位阻效应
溶剂化
金属锂
电解质
锂(药物)
电介质
金属
二甲氧基乙烷
溶剂
材料科学
阳极
无机化学
化学
光电子学
有机化学
物理化学
内分泌学
医学
电极
作者
Eunseok Park,Jong‐Seok Park,Kyunam Lee,Yan Zhao,Tianhong Zhou,Gyuleen Park,Moon Sik Jeong,Min‐Koo Choi,Dong‐Joo Yoo,Hun‐Gi Jung,Ali Coskun,Jang Wook Choi
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-12-04
卷期号:8 (1): 179-188
被引量:42
标识
DOI:10.1021/acsenergylett.2c02003
摘要
1,2-Dimethoxyethane (DME) has been widely used as an electrolyte solvent for lithium metal batteries on account of its intrinsic reductive stability; however, its low oxidative stability presents a major challenge for use in high-voltage Li metal batteries (LMBs). In this direction, herein, we introduce a new low-dielectric solvent, 1,2-dimethoxypropane (DMP), as an electrolyte solvent. Compared to DME, DMP has decreased solvation power owing to its increased steric effects, thus promoting anion–Li+ interactions. This controlled solvation structure of the 2 M LiFSI-in-DMP electrolyte facilitated the formation of an anion-driven, stable interface at the lithium metal anode and oxidative stability for compatibility with widely adopted cathodes to afford Li|LiFePO4 and Li|LiNi0.8Co0.1Mn0.1O2 cells with decent cycling stability. These results imply the usefulness of steric control as an alternative strategy to commonly used fluorination to fine-tune the solvation power and, in general, the design of new solvents for practical lithium metal batteries.
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