive electrode were analyzed using Raman, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy.

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