Growth of polyaniline on rGO-Co3S4 nanocomposite for high-performance supercapacitor energy storage

被引:64
|
作者
Tabrizi, Amin Goljanian [1 ]
Arsalani, Nasser [1 ]
Naghshbandi, Zhwan [1 ]
Ghadimi, Laleh Saleh [1 ]
Mohammadi, Abdolkhaled [2 ]
机构
[1] Univ Tabriz, Fac Chem, Dept Organ & Biochem, Res Lab Polymer, Tabriz, Iran
[2] Univ Tabriz, Fac Chem & Petr Engn, Res Lab Polymer, Tabriz, Iran
关键词
Supercapacitor; Graphene; Cobalt sulfide; Polyaniline; GRAPHENE OXIDE; REDUCED-GRAPHENE; TERNARY COMPOSITE; ASYMMETRIC SUPERCAPACITORS; FACILE SYNTHESIS; ANODE MATERIAL; ELECTROCHEMICAL PERFORMANCES; HIERARCHICAL NANOCOMPOSITES; ASSISTED SYNTHESIS; NANOSHEET ARRAYS;
D O I
10.1016/j.ijhydene.2018.04.129
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
Recently, since the supercapacitors have drawn considerable attention, a vast study have been triggered in order to develop efficient electrodes for responding to the increasing demand of supercapacitors. In this report, a possible approach have been used to prepare a ternary nanocomposite, polyaniline/reduced graphene oxide-cobalt sulfide (PANI/rGO-Co3S4). At first, a simple and inexpensive hydrothermal route has been used for the preparation of cobalt sulfide (Co3S4) on the surface of graphene oxide sheets (rGO-Co3S4). Then, the polyaniline nanorods have been flourished on the surface of rGO-Co3S4 sheets via in situ chemical polymerization of aniline which was synergistically adjoined to the graphene surface. Polyaniline has uniformly covered the surface of the rGO-Co3S4 due to the rational combination of two components. Combining of PANI with rGO-Co3S4 electrode material amplify its electrochemical efficiency in terms of a high specific capacitance of 767 F g(-1) at 1 A g(-1) and 81.7% of specific capacitance maintenance after 5000 cycles due to the creation of synergistic effect. Therefore, the ternary nanocomposite of PANI/rGO-Co3S4 provides a new promising pathway for the expanding of high-performance electrode materials for supercapacitors. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12200 / 12210
页数:11
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