Promising Au&CNTs@N-Doped Hierarchical Carbon Composite for High-Performance Lithium-Sulfur Batteries

被引:1
作者
Jin, Hong [1 ]
Bai, Yilu [2 ]
Kong, Zhao [2 ]
Pu, Fangzhao [1 ]
Yang, Zhimao [1 ]
Kong, Chuncai [1 ]
Wang, Keliang [3 ]
Xu, Hui [2 ]
机构
[1] Xi An Jiao Tong Univ, Sch Phys, Shaanxi Prov Key Lab Adv Funct Mat & Mesoscop Phys, Minist Educ,Key Lab Nonequilibrium Synth & Modulat, Xian 710049, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Suzhou Acad, Suzhou 215123, Jiangsu, Peoples R China
[3] Michigan State Univ, Fraunhofer USA Ctr Coatings & Diamond Technol, E Lansing, MI 48824 USA
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
POROUS CARBON; NITROGEN; CATHODE; IMMOBILIZER; GRAPHENE;
D O I
10.1021/acs.energyfuels.2c02783
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
A lithium-sulfur battery with an ultrahigh specific capacity of 1675 mAh g(-1) is witnessed to be one of the most promising high-energy-density storage devices. However, the commercialization is restricted by the poor conductivity of sulfur, the "shuttle effect" of polysulfides, and the volume expansion during the charge/discharge process. Herein, Au&CNTs@N-doped hierarchical porous carbon material was prepared in view of structural design, chemical modification, and metal catalysis. Sulfur can be effectively accommodated and protected in the hierarchical porous carbon host; besides, the overall conductivity and structural stability of the carbon/sulfur composite are able to be enhanced by carbon nanotubes interconnected between hollow carbon spheres. Furthermore, the redox reaction kinetics of lithium polysulfides and the chemical adsorption to polysulfide are enhanced by Au atoms and doped N heteroatoms. As a result of the multifunctional features, Au&CNTs@ND-C/S exhibits an initial discharge capacity of 1256 mAh g(-1) at the current density of 0.8 A g(-1), with 1031 mAh g(-1) remaining after 50 cycles. Overall, the multifunctional Au&CNTs@N-doped hierarchical carbon materials can effectively facilitate the electrochemical performance of the sulfur cathode through physical confinement, chemical adsorption, and catalytic enhancement.
引用
收藏
页码:13327 / 13336
页数:10
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