研究目的
To investigate the structural and electrical properties of porous BaTiO3 and Ba(Ti0.96SnxZr0.04-x)O3 (x=0.02-0.04) ceramics prepared by solid-state and mechanochemical technique, and to evaluate the effect of porosity on the ceramics material for MLCC and thermistor applications.
研究成果
Porous BaTiO3 and Ba(Ti0.96SnxZr0.04-x)O3 (x=0.02-0.04) ceramics with nanocrystalline structure were obtained by mechanochemical synthesis method. The effects of the porosity of the ceramics on their microstructural and dielectric properties were investigated. It was found that porosity of the ceramics could be tailored by varying the dopant content. X-ray analysis confirms the cubic and tetragonal structure at room temperature for pristine and Zr and Sn codoped barium titanate, respectively. FESEM images indicated that the particles possess a porous structure. The temperature dependence dielectric study revealed a normal ferroelectric behavior in the material. Room temperature dielectric constant increased with Sn and Zr content, while dielectric loss decreased. Electrical parameters such as the real part of impedance (Z'), the imaginary part of impedance (Z'') as a function of both frequency and temperature have been studied through impedance spectroscopy. Nyquist plots of Ba(Ti0.96Sn0.02Zr0.02)O3 ceramic show both bulk and grain boundary effects at 400°C which indicates the NTCR behavior of the sample. Therefore, Ba(Ti0.96Sn0.02Zr0.02)O3 ceramic is considered as a promising low-cost material for thermistor applications. The electrical relaxation process occurring in the material has been found to be temperature dependent.
研究不足
The high costs and difficulty in process control in some routes necessitated the development of alternative options for the synthesis of porous BaTiO3 nanoparticles. The presence of porosity can lead to dielectric permittivity that is lower than that of the solid material.
1:Experimental Design and Method Selection:
The samples were prepared by conventional solid state and mechanochemical technique from fine powders of metal oxides or metal carbonates. The nominal purity of the initial powders, as well as their manufacturers are given in Table
2:Sample Selection and Data Sources:
Analytical grade high-purity (
3:9%) oxide precursors, BaCO3, ZrO2, TiO2 and SnO2 were used. List of Experimental Equipment and Materials:
X-ray diffractometer with monochromatic Cu-Kα radiation (λ=
4:54178 ?) under 40 kV/30 mA, Electronic Densimeter MD-3005 ALFA MIRAGE, field-emission scanning electron microscopy (FE-SEM) (JEOL 7600F) operated at 15 kV, Precision LC material analyzer (Radiant, U.S.A), Agilent 4294A Impedance Analyzer. Experimental Procedures and Operational Workflow:
Stoichiometric amounts of the oxides were weighed according to nominal composition and ball-mixed for 12 h in alcohol. The mixture was dried in an oven and calcined in an alumina crucible at 1050°C for 4 h in the air. The calcined powders were ball-milled in an isopropyl alcohol as wetting medium using SPEX 8000 Mixer/Mills (60 Hz model) at room temperature for 7 h. The milled powder was compacted at 5 ton to make pellets of size 15 mm in diameter and
5:5 mm in thickness using polyvinyl alcohol (PVA) as a binder. After burning off the binder (PVA), the pellets were sintered in a programmable furnace at temperatures of 1190°C for 2 h in alumina crucibles. Data Analysis Methods:
Phase identification of calcined and sintered powders was carried out using X-ray diffractometer. The experimental densities of the samples were calculated using Electronic Densimeter MD-3005 ALFA MIRAGE. The morphological studies of the sintered sample were carried out using field-emission scanning electron microscopy (FE-SEM). The polarization-electric field (P–E) hysteresis characteristics of the samples were determined using a Precision LC material analyzer. The dielectric and impedance measurement was carried out for the sintered sample using an Agilent 4294A Impedance Analyzer in the frequency and temperature range of 40 Hz–1 MHz and 30–400°C, respectively.
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