Adsorption-catalysis synergy within pyrrolic-N-rich carbon nanosheets: Propelling electrochemical kinetics and shielding polysulfides for lithium-sulfur batteries

被引:9
|
作者
Yang, Jingwen [1 ,2 ]
Cao, Chaochao [2 ,3 ]
Li, Zexia [1 ,2 ]
Wang, Peng [1 ,2 ]
Li, Bo [1 ,2 ]
Wu, Weilong [1 ,2 ]
Tang, Chengchun [1 ,2 ]
Xue, Yanming [1 ,2 ]
机构
[1] Hebei Univ Technol, Sch Mat Sci & Engn, Tianjin 300130, Peoples R China
[2] Hebei Univ Technol, Hebei Key Lab Boron Nitride Micro & Nano Mat, Tianjin 300130, Peoples R China
[3] Hebei Univ Technol, Sch Chem Engn & Technol, Hebei Key Lab Funct Polymers, Tianjin 300130, Peoples R China
关键词
Li-S batteries; Pyrrolic-N-rich carbon nanosheets; Synergistic adsorption-catalysis function; Electrochemical kinetics; LI-S BATTERIES; ENHANCED PERFORMANCE;
D O I
10.1016/j.cej.2023.146532
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The practical applications of lithium-sulfur (Li-S) batteries are rather limited by the shuttle effect of lithium polysulfides (LiPSs) and sluggish redox reaction kinetics. Here, a kind of pyrrolic-N-rich carbon nanosheets (Npr- CNs) are prepared by introducing melamine cyanurate (MCA) into the carbonization process of polyacrylonitrile (PAN). As a mediator in Li-S batteries, hierarchical pores, dominant pyrrolic-N-doping, disorder/defective structures and unique electronic states endow Npr-CNs with synergistic adsorption-catalysis function for S species. Specifically, they can effectively inhibit LiPSs shuttle, catalyze the conversion of both liquid-phase LiPSs and solid-phase Li2S, reduce the charge transfer resistance and enhance Li-ions migration rate. Hence, it can make the Li-S batteries deliver excellent rate performance and cycling stability. The battery can reach ultrahigh discharge capacity of 932.0 mAh g-1 at the beginning under current density of 1C and even liberate a capacity as high as 1109.4 mAh g-1 at 0.2C with high sulfur loading of 3.8 mg cm-2.
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页数:10
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