4.7 Article

NiFe2O4-Ni3S2 nanorod array/Ni foam composite catalyst indirectly controlled by Fe3+ immersion for an efficient oxygen evolution reaction

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 27, Pages 14407-14417

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.01.221

Keywords

Oxygen evolution reaction; Ni3S2; NiFe2O4; Morphological control; Nanorod array structure; Fe3+ immersion

Funding

  1. National Natural Science Foundation of China [21878202, 21975175]
  2. Shanxi Scholarship Council of China [2017-041]
  3. Natural Science Foundation of Shanxi Province [201801D121052]

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NiFe2O4-Ni3S2 nanorods and nanosheets composite catalysts were successfully prepared using cathodic electrode position and hydrothermal sulfuration methods, showing excellent oxygen evolution performance and long-term stability in 1.0 M KOH electrolyte.
A NiFe alloy was designed on nickel foam (NF) as a precursor using cathodic electrode position. NiFe2O4-Ni3S2 nanorods (NRs) composite catalysts were prepared by Fe3+ impregnation and further hydrothermal sulfuration methods. NiFe2O4-Ni3S2 nanosheets (NSs) were also prepared by direct hydrothermal sulfuration of the NiFe alloy for comparison. Compared to the dense NS structure of the NiFe2O4-Ni3S2 NSs/NF, the NiFe2O4-Ni3S2 NRs/NF showed better oxygen evolution performance due to its unique weed-like NR array structure composed of additional oxygen evolution reaction (OER) active sites, with a strong electron interaction for Ni and Fe and the active sulfide synergistic effect with oxides. Therefore, Driving a current density of 10 mA cm(-2) only requires an overpotential of 189 mV and the catalyst could provide 100 mA cm(-2) continuously and be constant for more than 80 h in 1.0 M KOH. This experiment indicated that Fe3+ immersion had an indirect regulating effect on the morphological growth of the catalyst, which provided a novel concept for designing better OER catalysts. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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