Confining small sulfur molecules in peanut shell-derived microporous graphitic carbon for advanced lithium sulfur battery

被引:76
作者
Zhou, Jingjing [1 ]
Guo, Yongsheng [2 ]
Liang, Chengdu [2 ]
Yang, Jun [1 ]
Wang, Jiulin [1 ]
Nuli, Yanna [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai Electrochem Energy Devices Res Ctr, Shanghai 200240, Peoples R China
[2] Ningde Contemporary Amperex Technol Co Ltd, Res Inst, Ningde 352100, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Peanut shell; Microporous graphitic carbon; Small sulfur molecules; Lithium sulfur battery; Carbonate electrolyte; ELECTRODE MATERIALS; PERFORMANCE; CATHODE; STABILITY; COMPOSITES; POLYHEDRA; LIFE;
D O I
10.1016/j.electacta.2018.04.021
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this work, small sulfur molecules (S2-4) confined in microporous graphitic carbon (MGC) demonstrates excellent performance in Li-S battery with carbonate-based electrolyte. The MGC is synthesized via the simultaneous activation and graphitization of peanut shell char promoted by K2FeO4, which possesses ultra-micropore (pore width <0.7 nm) volume as high as 0.65 cm(3) g(-1) and the predominant pore width less than 0.4 nm. After sulfur infusion, the S/MGC composite with 50.5 wt% sulfur loading exhibits superior long-term cycling stability and rate performance in S/MGC vertical bar Li full cell. The cell delivers high capacity of 1146 mAh g(-1) at 0.1 C and 570 mAh g(-1) even at 4 C. Moreover, the capacities of 826 and 571 mAh g(-1) remain after 1000 cycles at 1 C and 2 C, respectively. In addition, the cell exhibits good storage property. The well confined S2-4 inside the interconnected ultra-micropores with graphitic carbon walls endows the S/MGC composite with good electronic conductivity and stability, while unoccupied pores within the S/MGC facilitate fast Lithorn transport and kinetics of electrochemical reactions. This work offers a green and sustainable route to promote the application of Li-S batteries. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
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