Electronic structure and formation mechanism of complex Ti–Nb oxide
Two-layer thin film specimens of Nb2O5 and TiO2 were deposited on optical-grade quartz and n-type single crystalline silicon substrates with (100) crystallographic orientation by a magnetron deposition source under high vacuum. All samples were subjected to 1–5h of resistive heating at ultra high va...
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Published in | Thin solid films Vol. 520; no. 14; pp. 4797 - 4799 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.05.2012
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Subjects | |
Online Access | Get full text |
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Summary: | Two-layer thin film specimens of Nb2O5 and TiO2 were deposited on optical-grade quartz and n-type single crystalline silicon substrates with (100) crystallographic orientation by a magnetron deposition source under high vacuum. All samples were subjected to 1–5h of resistive heating at ultra high vacuum, and in situ X-ray diffraction measurements (XRD) were made in the temperature range of 300–1373K. Analysis of the XRD data confirmed the growth of TiNbO4 during cooling of the two-layered specimens which had been previously heated to 1373K. Optical measurements revealed a band gap value of 3.78eV for the direct transition and 3.29eV for the indirect one. The samples had a transmittance of 85% in the visible range. Electrophysical measurements in high vacuum established the electroresistivity vs. temperature dependence in the range of 300–773K, from 7.3⁎10−1 to 3.9⁎10−2Ω cm, respectively. X-ray photoelectron spectroscopy measurements were used to examine the chemical shift for Nb 3d, with a value of −1.1eV in comparison with Nb5+ and matched to Nb4+[1], while the Ti lines correspond to Ti4+[2]. |
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ISSN: | 0040-6090 1879-2731 |
DOI: | 10.1016/j.tsf.2011.10.130 |