Journal
APPLIED SURFACE SCIENCE
Volume 309, Issue -, Pages 181-187Publisher
ELSEVIER
DOI: 10.1016/j.apsusc.2014.04.215
Keywords
Zirconium oxinitride; Radio frequency sputtering; Texture
Categories
Funding
- Foundation for the Promotion of Research and Technology Bank of the Republic of Colombia
- Corrosion and Protection Laboratory of the University of Cadiz (LABCYP) and International Physics Center CIF
- Research Directorate the National University of Colombia, Bogota, Colombia DIB
- Spanish Ministry of Economy and Competitiveness [MAT2010-3804-C04-01]
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This paper reports the influence of substrate temperature on the structure, morphology and corrosion resistance of ZrOxNy/ZrO2 thin films deposited on 304 stainless steel using radio frequency sputtering (RF sputtering). Structural analysis was carried out by X-ray diffraction (XRD); morphological analysis was performed using scanning electron microscopy (SEM) and atomic force microscopy (AFM) and surface chemical analysis was determined using X-ray photoelectron spectroscopy (XPS). XRD data showed that the films deposited at 300 degrees C (573 K) and 350 degrees C (623 K) result in the growth of a monoclinic zirconium oxynitride phase with preferential orientation along the (-1 1 1) plane, while at 14 degrees C (287 K) the predominant phase is of polycrystalline ZrO2. The corrosion results indicate that the coatings provide good resistance to corrosion in chloride-containing media, being better in the film deposited at 350 degrees C (623 K). SEM analysis demonstrated the homogeneity of the films deposited at the three temperatures; AFM studies established the average roughness of the films to be 4.25 nm. The binding energies of the Zr 3d, N 1s, and O 1s core levels determined by XPS were all compatible with the formation of a zirconium oxynitride and zirconium oxide in the surface of the film. ZrOxNy/ZrO2 thin films are promising candidates for increasing the corrosion resistance of the steels in chloride-rich environments. (C) 2014 Elsevier B.V. All rights reserved.
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