DEGRADATION MECHANISM OF ALKYL CARBONATE SOLVENTS USED IN LITHIUM-IONCELLS DURING INITIAL CHARGING

Citation
H. Yoshida et al., DEGRADATION MECHANISM OF ALKYL CARBONATE SOLVENTS USED IN LITHIUM-IONCELLS DURING INITIAL CHARGING, Journal of power sources, 68(2), 1997, pp. 311-315
Citations number
6
Journal title
ISSN journal
03787753
Volume
68
Issue
2
Year of publication
1997
Pages
311 - 315
Database
ISI
SICI code
0378-7753(1997)68:2<311:DMOACS>2.0.ZU;2-R
Abstract
The degradation mechanism of electrolytes in the lithium-ion cell with LiCoO2 and graphite electrodes was investigated by analyzing: (i) the composition of generated gases; (ii) thin films formed on the electro de, and (iii) the compositional change of the electrolyte during the i nitial charging. The solvents in this work were ethylene carbonate (EC ), dimethyl carbonate (DMC), ethylmethyl carbonate (EMC) and diethyl c arbonate (DEC). LiPF6 was used as a salt. In the one- to three-compone nt systems containing EC, carbon monoxide and ethane were detected, wh ereas Li2CO3, RCOOLi and (CH2OLi)(2) were the main components of the s urface film on the negative electrode. From these results, it can be a ssumed that the decomposition of the systems was mainly due to the red uctive reaction of EC at the initial charging. Through the additional analysis of the electrolyte composition, it was confirmed that the dia lkyl-2,5-dioxahexane carboxylate was produced in the electrolyte after initial charging. This suggests the occurrence of trans-esterificatio n. (C) 1997 Elsevier Science S.A.