Mechanical properties and oxidation resistance of CrAlN/BN nanocomposite coatings prepared by reactive dc and rf cosputtering
Mechanical properties and oxidation resistance of CrAlN/BN nanocomposite coatings prepared by reactive dc and rf cosputtering
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DOI:
10.1016/j.surfcoat.2011.02.044
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发表时间:
2011-07-25
影响因子:
5.4
通讯作者:
Ikeno, S.
中科院分区:
文献类型:
--
作者:
Nose, M.;Kawabata, T.;Ikeno, S.
CrAlN/BN nanocomposite coatings were deposited through reactive cosputtering, i.e., pulsed dc and rf sputtering, of CrAl and h-BN targets, respectively. X-ray diffraction (XRD) and selected area electron-diffraction (SAED) analysis indicated that the CrAlN/BN coating consists of very fine grains of B1 structured CrAlN phase. With an increasing BN volume fraction of over 8 vol.%, the nanocrystalline nature of the grains is revealed through a dispersion of fine grains in the CrAlN/BN coating. A cross-sectional observation using a transmission electron microscope (TEM) clarified that the coating demonstrating the highest level of hardness has a fiber-like structure consisting of grains that are similar to 20 nm in width and similar to 50 nm in length. X-ray photoelectron spectroscopy (XPS) analysis revealed that the coating consists mainly of CrAlN and h-BN phase. The indentation hardness (H-IT) and effective Young's modulus (E*) of the coatings increased with the BN phase ratio, reaching a maximum value of similar to 46 and similar to 440 GPa at similar to 7 vol.% of BN phase; it then decreased moderately to similar to 40 and similar to 350 GPa at 18 vol.% of BN, respectively. Furthermore, CrAlN/BN coatings showed superior oxidation resistance compared with CrAlN coatings. After annealing at 800 degrees C in air for 1 h, the indentation hardness of CrAlN coatings decreased to 50% of the as-deposited hardness; in contrast, the hardness of CrAlN/BN nanocomposite coatings either stayed the same or increased, attaining a value of about 46 GPa. After annealing at 900 degrees C for 1 h, the hardness of all the coatings decreased to about 40%. (C) 2011 Elsevier B.V. All rights reserved.