TPD-GC/MS analysis of the solid electrolyte interface (SEI) on a graphite anode in the propylene carbonate/ethylene sulfite electrolyte system for lithium batteries

被引:83
作者
Ota, H
Sato, T
Suzuki, H
Usami, T
机构
[1] Ctr Analyt Chem & Sci Inc, Tsukuba Lab, Ami, Ibaraki 3000332, Japan
[2] Mitsubishi Chem Corp, Tsukuba Res Ctr, Ami, Ibaraki 3000332, Japan
关键词
TPD-GC/MS; solid electrolyte interfaces; graphite anode; ethylene sulfite; additive;
D O I
10.1016/S0378-7753(01)00738-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The solid electrolyte interface (SEI) formed on a graphite electrode in the electrolyte system consisting of propylene carbonate (PC) and ethylene sulfite (ES) was investigated by temperature programmed desorption or decomposition-gas chromatography/mass spectrometry (TPD-GC/MS), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), and chemical analysis in order to analyze the detailed structure of the SEI. It was proved that a lithium-oxy-sulfite film (Li2SO3 and/or ROSO2Li) was generated by the reductive decomposition of ES in advance of the decomposition of PC and the structure of the SEI structure significantly depends upon current density. In case of the high current density, the inorganic SEI was first formed at high potential and, around the potential where the intercalation of lithium occurs, the organic SEI was formed later. On the other hand, at a low current density, the SEI composed of only an organic component was immediately formed from the starting potential (1.5 V versus Li/Li+). Asa result, it has become clear that the SEI created by the additive at the initial stage of the potential suppressed the reductive decomposition of PC and plays an important role in the effective SEI formation for intercalation. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:107 / 113
页数:7
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