Activating Ni/Co Sites in NiCo‐MOF via V <sub>2</sub> O <sub>5</sub> Nanosheet Integration for Enhanced Water Oxidation Reaction

Abstract A composite with enhanced electrochemical performance for the oxygen evolution reaction (OER) was prepared by forming a heterostructured NiCo metal–organic framework (MOF) on V 2 O 5 nanosheets using a simple two‐step hydrothermal approach. Detailed microstructural and surface analyses revealed a uniform distribution of NiCo MOF microplates on the V 2 O 5 nanosheets, confirming the structural modification responsible for faster charge transfer kinetics. The optimal NiCo MOF/V 2 O 5 electrocatalyst exhibited an OER overpotential of 280 mV at 20 mA cm −2 , a Tafel slope of 77.5 mV dec −1 , and a low charge transfer resistance ( R ct = 9.2 Ω). These quantitative improvements in OER performance were attributed to synergistic interfacial interactions, which increased the exposure of Ni/Co active sites to the electrolyte. The catalyst maintained a stable activity over 5000 cyclic voltammetry (CV) cycles and a 55‐h chronopotentiometry (CP) test, demonstrating its electrochemical durability. Furthermore, an asymmetric electrolyzer (Pt/C||NiCo MOF/V 2 O 5 ) incorporating the present catalyst achieved a cell voltage of 1.625 V at 10 mA cm −2 and maintained a stable performance during extended operation, confirming its potential for practical water splitting applications.

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Publication Details

Journal
ChemCatChem
Published
2025-12-02
DOI
https://doi.org/10.1002/cctc.202501409
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.00

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article

Activating Ni/Co Sites in NiCo‐MOF via V 2 O 5 Nanosheet Integration for Enhanced Water Oxidation Reaction

Tae Hwan Oh, Mohammad Kashif
ChemCatChem
Electrocatalysts for Energy Conversion
article

Activating Ni/Co Sites in NiCo‐MOF via V 2 O 5 Nanosheet Integration for Enhanced Water Oxidation Reaction

Tae Hwan Oh, Mohammad Kashif
article en

Abstract

Abstract A composite with enhanced electrochemical performance for the oxygen evolution reaction (OER) was prepared by forming a heterostructured NiCo metal–organic framework (MOF) on V 2 O 5 nanosheets using a simple two‐step hydrothermal approach. Detailed microstructural and surface analyses revealed a uniform distribution of NiCo MOF microplates on the V 2 O 5 nanosheets, confirming the structural modification responsible for faster charge transfer kinetics. The optimal NiCo MOF/V 2 O 5 electrocatalyst exhibited an OER overpotential of 280 mV at 20 mA cm −2 , a Tafel slope of 77.5 mV dec −1 , and a low charge transfer resistance ( R ct = 9.2 Ω). These quantitative improvements in OER performance were attributed to synergistic interfacial interactions, which increased the exposure of Ni/Co active sites to the electrolyte. The catalyst maintained a stable activity over 5000 cyclic voltammetry (CV) cycles and a 55‐h chronopotentiometry (CP) test, demonstrating its electrochemical durability. Furthermore, an asymmetric electrolyzer (Pt/C||NiCo MOF/V 2 O 5 ) incorporating the present catalyst achieved a cell voltage of 1.625 V at 10 mA cm −2 and maintained a stable performance during extended operation, confirming its potential for practical water splitting applications.

ChemCatChemVol. 18(1)
Yeungnam University (KR)
National Research Foundation, Ministry of Trade, Industry and Energy, Korea Basic Science Institute, National Research Foundation of Korea
Openalex Percentile: Top 72%
Electrocatalysts for Energy Conversion
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