期刊
ACS APPLIED POLYMER MATERIALS
卷 3, 期 3, 页码 1573-1582出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsapm.0c01398
关键词
polymer electrolyte; PEO architectures; vinyl ether with PEO side chains; grafting-to; thermal and electrochemical properties; Li+ conductivity
资金
- German Federal Ministry of Education and Research (BMBF) [13XP0175A]
- Helmholtz Association
This study investigates the synthesis of vinyl ether-based poly(ethylene oxide) (PEO) side-chain copolymers to reduce PEO crystallization. The research explores the impact of different PEO side chain lengths, grafting densities, and LiTFSI ratios on T-g, crystallinity, and ionic conductivity. Copolymers with longer PEO side chains and higher grafting densities exhibit higher crystallization tendencies with reduced T-g, while the addition of LiTFSI decreases crystallization but increases T-g, directly affecting ionic conductivity. Balancing these factors is crucial for the potential application of PEO side-chain copolymers as polymer electrolytes.
Herein, we report on the synthesis of a systematic library of vinyl ether-based poly(ethylene oxide) (PEO) side-chain copolymers in order to reduce the crystallization of PEO. The influence of different grafted PEO side chain lengths, the grafting density, and the [Li+]:[EO] ratio after mixing with LiTFSI on the glass transition temperature (T-g), the crystallinity, and the resulting ionic conductivity was examined. Copolymers bearing longer PEO side chains and higher grafting densities show higher crystallization tendencies while their T-g is reduced at the same time. Furthermore, the addition of LiTFSI reduces crystallization but increases T-g. Because these effects are directly impacting the ionic conductivity, we demonstrate that the different parameters need to be carefully adjusted in order to balance their influence. In this way, a fundamental view that shows the potential of PEO side-chain copolymers for their applications as polymer electrolytes is provided.
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