阴极
材料科学
硫黄
电极
聚合物
金属
电池(电)
硫化物
钝化
锂(药物)
化学工程
氧化还原
锂硫电池
复合材料
无机化学
化学
电化学
冶金
物理化学
医学
功率(物理)
物理
图层(电子)
量子力学
工程类
内分泌学
作者
Qiaomeng Gao,Zhengyuan Shen,Zhijie Guo,Minggang Li,Jun Wei,Jinling He,Yong Zhao
出处
期刊:Small
[Wiley]
日期:2023-03-27
卷期号:19 (28)
被引量:7
标识
DOI:10.1002/smll.202301344
摘要
The construction of high sulfur (S) loading cathode is one of the critical parameters to obtain lithium-sulfur (Li-S) batteries with high energy density, but the slow redox reaction rate of high S loading cathode limits the development process. In this paper, a metal coordinated polymer-based three-dimensional network binder, which can improve the reaction rate and stability of S electrode. Compared with traditional linear polymer binders, the metal coordinated polymer binder can not only increase the load amount of S through the three-dimensional cross-linking, but also promote the interconversion reactions between S and lithium sulfide (Li2 S), avoiding the passivation of electrode and improving the stability of the positive electrode. At an S load of 4-5 mg cm-2 and an E/S ratio of 5.5 µL mg-1 , the discharged voltage in the second platform is 2.04 V and the initial capacity is 938 mA h g-1 with metal coordinated polymer binder. Moreover, the capacity retention rate approaches 87% after 100 cycles. In comparison, the discharged voltage in the second platform is lost and the initial capacity is 347 mA h g-1 with PVDF binder. It demonstrates the advanced properties of metal-coordinated polymer binders for improving the performance of Li-S batteries.
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