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Polarization properties of nonpolar ZnO films grown on R-sapphire substrates using high-temperature H2O generated by a catalytic reaction
Nonpolar ZnO films were grown on r-plane sapphire substrates through the reaction between dimethylzinc (DMZn) and high-temperature H2O, the latter produced by the Pt-catalyzed reaction between H2 and O2. The resulting ZnO films were characterized using atomic force microscopy, X-ray diffraction, and...
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Published in: | Thin solid films 2017-12, Vol.644, p.29-32 |
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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: | Nonpolar ZnO films were grown on r-plane sapphire substrates through the reaction between dimethylzinc (DMZn) and high-temperature H2O, the latter produced by the Pt-catalyzed reaction between H2 and O2. The resulting ZnO films were characterized using atomic force microscopy, X-ray diffraction, and photoluminescence (PL) measurements. They were found to have an anisotropic surface morphology with stripe arrays, and exhibited a diffraction peak associated with ZnO (11-20) index planes. The PL spectra indicated anisotropy in polarization between the directions parallel and perpendicular to the c-axis. The band-edge luminescence at 3.3eV exhibited a maximum when the electric field vector E was perpendicular to the c-axis (parallel to the [1-100] direction) and another minimum when E was parallel to the c-axis. The angular dependence of the linear polarization of the band-edge luminescence was large for ZnO films grown at low temperatures. The large degree of polarization observed for low-temperature growth is thought to be due to the film geometry.
•ZnO films were grown on r-plane sapphire substrates by CVD using a catalytic reaction.•Crystallinity, morphology, PL properties were measured for a-plane ZnO films.•The polarization of the luminescence was shown to highly anisotropic. |
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ISSN: | 0040-6090 1879-2731 |
DOI: | 10.1016/j.tsf.2017.06.062 |