电解质
材料科学
离子电导率
热稳定性
化学工程
聚合物
法拉第效率
阳离子聚合
玻璃化转变
锂(药物)
聚合
电极
高分子化学
化学
复合材料
医学
物理化学
工程类
内分泌学
作者
Wei Zhang,Taewook Ryu,Sujin Yoon,Lei Jin,Giseok Jang,Wansu Bae,Whangi Kim,Faiz Ahmed,Hohyoun Jang
出处
期刊:Membranes
[Multidisciplinary Digital Publishing Institute]
日期:2022-04-18
卷期号:12 (4): 439-439
被引量:14
标识
DOI:10.3390/membranes12040439
摘要
The polymer electrolytes are considered to be an alternative to liquid electrolytes for lithium-ion batteries because of their high thermal stability, flexibility, and wide applications. However, the polymer electrolytes have low ionic conductivity at room temperature due to the interfacial contact issue and the growing of lithium dendrites between the electrolytes/electrodes. In this study, we prepared gel polymer electrolytes (GPEs) through an in situ thermal-induced cationic ring-opening strategy, using LiFSI as an initiator. As-synthesized GPEs were characterized with a series of technologies. The as-synthesized PNDGE 1.5 presented good thermal stability (up to 150 °C), low glass transition temperature (Tg < −40 °C), high ionic conductivity (>10−4 S/cm), and good interfacial contact with the cell components and comparable anodic oxidation voltage (4.0 V). In addition, PNGDE 1.5 exhibited a discharge capacity of 131 mAh/g after 50 cycles at 0.2 C and had a 92% level of coulombic efficiency. Herein, these results can contribute to developing of new polymer electrolytes and offer the possibility of good compatibility through the in situ technique for Li-ion batteries.
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