碳酸乙烯酯
电解质
环氧乙烷
化学
碳酸二甲酯
化学分解
盐(化学)
分解
碳酸盐
锂(药物)
降级(电信)
无机化学
氧化物
化学工程
甲醇
有机化学
聚合物
电极
物理化学
共聚物
内分泌学
工程类
电信
医学
计算机科学
作者
Grégory Gachot,Sylvie Grugeon,Michel Armand,Serge Pilard,Pierre Guénot,Marie‐Liesse Doublet,Stéphane Laruelle
标识
DOI:10.1016/j.jpowsour.2007.11.110
摘要
Electrolytes are crucial to the safety and long life of Li-ion batteries, however, the understanding of their degradation mechanisms is still sketchy. Here we report on the nature and formation of organic/inorganic degradation products generated at low potential in a lithium-based cell using cyclic and linear carbonate-based electrolyte mixtures. The global formation mechanism of ethylene oxide oligomers produced from EC/DMC (1/1 w/w)–LiPF6 salt (1 M) electrolyte decomposition is proposed then mimicked via chemical tests. Each intermediary product structure/formula/composition is identified by means of combined NMR, FTIR and high resolution mass spectrometry (ESI-HRMS) analysis. The key role played by lithium methoxide as initiator of the electrolyte degradation is evidenced, but more importantly we isolated for the first time lithium methyl carbonate as a side product of the ethylene oxide oligomers chemical formation. The same degradation mechanism was found to hold on for another cyclic and linear carbonate-based electrolyte such as EC/DEC (1/1 w/w)–LiPF6 salt (1 M). Such findings have important implications in the choice of chemical additives for developing highly performing electrolytes.
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