A sulfur host based on titanium monoxide@carbon hollow spheres for advanced lithium-sulfur batteries

被引:611
|
作者
Li, Zhen [1 ]
Zhang, Jintao [1 ]
Guan, Buyuan [1 ]
Wang, Da [2 ]
Liu, Li-Min [2 ]
Lou, Xiong Wen [1 ,3 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
[2] Beijing Computat Sci Res Ctr, Beijing 100084, Peoples R China
[3] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 320027, Zhejiang, Peoples R China
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
关键词
POLYSULFIDE MEDIATOR; CATHODES; GRAPHENE; PERFORMANCE; SHELL; ENCAPSULATION; COMPOSITES; HYDROXIDES; NANOSHEETS; BINDING;
D O I
10.1038/ncomms13065
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lithium-sulfur batteries show advantages for next-generation electrical energy storage due to their high energy density and cost effectiveness. Enhancing the conductivity of the sulfur cathode and moderating the dissolution of lithium polysulfides are two key factors for the success of lithium-sulfur batteries. Here we report a sulfur host that overcomes both obstacles at once. With inherent metallic conductivity and strong adsorption capability for lithium-polysulfides, titanium monoxide@carbon hollow nanospheres can not only generate sufficient electrical contact to the insulating sulfur for high capacity, but also effectively confine lithium-polysulfides for prolonged cycle life. Additionally, the designed composite cathode further maximizes the lithium-polysulfide restriction capability by using the polar shells to prevent their outward diffusion, which avoids the need for chemically bonding all lithium-polysulfides on the surfaces of polar particles.
引用
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页数:11
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