Design of organic-inorganic solid polymer electrolytes: synthesis, structure, and properties

被引:48
|
作者
Bronstein, LM [1 ]
Karlinsey, RL
Ritter, K
Joo, CG
Stein, B
Zwanziger, JW
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[2] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
关键词
D O I
10.1039/b401826e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This paper reports the synthesis, structure, and properties of novel hybrid solid polymer electrolytes (SPEs) consisting of organically modified aluminosilica (OM-AlSi), formed within a poly(ethylene oxide)-in-salt (Li triflate) phase. To alter the structure and properties of these polymer electrolytes, we used functionalized silanes containing poly(ethylene oxide) (PEO) tails or CN groups. The SPEs described here were studied using differential scanning calorimetry, Raman spectroscopy, X-ray powder diffraction, and AC impedance spectroscopy. The size of the OM-AlSi domains was estimated using transmission electron microscopy and comparing the sizes of AlSi nanoparticles, obtained via calcination of the hybrid SPE. The conductivity enhancement, caused by incorporation of PEO tails or CN groups in the hybrid materials based on 600 Da poly(ethylene glycol), can be ascribed to a decrease of OM-AlSi domain size accompanied by an increase of the OM-AlSi/PEO + LiTf interface. For the CN modifier, increase of this interface increases the amount of CN groups exposed to PEO + LiTf phase, thus increasing the effective dielectric constants of the materials and their conductivity, although this dependence is not linear. In the case of the PEO modifier, different effects are observed for 600 Da PEG and 100 kDa PEO. For 100 kDa PEO, incorporation of the silane with a PEO tail caused a decrease of conductivity. Here, AlSi particle size remains basically unchanged with addition of silane-modifier, and the decrease of conductivity can be attributed to formation of a crystalline phase at the OM-AlSi/PEO + LiTf interface.
引用
收藏
页码:1812 / 1820
页数:9
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