材料科学
超级电容器
电解质
离子键合
电化学
电极
化学工程
小提琴手
离子电导率
储能
离子
功率密度
聚合物
多孔性
离子液体
多孔介质
纳米技术
复合材料
有机化学
功率(物理)
化学
物理化学
工程类
催化作用
物理
量子力学
作者
A M Mahmudul Hasan,Saptasree Bose,Rupam Roy,J. Márquez,Chaitanya Sharma,Juan C. Nino,Kent O. Kirlikovali,Omar K. Farha,Austin M. Evans
标识
DOI:10.1002/adma.202405924
摘要
Abstract Here, an ionic polymer of intrinsic microporosity (PIM) as a high‐functioning supercapacitor electrode without the need for conductive additives or binders is reported. The performance of this material is directly related to its large accessible surface area. By comparing electrochemical performance between a porous viologen PIM and a nonporous viologen polymer, it is revealed that the high energy and power density are both due to the ability of ions to rapidly access the ionic PIM. In 0.1 m H 2 SO 4 electrolyte, a pseudocapacitve energy of 315 F g −1 is observed, whereas in 0.1 m Na 2 SO4, a capacitive energy density of 250 F g −1 is obtained. In both cases, this capacity is retained over 10 000 charge–discharge cycles, without the need for stabilizing binders or conductive additives even at moderate loadings (5 mg cm −2 ). This desirable performance is maintained in a prototype symmetric two‐electrode capacitor device, which has >99% Coloumbic efficiency and a <10 mF capacity drop over 2000 cycles. These results demonstrate that ionic PIMs function well as standalone supercapacitor electrodes and suggest ionic PIMs may perform well in other electrochemical devices such as sensors, ion‐separation membranes, or displays.
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