journal article·2008-03

Deciphering the multi-step degradation mechanisms of carbonate-based electrolyte in Li batteries

Gregory Gachot, Sylvie Grugeon, Michel Armand, Serge Pilard, Pierre Guenot, Jean-Marie Tarascon, Stephane Laruelle

Journal of Power Sources· Volume 178· Issue 1
Publisher page

Abstract

Abstract Electrolytes are crucial to the safety and long life of Li-ion batteries, however, the understanding of their degradation mechanisms is still sketchy. Here we report on the nature and formation of organic/inorganic degradation products generated at low potential in a lithium-based cell using cyclic and linear carbonate-based electrolyte mixtures. The global formation mechanism of ethylene oxide oligomers produced from EC/DMC (1/1 w/w)–LiPF 6 salt (1 M) electrolyte decomposition is proposed then mimicked via chemical tests. Each intermediary product structure/formula/composition is identified by means of combined NMR, FTIR and high resolution mass spectrometry (ESI-HRMS) analysis. The key role played by lithium methoxide as initiator of the electrolyte degradation is evidenced, but more importantly we isolated for the first time lithium methyl carbonate as a side product of the ethylene oxide oligomers chemical formation. The same degradation mechanism was found to hold on for another cyclic and linear carbonate-based electrolyte such as EC/DEC (1/1 w/w)–LiPF 6 salt (1 M). Such findings have important implications in the choice of chemical additives for developing highly performing electrolytes.
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research

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References (24)

Show source-provided references
1. Peled · J. Electrochem. Soc. · 1979 · 126 · 204710.1149/1.2128859 ↗
2. Laruelle · J. Electrochem. Soc. · 2004 · 151 · A120210.1149/1.1760992 ↗
3. Dedryvère · Chem. Mater. · 2004 · 16 · 105610.1021/cm0311269 ↗
4. Grugeon · Chem. Mater. · 2005 · 17 · 504110.1021/cm0511825 ↗
5. Vollmer · J. Electrochem. Soc. · 2004 · 151 · A17810.1149/1.1633765 ↗
6. Aurbach · J. Electrochem. Soc. · 1987 · 134 · 161110.1149/1.2100722 ↗
7. Aurbach · J. Electroanal. Chem. · 1992 · 339 · 45110.1016/0022-0728(92)80467-I ↗
8. Aurbach · J. Electrochem. Soc. · 1994 · 141 · L110.1149/1.2054718 ↗
9. Aurbach · J. Electrochem. Soc. · 1994 · 141 · 60310.1149/1.2054777 ↗
10. Aurbach · J. Electrochem. Soc. · 1995 · 142 · 288210.1149/1.2048659 ↗
11. Zuang · J. Phys. Chem. B · 2005 · 109 · 1756710.1021/jp052474w ↗
12. Xu · J. Phys. Chem. B · 2006 · 110 · 770810.1021/jp0601522 ↗
13. Takeuchi · J. Electrochem. Soc. · 1997 · 144 · 194410.1149/1.1837726 ↗
14. Aurbach · J. Power Sources · 1997 · 68 · 9110.1016/S0378-7753(97)02575-5 ↗
15. Yoshida · J. Power Sources · 1997 · 68 · 31110.1016/S0378-7753(97)02635-9 ↗
16. Ein-Ely · Electrochem. Solid-State Lett. · 1999 · 2 · 21210.1149/1.1390787 ↗
17. Sasaki · J. Power Sources · 2005 · 150 · 20810.1016/j.jpowsour.2005.02.021 ↗
18. Gireaud · J. Electrochem. Soc. · 2005 · 152 · A85010.1149/1.1872673 ↗
19. Dedryvère · J. Electrochem. Soc. · 2005 · 152 · A68910.1149/1.1861994 ↗
20. Andersson · J. Electrochem. Soc. · 2001 · 148 · A110010.1149/1.1397771 ↗
21. Sloop · J. Power Sources · 2003 · 119–121 · 33010.1016/S0378-7753(03)00149-6 ↗
22. Grugeon · Anal. Chem. · 2006 · 78 · 368810.1021/ac051987w ↗
23. Radvel · J. Power Sources · 2003 · 119–121 · 805
24. Dedryvère · J. Phys. Chem. B · 2005 · 109 · 1586810.1021/jp051626k ↗