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
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.