环氧乙烷
单体
聚合物
材料科学
电解质
离子电导率
乙二醇
阳极
互穿聚合物网络
乙二醇二甲基丙烯酸酯
共聚物
化学工程
复合材料
高分子化学
化学
物理化学
工程类
电极
甲基丙烯酸
作者
Zhuoran Ao,Youlan Zou,Huiyao Li,Nantao Chen,Yuxing Huang,Yaru Liang
标识
DOI:10.1016/j.susmat.2023.e00712
摘要
Lithium–sulfur (Li-S) battery attracts numerous study due to its high theoretical specific capacity. Unfortunately, the notorious shuttle effect and the safety issue of lithium anode limit the development. The application of solid-state electrolyte is regarded as one of the solutions. Herein, a UV-cured polymer network is introduced in poly(ethylene oxide) (PEO)-based solid polymer electrolyte (SPE) to enhance the performance of Li-S battery. Poly(ethylene glycol) dimethacrylate (PEGDMA) was used as the main crosslinking monomer. The abundant -C-C-O- long chain can provide a fast channel for Li+ transfer. Trimethylolpropane ethoxylate triacrylate (TMPETA) is used as the crosslinker, which made the linear copolymer formed by single monomer transform into interpenetrating polymer network. Hence, an interpenetrating UV-cured network was synthesized and combined with PEO. This elaborately designed structure enhances the ionic conductivity and the mechanical properties of PEO SPE as well as hinder the lithium polysulfides (LiPSs) migration. As a result, the symmetric Li cells with this SPE can stably cycle for >1600 h at the current density of 0.1 mA cm−2. Moreover, the Li-S cells can deliver an initial capacity of 1131 mAh g−1 at 0.1C. It provides a thread to design the polymer network of SPE.
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