Poly(ethylene oxide) (PEO)/salt hybrids having sulfonamide groups on the PEO chain ends (PEOlooo -(SAR)2M2; R = -CF 3, -CH 3 and -C6H5; M = Li, Na, K, Rb and Cs) were prepared, and the bulk ionic conductivity was measured as a new type of ion conductive matrix. Among these, the salt having a trifluo
Polyether/salt hybrid (IV). Effect of benzenesulfonate group(s) and PEO molecular weight on the bulk ionic conductivity
โ Scribed by Kaori Ito; Yoichi Tominaga; Hiroyuki Ohno
- Book ID
- 104115008
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 985 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
Benzenesulfonate (Bs) groups were introduced to the terminal of poly(ethylene oxide) (PEO) and poly(propylene oxide) (PPO) oligomers with molecular weight (MW) of 30&6000 to design an ion conductive amorphous matrix. The phase of these PEO-salt hybrids was mainly influenced by the MW of the polyethers. PEO oligomers having benzenesulfonate group(s) with MW less than 600 showed amorphous phase in the bulk in a wide temperature range (-120 -+ 150ยฐC). The ionic conductivity of these amorphous salts was considerably influenced by the glass transition temperature (r,). The Tg of these PEO-salt hybrids was influenced by the fraction of salt group in the matrix. Among totally amorphous salts, the best ionic conductivity of 2.95 x 10e5 S cm-', at 50ยฐC was obtained in the PEOsso-BsCs. Though PE03so-BsM was also an amorphous salt, lower ionic conductivity was observed because of higher TB than that of PEO~X~-BSM. However, PEO~~O-BSM was useful as electrolyte in PEO oligomers because of excellent compatibility with the PEO oligomers. The ionic conductivity of PEOX~-BsM in PEO~W (MW of 300) was 40 times higher than that of PE0350-BsM in the bulk. Since PE0350-BsM was inherently ion conductive, the ionic conductivity for PE03so-BsM/PE0300 was kept high regardless of the salt concentration.
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