Synthesis, Structural Characterization and Morphological Studies of Nanocrystalline CdO by Wet-Chemical Method

Author:

Hassan Israr Ul1,John Liji2,Joseyphus R. Selwin2,Joe I. Hubert3,Amritha R. S2,Naikoo Gowhar Ahmad1

Affiliation:

1. Department of Mathematics and Sciences, College of Arts and Applied Sciences, Dhofar University, Salalah, Oman

2. Department of Chemistry, Mar Ivanios College (Autonomous), Thiruvannathapuram 695015, Kerala, India

3. Centre for Molecular and Biophysics Research, Department of Physics, Mar Ivanios College (Autonomous), Thiruvananthapuram 695015, Kerala, India

Abstract

Synthesis of nanocrystalline cadmium oxide particles were explored by the reaction of inorganic precursor (cadmium chloride) and alkali (sodium hydroxide) via modified wet-chemical method followed by annealing at various temperatures (250, 500 and 750 °C). The structural, optical and morphological studies of cadmium oxide samples were carried out by X-ray diffraction, infrared, ultraviolet-visible, and scanning electron microscope techniques. From X-ray diffraction analysis, it was confirmed that cadmium oxide particles furnish a face centred cubic phase structure and revealing a grain size of around 59 nm. The scanning electron microscope micrographs admit that cadmium oxide samples are agglomerated and have spherical shapes. The bonding deformation and stretching frequency results of cadmium oxide samples were obtained from infrared spectra. The corresponding increase in calcination temperatures has shown an increase in particle size while as no change was found in band gape. These results attribute that the variation in annealing temperature has a significant role on the crystalline nature, grain size and its optical properties. Furthermore, the synthesized cadmium oxide samples were examined for bioactivity analysis.

Publisher

American Scientific Publishers

Subject

General Energy,General Engineering,General Environmental Science,Education,General Mathematics,Health (social science),General Computer Science

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