共价键
分离器(采油)
共价有机骨架
吸附
Boosting(机器学习)
硫黄
有机自由基电池
电解质
材料科学
氧化还原
无机化学
化学
化学工程
工程类
电极
计算机科学
有机化学
物理
热力学
物理化学
机器学习
作者
Qing Xu,Kailong Zhang,Jing Qian,Yu Guo,Xiaokai Song,Honglin Pan,Di Wang,Xiaopeng Li
标识
DOI:10.1021/acsaem.9b00920
摘要
Lithium–sulfur batteries are getting more attention in energy storage and conversion fields due to their high theoretical capacity and specific energy density. Nevertheless, the dissolution of polysulfides results in their poor cycle stability, which is the major issue in practical use. To overcome the challenge, we report a new strategy by employing a redox-active covalent organic framework as the separator in lithium–sulfur batteries. The one-dimensional pore channels of the covalent organic framework provide a fast transport pathway for the lithium ion. And the pyridine units of the framework not only enhance the chemical adsorption of sulfur but also catalyze the charge and discharge processes. By virtue of these features, the specific capacity at 0.2 C is 977 mAh g–1 after 100 cycles, which is 5.2 times higher than that of the pristine separator-based battery. Additionally, the specific capacity achieves 826 mAh g–1 at 1 C after 250 cycles.
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