Double-oxide sulfur host for advanced lithium-sulfur batteries

被引:101
作者
Xue, Weijiang [1 ,2 ,3 ]
Yan, Qing-Bo [2 ,3 ,4 ]
Xu, Guiyin [2 ,3 ]
Suo, Liumin [2 ,3 ]
Chen, Yuming [2 ,3 ]
Wang, Chao [2 ,3 ]
Wang, Chang-An [1 ]
Li, Ju [2 ,3 ]
机构
[1] Tsinghua Univ, Sch Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
[2] MIT, Dept Nucl Sci & Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[4] Univ Chinese Acad Sci, Coll Mat Sci & Optoelect Technol, Beijing 100049, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金; 中国博士后科学基金;
关键词
Polysulfides adsorption; Double-oxide sulfur host; Sulfur cathode; Secondary particle; ION BATTERY; PERFORMANCE; COMPOSITE; CATHODE; POLYSULFIDES; CHEMISTRY; DESIGN; PAPER; LIFE;
D O I
10.1016/j.nanoen.2017.05.041
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Although lithium-sulfur batteries show fascinating potential for high-capacity energy storage, their practical applications are hindered by the fast capacity decay and low sulfur utilization at high sulfur loading. Herein we report an efficient sulfur host based on two oxides, in which SiO2 hollow spheres with radial meso-channels are covered by a thin TiO2 coating. SiO2 spheres not only yield high sulfur loading as high as 80 wt% but also possess strong lithium polysulfides (LiPS) adsorption capability. The thin TiO2 coating can effectively prevent the LiPS outward diffusion, giving rise to a long-term stability. Meanwhile, the oxide-supported carbon from the carbonization of surfactants enables good electrical conductivity to facilitate electron access and improve sulfur utilization. Experimental and theoretical studies show the strong adsorption of LiPS by SiO2. Benefitting from the unique structural and compositional advantages, we achieve a high sulfur loading up to 80 wt% with similar to 65.5% and 33% capacity retentions over 500 and 1000 cycles when tested at 0.5 C and 1 C, respectively.
引用
收藏
页码:12 / 18
页数:7
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