电解质
离子电导率
离子液体
离子键合
反离子
单体
介电谱
高分子化学
线性扫描伏安法
烷基
电化学
聚合
化学
材料科学
聚合物
循环伏安法
无机化学
化学工程
有机化学
离子
电极
物理化学
催化作用
工程类
作者
Lisa Ehrlich,Doris Pospiech,Upenyu L. Muza,Albena Lederer,Julia Muche,Dieter Fischer,Petra Uhlmann,Felix Tzschöckell,Simon Muench,Martin D. Hager,Ulrich S. Schubert
标识
DOI:10.1002/macp.202200317
摘要
Organic, solid-state batteries require efficient solid electrolytes able to provide stable ion conduction. Here, we present solid electrolytes based on ionic liquid (IL) polymers with chloride counterions as electrolyte materials for batteries. Acrylic monomers with imidazolium substituents with alkyl side groups that are linked by alkyl spacers to the acrylic group are employed. The IL monomers with chloride counterions are either converted by thermally initiated radical polymerization into linear homopolymers or incorporated into polymer networks by UV-initiated copolymerization utilizing a bifunctional, non-ionic crosslinker. Both procedures successfully yielded the desired materials, which was confirmed by NMR spectroscopy (linear homopolymers) or Raman spectroscopy (IL networks). The ionic conductivities at room temperature were measured by Electrochemical Impedance Spectroscopy. The ionic conductivities of the linear homopolymers are in the range of 10−4 to 10−6 S cm−1, while those of the IL networks were about two orders of magnitude lower. They increase to 10−4 S cm−1 at 70°C. The electrochemical stability was examined by Linear Sweep Voltammetry and is proven in the voltage range of -2 to +2 V. The results reveal that the materials represent promising electrolytes for potential solid-state battery applications. This article is protected by copyright. All rights reserved
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