Thermal stability of amorphous molybdenum trioxide films prepared at different oxygen partial pressures by reactive DC magnetron sputtering
Thin films of MoO 3 were prepared on quartz and Si (1 0 0) substrates by reactive dc magnetron sputtering of a Mo target in an oxygen and argon atmosphere. The structural and optical changes induced in the films due to post-growth annealing have been systematically studied by Rutherford backscatteri...
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Published in | Vacuum Vol. 81; no. 5; pp. 636 - 643 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
05.01.2007
|
Subjects | |
Online Access | Get full text |
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Summary: | Thin films of MoO
3 were prepared on quartz and Si (1
0
0) substrates by reactive dc magnetron sputtering of a Mo target in an oxygen and argon atmosphere. The structural and optical changes induced in the films due to post-growth annealing have been systematically studied by Rutherford backscattering (RBS), X-ray diffraction (XRD), X-ray reflectivity (XRR) and by optical methods. RBS studies reveal no change in composition of the films upon annealing at high temperatures. Grazing angle XRD studies show that the as-deposited films are amorphous and crystallize to
β-MoO
3 phase with small contribution of
α-MoO
3 upon annealing at 300
°C. The film prepared at 0.40
Pa transforms to
α-MoO
3 upon annealing at 650
°C, while the film deposited at 0.19
Pa still has some
β-MoO
3 phase contribution. XRR measurements reveal that the film thickness decreases upon annealing with simultaneous increase of film density. The surface roughness of the films strongly increases after crystallization. The contraction of the film deposited at 0.40
Pa is much greater than the contraction of the film prepared at 0.19
Pa. The mass variation of the film deposited at 0.19
Pa and that deposited at 0.40
Pa are completely different. The optical properties of MoO
3 films deposited at 0.19 and 0.40
Pa are changed strongly by annealing. |
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ISSN: | 0042-207X 1879-2715 |
DOI: | 10.1016/j.vacuum.2006.08.006 |