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Upgrading traditional liquid electrolyte via in situ gelation for future lithium metal batteries
Author(s) -
Feng-Quan Liu,
Wenpeng Wang,
YaXia Yin,
Shuaifeng Zhang,
JiLei Shi,
Lu Wang,
XuDong Zhang,
Yue Zheng,
Jianjun Zhou,
Lin Li,
YuGuo Guo
Publication year - 2018
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aat5383
Subject(s) - electrolyte , lithium metal , lithium (medication) , liquid metal , in situ , materials science , metal , chemical engineering , electrode , nanotechnology , chemistry , metallurgy , organic chemistry , engineering , medicine , endocrinology
High-energy lithium metal batteries (LMBs) are expected to play important roles in the next-generation energy storage systems. However, the uncontrolled Li dendrite growth in liquid electrolytes still impedes LMBs from authentic commercialization. Upgrading the traditional electrolyte system from liquid to solid and quasi-solid has therefore become a key issue for prospective LMBs. From this premise, it is particularly urgent to exploit facile strategies to accomplish this goal. We report that commercialized liquid electrolyte can be easily converted into a novel quasi-solid gel polymer electrolyte (GPE) via a simple and efficient in situ gelation strategy, which, in essence, is to use LiPF to induce the cationic polymerization of the ether-based 1,3-dioxolane and 1,2-dimethoxyethane liquid electrolyte under ambient temperature. The newly developed GPE exhibits elevated protective effects on Li anodes and has universality for diversified cathodes including but not restricted to sulfur, olivine-type LiFePO, and layered LiNiCoMnO, revealing tremendous potential in promoting the large-scale application of future LMBs.

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