溶剂化
锂(药物)
电解质
二甲氧基乙烷
金属锂
离子
金属
溶剂
化学
无机化学
离解(化学)
轨道能级差
相间
分子
化学工程
有机化学
物理化学
电极
内分泌学
工程类
生物
医学
遗传学
作者
Gyuleen Park,Kyunam Lee,Dong‐Joo Yoo,Jang Wook Choi
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-11-03
卷期号:7 (12): 4274-4281
被引量:35
标识
DOI:10.1021/acsenergylett.2c02399
摘要
A variety of electrolyte engineering strategies have been introduced to extend the cycle life of lithium metal batteries (LMBs). These strategies can be largely grouped into two categories: those that induce a solvent-driven vs those that induce an anion-driven solid electrolyte interphase (SEI) layer. Although each strategy has proven to be effective for SEI manipulation, they are not yet comprehensively understood. Here, lithium salts with different dissociation abilities are systematically screened. Among those screened, highly dissociative lithium bis(trifluoromethane) sulfonimide (LiTFSI) with a high lowest unoccupied molecular orbital (LUMO) level is found to have enhanced cyclability by promoting the reduction of the solvent, fluoroethylene carbonate (FEC). Moreover, 1,2-dimethoxyethane (DME) as a cosolvent induces free FEC from the solvation sheath to further improve the cycle life by forming an SEI layer with uniformly distributed fluorine-containing components. This study unveils the usefulness of free solvent molecules by manipulating the solvation environments in achieving high-performance LMBs.
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