电解质
电化学
电池(电)
原位
离子
氯化物
材料科学
电极
聚合
原位聚合
化学工程
无机化学
化学
复合材料
热力学
物理化学
冶金
物理
聚合物
工程类
有机化学
功率(物理)
作者
Yuling Xu,Tiantian Zhu,Haiyang Xu,Xiangyu Zhao
标识
DOI:10.1016/j.jmst.2024.04.050
摘要
Considering large volume variation and dissolution issues of some promising electrode materials for chloride ion batteries (CIB), the construction of solid polymer electrolytes (SPE) for efficient chloride ion transport is intriguing. However, this is hindered by low ionic conductivity of chloride SPEs and poor cycling performance of CIBs. Herein, an in-situ polymerized and cross-linked poly(ethylene glycol) diacrylate-based chloride SPE with a low plasticizer content of succinonitrile is designed, yielding a room-temperature ionic conductivity of 7.6 × 10−5 S cm−1, which is higher than that of previously reported SPEs for CIBs. Moreover, the use of the as-prepared SPE achieves an integrated organic cathode with significantly enhanced rate performance and capacity retention of 96.1% after 100 cycles at room temperature, which is much higher than 49.9% (80 cycles) of the cathode in the CIB with a sandwiched structure. These improved performance is also superior to that of other reported cathodes coupled with different chloride SPEs. The chloride ion transfer mechanism of the cathode is revealed by X-ray photoelectron spectroscopy and energy dispersive spectroscopy.
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