Zirconium fluoride-supported high-entropy fluoride: a catalyst for enhanced oxygen evolution reaction

Extended hydrogen initiatives promote the urgency of research on water splitting technologies and, therein, oxygen evolution reaction catalysts being developed. A route to access a ZrF4 supported high-entropy fluoride catalyst using a facile sol–gel route is presented. The high-entropy character of the catalyst was confirmed by scanning transmission electron microscopy and energy dispersive X-ray spectroscopy (STEM-EDX) as well as inductively coupled plasma-mass spectrometry (ICP-MS). Additional investigations on the local structure were performed using extended X-ray absorption fine structure spectroscopy (EXAFS) and pair distribution function (PDF) analysis. The catalyst shows significant potential for oxygen evolution reaction (OER) in alkaline media with a current density of 100 mA cm−2 at approximately 1.60 V, thus outperforming benchmark materials such as IrO2, despite a significant reduction in electrochemical mass loading. A potential mechanism is suggested based on free energy calculation using DFT calculations.

Publication Details

Journal
edoc Publication server (Humboldt University of Berlin)
Published
2025-04-01
DOI
https://doi.org/10.18452/34053
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
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article

Zirconium fluoride-supported high-entropy fluoride: a catalyst for enhanced oxygen evolution reaction

edoc Publication server (Humboldt University of Berlin)
Electrocatalysts for Energy Conversion
article

Zirconium fluoride-supported high-entropy fluoride: a catalyst for enhanced oxygen evolution reaction

article en

Abstract

Extended hydrogen initiatives promote the urgency of research on water splitting technologies and, therein, oxygen evolution reaction catalysts being developed. A route to access a ZrF4 supported high-entropy fluoride catalyst using a facile sol–gel route is presented. The high-entropy character of the catalyst was confirmed by scanning transmission electron microscopy and energy dispersive X-ray spectroscopy (STEM-EDX) as well as inductively coupled plasma-mass spectrometry (ICP-MS). Additional investigations on the local structure were performed using extended X-ray absorption fine structure spectroscopy (EXAFS) and pair distribution function (PDF) analysis. The catalyst shows significant potential for oxygen evolution reaction (OER) in alkaline media with a current density of 100 mA cm−2 at approximately 1.60 V, thus outperforming benchmark materials such as IrO2, despite a significant reduction in electrochemical mass loading. A potential mechanism is suggested based on free energy calculation using DFT calculations.

edoc Publication server (Humboldt University of Berlin)
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Electrocatalysts for Energy Conversion
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