Thermal decomposition route for synthesis of Mn3O4 nanoparticles in presence of a novel precursor

The synthesis of manganese oxide (Mn3O4) nanoparticles by using thermal decomposition and its physicochemical characterization are being reported in present investigation. As a new precursor, [bis(2-hydroxy-1-naphthaldehydato)manganese(II)] complex was used in the presence of oleylamine (C18H37N) as both surfactant and solvent to control the size of resulting nanoparticle. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and Raman spectrum. Synthesized manganese oxide nanoparticles have a tetragonal structure with average size of 9–24 nm. The phase pure samples were characterized by using X-ray photoelectron spectroscopy (XPS) for Mn 2p level. The values of binding energies are consistent with the relative values are reported in the literature. As a comparison between two methods, the novel precursor thermally was treated in solid state reaction in different temperature, 400, 500, and 600 °C and the products were characterized by SEM images. Magnetic property of the as-prepared Mn3O4 nanoparticle shows a ferromagnetic behavior with high saturation magnetization and coercivity.

The present investigation reports, the synthesis of Mn3O4 nanoparticles using thermal decomposition and its physicochemical characterization. The Mn3O4 nanoparticles have been prepared using [bis(2-hydroxy-1-naphthaldehydato)manganese(II)] complex as precursor. Synthesized manganese oxide nanoparticles have a tetragonal structure with average size of 9–24 nm. As a comparison between two methods, the novel precursor thermally was treated in solid state reaction in different temperature, 400, 500, and 600 °C and the products were characterized by SEM images.Figure optionsDownload as PowerPoint slide