Integrating Conductivity, Immobility, and Catalytic Ability into High-N Carbon/Graphene Sheets as an Effective Sulfur Host

被引:150
作者
Xu, Huifang [1 ]
Jiang, Qingbin [1 ]
Zhang, Bingkai [1 ]
Chen, Chao [1 ]
Lin, Zhan [1 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
catalytic ability; electrical conductivity; redox kinetics; strong binding; sulfur electrodes; POLYMER NETWORKS; BATTERIES; NITROGEN; POLYSULFIDE; PERFORMANCE; CONVERSION; ELECTROLYTE; COMPOSITES; KINETICS; SURFACE;
D O I
10.1002/adma.201906357
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur (Li-S) batteries are considered to be one of the most promising candidate systems for next-generation electrochemical energy storage. The major challenge of this system is the polysulfide shuttle, which results in poor cycling efficiency. In this work, a highly N-doped carbon/graphene (NC/G) sheet is designed as a sulfur host, which combines the merits of abundant N active sites and high electrical conductivity to achieve in situ anchoring-conversion of lithium polysulfides (LiPSs). Such a host not only has strong binding with LiPSs but also promotes redox kinetics, which are revealed by both experimental investigations and theoretical studies. The sulfur cathode based on the NC/G host exhibits a high initial capacity of 1380 mA h g(-1) and a superior cycle stability with a low capacity decay of 0.037% per cycle within 500 cycles at 2 C. Steady areal capacity with a high sulfur loading (5.6 mg cm(-2)) is also attained even without the addition of LiNO3 in the electrolyte. This work proposes and illustrates the importance of in situ anchoring-conversion of LiPSs, offering a new strategy to design multifunctional sulfur hosts for high-performance Li-S batteries.
引用
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页数:9
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