Determining Parasitic Reaction Enthalpies in Lithium-Ion Cells Using Isothermal Microcalorimetry

被引:20
作者
Glazier, S. L. [1 ]
Odom, S. A. [2 ]
Kaur, A. P. [2 ]
Dahn, J. R. [1 ]
机构
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS, Canada
[2] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
基金
加拿大自然科学与工程研究理事会;
关键词
ELECTROLYTE INTERPHASE FORMATION; FLUORINATED ELECTROLYTES; MOLECULAR-DYNAMICS; METHYL ACETATE; HEAT-FLOW; BATTERIES; CARBONATE; CHEMISTRY; LI+; CALORIMETRY;
D O I
10.1149/2.0761814jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Typical measurements of parasitic heat flow in lithium-ion cells can determine the magnitude of heat flow but cannot differentiate between different types of reactions. This causes difficulty when comparing cells that contain different coatings and solvent systems, which may affect parasitic reaction pathways. In this work, a new technique to measure the rate and net enthalpy change (Delta H) of parasitic reactions in lithium ion cells is introduced. Isothermal microcalorimetry and precision current measurements are used to make in-situ, non-destructive measurements of heat flow and parasitic current during high-voltage holds. The results are used to determine Delta H of parasitic processes in NMC532/graphite pouch cells. Effects of positive electrode coating, solvent, and upper cutoff voltage are explored. Solvent systems of organic carbonates with and without methyl acetate, and fluorinated carbonates are also investigated. Each solvent system yielded a unique trend of Delta H with increased voltage, and results were consistent between pair cells. Cells with organic carbonates showed consistent Delta H between voltages, while cells containing methyl acetate showed decreasing Delta H. Cells containing fluorinated carbonates showed increasing Delta H with increased voltage. The observed trends in Delta H and solvent systems as well as future developments of this method are discussed. (C) The Author(s) 2018. Published by ECS.
引用
收藏
页码:A3449 / A3458
页数:10
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