多硫化物
储能
共价键
硫黄
聚合
硫化物
材料科学
亚胺
化学工程
纳米技术
化学
有机化学
聚合物
电解质
工程类
催化作用
功率(物理)
物理化学
物理
量子力学
电极
作者
Fei Xu,Shuhao Yang,Xiong Chen,Qianhui Liu,Hejun Li,Hongqiang Wang,Bingqing Wei,Donglin Jiang
出处
期刊:Chemical Science
[The Royal Society of Chemistry]
日期:2019-01-01
卷期号:10 (23): 6001-6006
被引量:132
摘要
The aligned one-dimensional channels found in covalent organic frameworks offer a unique space for energy storage. However, physical isolation of sulfur in the channels is not sufficient to prevent the shuttle of lithium-sulfide intermediates that eventually results in a poor performance of lithium-sulfur energy storage. Herein, we report a strategy based on imine-linked frameworks for addressing this shuttle issue by covalently engineering polysulfide chains on the pore walls. The imine linkages can trigger the polymerization of sulfur to form polysulfide chains and anchor them on the channel walls. The immobilized polysulfide chains suppress the shuttle effect and are highly redox active. This structural evolution induces multifold positive effects on energy storage and achieves improved capacity, sulfur accessibility, rate capability and cycle stability. Our results suggest a porous platform achieved by pore wall engineering for tackling key issues in energy storage.
科研通智能强力驱动
Strongly Powered by AbleSci AI