The crystallographic properties and defects of hydrothat hydrothermal BaTiO 3 powders show structural peculiarities that are closely connected with a considerable content of water. thermally grown barium titanate crystallites are reported. When a precursor with a Ba:Ti molar ratio of 1.0 was used, On annealing the powders to 500ЊC, the water is gradually released and the normal structural properties of BaTiO 3 recur. cubic barium titanate crystallites were formed. However, when the precursor Ba:Ti molar ratio was 3.0, the product In this paper, systematic measurements of hydrothermal BaTiO 3 crystallites are presented. The formation of defects, the relationwas tetragonal. The defect concentration (including OH defects and barium vacancies) was higher in cubic crystalliship between defect content, the reaction conditions, and the crystallographic properties of the crystallites are discussed. tes than in tetragonal crystallites. Because of the defects in the crystallites, the displacement of Ba 2؉ cations and the deformation of the Ti-O 6 octahedrons was suppressed;II. Experimental Procedure thus, no phase transition from cubic to tetragonal occurred at the Curie point. When the defects were eliminated by (1) Hydrothermal Synthesis of BaTiO 3 Crystallites thermal treatment, the normal crystallographic propertiesThe hydrothermal experiments were performed in a platinumwere obtained. A high reaction temperature and a high lined tube-type autoclave with an internal diameter of 30 mm Ba:Ti molar ratio in the precursor were beneficial to limand a length of 450 mm. Many types of precursors were utiiting defect dormation in the crystallites; thus, tetragonal lized, including commercial TiO 2 (CP, Shanghai Institute of crystallites were obtained.Fine Chemicals) and Ba(OH) 2 и8H 2 O (AR, Shanghai Institute of Fine Ceramics) powders; hydrolysis product of tetrabutyl I. Introduction titanate and Ba(OH) 2 и8H 2 O powders; newly prepared barium titanium acetate gel 11 and barium titanium peroxide gel. 12 The N UMEROUS ceramic powders can be conveniently synthe-fill parameter of the hydrothermal reaction system was selected sized by the hydrothermal method. Hydrothermal synthesis in a range from 80% to 90%, the reaction temperature in a range makes it possible to prepare phase-pure products from inexpenfrom 75Њ to 400ЊC, and the reaction time (the time at the sive and easily accessible precursors in a single step. Also, reaction temperature) in a range from 4 to 72 h. The heating the synthesis can be performed at moderate temperature and rate for all experiments was fixed at 7ЊC/min. pressure using a simple autoclave. The conditions of hydrothermal reactions can be optimized by varying the chemical process(2) Characterization of the Crystallites variables, such as reagent concentrations, temperature, presAfter they were washed with distilled water and absolute sure, and pH. Traditionally, the process variables, with few ethanol several times, the hydrothermal products were dried in exceptions, 1,2 are adjusted empirically in a t...