Ion-Inserted Metal-Organic Frameworks Accelerate the Mass Transfer Kinetics in Lithium-Sulfur Batteries

被引:19
作者
Zhou, Mingjie [1 ]
Li, Yaoyao [1 ]
Lei, Tianyu [1 ]
Chen, Wei [1 ]
Rao, Gaofeng [1 ]
Xue, Lanxin [1 ]
Hu, Anjun [1 ]
Fan, Yuxin [1 ]
Huang, Jianwen [1 ]
Hu, Yin [1 ,2 ]
Wang, Xianfu [1 ]
Xiong, Jie [1 ]
机构
[1] Univ Elect Sci & Technol China, State Key Lab Elect Thin Films & Integrated Devic, Chengdu 610054, Peoples R China
[2] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 610054, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
functional separators; ion insertion; lithium-sulfur batteries; mass transfer kinetics; metal-organic frameworks; PERFORMANCE; SEPARATORS; CONVERSION;
D O I
10.1002/smll.202104367
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur battery promises great potential to promote the reform of energy storage field. Modified functional interlayer on separator has been recognized as efficient method to promote battery performances, mainly focusing on the entrapment and catalytic effect toward lithium polysulfide, while the mass transfer property across the interlayers has not been carefully considered. Herein, a dense layer composed of ion-inserted metal-organic frameworks is used to facilitate mass transfer across the layer and ensure high polysulfides entrapment efficiency. In situ Raman study reveals that the dense functional layer blocks the transfer of Li ions, while the ion-inserted layer can accelerate the ion-transfer kinetics and avoid the ion depletion caused polarization. As a result, a specific capacity of 742 mAh g(-1) is obtained at 2 C, with the decay rate of 0.089% per cycle at 1 C over 600 cycles, demonstrating great potential for the application in advanced Li-S batteries.
引用
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页数:7
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