Thermal stability of LiPF6 salt and Li-ion battery electrolytes containing LiPF6

被引:489
作者
Yang, Hui
Zhuang, Guorong V.
Ross, Philip N., Jr. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA
关键词
ethylene carbonate; lithium hexafuorophosphate; lithium ion battery;
D O I
10.1016/j.jpowsour.2006.03.058
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 thermal stability of the neat lithium hexafluorophosphate (LiPF6) salt and of 1 molal (m) solutions of LiPF6 in prototypical Li-ion battery solvents was studied with thermogravimetric analysis (TGA) and on-line Fourier transform infrared (FTIR). Pure LiPF6 salt is thermally stable up to 107 degrees C in a dry inert atmosphere, and its decomposition path is a simple dissociation producing lithium fluoride (LiF) as solid and PF5 as a gaseous products. In the presence of water (300 ppm) in the carrier gas, its decomposition onset temperature is lowered as a result of direct thermal reaction between LiPF6 and water vapor to form phosphorous oxyfluoride (POF3) and hydrofluoric acid (HF). No new products were observed in I m solutions of LiPF6 in ethylene carbonate (EC), dimethyl carbonate (DMC) and ethyl methyl carbonate (EMC) by on-line TGA-FTIR analysis. The storage of the same solutions in sealed containers at 85 degrees C for 300-420 h did not produce any significant quantity of new products as well. In particular. no alkylflurophosphates were found in the solutions after storage at elevated temperature. In the absence of either an impurity like alcohol or cathode active material that may (or may not) act as a catalyst, there is no evidence of thermally induced reaction between LiPF6 and the prototypical Li-ion battery solvents EC, PC, DMC or EMC. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:573 / 579
页数:7
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