电解质
碳酸锂
氟化物
锂(药物)
聚酯纤维
碳酸盐
聚合物
材料科学
聚合物电解质
化学工程
氟化锂
无机化学
化学
离子
有机化学
离子电导率
离子键合
复合材料
电极
冶金
物理化学
医学
工程类
内分泌学
作者
Da Xu,Doudou Zhao,Xiaoyang Niu,Tiantian Wang,Zhenglong Yang
标识
DOI:10.1016/j.cej.2024.151780
摘要
Polymer solid-state electrolytes have become one of the promising materials for constructing solid-state lithium batteries due to their excellent processability and good compatibility with electrode interfaces. However, their limited electrochemical performance and mechanical strength have hindered their widespread application. Through the adoption of an in-situ thermal curing method, we successfully prepared a poly(carbonate-fluoride) solid-state electrolyte, utilizing a polyester separator with abundant polar groups as a reinforcing framework. The introduction of ionic liquid into the solid polymer electrolyte not only enhances the mobility of polymer chain segments to improve ionic conductivity but also, in synergy with trifluoromethyl, promotes lithium salt dissociation while restricting the migration of lithium salt anions. Additionally, their reaction with the lithium metal anode generates the LiF-rich SEI, regulating the deposition of lithium dendrites. The resulting 31VPIF/OZ exhibited outstanding ionic conductivity (3.58 × 10−4 S cm−1 at 25 °C), Li-ion migration number (0.52), and electrochemical window (5.4 V). Li | 31VPIF/OZ | Li battery cycled for 1000 h at 0.1 mA cm−2 without short-circuiting. Importantly, Li | | LiFePO4 battery demonstrated a high capacity retention rate of 91.5 % after 600 cycles at 0.5C (25 °C). Thus, through the synergistic interplay of polymer structure design and fillers, we have successfully achieved stable cycling in solid-state lithium batteries, providing robust support for their application in rechargeable lithium battery technology.
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