电解质
离子
溶剂化
锂(药物)
碳酸丙烯酯
化学
无机化学
电导率
溶剂
离子电导率
四氢呋喃
二甲醚
冰点
化学工程
甲醇
热力学
物理化学
有机化学
电极
医学
内分泌学
物理
工程类
作者
Honglu Hu,Jinhan Li,Qiu Zhang,Guoyu Ding,Jiuding Liu,Dong Yang,Kang Zhao,Meng Yu,Huan Wang,Fangyi Cheng
标识
DOI:10.1016/j.cej.2023.141273
摘要
Tailoring the lithium-ion solvation structure of ether-based electrolyte to accelerate charge transfer is of significance in low-temperature lithium batteries but remains largely unexplored. Herein, we propose a strategy based on carbonates mediating the anion coordination to realize cold-resistant electrolyte with superior kinetics and improved anodic stability. The combination of computational and experimental methods reveals that decreasing anions in the Li+-solvation structure reduces the desolvation energy of Li+ and enhances low-temperature performance. A formulated electrolyte composed of 0.5 M lithium tetrafluoroborate in hybrid solvent of tetrahydrofuran and trifluoropropylene carbonate features a high ionic conductivity of 0.45 mS cm−1 at − 90 °C and an ultra-low freezing point of − 133 °C. Furthermore, in such electrolyte, the LiNi0.8Co0.1Mn0.1O2 cathode can be reversibly cycled at low temperature of − 40 °C and delivers a considerable specific capacity of 108.5 mAh/g at − 90 °C.
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