Synthesis and electrochemical characteristics of Ta-N thin films fabricated by cathodic arc deposition
- 1. Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100080 (China) and College of Science, Civil Aviation University of China, Tianjin 300300 (China)
- 2. Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100080 (China)
- 3. College of Science, Changchun University of Science and Technology, Changchun 130022, Jilin Province (China)
Description
Ta-N thin films were deposited on AISI 317L stainless steel (SS) substrates by cathodic arc deposition (CAD) at substrate biases of -50 and -200 V. The as-deposited films were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray analysis (EDX). The results show that stoichiometric TaN with hexagonal lattice (3 0 0) preferred orientation was achieved at the bias of -200 V. On the other hand, Ta-rich Ta-N thin film deposited at -50 V shows amorphous nature. According to the XPS result, Ta element in the films surface exist in bonded state, including the Ta-N bonds characterized by the doublet (Ta 4f7/2 = 23.7 eV and Ta 4f5/2 = 25.7 eV). Electrochemical properties of the Ta-N coated stainless steel systems were investigated using potentiodynamic polarization and electrochemical impedance spectroscope (EIS) in Hank's solution at 37 deg. C. For the Ta-N coated samples, the corrosion current (icorr) is two or three orders of magnitude lower than that of the uncoated ones, indicating a significantly improved corrosion resistance. Growth defects in the Ta-N thin films produced by CAD, however, play a key role in the corrosion process, especially the localised corrosion. Using the polarization fitting and the EIS modelling, we compared the polarization resistance (Rp) and the porosity (P) of the Ta-N coatings deposited at different biases. It seems that Ta-N film with comparatively lower bias (-50 V) shows better corrosion behavior in artificial physiological solution. That may be attributed to the effect of ion bombarding, which can be modulated by the substrate bias
Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2007.01.128;
- PII
- S0169-4332(07)00203-6;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 253
- Journal Issue
- 16
- Journal Page Range
- p. 6811-6816
- ISSN
- 0169-4332
- CODEN
- ASUSEE
Conference
- Title
- 4. international workshop on basic aspects of nonequilibrium plasmas interacting with surfaces - Negative ions, their function and designability; 4. EU-Japan joint symposium on plasma processes
- Dates
- 30 Jan - 1 Feb 2006
- Place
- Lake Kawaguchi (Japan)
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 39003099
- Subject category
- S36: MATERIALS SCIENCE;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ALUMINIUM COMPOUNDS; COATINGS; CORROSION; CORROSION RESISTANCE; CRYSTAL GROWTH; CRYSTAL STRUCTURE; CURRENTS; DEFECTS; DEPOSITION; HEXAGONAL LATTICES; IMPEDANCE; NITROGEN; POLARIZATION; POROSITY; SILICON COMPOUNDS; SIMULATION; SOLUTIONS; STAINLESS STEEL-317; STAINLESS STEELS; STOICHIOMETRY; SUBSTRATES; SURFACES; SYNTHESIS; TANTALUM; TANTALUM NITRIDES; THIN FILMS; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALLOYS; CARBON ADDITIONS; CHEMICAL REACTIONS; COHERENT SCATTERING; CRYSTAL LATTICES; CRYSTAL STRUCTURE; DIFFRACTION; DISPERSIONS; ELECTRON SPECTROSCOPY; ELEMENTS; FILMS; HIGH ALLOY STEELS; HOMOGENEOUS MIXTURES; IRON ALLOYS; IRON BASE ALLOYS; METALS; MIXTURES; NITRIDES; NITROGEN COMPOUNDS; NONMETALS; PHOTOELECTRON SPECTROSCOPY; PNICTIDES; REFRACTORY METAL COMPOUNDS; REFRACTORY METALS; SCATTERING; SPECTROSCOPY; STAINLESS STEELS; STEELS; TANTALUM COMPOUNDS; TRANSITION ELEMENT ALLOYS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.