4.7 Article

Two-dimensional Co3O4 thin sheets assembled by 3D interconnected nanoflake array framework structures with enhanced supercapacitor performance derived from coordination complexes

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 292, Issue -, Pages 1-12

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2016.02.009

Keywords

Co3O4 thin sheets; Coordination complex; Nanoflake; Hydrothermal synthesis; Supercapacitor; Electrochemical energy storage

Funding

  1. National Natural Science Foundation of China [21101176, 51464033, 21061011]
  2. Natural Science Foundation Project of CQ CSTC [2010BB4232]
  3. Fundamental Research Funds for the Central Universities [106112015CDJXY228801, DXWL-2012-014, DXWL-2012-037, CDJRC10220011]
  4. Large-scale Equipment Sharing Fund of Chongqing University
  5. National Undergraduate Innovative Experiment Training Project
  6. Chongqing University Postgraduates' Science and Innovation Project

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Two-dimensional (2D) Co3O4 thin sheets assembled by 3D interconnected nanoflake array framework structures were first synthesized from nanoflake array-assembled porous cobalt-oxalate coordination complex thin sheets by means of direct pyrolysis in the air and the synthesis is simple and facile to implement scale-up for various application. The products exhibit excellent pseudocapacitive performance in an alkaline medium, holding great promise in supercapacitors (SCs). The electrochemical properties of the obtained Co3O4 thin sheets were evaluated by cyclic voltammetry (CV), galvanostatic charge-discharge measurement (CP) and electrochemical impedance spectroscopy (EIS) in 2.0 M KOH solution. Temperature has an obvious effect on the performance of the products. Impressively, the thin sheets synthesized at 500 degrees C for 6 h used as electrode materials for SCs exhibit a specific capacitance as high as 1500 F g(-1) at 1 A g(-1) and even 828 F g(-1) at 10 A g(-1), as well as remarkable cycling stability with 99.3% of its initial capacitance retained after 2000 continuous charge-discharge cycles at a current density of 5 A g(-1). In addition, the assembled asymmetric system using the obtained Co3O4 thin sheets at 500 degrees C for 6 h as positive electrode and activated carbon as negative one can produce a high energy density of 15.4 Wh kg(-1) at a power density of 0.8 kW kg(-1). The hierarchical architectures of the products with hierarchical porosity and interconnected channels as well as the synergistic effect between their compositions provide several advantages including a large contact surface area, short ion diffusion path and good charge transport, which validate these thin sheets promising potential for a wide range of applications in energy storage. (C) 2016 Elsevier B.V. All rights reserved.

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