Cellulose-reinforced poly(cyclocarbonate-ether)-based composite polymer electrolyte and facile gel interfacial modification for solid-state lithium-ion batteries

材料科学 化学工程 电解质 分离器(采油) 碳酸乙烯酯 乙二醇 离子电导率 电化学 聚合物 离子液体 复合数 固化(化学) 高分子化学 复合材料 电极 有机化学 化学 催化作用 物理 热力学 物理化学 工程类
作者
Xiaojiao Zheng,Jiawei Wu,Xiaodong Wang,Zhenglong Yang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:446: 137194-137194 被引量:50
标识
DOI:10.1016/j.cej.2022.137194
摘要

Synthesizing high-performance solid electrolytes with simple methods and common materials has long been a desire for lithium-ion batteries. Here, easy-available composite polymer electrolytes (CPEs) were prepared via UV curing of novel P(VEC-co-EGDMA) matrix and ionic liquid (IL) with commercial cellulose separator (CL). Loose complexation environment enabled cyclic carbonate of vinyl ethylene carbonate (VEC) to have higher Li+ migration capacity than EO, and poly (ethylene glycol) dimethacrylate (PEGDMA) was introduced as a flexible crosslinker to avoid excessively rigid structure. Furthermore, the IL with high voltage stability and CL with polar groups on the surface achieved liquid plasticization and mechanical reinforcement of P(VEC-co-EGDMA) matrix, synergistically improving the electrochemical performance and safety of CPEs. The ionic conductivity, electrochemical stability window and tensile strength of the optimal sample (PI64/CL) even reached 3.60 × 10−4 S cm−1 (25 °C), 5.6 V and 4.50 MPa, respectively. Finally, a 5 μm-thick PEO-LLZTO-IL gel transition layer was added at the electrolyte/cathode interface by a facile casting-curing method to optimize their interfacial contact, enabling the assembled solid-state battery to exhibit impressive rate and cycle performance, its specific capacity reached 151.6 mAh g−1 (1C) at 40 °C with the 89.1% capacity retention rate after 280 cycles, corresponding to 148.6 mAh g−1 (0.5C), 98.7%, 120 cycles at room temperature.
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