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Aluminum-nitride codoped zinc oxide films prepared using a radio-frequency magnetron cosputtering system
Al-N codoped zinc oxide films were prepared using a radio-frequency magnetron cosputtering system at room temperature. AlN and ZnO materials were employed as the cosputtered targets. The as-deposited cosputtered films at various theoretical atomic ratios [ Al ∕ ( Al + Zn ) at. % ] showed n -type con...
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Published in: | Journal of applied physics 2007-08, Vol.102 (3), p.033516-033516-6 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Al-N codoped zinc oxide films were prepared using a radio-frequency magnetron cosputtering system at room temperature. AlN and ZnO materials were employed as the cosputtered targets. The as-deposited cosputtered films at various theoretical atomic ratios
[
Al
∕
(
Al
+
Zn
)
at.
%
]
showed
n
-type conductive behavior in spite of the N atoms exceeding that of the Al dopants, indicating that the N-related acceptors were still inactive. The crystalline structure was obviously correlated with the cosputtered AlN contents and eventually evolved into an amorphous structure for the Al-N codoped ZnO film at a theoretical Al doping level reaching 60%. With an adequate postannealing treatment, the N-related acceptors were effectively activated and the
p
-type ZnO conductive behavior achieved. The appearance of the
Zn
3
N
2
phase in the x-ray diffraction pattern of the annealed Al-N codoped ZnO film provided evidence of the nitrification of zinc ions. The redshift of the shallow level transition and the apparent suppression of the oxygen-related deep level emission investigated from the photoluminescence spectrum measured at room temperature were concluded to be influenced by the activated N-related acceptors. In addition, the activation of the N acceptors denoted as N-Zn bond and the chemical bond related to the
Zn
3
N
2
crystalline structure were also observed from the associated x-ray photoelectron spectroscopy spectra. |
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ISSN: | 0021-8979 1089-7550 |
DOI: | 10.1063/1.2768010 |