Heat-induced formation of porous and free-standing MoS2/GS hybrid electrodes for binder-free and ultralong-life lithium ion batteries

被引:132
作者
Wang, Ronghua [1 ]
Xu, Chaohe [1 ]
Sun, Jing [1 ]
Liu, Yangqiao [1 ]
Gao, Lian [1 ]
Yao, Heliang [1 ]
Lin, Chucheng [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphene; Molybdenum disulfide; Free-standing; Binder-free; Lithium ion batteries; HIGH-PERFORMANCE; REDUCED GRAPHENE; AQUEOUS DISPERSIONS; COMPOSITE ELECTRODE; ASSISTED SYNTHESIS; ANODE MATERIALS; LARGE-AREA; NANOPARTICLES; NANOSHEETS; ENERGY;
D O I
10.1016/j.nanoen.2014.05.009
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
Flexible and free-standing MoS2/GS films are constructed for the first time based on a novel heat-induced formation process, during which self-generated gaseous species successfully trigger the formation of porous structure, without the assistance of any templates or spacers. Graphene forms an open porous network, with few-layered MoS2 uniformly grown on the surface of GS. The fascinating structure provides several attractive features as anode material, including efficient ion transport, high conductivity and good structure durability. When used as free-standing and binder-free electrodes for lithium-ion batteries, the optimized hybrid film with graphene content of 32% exhibits superior rate capability (994, 880, and 598 mAh g(-1) at 0.5, 1, and 5 A g(-1), respectively) and outstanding cycling performance at high rates (retaining 100.6% of the initial capacity after 1000 cycles at 1000 mA g(-1)). Importantly, the electrochemical reaction kinetics and interfacial behavior of the hybrid electrode are also in-depth investigated by EIS and morphological study. The work described here can be extended to prepare various porous graphene-based hybrid films, for the application in a broad range of LIBs, electrochemical capacitors, sensors, and catalysts. (C) 2014 Published by Elsevier Ltd.
引用
收藏
页码:183 / 195
页数:13
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