等温微量热法
电解质
碳酸乙烯酯
碳酸盐
碳酸二乙酯
化学
等温过程
锂(药物)
碳酸二甲酯
无机化学
溶剂
化学工程
分析化学(期刊)
色谱法
有机化学
热力学
物理化学
电极
内分泌学
工程类
甲醇
物理
医学
焓
作者
L. E. Downie,S. R. Hyatt,Jeff R. Dahn
摘要
In an effort to better the understanding of the high voltage degradation of electrolytes in lithium ion cells, this work presents isothermal microcalorimetry results on LiNi 0.42 Mn 0.42 Co 0.16 O 2 (NMC442)/graphite pouch cells up to 4.7 V. The voltage and time dependent parasitic heat flow was determined for cells containing several electrolyte compositions based on carbonate solvents with several additive combinations, as well as a fluorinated carbonate solvent system. We have demonstrated that cells containing fluorinated carbonate-based electrolyte (1M LiPF 6 in 3:7 fluoroethylene carbonate: di-2,2,2-trifluoroethyl carbonate) showed a significantly decreased parasitic heat flow at voltages >4.4 V compared to ethylene carbonate-based cells, but limited advantage <4.4 V. However all cells, regardless of electrolyte composition, exhibited very large parasitic heat flows, and therefore parasitic reaction rates, at high voltages (>4.35 V). The results presented here also show that high voltage (>4.5 V) cycling results in an increase in parasitic heat flow of the subsequent lower voltage cycles, and is indicative of a change in the dominant reaction pathway.
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