Effect of annealing temperature on optical and electrical properties of ZrO sub(2)-SnO sub(2) nanocomposite thin films
ZrO sub(2)-SnO sub(2) nanocomposite thin films were deposited onto quartz substrate by sol-gel dip-coating technique. Films were annealed at 500, 800 and 1,200 degree C respectively. X-ray diffraction pattern showed a mixture of three phases: tetragonal ZrO sub(2) and SnO sub(2) and orthorhombic ZrS...
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Veröffentlicht in: | Journal of materials science. Materials in electronics 2013-11, Vol.24 (11), p.4340-4345 |
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Sprache: | eng |
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Zusammenfassung: | ZrO sub(2)-SnO sub(2) nanocomposite thin films were deposited onto quartz substrate by sol-gel dip-coating technique. Films were annealed at 500, 800 and 1,200 degree C respectively. X-ray diffraction pattern showed a mixture of three phases: tetragonal ZrO sub(2) and SnO sub(2) and orthorhombic ZrSnO sub(4). ZrSnO sub(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 sub(2)-SnO sub(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 sub(4). PL spectra of the films exhibited an increase in the emission intensity with increase in temperature which substantiates enhancement of ZrSnO sub(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. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-013-1408-7 |