电解质
异氰酸酯
碳酸丙烯酯
化学
锂(药物)
无机化学
电化学
傅里叶变换红外光谱
碳酸乙烯酯
聚合
单体
高分子化学
有机化学
化学工程
电极
聚合物
聚氨酯
物理化学
内分泌学
工程类
医学
作者
Christiane Korepp,Wolfgang Kern,Eva Lanzer,Peter Raimann,Jürgen Besenhard,Maozhu Yang,Kai‐Christian Möller,Deng Tswen Shieh,Martin Winter
标识
DOI:10.1016/j.jpowsour.2007.06.140
摘要
To avoid solvent co-intercalation into graphite, the presence of a solid electrolyte interphase (SEI) is required. This film is formed via the reductive decomposition of electrolyte species, i.e. a film forming electrolyte additives. In this contribution we focus on an isocyanate compound, ethyl isocyanate (EtNCO) which performs well in a propylene carbonate electrolyte at both graphite anode and LiCoO2 cathode. EtNCO is investigated by in situ Fourier transform infrared (FTIR) spectroscopy. We conclude that the formation of a radical anion via electrochemical reduction of the electrolyte additive is the initiating step of the SEI formation process. The electro-polymerization of isocyanate monomers in small additive amounts in the PC electrolyte is critically discussed.
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