Flower-like polyaniline/graphene hybrids for high-performance supercapacitor

被引:58
作者
Ke, Fuyou [1 ]
Liu, Yu [1 ]
Xu, Hongyao [1 ]
Ma, Yu [1 ]
Guang, Shanyi [1 ]
Zhang, Fayin [1 ]
Lin, Naibo [2 ]
Ye, Meidan [2 ]
Lin, Youhui [2 ]
Liu, Xiangyang [2 ,3 ]
机构
[1] Donghua Univ, Coll Mat Sci & Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[2] Xiamen Univ, Res Inst Soft Matter & Biomimet, Xiamen 361005, Peoples R China
[3] Natl Univ Singapore, Fac Sci, Dept Phys, 2 Sci Dr 3, Singapore 117542, Singapore
关键词
Polyaniline; Graphene; Supercapacitor; Flower-like nanostructure; REDUCED GRAPHENE OXIDE; FLEXIBLE SUPERCAPACITORS; NANOWIRE ARRAYS; COMPOSITE; ELECTRODE; NANOTUBE; NANOSTRUCTURE; CAPACITOR; PAPER;
D O I
10.1016/j.compscitech.2017.02.026
中图分类号
TB33 [复合材料];
学科分类号
摘要
A novel flower-like polyaniline/graphene hybrid (PANI-ATRGO) is prepared by a one-pot synthesis and used as electrode materials for supercapacitors. The structure, formation mechanism and electrochemical properties of such unique architecture are systematically investigated by combining Fourier transform infrared spectroscopy, Ultraviolet visible absorption spectroscopy, Raman spectroscope, X-ray diffraction and electrochemical techniques. The results suggest that "V-type" amino groups of ATRGO and supermolecular assembly between PANT chains play the key role in the formation of flower-like nanostructures. Compare to pristine PANI (487 F g(-1) at 1 A g(-1)), PANI-ATRGO electrode materials exhibit a remarkable improvement of the specific capacitance (1510 F g(-1) at 1 A g(-1)) for supercapacitor in addition to excellent rate capacity and long-term cycling stability. Moreover, it is found that flower-like PANI-ATRGO hybrids exhibit better electrochemical properties than the corresponding nanorod-array hybrids in our previous study. This reveals the significance of controlling the hierarchical structure of hybrid materials in the development of high-performance supercapacitor. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:286 / 293
页数:8
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