硫化钴
电催化剂
氧化还原
钴
化学工程
锂(药物)
咪唑酯
沸石咪唑盐骨架
催化作用
材料科学
无定形固体
无机化学
动力学
化学
吸附
电化学
电极
金属有机骨架
物理化学
有机化学
医学
量子力学
内分泌学
工程类
物理
作者
Junan Feng,Jiayi Li,Hongwei Zhang,Wendong Liu,Zenghui Lin,Tianyi Wang,Bing Sun,Xiaoxian Zhao,Fengyun Wang,Jianjun Song,Yuping Wu,Fangling Production
出处
期刊:Energy materials
[OAE Publishing Inc.]
日期:2023-01-01
卷期号:3 (1): 300001-300001
被引量:14
标识
DOI:10.20517/energymater.2022.62
摘要
The feasibility of the commercialization of lithium-sulfur (Li-S) batteries is troubled by sluggish redox conversion kinetics and the shuttle effect of polysulfides. Herein, a zeolitic imidazolate framework derived amorphous CoP combined with carbon nanotubes conductive network composites (aCoP@CNTs) has been synthesized as an effective dual-electrocatalyst for accelerating the redox kinetics of polysulfides to prolong the lifespan of Li-S batteries. Compared with crystalline CoP, unsaturated Co atoms of aCoP@CNTs exhibit stronger chemical adsorption capacity for polysulfides and serve as catalytic centers to accelerate the conversion from soluble polysulfides to solid-state lithium sulfide. Meanwhile, the 3D porous conductive network not only facilitates ion/electron transportation but also forms a physical barrier to limit the migration of polysulfides. Benefiting from the above preponderances, the batteries with aCoP@CNTs modified interlayer exhibited excellent cycle stability (initial discharge capacity of 1227.9 mAh g-1 at 0.2 C), rate performance (795.9 mAh g-1 at 2.5 C), long-term cycle reliability (decay rate of 0.049% per cycle at 1 C over 1000 cycles), and superior high-loading performance (high initial discharge capacity of 886 mAh g-1 and 753.6 mAh g-1 at 1 C under high S loading of 3 mg cm-2 and 4 mg cm-2).
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