MoS2 anchored free-standing three dimensional vertical graphene foam based binder-free electrodes for enhanced lithium-ion storage

被引:28
作者
Ouyang, Bo [1 ]
Wang, Ying [2 ]
Zhang, Zheng [3 ]
Rawat, R. S. [1 ]
机构
[1] Nanyang Technol Univ, Natl Inst Educ, Nat Sci & Sci Educ, Singapore 637616, Singapore
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 637371, Singapore
[3] ASTAR, Inst Mat Res & Engn, 3 Res Link, Singapore 117602, Singapore
关键词
Three dimensional vertical graphene; Free-standing; MoS2 anchored architecture; Binder-free electrode; Lithium-ion storage; ENERGY-STORAGE; CARBON NANOFIBERS; FACILE SYNTHESIS; ANODE MATERIAL; METAL-OXIDES; PERFORMANCE; FABRICATION; GROWTH; NANOSTRUCTURES; NANOCOMPOSITE;
D O I
10.1016/j.electacta.2016.02.120
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The vertical graphene with hierarchical three-dimensional network architecture is a promising substrate for high energy and power density Li-ion battery due to its large surface area, inherent three-dimensional network and excellent ion transport property. Three dimensional vertical graphene (3DVG) is synthesized via plasma enhanced chemical vapor deposition (PECVD) using cost-effective and environment-friendly natural oil of M. alternifolia as precursor. The MoS2 nanosheets are then anchored on free-standing 3DVG by hydrothermal method to make the binder free MoS2@3DVG anode of a Li-ion battery. The MoS2@3DVG electrodes deliver an enhanced capacity of 670 mAh g(-1) with the capacity retention of 99% after 30 cycles at 100 mA g(-1), much better than that of the reference sample of MoS2@3DG (550 mAh g(-1) at 100 mA g(-1)) which uses 3D planar graphene. Superior performance of the vertical graphene based electrode is attributed to the unique hierarchical structure and densely packed reactive edges of the as-synthesized 3DVG. The versatility of plasma-assisted natural precursor based vertical graphene as functional nano-structured substrate for MoS2, as active material, for advanced energy storage devices is demonstrated. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:151 / 160
页数:10
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