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Structural and magnetic study of undoped and cobalt doped TiO(2) nanoparticles

The present study investigates the influence of cobalt doping on the structural and magnetic properties of TiO(2) nanoparticles prepared by a simple wet chemical method. The single phase anatase structure of Co-doped TiO(2) nanoparticles was confirmed by X-ray powder diffraction. A morphological stu...

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Detalles Bibliográficos
Autores principales: Chanda, Anupama, Rout, Kumarmani, Vasundhara, M., Joshi, Shalik Ram, Singh, Jai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087881/
https://www.ncbi.nlm.nih.gov/pubmed/35548180
http://dx.doi.org/10.1039/c8ra00626a
Descripción
Sumario:The present study investigates the influence of cobalt doping on the structural and magnetic properties of TiO(2) nanoparticles prepared by a simple wet chemical method. The single phase anatase structure of Co-doped TiO(2) nanoparticles was confirmed by X-ray powder diffraction. A morphological study using scanning electron microscopy and transmission electron microscopy indicates the formation of TiO(2) nanoparticles of sizes 6–10 nm. The high resolution TEM image shows clear lattice fringes indicating the highly crystalline nature of the nanoparticles which was further analysed by selected area electron diffraction pattern which indicates a polycrystalline nature of anatase TiO(2). The shifting and broadening of the most intense E(g) (1) mode in micro-Raman study of Co-doped TiO(2) nanoparticles and XPS spectra indicate the incorporation of Co in TiO(2). Magnetic measurement shows ferromagnetic behavior at room temperature in undoped TiO(2) which has originated due to the presence of oxygen vacancies which are intrinsic in nature. But the M–H curve of Co-doped TiO(2) shows the coexistence of ferromagnetic and paramagnetic phases with enhanced magnetization. The enhancement in magnetization has arisen due to Co doping and the paramagnetism may be due to the presence of some undetected clusters of oxides of cobalt.