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

碳酸乙烯酯 化学 碳酸二甲酯 热重分析 热稳定性 电解质 惰性气体 无机化学 二甲氧基乙烷 热分解 氢氟酸 锂(药物) 傅里叶变换红外光谱 化学工程 工程类 有机化学 催化作用 电极 物理化学 内分泌学 医学
作者
Hui Yang,Guorong V. Zhuang,Philip N. Ross
出处
期刊:Journal of Power Sources [Elsevier BV]
卷期号:161 (1): 573-579 被引量:559
标识
DOI:10.1016/j.jpowsour.2006.03.058
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 °C in a dry inert atmosphere, and its decomposition path is a simple dissociation producing lithium fluoride (LiF) as solid and PF5 as 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 1 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 °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.
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