电解质
材料科学
离子电导率
共晶体系
锂(药物)
聚合物
化学工程
电池(电)
电导率
快离子导体
复合材料
化学
电极
物理化学
微观结构
量子力学
医学
功率(物理)
物理
工程类
内分泌学
作者
Yanqing Wang,Rui Xu,Bowen Xiao,Dong Lv,Peng Yu,Yun Zheng,Yanghuan Shen,Jingchao Chai,Xiaohua Lei,Shiyu Luo,Xinyi Wang,Xinmiao Liang,Jiwen Feng,Zhihong Liu
标识
DOI:10.1016/j.mtphys.2022.100620
摘要
Solid-state polymer electrolytes have recently drawn intense attention as alternatives to traditional liquid electrolytes in lithium batteries due to their high energy-density and reliable safety. Unfortunately, current all-solid-state polymer electrolytes suffer from the low ionic conductivity, limiting the power density of energy storage batteries. Here, we propose a deep-eutectic electrolyte, formed directly by the interaction between poly (1,3-dioxolane) and lithium salt without other auxiliary solvents. The ionic conductivity of the designed deep-eutectic polymer electrolyte can approach to 1.5 × 10−5 S/cm at ambient temperature, which is twenty times higher than that of polyethylene oxide-based electrolytes. Specifically, solid-state NMR verifies the interaction between oxygen in poly (1,3-dioxolane) and lithium ion. The LiFePO4/Li battery assembled with deep-eutectic polymer electrolyte delivers a discharge capacity of 139.6 mAh/g at 0.1 C and a capacity retention of 90% after 200 cycles at 0.2 C. Pouch LiFePO4/Li batteries also present excellent safety performances. This finding provides a new approach for materials engineering of polymer electrolytes for advanced lithium batteries.
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