4.6 Article

Co(OH)2@FeCo2O4 as electrode material for high performance faradaic supercapacitor application

Journal

ELECTROCHIMICA ACTA
Volume 299, Issue -, Pages 312-319

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2019.01.017

Keywords

Co(OH)(2)@FeCo2O4; Hydrothermal synthesis; Supercapacitors; Mesoporous structure

Funding

  1. Department of Science and Technology of Yunnan Province via the Key Project for the Science and Technology [2017FA025]
  2. National Natural Science Foundation of China [61761047, 41876055]
  3. Program for Innovative Research Team (in Science and Technology) in University of Yunnan Province

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Co(OH)(2)@FeCo2O4 nanocomposite was successfully synthesized via a facile one-step hydrothermal reaction without thermal treatment. The structure and chemical composition of as-synthesized Co(OH)(2)@FeCo2O4 was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS), respectively. The results show the FeCo2O4 nanosheets are covered with the Co(OH)(2) nanoparticles and the BET show the nanocomposite possess the mesoporous structure with specific surface area and total pore volume are 93.071m(2) g(-1) and 0.37 cm(3) g(-1), respectively. In addition, the electrochemical performances were investigated in a three-electrode system to evaluate the material. The as-synthesized Co(OH)(2)@FeCo2O4 nanocomposite exhibits a high specific capacitance of 1173.43 F g(-1) at 1 A g(-1) and remarkable cycling stability with 95.4% capacitance retention after 5000 cycles. The results show the higher capacitance and longer cycle performance, compared with the Co(OH)(2) and FeCo2O4, respectively. This remarkable electrochemical performances were mainly due to mesoporous structure and the synergistic effect of Co(OH)(2) and FeCo2O4. It means that this nanostructure Co(OH)(2)@FeCo2O4 synthesized by this simple and cost-effective method would have more hopeful prospects in energy storage applications. (C) 2019 Elsevier Ltd. All rights reserved.

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