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dc.contributor.authorTucker, Mark
dc.contributor.authorBilek, M.
dc.contributor.authorMcKenzie, D.
dc.date.accessioned2017-01-30T12:06:21Z
dc.date.available2017-01-30T12:06:21Z
dc.date.created2014-05-07T20:00:21Z
dc.date.issued2014
dc.identifier.citationTucker, Mark D. and Bilek, Marcela M.M. and McKenzie, David R. 2014. A combinatorial investigation of sputtered Ta-Al-C thin films. Thin Solid Films. 558: pp. 99-103.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/18171
dc.identifier.doi10.1016/j.tsf.2014.02.086
dc.description.abstract

We describe a combinatorial experiment investigating the Ta–Al–C material system, conducted with the aim of determining why the tantalum-containing Mn + 1AXn phases have so far proved to be not amenable to thin-film synthesis. Samples were deposited onto (0001) Al2O3 wafers at 850 °C and characterized by X-ray diffraction wafer maps, scanning electron microscopy, and surface optical scattering. Elemental Ta, the binary phases TaC, Ta2C, and TaAl3, and the ternary phases Ta3Al2C and Ta5Al3C were identified. The morphology, phase composition and preferred orientation of the films deposited were found to be highly sensitive to the Ta fraction of the incident flux during deposition. No MAX phase material was observed, indicating that the Ta-containing MAX phases do not form under the deposition conditions investigated. Explanations associated with inadequate coverage of stochiometries, preferential sputtering, and thermodynamic instability have been ruled out. An explanation based on reduced surface diffusion of Ta during growth is proposed. A substantially higher substrate temperature during deposition is likely to be required to synthesize Ta-containing MAX phases.

dc.publisherElsevier S.A.
dc.subjectCombinatorial
dc.subjectTantalum
dc.subjectMAX phase
dc.titleA combinatorial investigation of sputtered Ta-Al-C thin films
dc.typeJournal Article
dcterms.source.volume558
dcterms.source.startPage99
dcterms.source.endPage103
dcterms.source.issn0040-6090
dcterms.source.titleThin Solid Films
curtin.note

NOTICE: this is the author’s version of a work that was accepted for publication in Thin Solid Films. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Thin Solid Films, Vol. 558 (2014). DOI: 10.1016/j.tsf.2014.02.086

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curtin.accessStatusOpen access


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