4.8 Article

Hierarchical trimetallic Co-Ni-Fe oxides derived from core-shell structured metal-organic frameworks for highly efficient oxygen evolution reaction

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 287, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2021.119953

Keywords

Ion exchange; Hierarchical structured MOFs; Co-Ni-Fe spinet oxides; Electronic modulation; Oxygen evolution reaction

Funding

  1. Taishan Scholar Project of Shandong Province
  2. National Natural Science Foundation of China [21805308]
  3. Key Research and Development Project of Shandong Province [2019GSF109075]
  4. Fundamental Research Funds for the Central Universities [18CX06065A, 20CX06022A]

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The study successfully synthesized a hierarchically structured Co-Ni-Fe spinet oxide-carbonitrides hybrid electrocatalyst with excellent OER performance through a unique ion-exchange strategy. This method may serve as a versatile platform for rational design and synthesis of multi-metallic MOF derived electrocatalysts.
Metal-organic frameworks (MOFs) have recently emerged as promising precursors to construct efficient nonnoble metal electrocatalyst for oxygen evolution reaction (OER). Herein, a Co-Ni-Fe spinet oxide-carbonitrides hybrids (CoNiFeOx-NC) electrocatalyst with hierarchical structure was synthesized from Fe-MIL-101-NH2 through a unique ion-exchange based strategy. The ion exchange of Fe-MIL-101-NH2 with both Ni and Co ions induced a hierarchically structured 2-D ternary metal MOF shell layer encapsulated 3-D octahedral MOF crystals as a core. This prevents the collapse of MOF frameworks during the air calcination process and affords highly porous structure and large surface area. Additionally, the unique combination of Co-Ni-Fe in spinet oxides derived from calcination of the hierarchically structured core-shell MOF provides a favorable electronic environment for the adsorption of OER intermediates, which was further verified by the XPS characterizations and DFT calculations. DFT study revealed the Ni-Co coordinated O-h sites in the MFe2O4 reverse spinet structures as the main active sites, which tuned the binding strength of oxygen species with a catalyst through electron transfer of Fe -> Co -> Ni, thereby lowered the energy barriers for OER. As a result, the rationally designed CoNiFeOx-NC catalyst manifests superior OER performance with a low overpotential of 265 mV at 50 mA cm(-2) and a decent Tafel slope of 64.1 mV dec(-1). The ion-exchange based strategy may serve as a versatile platform for rational design and synthesis of multi-metallic MOF derived electrocatalysts.

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