4.6 Article

Rapid construction of three-dimensional sulfur doped graphene supported by NiFeS2 interconnected networks as convenient electron/ion transport channels for flexible supercapacitors

Journal

ELECTROCHIMICA ACTA
Volume 309, Issue -, Pages 1-10

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2019.04.079

Keywords

Three-dimensional sulfur-doping graphene; Nickel-iron bimetallic sulfides; Mercaptoacetic acid; In-situ generation; Supercapacitor

Funding

  1. China Postdoctoral Science Foundation [2017M621656]
  2. Jiangsu Planned Projects for Postdoctoral Research Funds [1701170C]

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Developing a convenient synthetic strategy to achieve graphene based composites with ideal electrochemical properties is still a huge challenge. In this work, three-dimensional sulfur doped graphene supported by nickel-iron bimetallic sulfides (NiFeS2/3DSG) as high performance supercapacitors electrode are fabricated by one-step microwave alcohothermal method, in which mercaptoacetic acid is applied as sulfur source of doped graphene as well as precursor of nickel-iron sulfide. The 3DSG not only exhibits space laminated structure with ideally pore sizes and large specific surface area, but also increases the binding of nickel-iron precursor through chemical bonds of sulfur. NiFeS2/3DSG electrode has reflected in the specific capacitance of 643.9 C g(-1 )(1073.2 F g(-1)) at the current density of 1 A g(-1) in 6.0 M KOH electrolyte. Furthermore, the asymmetric supercapacitor device is constructed of NiFeS2/3DSG electrode as positive electrode and 3DSG as negative electrode (NiFeS2/3DSG//3DSG), which delivers a superior energy density of 45.7 Wh kg(-1) at a power density of 222 W kg(-1) under a wide potential range of 1.6 V. After 5000 cycles of charge and discharge, the specific capacitance of this device hold the retention rate of 82%. These results indicate that the graphene based hybrid with outstanding electrochemical performance could be a strong competitive prospect in the applications of supercapacitor. (C) 2019 Elsevier Ltd. All rights reserved.

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