电解质
离子电导率
纤维素
锂(药物)
电导率
离子
材料科学
聚合物
快离子导体
化学工程
离子键合
电池(电)
准固态
溶剂
化学
有机化学
电极
复合材料
工程类
物理化学
功率(物理)
内分泌学
物理
医学
量子力学
色素敏化染料
作者
Yonglin Xu,Jinghao Cui,Binhui Guo,Zhenghao Li,W.Z. Wang,Wei Li
标识
DOI:10.1016/j.cej.2024.151783
摘要
It is known that the low ionic conductivity of solid-state polymer electrolytes at room temperature (RT) has severely restricted their practical application in lithium-ion batteries. Although eutectogel (ETG) electrolytes could solve this problem to some extent, highly compatible deep eutectic solvent (DES)/polymer systems are desirable to further enhance ion conduction. Herein, we designed cellulose-based ETG (CETG) with dual channels through "hopping" and "vehicle" mechanisms by hydroxyethyl cellulose (HEC) molecular chains and N-methylacetamide (NMA)/LiTFSI-derived DES, respectively. Thanks to the strong molecular interactions between HEC and DES, the highest DES content in the ETG could achieve 90 %, which endowed the CETG with an excellent ionic conductivity of 2.04 × 10–3 S cm−1 at 30 °C. Additionally, our designed CETG displayed good self-healing and fire retardant properties. The assembled Li/LiFePO4 cell showed a capacity retention of 91.8 % after 200 cycles at 0.2 C under RT with an initial discharge capacity of 156.2 mAh g−1. In particular, the capacity retention rates of the assembled batteries reached 95.2 % and 92.1 %, respectively, after 100 cycles at 0.2 C under 60 °C and 50 cycles at 0.2 C under 100 °C. Our fabrication strategy would provide a novel idea for the design of green, safe and efficient solid-state polymer electrolytes for lithium-ion batteries.
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