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Direct MOCVD Growth of Iron Oxide on Three-Dimensional Nickel Foam as Electrode for the Oxygen Evolution Reaction.


ABSTRACT: Iron oxide thin films were grown directly on three-dimensional nickel foam via metalorganic chemical vapor deposition (MOCVD) in the temperature range of 250-450?°C using Fe(CO)5 as precursor. Iron oxide (?-Fe2 O3 ) films were formed at low substrate temperatures (250-350?°C), whereas the additional growth of an underlying NiO film occurred at substrate temperatures above 350?°C. The electrochemical activities of the as-formed binder-free and noble metal-free electrodes were tested for the oxygen evolution reaction (OER) in alkaline media. An overpotential reduced by 250?mV at a current density of 50?mA?cm-2 and a lower Tafel slope of 55?mV?dec-1 compared to bare nickel foam were found for the best-performing electrocatalyst, while the long-term stability of the as-formed electrodes was proven by chronopotentiometry. The surface morphology of the iron oxide films was characterized by scanning electron microscopy, whereas the crystallographic phase as well as the elemental composition were determined by X-ray diffraction, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and time-of-flight secondary ion mass spectrometry in the pre- and the post-catalytic state.

SUBMITTER: Stienen C 

PROVIDER: S-EPMC7756718 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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Direct MOCVD Growth of Iron Oxide on Three-Dimensional Nickel Foam as Electrode for the Oxygen Evolution Reaction.

Stienen Christian C   Bendt Georg G  

ChemSusChem 20200930 22


Iron oxide thin films were grown directly on three-dimensional nickel foam via metalorganic chemical vapor deposition (MOCVD) in the temperature range of 250-450 °C using Fe(CO)<sub>5</sub> as precursor. Iron oxide (α-Fe<sub>2</sub> O<sub>3</sub> ) films were formed at low substrate temperatures (250-350 °C), whereas the additional growth of an underlying NiO film occurred at substrate temperatures above 350 °C. The electrochemical activities of the as-formed binder-free and noble metal-free ele  ...[more]

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