材料科学
分离器(采油)
共价键
膜
离子键合
硫黄
锌
锂硫电池
无机化学
电池(电)
纳滤
化学工程
离子
电化学
电极
有机化学
化学
冶金
物理化学
生物化学
物理
功率(物理)
量子力学
工程类
热力学
作者
Liyao Wang,Xu Yan,Linyu Xiao,Yang Liu,Lixinyu Wang,Shangwen Zha,Shenxiang Zhang,Jian Jin
标识
DOI:10.1021/acsami.4c11422
摘要
Zinc-sulfur (Zn-S) batteries exhibit a high theoretical energy density, nontoxicity, and cost-effectiveness, demonstrating significant potential for integration into large-scale energy storage systems. However, the phenomenon of polysulfide (including dissolved S 8 and S x 2– ) shuttling is a major issue that results in rapid capacity decay and a short lifespan, limiting the practical performance of sulfur-based batteries. Herein, we fabricated an ionic covalent organic framework (iCOF) membrane as an active separator for the Zn-S battery. Sulfonic acid groups were introduced to the COF membrane, providing abundant negative charge sites in its pore wall. By combining size sieving and charge interaction between the polysulfide and pore wall, the iCOF membrane inhibited the crossover of polysulfides to the Zn metal anode without affecting the transport of metal ions. The Zn-S battery with the iCOF membrane as the separator shows a high-performance and low attenuation rate of 0.05% per cycle over 300 cycles at 2.5 A g –1 . This study emphasizes the significance of separator design in enhancing Zn-S batteries and showcases the potential of functionalized framework materials for the development of high-performance energy storage systems.
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