材料科学
化学工程
双金属片
氧化还原
阳极
催化作用
分离器(采油)
煅烧
涂层
氧化物
钼酸盐
非阻塞I/O
无机化学
纳米技术
电极
化学
冶金
物理化学
工程类
物理
热力学
生物化学
作者
Tingyi Wu,Huanglin Dou,Zhenxin Zhao,Junliang Zhou,Xiaomin Wang
出处
期刊:ChemNanoMat
[Wiley]
日期:2023-04-21
卷期号:9 (7)
被引量:10
标识
DOI:10.1002/cnma.202300087
摘要
Abstract Lithium‐sulfur (Li−S) batteries are considered to be the most promising candidates for achieving low‐cost, high‐energy density systems. The serious shuttle effect of polysulfides (LiPS) and the sluggish redox kinetics have become major obstacles to the practical application of Li−S batteries. Herein, a hollow microsphere structure of transition bimetallic oxide nickel molybdate (NiMoO4) was prepared by hydrothermal reaction and calcination method. It was used as a separator coating material to inhibit LiPS shuttle and promote efficient redox conversion of sulfur species. The hollow microsphere structure not only possesses a large internal space to physically confine LiPS but also exposes abundant active sites to enhance the redox kinetics of LiPS. The NiMoO4 shows superior adsorption ability for LiPS and accelerated ion/electron transport rates compared to NiO, thus facilitating the anchoring‐conversion‐diffusion processes of polysulfides. Benefiting from this versatility, the Li−S batteries with NiMoO4‐PP exhibit a high discharge specific capacity of 1354.5 mAh g−1 at 0.1 C. In addition, the battery exhibits excellent cycling stability with a capacity decay rate of 0.027% for 500 cycles at 2 C. These results demonstrate the potential application of NiMoO4‐based electrocatalysts in high‐performance Li−S batteries.
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