Synergistic sulfur-selenium cathodes for lithium-sulfur batteries

被引:6
|
作者
Wei, Shanyue [1 ,2 ]
Chen, Huixin [2 ,3 ]
Yu, Fuda [1 ]
Wu, Xiaowei [2 ,3 ]
Que, Lanfang [1 ]
Hu, Ting [2 ,3 ]
Wang, Jiangli [3 ]
Huang, Miaoliang [1 ]
Lu, Can-Zhong [2 ,3 ]
Xie, Yiming [1 ]
机构
[1] Huaqiao Univ, Coll Mat Sci & Engn, Engn Res Ctr Environm Friendly Funct Mat, Minist Educ, Xiamen 361021, Fujian Province, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, CAS Key Lab Design & Assembly Funct Nanostruct, Fujian Prov Key Lab Nanomat, Fuzhou 350002, Fujian Province, Peoples R China
[3] Chinese Acad Sci, Xiamen Inst Rare Earth Mat, Haixi Inst, Xiamen 361021, Fujian Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon nanosheets; Adsorption; CNSs-Se@S; Li-S batteries; LI-S; HIGH-PERFORMANCE; POROUS CARBON; CONVERSION; COMPOSITE; SINGLE; LAYER;
D O I
10.1016/j.jpowsour.2024.234193
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
Lithium-sulfur batteries are promising for next -generation energy storage but face challenges such as the polysulfide shuttle effect, slow kinetics, and lithium dendrite growth. Here we report a novel approach utilizing twodimensional carbon nanosheets for the encapsulation of sulfur and selenium materials. Furthermore, we employed a high-temperature selenization process to facilitate the ingress of a larger number of Se atoms into the mesopores and macropores of the two-dimensional carbon nanosheets, thereby providing comprehensive protection for Se within the carbon nanosheets. The cathode exhibits a high initial capacity of 1418 mAh/g at 0.1 C and low-capacity decay rates of 0.11 % for 500 cycles at 1 C, and 0.101 % for 400 cycles at 2 C, respectively. Xray photoelectron spectroscopy (XPS) and Density functional theory calculations (DFT) show that there is a strong adsorption effect between sulfur, selenium and the substrate material, which can inhibit the generation of shuttle effects. Our work provides a scalable and viable strategy for long-term lithium storage applications.
引用
收藏
页数:11
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