Structural, optical and magnetic properties of Sn doped ZnS nano powders prepared by solid state reaction
Autor: | N. Madhusudhana Rao, G. Venugopal Rao, S. Kaleemulla, K. Chaitanya Kumar |
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Rok vydání: | 2017 |
Předmět: |
010302 applied physics
Photoluminescence Materials science Scanning electron microscope Band gap Doping Analytical chemistry 02 engineering and technology 021001 nanoscience & nanotechnology Condensed Matter Physics 01 natural sciences Electronic Optical and Magnetic Materials Paramagnetism Magnetization 0103 physical sciences Crystallite Electrical and Electronic Engineering 0210 nano-technology Diffractometer |
Zdroj: | Physica B: Condensed Matter. 522:75-80 |
ISSN: | 0921-4526 |
DOI: | 10.1016/j.physb.2017.07.071 |
Popis: | Tin doped ZnS powders (Zn 1−x Sn x S, x = 0.00, 0.02, 0.05&0.08) were synthesized by a simple Solid state reaction and were characterized by Powder X-ray diffractometer (XRD), UV–Vis–NIR diffuse reflectance spectrophotometer, fluorescence spectrophotometer, scanning electron microscope (SEM) and vibrating sample magnetometer (VSM). The XRD studies revealed that no change in crystal structure was observed by the substitution of Sn into ZnS lattice. The crystallite size was calculated by Scherrer's formula and found that the crystallize size of Sn doped ZnS powders were in the range of 35–45 nm. From the diffused reflectance spectra, the band gap values of Zn 1−x Sn x S powders were estimated, and they were found to be in the range of 3.53–3.58 eV. The pure ZnS particles showed higher optical absorption in visible region than that of Sn doped ZnS nano particles. The Photoluminescence (PL) spectra of Zn 1−x Sn x S powders were recorded in the range of 400–700 nm with an excitation wavelength of 360 nm. The Zn 1−x Sn x S powders exhibited ferromagnetism at low temperature (100 K) and super paramagnetism at room temperature (300 K). The strength of magnetization increased with increase of Sn doping concentration from 0.015 emu/g to 0.18 emu/g, when x increased from 0.00–0.05. |
Databáze: | OpenAIRE |
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