Wet-chemical synthesis of magnesium niobate nanoparticles powders

Nanosized and highly reactive magnesium niobate (image) powders were successfully synthesized by a new wet-chemical method by means of the dissolution of image and in a solution of oxalic acid followed by the addition of stoichiometric amounts of magnesium carbonate. The Nb–Mg–oxalic acid solution was evaporated resulting in a dry and amorphous powder that was calcined in the temperature range from 200 to 900 °C for 2 h. The crystallization process from the amorphous state to the crystalline image was followed by thermal analysis. The calcined powders characterized by FT-Raman spectroscopy, X-ray diffraction (XRD) and their morphology examined by high resolution scanning electron microscopy (HR-SEM). Pure image, free from the second phases and obtained at 800 °C was confirmed by a combined analysis using XRD and FT-Raman. The average diameter of the particles was calculated from the HR-SEM image as 70 nm approximately. This technique allows a better mixing of the constituent elements and thus a better reactivity of the mixture to obtain pre-reaction products with high purity at lower temperatures and reducing cost. It can offer a great advantage in the PMN-PT formation with respect to the solid-state synthesis.