电介质
材料科学
结构精修
凝聚态物理
陶瓷
介电常数
居里温度
居里-维斯定律
分析化学(期刊)
核磁共振
晶体结构
结晶学
化学
物理
光电子学
铁磁性
色谱法
复合材料
作者
Shahid Anwar,Pankaj R. Sagdeo,N. P. Lalla
标识
DOI:10.1016/j.solidstatesciences.2007.07.023
摘要
Abstract The influence of Hf doping on the structure and dielectric properties of BaTiO3 has been studied. For this purpose Ba(Ti1−xHfx)O3 ceramics were prepared through solid-state reaction route at close compositions, having x = 0.20, 0.22, 0.23 and 0.30. The study was aimed to locate the exact hafnium concentration for normal to relaxor crossover in these ceramics. X-ray diffraction followed by Rietveld refinement, reveals the formation of single phase with Pm3m cubic structure. Temperature and frequency dependence of real (ɛ′) and imaginary (ɛ″) parts of the dielectric permittivity have been studied in the temperature range of 90–350 K, at frequencies between 0.1 kHz and 100 kHz. The dielectric permittivity variations with temperature show deviation from Curie–Weiss behavior and strong frequency dispersion. The deviation from Curie–Weiss behavior, discontinuous jump along with the change in the slope of Tm vs Hf concentration plot, and the degree of relaxation (γ) approaching ∼2, indicate a crossover from normal to relaxor ferroelectrics. Substitution of Hf4+ for Ti4+ in BaTiO3 introduces structural disorder, causing perturbations like local electric and strain fields. These perturbations reduce the long-range polar order resulting in relaxor behavior.
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