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Use of Ionic Liquids in Rod-Coil Block Copolyimides for Improved Lithium Ion ConductionSolvent-free, solid polymer electrolytes (SPE) have the potential to improve safety, increase design flexibility and enhance performance of rechargeable lithium batteries. Solution based electrolytes are flammable and typically incompatible with lithium metal anodes, limiting energy density. We have previously demonstrated use of polyimide rod coil block copolymers doped with lithium salts as electrolytes for lithium polymer batteries. The polyimide rod blocks provide dimensional stability while the polyethylene oxide (PEO) coil portions conduct ions. Phase separation of the rods and coils in these highly branched polymers provide channels with an order of magnitude improvement in lithium conduction over polyethylene oxide itself at room temperature. In addition, the polymers have been demonstrated in coin cells to be compatible with lithium metal. For practical use at room temperature and below, however, at least an order of magnitude improvement in ion conduction is still required. The addition of nonvolatile, room temperature ionic liquids has been shown to improve the ionic conductivity of high molecular weight PEO. Herein we describe use of these molten salts to improve ionic conductivity in the rod-coil block copolymers.
Document ID
20070006481
Acquisition Source
Glenn Research Center
Document Type
Conference Paper
Authors
Meador, Mary Ann B.
(NASA Glenn Research Center Cleveland, OH, United States)
Tigelaar, Dean M.
(Ohio Aerospace Inst. Cleveland, OH, United States)
Chapin, Kara
(NASA Glenn Research Center Cleveland, OH, United States)
Bennett, William R.
(QSS Group, Inc. Cleveland, OH, United States)
Date Acquired
August 24, 2013
Publication Date
January 1, 2007
Subject Category
Inorganic, Organic And Physical Chemistry
Meeting Information
Meeting: American Chemical Society Meeting
Location: Chicago, IL
Country: United States
Start Date: March 1, 2007
Funding Number(s)
WBS: WBS 083229.04.15.01.01.01
Distribution Limits
Public
Copyright
Public Use Permitted.
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