Electro-Oxidation of Ni42 Steel: A Highly Active Bifunctional Electrocatalyst

Autor(en): Schaefer, Helmut
Chevrier, Daniel M.
Zhang, Peng
Stangl, Johannes
Mueller-Buschbaum, Klaus
Hardege, Jorg D.
Kuepper, Karsten 
Wollschlaeger, Joachim 
Krupp, Ulrich
Duehnen, Simon
Steinhart, Martin 
Walder, Lorenz 
Sadaf, Shamaila
Schmidt, Mercedes
Stichwörter: Chemistry; Chemistry, Multidisciplinary; Chemistry, Physical; ELECTROCHEMICAL EVOLUTION; EVOLVING CATALYST; HYDROGEN EVOLUTION; IN-SITU; IRON ELECTRODES; Materials Science; Materials Science, Multidisciplinary; Nanoscience & Nanotechnology; OXYGEN EVOLUTION REACTION; Physics; Physics, Applied; Physics, Condensed Matter; RUTHENIUM DIOXIDE; Science & Technology - Other Topics; STAINLESS-STEEL; THIN-FILM; WATER-OXIDATION CATALYSTS
Erscheinungsdatum: 2016
Herausgeber: WILEY-V C H VERLAG GMBH
Journal: ADVANCED FUNCTIONAL MATERIALS
Volumen: 26
Ausgabe: 35
Startseite: 6402
Seitenende: 6417
Zusammenfassung: 
Janus type water-splitting catalysts have attracted highest attention as a tool of choice for solar to fuel conversion. AISI Ni42 steel is upon harsh anodization converted into a bifunctional electrocatalyst. Oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are highly efficiently and steadfast catalyzed at pH 7, 13, 14, 14.6 (OER) and at pH 0, 1, 13, 14, 14.6 (HER), respectively. The current density taken from long-term OER measurements in pH 7 buffer solution upon the electro-activated steel at 491 mV overpotential (eta) is around four times higher (4 mA cm(-2)) in comparison with recently developed OER electrocatalysts. The very strong voltage-current behavior of the catalyst shown in OER polarization experiments at both pH 7 and at pH 13 are even superior to those known for IrO2 center dot RuO2. No degradation of the catalyst is detected even when conditions close to standard industrial operations are applied to the catalyst. A stable Ni-, Fe-oxide based passivating layer sufficiently protects the bare metal for further oxidation. Quantitative charge to oxygen (OER) and charge to hydrogen (HER) conversion are confirmed. High-resolution XPS spectra show that most likely gamma-NiO(OH) and FeO(OH) are the catalytic active OER and NiO is the catalytic active HER species.
ISSN: 1616301X
DOI: 10.1002/adfm.201601581

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