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Gel polymer electrolytes prepared by in situ polymerization of vinyl monomers in room-temperature ionic liquids

机译:通过在室温离子液体中原位聚合乙烯基单体制备的凝胶聚合物电解质

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摘要

In situ free radical polymerization of compatible vinyl monomers (methyl methacrylate, MMA) in a room temperature ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate, BMIPF_6), obtained a novel series of gel polymer electrolytes (GPEs) with high ionic conductivity. The resulting polymer gels were flexible, transparent and high conductive films. Their glass transition temperatures decreased with increasing mass fraction of BMIPF_6 and behaved as a completely compatible binary system. Analysis of FT-IR spectra showed that there existed an interaction between BMIPF6 and PMMA polymer matrix in the GPEs. The temperature dependence of the ionic conductivity of the polymer electrolyte films followed the Vogel-Tamman-Fulcher (VTF) equation, and the ionic conductivity at ambient temperature reached a value close to 10~(-3) S cm~(-1). Then the performance of capacitors applying the GPEs was determined by cyclic voltammetry, impedance spectroscopy and galvanostatic charging and discharging.
机译:相容性乙烯基单体(甲基丙烯酸甲酯,MMA)在室温离子液体(1-丁基-3-甲基咪唑六氟磷酸盐,BMIPF_6)中的原位自由基聚合,获得了一系列具有高离子电导率的新型凝胶聚合物电解质(GPE)。所得的聚合物凝胶是柔性的,透明的和高导电的膜。它们的玻璃化转变温度随着BMIPF_6质量分数的增加而降低,并表现为完全兼容的二元体系。红外光谱分析表明,GPE中BMIPF6与PMMA聚合物基体之间存在相互作用。聚合物电解质膜离子电导率的温度依赖性遵循Vogel-Tamman-Fulcher(VTF)方程,在室温下离子电导率达到接近10〜(-3)S cm〜(-1)的值。然后,通过循环伏安法,阻抗谱法和恒电流充放电确定了应用GPE的电容器的性能。

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