Effect of annealing temperature on optical and electrical properties of ZrO2–SnO2 nanocomposite thin films

ZrO 2 –SnO 2 nanocomposite thin films were deposited onto quartz substrate by sol–gel dip-coating technique. Films were annealed at 500, 800 and 1,200 °C respectively. X-ray diffraction pattern showed a mixture of three phases: tetragonal ZrO 2 and SnO 2 and orthorhombic ZrSnO 4 . ZrSnO 4 phase and...

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Veröffentlicht in:Journal of materials science. Materials in electronics 2013-11, Vol.24 (11), p.4340-4345
Hauptverfasser: Anitha, V. S., Lekshmy, S. Sujatha, Joy, K.
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Sprache:eng
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Zusammenfassung:ZrO 2 –SnO 2 nanocomposite thin films were deposited onto quartz substrate by sol–gel dip-coating technique. Films were annealed at 500, 800 and 1,200 °C respectively. X-ray diffraction pattern showed a mixture of three phases: tetragonal ZrO 2 and SnO 2 and orthorhombic ZrSnO 4 . ZrSnO 4 phase and grain size increased with annealing temperature. Fourier transform infra-red spectroscopy spectra indicated the reduction of –OH groups and increase in ZrO 2 –SnO 2 , by increasing the treatment temperature. Scanning electron microscopy observations showed nucleation and particle growth on the films. The electrical conductivity decreased with increase in annealing temperature. An average transmittance greater than 80 % (in UV–visible region) was observed for all the films. The optical constants of the films were calculated. A decrease in optical band gap from 4.79 to 4.59 eV was observed with increase in annealing temperature. Photoluminescence (PL) spectra revealed an emission peak at 424 nm which indicates the presence of oxygen vacancy in ZrSnO 4 . PL spectra of the films exhibited an increase in the emission intensity with increase in temperature which substantiates enhancement of ZrSnO 4 phase and reduction in the non-radiative defects in the films. The nanocomposite modifies the structure of the individual metal oxides, accompanied by the crystallite size change and makes it ideal for gas sensor and optical applications.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-013-1408-7