In Situ Self-Polymerization to Form Hollow Graphitized Carbon Nanocages with Embedded Cobalt Nanoparticles for High-Performance Lithium-Sulfur Batteries

被引:5
作者
Lei, Feifei [1 ]
Cao, Yuqing [1 ]
Fu, Yifang [1 ]
Li, Yunliang [1 ]
Wang, Runwei [1 ]
Qiu, Shilun [1 ]
Zhang, Zongtao [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
catalysis; cobalt nanoparticles; high energy density; hollow graphitic carbon materials; lithium-sulfur batteries; METAL-ORGANIC FRAMEWORKS; EFFICIENT POLYSULFIDE MEDIATOR; ENERGY-STORAGE; CATHODE; COMPOSITES; ELECTRODES; CHEMISTRY; HOSTS;
D O I
10.1002/chem.202002487
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur batteries, owing to the multi-electron participation in the redox reaction, possess enormous energy density, which has aroused much attention. Nevertheless, the detrimental shuttle effect, volume expansion, and electrical insulation of sulfur, have hindered their application. To improve the cyclability, a functional host, consisting of Co nanoparticles and N-doped hollow graphitized carbon (Co-NHGC) material, is elaborated, which has the advantages of: 1) the graphitized carbon material working as an electronic matrix to improve the utilization rate of sulfur; 2) the hollow structure relieving the stress change caused by volume expansion; 3) the rich active sites catalyze the electrochemical reaction of sulfur and entrap polysulfides. These advantages significantly improve the performance of the lithium-sulfur batteries. Accordingly, the S@Co-NHGC cathode exhibits excellent initial specific capacity, high coulombic efficiency, and excellent rate performance. This work utilizes a novel method of dopamine in situ etching of a metal-organic framework to synthetize the Co-NHGC host of sulfur, which will hopefully provide inspiration for other energy materials.
引用
收藏
页码:13295 / 13304
页数:10
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