电解质
锂(药物)
分解
金属锂
金属
材料科学
无机化学
化学工程
化学
电极
冶金
有机化学
工程类
物理化学
医学
内分泌学
作者
Zehao Cui,Zhiao Yu,Hao Lyu,Zhenan Bao,Arumugam Manthiram
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-07-15
卷期号:10 (8): 3827-3833
被引量:5
标识
DOI:10.1021/acsenergylett.5c01433
摘要
Lithium (Li)-metal batteries with high-voltage cathodes are promising next-generation, high-energy automotive batteries. While ether-based electrolytes are known for their high reductive stability, their limited oxidative stability against high-voltage cathodes remains a key barrier to long-term service life. Here, we present a methodology enabling a comprehensive, quantitative assessment of cathode–electrolyte reactions, based on a model fluorinated 1,2-diethoxyethane-based electrolyte and LiNiO2 cathode. Online electrochemical mass spectroscopy at varying temperatures reveals both the thermodynamic and kinetic features of the electrolyte oxidative decomposition by quantifying gaseous byproducts and the reaction activation energy. Nuclear magnetic resonance spectroscopic results unveil alcohol and alkoxy acetic acid species as soluble decomposition products of ether electrolytes. Time-of-flight secondary ion mass spectrometry, combined with region-of-interest and spatial normalized standard deviation analyses, quantitatively determines the thickness and spatial and chemical homogeneity of the cathode–electrolyte interphase. This work establishes a quantitative methodology to assess gaseous, soluble, and solid cathode–electrolyte decomposition products.
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