Desorption of Al and Phase Transformation of Ti2AlN MAX Thin Film upon Annealing in Ultra-High-Vacuum

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Desorption of Al and Phase Transformation of Ti2AlN MAX Thin Film upon Annealing in Ultra-High-Vacuum
Title:
Desorption of Al and Phase Transformation of Ti2AlN MAX Thin Film upon Annealing in Ultra-High-Vacuum
Journal Title:
The Journal of Physical Chemistry C
Publication Date:
14 August 2014
Citation:
Zhang, Z., Jin, H., Chai, J., Shen, L., Seng, H. L., Pan, J., … Wang, S. J. (2014). Desorption of Al and Phase Transformation of Ti2AlN MAX Thin Film upon Annealing in Ultra-High-Vacuum. The Journal of Physical Chemistry C, 118(36), 20927–20939. doi:10.1021/jp505428a
Abstract:
Phase stability of single-crystalline Ti2AlN thin film in ultra-high vacuum has been studied in situ by X-ray photoelectron spectroscopy as a function of annealing temperature and ex situ by atomic force microscopy, secondary ion mass spectroscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, and nanoindentation. Ti2AlN is stable up to 600 °C. At 700 °C, Al is preferentially desorbed from the surface and becomes nearly undetected at 900 °C by XPS, where single-crystalline Ti2AlN with terrace morphology transforms into polycrystalline δ-TiN1–x and ξ-TiN0.75–y phases with voids on the surface and reduced film thickness. Mechanical properties including hardness and Young’s modulus are also observed to have deteriorated. Density functional theory calculation shows that Al atoms prefer to diffuse out from the Ti2AlN horizontally along the Al basal planes. The subsequent desorption of Al from surface due to its high vapor pressure results in the decreased Al composition, the void formation on the surface, and the decomposition of Ti2AlN. A kinetic model involving diffusion and desorption processes is proposed to describe the Al behavior and voids formation above 700 °C.
License type:
Publisher Copyright
Funding Info:
There was no specific funding for the research done
Description:
This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Physical Chemistry C, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see 10.1021/jp505428a
ISSN:
1932-7447
1932-7455
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