流动电池
化学
钝化
电池(电)
氧化还原
碘化物
膜
离子
储能
锂离子电池
多硫化物
无机化学
化学工程
电极
功率(物理)
有机化学
电解质
物理
工程类
物理化学
量子力学
生物化学
图层(电子)
作者
Wei Huang,Qingli Zou,Yi‐Chun Lu
标识
DOI:10.1002/batt.201900107
摘要
Abstract Highly concentrated polysulfide‐ (PS) and iodide‐based (I3−/I−) redox couples are promising active materials for redox flow battery applications owing to their high volumetric capacity. However, their applications in lithium redox flow batteries suffer from severe shuttle of iodine and PS and thus require the use of an ion‐selective ceramic membrane for stable operation. This inherent challenge critically limits the practical current density of the flow battery (<1 mA cm−2). Herein, we developed a dual PS‐LiI catholyte to simultaneously alleviate the shuttling of iodine and the passivation of Li2S, demonstrating stable ion‐selective membrane‐free Li‐catholyte cells achieving volumetric capacity between 30–60 Ah L−1catholyte with long cycle life (>150 cycles) at high current densities (3.8 mA cm−2 and 5.4 mA cm−2). The dual PS‐LiI catholyte not only increases the volumetric capacity and stability, but also removes the resistive and high‐cost ion‐selective membrane for low‐cost, high‐energy and high‐power flow battery applications.
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