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The synthesis of spherical BaTiO 3 particles was attempted by a new technique, the “gel–sol method,” at 45°C. The (Ba–Ti) gel used as a starting material was prepared by aging mixtures of titanyl acylate with a barium acetate aqueous solution ([glacial acetic acid (AcOH)]/[titanium isopropoxide (TIP)] = 4, [barium acetate]/[TIP] = 1) at 45°C for 48 h. Potassium hydroxide (KOH) was used as a catalyst for the formation of BaTiO 3 . Powder X‐ray diffractometry (XRD) results and Fourier‐transform infrared (FT‐IR) measurements for the (Ba–Ti) gel showed that the gel was amorphous, but the spatial arrangement of barium and titanium in the (Ba–Ti) gel is similar to that in crystalline BaTiO 3 particles. Fully crystallized spherical BaTiO 3 powder with a particle size of 40–250 nm formed at the very low reaction temperature of 45°C. Scanning electron microscopy images showed that the final particles formed via aggregation of the fine particles that seem to be the primary particles of bulk (Ba–Ti) gel. From the XRD, FT‐IR, and Raman spectroscopy analysis, it was found that the crystal structure of the as‐prepared particles continuously transformed from cubic to tetragonal as the calcination temperature increased, and high crystalline tetragonal BaTiO 3 phase was obtained at 1000°C after 1 h of heat treatment.
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Hwang et al. (2004) studied this question.
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