Corrosion-Guided Surface Engineering of Permalloy for Efficient Alkaline Oxygen Evolution Reaction
Sara Fidha C M1, Sethumathavan Vadivel1, Anantharaj Sengeni2
1Department of Chemistry, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, Chennai 603203, Tamil Nadu, India.
Langmuir : the ACS Journal of Surfaces and Colloids
|August 26, 2025
Summary
This study presents an advanced electrocatalyst for the oxygen evolution reaction (OER) using an unconventional acid activation of permalloy. This cost-effective method enhances hydrogen production efficiency in water electrolysis.
Area of Science:
- Electrochemistry
- Materials Science
- Energy Conversion
Background:
- Water electrolysis for hydrogen production is hindered by the slow oxygen evolution reaction (OER).
- Non-noble metal catalysts are effective for alkaline OER.
- Developing efficient and cost-effective OER catalysts is crucial.
Purpose of the Study:
- To develop an advanced oxygen evolution reaction (OER) electrocatalyst.
- To utilize an unconventional electrochemical anodization method for catalyst development.
- To enhance hydrogen production efficiency in water electrolysis.
Main Methods:
- Unconventional electrochemical anodization in acid (pH 0) of permalloy (Ni0.8Fe0.2).
- Characterization of the activated permalloy for OER performance in alkaline media (1.0 M KOH).
- Analysis of surface morphology and kinetics.
Main Results:
- The activated permalloy demonstrated high OER activity (10 mA cm-2 at 264 mV) with excellent stability (95% retention after 12 h).
- The catalyst exhibited ultrafast OER kinetics, indicated by a low Tafel slope (38 mV dec-1).
- Acid activation increased surface roughness and formed active NiFeOOH nanostructures.
Conclusions:
- Unconventional acid activation transforms inexpensive permalloy into a high-performance OER electrocatalyst.
- This method offers a cost-effective approach to enhance hydrogen production via water electrolysis.
- The electrochemical activation strategy can be applied to other substrates for various electrocatalytic reactions.
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