Abstract
The crystalline structure, surface morphology, dielectric and ferroelectric properties of 0~10wt% Ho2O3 doped (Ba0.75Sr0.25) TiO3 ceramics prepared by conventional solid state method were studied using X-ray diffractometer, scanning electron microscopy, LCR measuring system and ferroelectric property test systems aiming for ceramic capacitor applications. It is found that proper amount of Ho2O3 can refine grains of the system. With the increase of Ho2O3 doping content, the average grain size of (Ba0.75Sr0.25) TiO3 ceramics decreases. When Ho2O3>8 wt%, (Ba0.75Sr0.25) TiO3 based ceramic samples are multi-phase compounds with typical perovskite structure accompanied by the appearance of cylindrical grains. The Ho3+ ions substitute the host A sites and B sites of (Ba0.75Sr0.25) TiO3 perovskite lattice, resulting in the lattice distortion of the system and the change of the relative dielectric constant and dielectric loss at room temperature. With the increase of Ho2O2 doping content, the relative dielectric constant at room temperature of the system increases first and then decreases. The maximum of relative dielectric constant at room temperature can be found in the 1 wt% Ho2O3 doped (Ba0.75Sr0.25) TiO3 ceramics. When Ho2O3＞1 wt%, the maximum of relative dielectric constant ermax decreases and the temperature corresponding to the maximum of relative dielectric constant Tm shifts toward lower temperature with the increase of Ho2O3 doping content. The (Ba0.75Sr0.25) TiO3 ceramics with high Ho2O3 content show relaxor-like behavior which is characterized by the typical diffuse phase transition and frequency dispersion of dielectric constant. However, the (Ba0.75Sr0.25) TiO3 ceramics with low Ho2O3 content do not exhibit permittivity frequency dispersion. According to the P-E hysteresis loops of Ho2O3 doped (Ba0.75Sr0.25) TiO3 ceramics, the ferroelectricity was increased and then decreased with the increase of Ho2O3 doping content. With the increase of Ho2O3 doping content, the P-E relationships turn out to be straight lines, implying the paraelectric phase for (Ba0.75Sr0.25) TiO3 ceramics with high Ho2O3 content.
Highlights
Barium strontium titanate ((Ba1-xSrx) TiO3, BST), as an infinite solid solution of BaTiO3 and SrTiO3, maintains perovskite structure (ABO3) similar to BaTiO3, and has outstanding properties such as high dielectric constant, low dielectric loss and excellent ferroelectric properties [1,2]
0~10 wt% Ho2O3 doped (Ba0.75Sr0.25) TiO3 ceramics were prepared by solid state reaction method
No obvious secondary phase is found even for the 10 wt% Ho2O3 doped (Ba0.75Sr0.25) TiO3 ceramics based on the XRD patterns
Summary
Barium strontium titanate ((Ba1-xSrx) TiO3, BST), as an infinite solid solution of BaTiO3 and SrTiO3, maintains perovskite structure (ABO3) similar to BaTiO3, and has outstanding properties such as high dielectric constant, low dielectric loss and excellent ferroelectric properties [1,2]. Sinclair et al studied the rare earth metal ions RE3+ doped barium titanate ceramics, and proposed that when the RE3+ ions enter the A site of the perovskite lattice, charge imbalance is created which must be compensated by either cation vacancies on the A or B site (ionic compensation), or by electrons Y. Li et al studied on the dielectric properties of Sm2O3 doped Ba0.68Sr0.32TiO3 ceramics, and proposed that the substitution preference of Sm3+ in the lattice depends on Sm2O3 doping content [13]. Some researchers studied the effect of grain size on dielectric and ferroelectric properties of Ba0.80Sr0.20TiO3 ceramics [15,16]. The substitution characteristics of Ho3+ ions in (Ba0.75Sr0.25) TiO3 perovskite lattice will be determined and the interrelationship between the macroscopic dielectric constant, dielectric loss, temperature-dependent properties and microscopic defect behavior will be established
Sign-in/Register to view highlights & summary Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: International Journal of Materials Science and Applications
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
