Novel polysilsesquioxane hybrid polymer electrolytes for lithium ion batteries

Authors
Lee, Albert Sung SooLee, Jin HongLee, Jong-ChanHong, Soon ManHwang, Seung SangKoo, Chong Min
Issue Date
2014-01
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.2, no.5, pp.1277 - 1283
Abstract
A novel inorganic-organic hybrid crosslinker was prepared through synthesis of a fully condensed, high molecular weight ladder-like poly(methacryloxypropyl) silsesquioxane (LPMASQ) in one pot with a facile, base-catalysed system. The fully condensed LPMASQ revealed good thermal (similar to 380 degrees C) and electrochemical stability (similar to 5.0 V) due to the absence of uncondensed silanol groups. LPMASQ also revealed good solubility in various organic solvents and fully gelated 1 M LiPF6 in ethyl carbonate-diethyl carbonate (EC-DEC, 3/7, v/v) electrolyte solution through fast thermal and photocuring even at a very low concentration of 2 wt%. These observations were attributed to the polymeric nature of LPMASQ containing over one hundred methacryl moieties on the rigid double-stranded siloxane backbone. To the best of our knowledge, formation of a gel polymer electrolyte with 2 wt% gelator is the smallest gelation concentration that has ever been reported. This leads to high ionic conductivity (similar to 6.0 mS cm(-1)), excellent Coulombic efficiency and battery cell performance, comparable with those of the neat liquid electrolyte. The small crosslinker content, thermal and electrochemical stability, fast thermal and photocuring and facile processing of the LPMASQ based GPEs, as well as excellent Li battery cell performances strongly hold great promise for future industrial battery applications.
Keywords
CHEMICAL CROSS-LINKING; SOL-GEL MATERIALS; CYCLING PERFORMANCES; LIQUID; CHEMICAL CROSS-LINKING; SOL-GEL MATERIALS; CYCLING PERFORMANCES; LIQUID; Ion conduction; Hybrid type gel electrolyte
ISSN
2050-7488
URI
https://pubs.kist.re.kr/handle/201004/127270
DOI
10.1039/c3ta14290f
Appears in Collections:
KIST Article > 2014
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