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Cited 22 time in webofscience Cited 27 time in scopus
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Electrochemical characterization of poly(vinylidene fluoride-co-hexafluoro propylene) based electrospun gel polymer electrolytes incorporating moth temperature ionic liquids as green electrolytes for lithium batteries

Authors
Raghavan, PrasanthZhao, XiaohuiChoi, HyunjiLim, Du-HyunKim, Jae-KwangMatic, AleksandarJacobsson, PerNah, ChangwoonAhn, Jou-Hyeon
Issue Date
1-Sep-2014
Publisher
ELSEVIER SCIENCE BV
Keywords
Electrospinning; Nanofibrous membrane; Gel polymer electrolyte; Room temperature ionic liquid; 1-Alkyl-3-methylimidazolium; bis(trifluoromethylsulfonyl)imide
Citation
SOLID STATE IONICS, v.262, pp 77 - 82
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
SOLID STATE IONICS
Volume
262
Start Page
77
End Page
82
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/18793
DOI
10.1016/j.ssi.2013.10.044
ISSN
0167-2738
1872-7689
Abstract
A series of gel polymer electrolytes (GPEs) based on electrospun membranes of poly(vinylidene fluoride-co-hexafluoropropylene) [P(VdF-co-HFP)] incorporating room temperature ionic liquids (RTILs), 1-alkyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide complexed with lithium bis(trifluoromethylsulfonyl) inside (LiTFSI) as electrolytes have been prepared and their fundamental electrochemical properties were investigated. The morphology of electrospun membranes was examined by a field emission scanning electron microscope (FE-SEM). The membranes show uniform morphology with an average fiber diameter of 780 nm, high porosity and high electrolyte uptake. GPEs were prepared by soaking the electrospun membranes in 1 M LiTFSI in RTILs for 1 h and exhibit a high ionic conductivity of 2.4 x 10(-3)-4.5 x 10(-3) S cm(-1) at 25 degrees C. A Li/GPEs/LiFePO4 cell using these RTILs delivers high discharge capacity (similar to 140 mAh g(-1)) when evaluated at 25 degrees C at 0.1 C-rate and exhibits a very stable discharge capacity under continuous cycling. Among the GPEs, EMITFSI shows the highest electrochemical properties although the solid electrolyte interface (SEI) layer was not formed. (C) 2013 Elsevier B.V. All rights reserved.
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