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Nanoporous Anodic Aluminum-Iron Oxide with a Tunable Band Gap Formed on the FeAl3 Intermetallic Phase.

ABSTRACT: Nanostructured anodic oxide layers on an FeAl3 intermetallic alloy was prepared by two-step anodization in 20 wt.% H2SO4 at 0 °C. The obtained anodic oxide coating was subjected to phase and chemical composition analysis using XPS and XRD techniques. An analysis of the band gap of individual coatings was also performed. The applied parameters of the anodization process were determined, enabling the formation of a nanostructured coating on the FeAl3 intermetallic alloy. Tests were carried out on samples produced at a voltage between 10 V and 22.5 V in 2.5 V steps. The produced coatings were subjected to an annealing process at 900 °C for 2 h in an argon protective atmosphere. Moreover, the influence of the substrate chemical composition on the chemical and phase composition of the anodic oxide are discussed. Band gaps of 2.37 eV at 22.5 V and 2.64 eV at 10 V were obtained directly after the anodizing process. After applying the heat treatment, band gap values of 2.10 eV at 22.5 Vand 2.48 eV for the coating produced at 10 V were obtained.

SUBMITTER: Chilimoniuk P

PROVIDER: S-EPMC7475830 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Nanoporous Anodic Aluminum-Iron Oxide with a Tunable Band Gap Formed on the FeAl3 Intermetallic Phase.

Chilimoniuk Paulina P Socha Robert P RP Czujko Tomasz T

Materials (Basel, Switzerland) 20200806 16

Nanostructured anodic oxide layers on an FeAl3 intermetallic alloy was prepared by two-step anodization in 20 wt.% H2SO4 at 0 °C. The obtained anodic oxide coating was subjected to phase and chemical composition analysis using XPS and XRD techniques. An analysis of the band gap of individual coatings was also performed. The applied parameters of the anodization process were determined, enabling the formation of a nanostructured coating on the FeAl3 int ...[more]

PMID: 32781714

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Project description:This work for the first time unfurls the fundamental mechanisms and sets the stage for an approach to derive electrocatalytic activity, which is otherwise not possible, in a traditionally known wide band-gap oxide material. Specifically, we report on the tunable optical properties, in terms of wide spectral selectivity and red-shifted band gap, and electrocatalytic behavior of iron (Fe)-doped gallium oxide (?-Ga2O3) model system. X-ray diffraction (XRD) studies of sintered Ga2-x Fe x O3 (GFO) (0.0 ? x ? 0.3) compounds provide evidence for the Fe3+ substitution at Ga3+ site without any secondary phase formation. Rietveld refinement of XRD patterns reveals that the GFO compounds crystallize in monoclinic crystal symmetry with a C2/m space group. The electronic structure of the GFO compounds probed using X-ray photoelectron spectroscopy data reveals that at lower concentrations, Fe exhibits mixed chemical valence states (Fe3+, Fe2+), whereas single chemical valence state (Fe3+) is evident for higher Fe content (x = 0.20-0.30). The optical absorption spectra reveal a significant red shift in the optical band gap with Fe doping. The origin of the significant red shift even at low concentrations of Fe (x = 0.05) is attributed to the strong sp-d exchange interaction originated from the 3d5 electrons of Fe3+. The optical absorption edge observed at ?450 nm with lower intensity is the characteristic of Fe-doped compounds associated with Fe3+-Fe3+ double-excitation process. Coupled with an optical band-gap red shift, electrocatalytic studies of GFO compounds reveal that, interestingly, Fe-doped Ga2O3 compound exhibits electrocatalytic activity in contrast to intrinsic Ga2O3. Fe-doped samples (GFO) demonstrated appreciable electrocatalytic activity toward the generation of H2 through electrocatalytic water splitting. An onset potential and Tafel slope of GFO compounds include ?900 mV, ?210 mV dec-1 (x = 0.15) and ?1036 mV, ?290 mV dec-1 (x = 0.30), respectively. The electrocatalytic activity of Fe-doped Ga-oxide compounds is attributed to the cumulative effect of different mechanisms such as doping resulting in new catalytic centers, enhanced conductivity, and electron mobility. Hence, in this report, for the first time, we explored a new pathway; the electrocatalytic behavior of Fe-doped Ga2O3 resulted due to Fe chemical states and red shift in the optical band gap. The implications derived from this work may be applicable to a large class of compounds, and further options may be available to design functional materials for electrocatalytic energy production.

Dataset Information

Nanoporous Anodic Aluminum-Iron Oxide with a Tunable Band Gap Formed on the FeAl3 Intermetallic Phase.

Publications

Nanoporous Anodic Aluminum-Iron Oxide with a Tunable Band Gap Formed on the FeAl<sub>3</sub> Intermetallic Phase.

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