Electrochemical stability of bis(trifluoromethanesulfonyl)imide-based ionic liquids at elevated temperature as a solvent for a titanium oxide bronze electrode
Cited 32 times in
Cited 32 times in
- Title
- Electrochemical stability of bis(trifluoromethanesulfonyl)imide-based ionic liquids at elevated temperature as a solvent for a titanium oxide bronze electrode
- Author
- Mun, Junyoung; Jung, Yoon Seok; Yim, Taeeun; Lee, Hyun Yeong; Kim, Hyo-Jin; Kim, Young Gyu; Oh, Seung M.
- Keywords
- Lithium-ion battery; Room-temperature ionic liquids; Titanium oxide bronze; Thermal stability; Cathodic stability; Electrolyte decomposition
- Issue Date
- 2009-12
- Publisher
- ELSEVIER SCIENCE BV
- Citation
- JOURNAL OF POWER SOURCES, v.194, no.2, pp.1068 - 1074
- Abstract
- Four different electrolytes are prepared by dissolving a Li salt in three different room-temperature ionic liquids (RTILs) and also in a conventional organic solvent. The cathodic (electrochemical reduction) stability of these electrolytes is compared at both ambient and elevated temperature by potential cycling on a TiO2-B electrode. At room temperature, the stability of pyrrolidinium- and piperidinium-based RTILs is comparable with that of the carbonate-based organic solvent, which is in contrast to the severely decomposed imidazolium-based RTIL. At elevated temperature (120 °C), the imidazolium-based RTIL undergoes even more significant cathodic decomposition that results in the deposition of a resistive surface film and leads to eventual cell degradation. By contrast, the cathodic decomposition and concomitant film deposition are not serious with pyrrolidinium- and piperidinium-based RTILs even at this high-temperature, so that the TiO2-B/Li cell operates with reasonably good cycle performance. The latter two RTILs appear to be promising solvents for lithium-ion batteries that are durable against occasional exposure to high-temperature.
- URI
- ; Go to Link
- DOI
- 10.1016/j.jpowsour.2009.05.048
- ISSN
- 0378-7753
- Appears in Collections:
- ECHE_Journal Papers
- Files in This Item:
-
1-s2.0-S0378775309010118-main.pdf
Download
can give you direct access to the published full text of this article. (UNISTARs only)
Show full item record
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.