A Study of Three Ester Co-Solvents in Lithium-Ion Cells
Source abstract
Abstract
The effects of three esters incorporated as co-solvents in 1.2 M LiPF 6 EC:EMC:DMC (25:5:70 by volume %) electrolyte were studied in Li[Ni 1-x-y Co x Al y ]O 2 /Graphite-SiO pouch cells. The esters: methyl propionate (MP), ethyl acetate (EA) and methyl butyrate (MB) were compared in a variety of tests on the cells. Storage tests at 60°C at both 4.2 V and 2.5 V demonstrated that MB and MP outperformed EA and cells containing 20% MP showed the least voltage drop during the 500 h storage period. In long-term cycling tests at 40°C, cells containing up to 20% ester exhibited similar capacity retention compared to cells with only EC:EMC:DMC solvent. Unwanted lithium plating could be suppressed in cells with 20% MP during charging above 2C compared to ester-free cells, which showed the onset of unwanted lithium plating at 1.8C. This improvement is due to the increased Li + conductivity of electrolytes containing MP. In addition, the use of up to 40% MP did not enhance reactivity between the charged electrode materials and electrolyte at elevated temperatures according to accelerating rate calorimetry measurements.
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Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (29)
Show source-provided references
1. 10.1016/j.progsolidstchem.2014.04.00610.1016/j.progsolidstchem.2014.04.006 ↗
2. 10.1016/j.mattod.2014.10.04010.1016/j.mattod.2014.10.040 ↗
3. http://www.molicel.com/hq/product/products12.html.
4. 10.1149/1.350123610.1149/1.3501236 ↗
5. 10.1016/S0378-7753(99)00470-X10.1016/S0378-7753(99)00470-X ↗
6. 10.1016/S0378-7753(99)00434-610.1016/S0378-7753(99)00434-6 ↗
7. 10.1016/S0378-7753(01)00670-X10.1016/S0378-7753(01)00670-X ↗
8. 10.1016/0378-7753(94)02031-W10.1016/0378-7753(94)02031-W ↗
9. 10.1149/1.145340710.1149/1.1453407 ↗
10. 10.1149/1.139257710.1149/1.1392577 ↗
11. 10.1016/0013-4686(95)00004-X10.1016/0013-4686(95)00004-X ↗
12. Herreyre S. Biensan P. Perton F. Barusseau S. , US6399255 B2 (1998).
13. 10.1016/j.electacta.2014.12.08410.1016/j.electacta.2014.12.084 ↗
14. 10.1016/j.electacta.2014.12.09310.1016/j.electacta.2014.12.093 ↗
15. Smallwood I. M. , Handbook of organic solvent properties, John Wiley & Sons, New York (1996).
16. 10.1021/cr030203g10.1021/cr030203g ↗
17. https://www.cdc.gov/niosh/ipcsneng/neng0816.html.
18. http://www.chemspider.com/Chemical-Structure.8305456.html.
19. Jow T. R. Xu K. Borodin O. Ue M. , Electrolytes for Lithium and Lithium-ion batteries, Springer, New York (2014).10.1007/978-1-4939-0302-3 ↗
20. 10.1149/2.1081706jes10.1149/2.1081706jes ↗
21. Beaulieu L. Y. Logan E. R. Gering K. L. Dahn J. R. , An Automated System for Performing Continuous Viscosity versus Temperature Measurements of Fluids Using an Ostwald Viscometer, submitted to Rev. Sci. Instrum. June 2017.10.1063/1.4990134 ↗
22. 10.1016/j.jpowsour.2016.07.03910.1016/j.jpowsour.2016.07.039 ↗
23. 10.1149/1.212885910.1149/1.2128859 ↗
24. 10.1149/2.031310jes10.1149/2.031310jes ↗
25. 10.1149/1.348935310.1149/1.3489353 ↗
26. 10.1149/2.007111jes10.1149/2.007111jes ↗
27. 10.1149/2.0191503jes10.1149/2.0191503jes ↗
28. 10.1149/2.0191701jes10.1149/2.0191701jes ↗
29. 10.1039/C6RA19482F10.1039/C6RA19482F ↗