材料科学
水溶液
锌
阳离子聚合
多孔性
聚合物
阴极
复合数
原位
化学工程
离子
无机化学
复合材料
高分子化学
冶金
有机化学
物理化学
化学
工程类
作者
Shoubing Chen,Xuewu Gao,Renyao Huang,Sha Fang,Xianghe Peng,Mengke Li,Yi Feng,Xiongwei Qu,Xiaojie Zhang
标识
DOI:10.1002/adfm.202521459
摘要
Abstract Manganese‐based oxides are promising cathode materials for aqueous zinc ion batteries (AZIBs) due to their high energy density and low cost. However, the cycling stability is severely limited by the sluggish reaction kinetics as well as the manganese dissolution. In this work, two pyridinium ionic porous organic polymers (iPOPs) composite ɛ‐MnO 2 cathode materials, CN‐POP@MnO 2 and PN‐POP@MnO 2 , are prepared by an in situ composite method. The stable skeleton of iPOPs effectively prevents the structural collapse of the cathode. Its ionic sites and rigid network framework work together to disrupt the coordination environment of hydrated zinc ions, accelerating reaction kinetics and reducing cathode polarization. Therefore, the resultant batteries based on CN‐POP@MnO 2 and PN‐POP@MnO 2 cathodes exhibit excellent electrochemical performance. Especially for PN‐POP‐based batteries, the specific capacity is maintained at ≈96 mAh g −1 after 1500 cycles at 1 C, and the capacity attenuation rate is 0.017% per cycle.
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