金属锂
四氢呋喃
锂(药物)
电解质
盐(化学)
对偶(语法数字)
金属
材料科学
固态
化学工程
无机化学
化学
电极
有机化学
冶金
物理化学
工程类
医学
艺术
文学类
溶剂
内分泌学
作者
Zhiyong Li,Zhiyong Li,Zhuo Li,Zhuo Li,Rui Yu,Xin Guo
标识
DOI:10.1016/j.jechem.2024.04.044
摘要
The stable operation of solid-state lithium metal batteries at low temperatures is plagued by severe restrictions from inferior electrolyte-electrode interface compatibility and increased energy barrier for Li+ migration. Herein, we prepare a dual-salt poly(tetrahydrofuran)-based electrolyte consisting of lithium hexafluorophosphate and lithium difluoro(oxalato)borate (LiDFOB). The Li-salt anions (DFOB−) not only accelerate the ring-opening polymerization of tetrahydrofuran, but also promote the formation of highly ion-conductive and sustainable interphases on Li metal anodes without sacrificing the Li+ conductivity of electrolytes, which is favorable for Li+ transport kinetics at low temperatures. Applications of this polymer electrolyte in Li||LiFePO4 cells show 82.3% capacity retention over 1000 cycles at 30 °C and endow stable discharge capacity at −30 °C. Remarkably, the Li||LiFePO4 cells retain 52% of their room-temperature capacity at −20 °C and 0.1 C. This rational design of dual-salt polymer-based electrolytes may provide a new perspective for the stable operation of quasi-solid-state batteries at low temperatures.
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