电解质
碳酸乙烯酯
溶解度
电池(电)
碳酸二甲酯
材料科学
有机自由基电池
聚合物
电化学
化学工程
碳酸盐
氧化还原
无机化学
电极
有机化学
化学
催化作用
物理化学
热力学
功率(物理)
复合材料
冶金
工程类
物理
作者
Verena Perner,Diddo Diddens,Fabian Otteny,Verena Küpers,Peter Bieker,Birgit Esser,Martin Winter,Martin Kolek
标识
DOI:10.1021/acsami.0c20012
摘要
Organic materials are promising candidates for next-generation battery systems. However, many organic battery materials suffer from high solubility in common battery electrolytes. Such solubility can be overcome by introducing tailored high-molecular-weight polymer structures, for example, by cross-linking, requiring enhanced synthetic efforts. We herein propose a different strategy by optimizing the battery electrolyte to obtain insolubility of non-cross-linked poly(3-vinyl-N-methylphenothiazine) (PVMPT). Successive investigation and theoretical insights into carbonate-based electrolytes and their interplay with PVMPT led to a strong decrease in the solubility of the redox polymer in ethylene carbonate/ethyl methyl carbonate (3:7) with 1 M LiPF6. This allowed accessing its full theoretical specific capacity by changing the charge/discharge mechanism compared to previous reports. Through electrochemical, spectroscopic, and theoretical investigations, we show that changing the constituents of the electrolyte significantly influences the interactions between the electrolyte molecules and the redox polymer PVMPT. Our study demonstrates that choosing the ideal electrolyte composition without chemical modification of the active material is a successful strategy to enhance the performance of organic polymer-based batteries.
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