共轭体系
磺胺
材料科学
电极
聚合物
锂(药物)
电池(电)
电导率
导电聚合物
有机自由基电池
离子
纳米技术
化学工程
有机化学
化学
复合材料
电解质
功率(物理)
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Jiang Tian Liu,Eloi Grignon,Alicia M. Battaglia,Muhammad Imran,Christopher Copeman,Harrison A. Mills,Ashlee J. Howarth,Edward H. Sargent,Dwight S. Seferos
标识
DOI:10.1021/acs.chemmater.3c02105
摘要
Organic electrode materials have emerged as promising solutions for numerous energy applications. However, their full utility is impeded by their limited stability and inherently poor conductivity. To address these issues, one approach is to use functional conjugated polymers to replace the conventional insulating poly(vinylidene fluoride) (PVDF) binder that may facilitate ion/electron transport and stabilize the electrode. In this study, we report the synthesis of a series of sulfonamide π-conjugated small molecules, linear oligomers, and two-dimensional polymers and their subsequent use as binder materials for organic electrodes. We observe an enhanced specific capacity in a perylenetetracarboxylic dianhydride (PTCDA) composite electrode. The impact of dimensionality is evaluated through the battery performance. The two-dimensional sulfonamide polymer affords a 3-fold improvement in capacity retention compared to PVDF. The results presented in this work highlight that sulfonamide-containing materials are promising candidates as metal ion battery binders and that dimensionality is a key parameter for their use in lithium-ion batteries.
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