4.7 Article

Template-Assisted Fabrication of ZnO/Co3O4 One-Dimensional Metal-Organic Framework Array Decorated with Amorphous Iron Oxide/Hydroxide Nanoparticles as an Efficient Electrocatalyst for the Oxygen Evolution Reaction

Journal

ENERGY & FUELS
Volume 34, Issue 6, Pages 7716-7725

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.energyfuels.0c01101

Keywords

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Funding

  1. National Research Foundation of Korea (NRF) - Korea Government (MISP) [2014R1A4A1008140]
  2. NRF - Ministry of Education ICT [2017H1D8A2030449]
  3. National Research Foundation of Korea [2014R1A4A1008140] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The construction of new electrocatalysts for effective and low-cost water electrolysis continues to be an important conceptual barrier for clean renewable energy technologies. Herein, we fabricate a unique approach to a stable metal-organic framework (MOF) based on zinc oxide/cobalt oxide (MOF ZnO/Co3O4) array synthesis aided by a sacrificial template technique and followed by the decoration of three-dimensional MOF arrays using amorphous iron oxide/hydroxide (FeOOH) nanoparticles. The highly active FeOOH nanoparticles are tightly bound to the surface of the MOF ZnO/Co3O4 array. These integrated heterostructures provide copious active sites, a large electrochemical surface area, an effective charge-mass transfer, and a strong integration between MOF ZnO/Co3O4 and FeOOH nanoparticles. Ascribed to all such aspects, FeOOH @ MOF ZnO/Co3O4 nanorods supported on nickel foam show an oxygen evolution reaction activity order of magnitude higher than that of individual entities in an alkaline solution with an overpotential of 260 mV achieved at a current density of 50 mA.cm(-2) and a Tafel slope of 48 mV dec(-1). This behavior can be ascribed to the effect of amorphous FeOOH nanoparticles being tightly anchored on the MOF ZnO/Co3O4 surface, which not only synergistically enriches the electrochemical surface area but also enhances the active sites. This work offers to open a new strategy to design and fabricate advanced electrode materials for the water electrolysis process.

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