کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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634722 | 1456073 | 2013 | 8 صفحه PDF | دانلود رایگان |
It is a compelling challenge to develop solid polymer electrolyte membranes for rechargeable battery with both high ionic conductivity and superior mechanical performance. In this study, we first prepare a new type of all-solid-state composite polymer electrolyte from lithium bis-trifluoromethanesulphonimide (LiTFSI), succinonitrile (SN) and poly(ethylene oxide) segmented polysulfone copolymers (PSF–PEO) with various PEO contents in low molecular weight (Mn=1500 Da), which are synthesized by condensation polymerization. The optimized composite polymer electrolyte PSF–PEO35+LiTFSI+SN membrane exhibits a remarkable amorphous state; leading to its ionic conductivity of 1.6×10−4 S cm−1 at room temperature. Especially, the tensile strength of the PSF–PEO35+LiTFSI+SN electrolyte membrane is still more than 4.3 MPa at 80 °C, indicating its excellent mechanical property and high thermal stability in a wide temperature range. Li symmetric cell and Li/LiFePO4 cell with the above electrolyte display low voltage polarization and good rechargeability. The test results indicate that the solid PSF–PEO35+LiTFSI+SN composite electrolyte membrane is a promising candidate for future applications in rechargeable lithium batteries.
A new type of composite polymer electrolyte is prepared by using poly(ethylene oxide) segmented polysulfone copolymer and succinonitrile. It shows high mechanical strength in a wide temperature range and good electrochemical performance.Figure optionsDownload high-quality image (264 K)Download as PowerPoint slideHighlights
► We first utilize PSF–PEO copolymers to prepare solid polymer electrolyte.
► This electrolyte shows superior mechanical properties in a wide temperature range.
► PSF–PEO35+LiTFSI+SN electrolyte has good compatibility toward Li electrode.
► Li/LiFePO4 cell using this electrolyte displays good electrochemical behavior.
Journal: Journal of Membrane Science - Volumes 425–426, 1 January 2013, Pages 105–112