Ionic conductivity and morphology of semi‐interpenetrating‐type polymer electrolyte entrapping poly(siloxane‐g‐allyl cyanide) |
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Authors: | Ki Hong Min Dae Beom Kim Yong Ku Kang Dong Hack Suh |
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Affiliation: | 1. School of Chemical Engineering, Hanyang University, Haengdang 1‐Dong, Seongdong‐Gu, Seoul 133‐791, Korea;2. Advanced Materials Division, Korea Research Institution of Chemical Technology, Yusong Taejon 305‐600, Korea |
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Abstract: | We prepared a semi‐IPN (interpenetrating network)‐type solid polymer electrolyte (SPE) using poly (ethylene glycol)dimethacrylate (PEGDMA) as a polymer matrix containing a monocomb‐type poly(siloxane‐g‐allyl cyanide) and poly(ethylene glycol)dimethylether (PEGDME) for the lithium secondary battery. The poly(siloxane‐g‐allyl cyanide)s were prepared by a hydrosilation reaction of poly (methyl hydrosiloxane) with allyl cyanide and characterized by 1H NMR and FTIR. The semi‐IPN‐type electrolyte was prepared by thermal curing, and conductivities of samples were measured by impedance spectroscopy using an indium tin oxide (ITO) electrode. The ionic conductivity of the semi‐IPN‐polymer electrolyte was about 1.05 × 10?5 S cm?1 with 60 wt % of the poly(siloxane‐g‐allyl cyanide) and 6.96 × 10?4 S cm?1 with 50 wt % of the PEGDME and 10 wt % of the poly(siloxane‐g‐allyl cyanide) at 30°C. The SEM morphology of the cross section of the semi‐IPN‐polymer electrolyte film was changed from discontinuous network to continuous network as increasing the PEGDME content and decreasing the poly(siloxane‐g‐allyl cyanide) content. The mechanical stability was also enhanced when increasing the PEGDME content. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 |
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Keywords: | polymer electrolyte polysiloxane allyl cyanide semi‐IPN |
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