Abstract
This paper describes studies of the interface between lithium electrodes and solid electrolyte systems using in situ FTIR spectroscopy in a single internal reflectance mode. In this method, the masking effect of the electrolyte matrix components is largely avoided. We studied gel electrolytes based on polyvinylidene difluoride-hexafluoropropylene with cyclic alkyl carbonates as plasticizers, suitable for ambient temperatures, and a solvent free polymer, derivatives of polyethylene oxide (PEO) with a branched structure: poly[ethyleneoxide-2-(2-methoxyethoxy)ethyl glycidyl ether] at elevated temperatures. We found that the surface chemistry of Li electrodes in contact with the gel matrixes is dominated by alkyl carbonate solvent reduction to ROCO2Li surface species. In the case of the PEO-based polymer, the surface reactions of Li electrodes are dominated by salt and trace water reduction. The polymer itself seems to be stable with lithium even at 60°C.
Original language | English |
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Pages (from-to) | 632-636 |
Number of pages | 5 |
Journal | Journal of Power Sources |
Volume | 97-98 |
DOIs | |
Publication status | Published - 2001 Jul |
Event | 10th International Meeting on Lithium Batteries - Como, Italy Duration: 2001 May 28 → 2001 Jun 2 |
Keywords
- Combed-branched PEO-based polymers
- Gel electrolytes
- In situ FTIR spectroscopy
- Li electrodes
- SIR mode
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- Energy Engineering and Power Technology
- Physical and Theoretical Chemistry
- Electrical and Electronic Engineering