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September 5, 2025Catalysts5 citationsOpen Access

Tuning High-Entropy Oxides for Oxygen Evolution Reaction Through Electrocatalytic Water Splitting: Effects of (MnFeNiCoX)3O4 (X = Cr, Cu, Zn, and Cd) on Electrocatalytic Performance

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MSMilad Zehtab SalmasiANAmir NarimaniAOAli Omidkar

Key Points

  • The Cr-containing catalyst showed a low overpotential of 323 mV at 10 mA/cm2 in 1.0 M KOH, indicating superior performance.
  • With the smallest Tafel slope of 56 mV/dec, the catalyst exhibits efficient charge transfer characteristics, supporting optimal performance.
  • Electrochemical characterization confirms the (MnFeNiCoCr)3O4 composition has the highest double-layer capacitance and extensive active surface area.
  • Tailoring the fifth metal in high-entropy oxides opens avenues for enhancing water oxidation catalysis and overall electrochemical efficiency.

Abstract

This research presents the development of spinel-type high-entropy oxide (HEO) catalysts with the general composition (MnFeNiCoX)3O4, where X represents Cr, Cu, Zn, and Cd, synthesized through a solution combustion method. The impact of the fifth metal element on the oxygen evolution reaction (OER) was systematically explored using structural, morphological, and electrochemical characterization techniques. Among the various compositions, the Cr-containing catalyst, (MnFeNiCoCr)3O4, displayed outstanding electrocatalytic behavior, delivering a notably low overpotential of 323 mV at a current density of 10 mA/cm2 in 1.0 M KOH—surpassing the performance of benchmark RuO2. Additionally, this material exhibited the smallest Tafel slope (56 mV/dec), the greatest double-layer capacitance (3.35 mF/cm2), and the most extensive electrochemically active surface area, all indicating enhanced charge transfer capability and high catalytic proficiency. The findings highlight the potential of element tailoring in HEOs as a promising strategy for optimizing water oxidation catalysis.

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Cite This Study

Salmasi et al. (2025) studied this question.

synapsesocial.com/papers/68bb5f586d6d5674bcd03885https://doi.org/10.3390/catal15090827
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