CuFeO2 prepared by electron cyclotron wave resonance-assisted reactive HiPIMS with two magnetrons and radio frequency magnetron sputtering

Author:

Písaříková A.12ORCID,Olejníček J.1ORCID,Venkrbcová I.1ORCID,Nožka L.2ORCID,Cichoň S.1ORCID,Azinfar A.3ORCID,Hippler R.13ORCID,Helm C. A.3ORCID,Mašláň M.4ORCID,Machala L.4ORCID,Hubička Z.1ORCID

Affiliation:

1. Institute of Physics, Czech Academy of Sciences 1 , Na Slovance 2, 18200 Prague, Czech Republic

2. Joint Laboratory of Optics, Palacky University Olomouc 2 , Av. 17. listopadu 50A, 77207 Olomouc, Czech Republic

3. Institut für Physik, Universität Greifswald 3 , Felix-Hausdorff-Str. 6, 17489 Greifswald, Germany

4. Department of Experimental Physics, Faculty of Science, Palacky University in Olomouc 4 , 17. listopadu 12, 77207 Olomouc, Czech Republic

Abstract

In this study, thin films of CuFeO2 were prepared using radio frequency reactive sputtering (RF) and reactive high-power impulse magnetron sputtering combined with electron cyclotron wave resonance plasma (HiPIMS-ECWR). The plasma was characterized using an RF ion probe. Plasma density, tail electron energy, and electron temperature were extracted from the measured data. The films were deposited on fluorine-doped tin oxide-coated glass and quartz glass, with the substrates being heated during the deposition process. The final delafossite CuFeO2 structure was formed after annealing in an argon gas flow at 550–600 °C. The ideal deposition conditions were found to be with a stoichiometric ratio of Cu:Fe = 1:1, which was the optimal condition for creating the delafossite CuFeO2 structure. The measured optical bandgap of CuFeO2 was 1.4 eV. The deposited CuFeO2 films were subjected to photoelectrochemical measurements in the cathodic region to investigate their potential application in solar photocatalytic water splitting. The films showed photocatalytic activity, with a photocurrent density of around 70 μA/cm2 (under an incident light irradiation of 62 mW/cm2, AM 1.5 G). The electrochemical properties of the layers were studied using open circuit potential, linear voltammetry, and chronoamperometry. The surface morphology and chemical composition of the layers were analyzed by atomic force microscopy and energy-dispersive x-ray spectroscopy, respectively. The crystalline structure was determined using XRD and Raman spectroscopy. The results of these methods are presented and discussed in this article.

Publisher

American Vacuum Society

Subject

Surfaces, Coatings and Films,Surfaces and Interfaces,Condensed Matter Physics

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