The conditions for the topochemical transformation of variously sized Bi 4 Ti 3 O 12 template plates into BaTiO 3 particles were studied in order to control their morphology, crystal structure, and preferential orientation. In the transformation from sub-200 nm-and μm-sized template plates in the presence of surplus BaCO 3 (Bi 4 Ti 3 O 12 /BaCO 3 = 1:10), the final BaTiO 3 particles retained a memory of the precursor size when the conversion reaction in the molten salt (NaCl/KCl) occurred at 660 and 900 °C, respectively. In both cases the side length of the template was well preserved, while the thicknesses of the final BaTiO 3 plates were larger compared to those of the templates. The morphology of the BaTiO 3 particles formed from micrometer-sized Bi 4 Ti 3 O 12 plates at 660 °C did not closely resemble the template shape because of the exfoliation and disintegration processes. Through the transformation of sub-200 nm Bi 4 Ti 3 O 12 plates at 900 °C the formed BaTiO 3 particles grew by Ostwald ripening, and thus also the shape of the final perovskite particles did not retain a memory of the template. We confirmed by Raman spectroscopy and X-ray diffraction that the BaTiO 3 plates formed at 900 °C exhibited a higher tetragonality than those prepared at 660 °C. Ferroelectric hysteresis and piezoelectric butterfly curves, as obtained using a piezo-force microscope, indicated the significant ferroelectric response of [001] preferentially oriented micrometer-sized and sub-micrometer-sized BaTiO 3 plates.