Low temperature, fast deposition of metallic titanium nitride films using plasma activated reactive evaporation
Titanium and titanium nitride thin films were deposited on silica glass and W substrates at a high coating growth rate by plasma-activated reactive evaporation (ARE). The crystal structure, preferred orientation and grain size of the coatings were determined by x-ray diffraction (XRD) technique usin...
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Veröffentlicht in: | Journal of vacuum science & technology. A, Vacuum, surfaces, and films Vacuum, surfaces, and films, 2005-05, Vol.23 (3), p.394-400 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Titanium and titanium nitride thin films were deposited on silica glass and
W
substrates at a high coating growth rate by plasma-activated reactive evaporation (ARE). The crystal structure, preferred orientation and grain size of the coatings were determined by x-ray diffraction (XRD) technique using
Cu
-
K
α
x rays. The analysis of the coating morphology was performed by field-emission scanning electron microscopy (FE-SEM). The composition of the films was analyzed by Auger electron spectroscopy (AES) and electron-probe microanalysis (EPMA). The titanium and titanium nitride condensates were collected on a carbon-coated collodion film then characterized by transmission electron microscopy (TEM) in order to study the structures of the deposits at very short deposition times. The resistivity of the films was measured by using the four-point-probe method. The titanium coatings were found to consist of very fine particles (
40
nm
in grain size) and to exhibit a strong (002) texture. The titanium nitride coatings were substoichiometric
(
TiN
x
,
x
<
1
)
, with an oxygen content ranging from 7 to 15 at. % depending on the deposition conditions. The deposits were found to exhibit a (111) preferred orientation. This behavior became stronger with coating thickness. In spite of the presence of oxygen, all the
TiN
x
coatings obtained at low temperature and a high growth rate in this work exhibited a rather high electrical conductivity. |
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ISSN: | 0734-2101 1520-8559 |
DOI: | 10.1116/1.1874152 |