The Impact of Electrolyte Composition on Parasitic Reactions in Lithium Ion Cells Charged to 4.7 V Determined Using Isothermal Microcalorimetry

被引:66
作者
Downie, L. E. [1 ]
Hyatt, S. R. [1 ]
Dahn, J. R. [1 ]
机构
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PROMOTE LONG LIFETIME; SITU GAS EVOLUTION; LI-ION; HIGH-VOLTAGE; FLUORINATED ELECTROLYTES; CYCLING PERFORMANCE; VINYLENE CARBONATE; TRIS(TRIMETHYLSILYL) PHOSPHITE; METHYLENE METHANEDISULFONATE; ADDITIVE MIXTURES;
D O I
10.1149/2.0081602jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
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 LiNi0.42Mn0.42Co0.16O2 (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 LiPF6 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. (C) The Author(s) 2015. Published by ECS.
引用
收藏
页码:A35 / A42
页数:8
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