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Updated: Nov 3, 2025
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Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Non-redox doping boosts oxygen evolution electrocatalysis on hematite
Huu Chuong Nguyën1, Felipe Andrés Garcés-Pineda1, Mabel de Fez-Febré1,2
1Institute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology Av. Països Catalans 16 Tarragona 43007 Spain nlopez@iciq.es jrgalan@iciq.es.
Zinc doping significantly enhances hematite
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- The oxygen evolution reaction (OER) is crucial for water electrolysis and renewable fuel production.
- Hematite (α-Fe2O3) is an abundant and inexpensive material with theoretical OER potential but exhibits poor activity.
- Current OER catalysts often rely on cobalt or nickel, driving research into alternatives.
Purpose of the Study:
- To investigate the effect of doping hematite with redox (Ni) and non-redox (Zn) active species to improve OER performance.
- To understand the mechanism behind the enhanced catalytic activity in doped hematite.
- To explore novel strategies for optimizing oxide catalysts for water splitting.
Main Methods:
- Synthesis and characterization of Ni-doped and Zn-doped hematite.
- Electrochemical testing of OER activity in alkaline media.
- Mechanistic studies to elucidate the role of dopants in the OER pathway.
Main Results:
- Zn-doped hematite demonstrates significantly higher OER activity than Ni-doped hematite and pristine hematite.
- Zn-doped hematite achieves state-of-the-art performance (10 mA cm⁻² at 350 mV overpotential at pH 13).
- Doping with Zn alters the OER mechanism, promoting a faster two-site reaction pathway.
Conclusions:
- Non-redox active Zn doping is a superior strategy for enhancing hematite's OER performance compared to redox active Ni doping.
- The enhanced activity of Zn-doped hematite is attributed to a modified reaction pathway involving adjacent metal centers.
- This study presents a new approach for optimizing oxide catalysts, particularly iron oxides, for efficient water electrolysis.
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