MOF-Derived Bifunctional Co0.85Se Nanoparticles Embedded in N-Doped Carbon Nanosheet Arrays as Efficient Sulfur Hosts for Lithium-Sulfur Batteries

被引:191
作者
Xie, Yonghui [1 ]
Cao, Jiaqi [1 ]
Wang, Xinghui [1 ,2 ,3 ]
Li, Wangyang [1 ]
Deng, Liying [1 ]
Ma, Shun [1 ]
Zhang, Hong [1 ]
Guan, Cao [4 ]
Huang, Wei [4 ]
机构
[1] Fuzhou Univ, Coll Phys & Informat Engn, Inst Micronano Devices & Solar Cells, Fuzhou 350108, Peoples R China
[2] Fujian Sci & Technol Innovat Lab Optoelect Inform, Fuzhou 350108, Fujian, Peoples R China
[3] Jiangsu Collaborat Innovat Ctr Photovolta Sci & E, Changzhou 213000, Peoples R China
[4] Northwestern Polytech Univ, Inst Flexible Elect, Xian Key Lab Flexible Elect, Xian 710072, Peoples R China
基金
中国国家自然科学基金;
关键词
metal-organic frameworks; metal selenide; sulfur cathode; lithium polysulfides; Li-S batteries; CONVERSION; FRAMEWORK; ELECTRODE; IMMOBILIZATION; POLYSULFIDES; CATHODE; SURFACE; ANODE; LIFE;
D O I
10.1021/acs.nanolett.1c02037
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur batteries possess the merits of low cost and high theoretical energy density but suffer from the shuttle effect of lithium polysulfides and slow redox kinetics of sulfur. Herein, novel Co0.85Se nanoparticles embedded in nitrogen-doped carbon nanosheet arrays (Co0.85Se/NC) were constructed on carbon cloth as the self-supported host for a sulfur cathode using a facile fabrication strategy. The interconnected porous carbonbased structure of the Co0.85Se/NC could facilitate the rapid electron and ion transfer kinetics. The embedded Co0.85Se nanoparticles can effectively capture and catalyze lithium polysulfides, thus accelerating the redox kinetics and stabilizing sulfur cathodes. Therefore, the Co0.85Se/NC-S cathode could maintain a stable cycle performance for 400 cycles at 1C and deliver a high discharge specific capacity of 1361, 1001, and 810 mAh g(-1) at current densities of 0.1, 1, and 3C, respectively. This work provides an efficient design strategy for high-performance lithium-sulfur batteries with high energy densities.
引用
收藏
页码:8579 / 8586
页数:8
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