Pb(Zr,Sn,Ti)O_3反铁电陶瓷场诱相变性能的改进

为了获得场诱反铁电 (AFEt)—铁电 (FER)相变临界电场Ef 小、电滞ΔE小、场致应变x适当的反铁电陶瓷 ,对Pb(Zr ,Sn ,Ti)O3 采用Ba2 置换Pb2 ,同时在四方反铁电相AFEt—三方铁电FER 相界附近调节Ti/Sn比 ,来控制FER AFEt,AFEt 顺电相 (FEC)之间的相变温度TFA,TC,最终实现了对场诱相变参量 (Ef,ΔE)和反铁电工作温区 (ΔT =TC-TFA)的优化与调节 .获得了ΔE =0 85kV/mm ,Ef=1 6kV/mm ,x =0 1% - 0 2 %可用作开关致动器的新型反铁电陶瓷 .借助于X射线衍射、介电温谱、去极化电流谱、电滞回线等手段得到了这一系统AFEt/FER相界附近的温度 Ti含量相图 .     

Pb(Zr,Sn,Ti)O3反铁电陶瓷的低温相变扩散与极化弛豫

用弱场介电温谱、热释电流谱、强场电滞回线和变温X射线衍射谱研究了微量La掺杂Pb(Zr,Sn,Ti)O₃(PZST)反铁电(AFEt)陶瓷在-100—180℃温区内的结构与电学特性.弱场介电温谱显示,AFEt陶瓷在低温段(-100—50℃)呈现介电频率弥散(0.1—100kHz)和扩散型相变的特征,而变温X射线衍射谱却表明材料在这一温区内保持四方相结构;低温下经强场作用后,AFEt被诱导为亚稳三方铁电态,介电频率弥散消失.基于多元复杂化合物的组分起伏理论,讨论了PZST AFEt陶瓷 关键词： Pb(Zr Sn 3反铁电陶瓷')" href="#">Ti)O₃反铁电陶瓷 反铁电弛豫 相变 变温X射线衍射     

La调节Pb(Zr,Sn,Ti)O_3反铁电陶瓷的相变与电学性质

利用X射线衍射、弱场介电温度谱、强场极化强度研究了不同La含量(Pb1-xLa2x3)(Zr06Sn03Ti01)O3(000≤x≤012)(PLZSnT)陶瓷的相变与电学特性.实验发现,随La含量增大,室温下材料由铁电三方相(x=000)转变为反铁电四方相(003≤x≤009)和立方相(x=012).介电测试表明,La含量增大,反铁电→顺电相变温度降低,峰值介电常量减小.在x=006的PLZSnT三元相图中,反铁电四方相区扩大到Ti含量约为18at%,该系统反铁电陶瓷具有“窄、斜”型双电滞回线和“三电滞回线”;在高Zr、高Sn区,反铁电→顺电相变呈现弥散相变和介电频率色散特征,即反铁电极化弛豫现象.从ABO3钙钛矿结构的容忍因子(t)和反铁电相的结构特征出发,讨论了La对Pb(Zr,Sn,Ti)O3相变与电学性质的影响机理 关键词： 场诱相变 弛豫型反铁电体 介电性能 La调节Pb(Zr Sn Ti)O3     

等静压和温度诱导的PbLa(Zr,Sn,Ti)O3反铁电陶瓷相变和介电性能研究

研究了等静压和温度诱导掺镧La的Pb(Zr,Sn,Ti)O₃(PLZST)陶瓷材料的铁电反铁电相变、介电压力谱和介电温度谱,研究了温度对压致相变和介电压力谱的影响,结果发现温度使铁电反铁电相变压力降低,介电压力谱具有明显的扩散相变和频率弥散的特点;研究了等静压对介电温度谱的影响,结果表明等静压使铁电反铁电相变温度降低,反铁电顺电相变温度升高.这些现象有利于丰富和拓宽人们对温度和压力诱导的多组元弛豫型铁电体和弛豫型反铁电体扩散相变和弛豫行为的认识和理解. 关键词： 等静压和压致相变 铁电反铁电相变 介电压力谱 介电温度谱     

脉冲电容器用细电滞回线铁电陶瓷材料的研究

采用低锆区的Pb(Zr_0.42Sn_0.40Ti_0.18)O₃(PZST42/40/18)铁电陶瓷为基, 通过少量La和Ba取代Pb同时Nb取代(Zr, Sn, Ti)复合取代的方法得到掺杂PZST42/40/18细电滞回线铁电陶瓷, 其最大极化强度P_max≈20.66μC/cm², 剩余极化强度P_r≈0.55μC/cm^{关键词： 细电滞回线 铁电陶瓷 PZST 脉冲电容器}     

PLZST反铁电陶瓷电场诱导相变与相稳定性的研究

在三方铁电(FE)-四方反铁(AFE)的准同型相界附近制备了一系列组份为(Pb_0.97La_0.02)(Zr_1-x-ySn_yTi_x)O₃(x=0.09或0.1;0.16≤y≤0.38)的反铁电陶瓷.研究了Sn含量y对电场诱导AFE→FE相变电场E_c、反铁电双电滞回线损耗ΔE、以及温度诱导FE→AFE相变温度T_FE，AFE→顺电(PE)相变温度T_c的影响.沿AFE-FE相界Ti含量一定的条件下，E_c随着Sn含量y的增加而增大，ΔE减小，T_FE与T_c均降低.场诱相变的回线参量E_c，ΔE与相变温度T_FE和T_c相关联.在直流偏压下用原位X-射线衍射表征了相变时晶格结构的变化，结果表明，当电场达到AFE→FE相变临界场时，伴随相变的发生，晶格结构由四方相转变为三方相，晶胞体积增大. 关键词：     

(Pb0.97La0.02)(Zr0.65Sn0.35-xTi x)O3反铁电陶瓷的热膨胀性质

在-100—200℃温度范围内，测量了(Pb_0.97La_0.02)(Zr_{0.65< /sub>Sn0.35-xTix)O3(PZST，0.1≤x≤0.14)反铁电陶 瓷的热膨胀性质.实验结果表明，组分在0.1 ≤x≤0.12的试样室温下为反铁电(AFEt)四方相，热膨胀系数(α)在低温段发生 “弯曲” ，而变温x射线衍射谱(XRD)显示材料保持四方相结构；当Ti含量在0.125≤x≤0.14时，室温 下是铁电三方相(FER)，温度升高时FER→AFEt相变体 积收缩，AFEt→立方顺电(PE c)相变体积增大；变温XRD谱证明了材料相结构随温度的转变过程.用多元复杂 化合物存在 纳米线度组分非均匀的观点解释了热膨胀性质随Ti含量演化的物理机理，并得到了该系统的 温度-Ti(x)含量相图. 关键词： 热膨胀性质 铁电/反铁电相界 反铁电陶瓷 PZST}     

La诱导(Pb(1-3x/2)Lax)(Zr0.5Sn0.3Ti0.2)O3反铁电介电弛豫研究

采用标准电子陶瓷工艺制备了(Pb_(1-3x/2)La_x)(Zr_0.5Sn_0.3Ti_0.2)O₃(PLZST,0.00≤x≤0.18)反铁电陶瓷,利用X射线衍射、不同频率下弱场介电温谱、强场下的极化强度-电场(P-E)测试研究了材料相结构和电学性能.实验结果发现,随La含量x增大,室温下材料由铁电三方相(关键词： 反铁电陶瓷 介电频率色散 相变弥散 介电弛豫     

基于相变换能机理的反铁电陶瓷水声换能器初探

阐述了改性锆锡钛酸铅Pb(Zr,Sn,Ti)O3(PZST)反铁电陶瓷作为一种基于相变换能机理的大应变电致伸缩材料的性能特征以及作为水声换能器新型有源材料的优势。采用掺镧改性锆锡钛酸铅PbLa(Zr,Sn,Ti)O3(PLZST)反铁电陶瓷材料首次设计制作了纵振式反铁电陶瓷水声换能器。试验结果表明,PLZST反铁电陶瓷用于水声换能器研制在技术上是可行的,与压电陶瓷换能器比较,目前反铁电换能器样品的等效发射电压灵敏度提高3~5dB以上。根据实验情况,认为在发射电压灵敏度和声源级方面具有进一步提升的潜力。     

PbLa(Zr,Sn,Ti)O_3反铁电陶瓷的静电场能存储特性北大核心CSCD

为了研究微量掺镧的反铁电陶瓷锆锡钛酸铅(PbLa(Zr,Sn,Ti)O_3,PLZST)的静态存储电场能量的特性,采用传统的氧化物固态反应的陶瓷制备工艺,制备了4个锆锡比不同的PLZST陶瓷样品,样品组分均位于PLZST相图中铁电-反铁电相界附近。通过等静压压致放电的实验方法研究了PLZST陶瓷放电特性。结果表明,经过充分极化的PLZST处于亚稳态的铁电相,在压力作用下,PLZST发生铁电反铁电相变,把在直流电场下极化时储存于PLZST陶瓷的静电场能量瞬间释放出来,从而得到极高功率的电脉冲。最终,样品完全退极化,最大放电电流密度达到5.0nA/cm^2,样品的静电场储能密度最高可达9.45J/cm^3,因此PLZST陶瓷是爆电换能电源的理想材料。     

Dynamics of birefringence properties in 17/30/70 PLZT ceramics

Birefringent properties of PLZT ceramics (Pb₈₃La₁₇)(Zr₃₀Ti₇₀)O₃ were investigated by measuring the transverse electrooptic effect in a 0.2 mm-thick wafer at various speeds of external voltage changes. At least two types of internal polarized microregions of different physical nature in charge of the electrooptical properties are observed.     

Dielectric properties and phase transitions of (Pb0.87La0.02Ba0.1)(Zr0.6Sn0.4−xTix)O3 ceramics with compositions near AFE/RFE phase boundary

The electrical properties and phase transition behavior of (Pb_0.87La_0.02Ba_0.1)(Zr_0.6Sn_0.4−xTi_x)O₃ solid solutions (PLBZST, 0.04≤x0.2) were investigated by the X-ray diffraction, permittivity, pyroelectric current, and P-E electric hysterisis loops. As the composition x increased from 0.04 to 0.2, the antiferroelectric ceramics (x≤0.07, AFE) with tetragonal phase changed to the ferroelectric relaxors (RFE, 0.09≤x). AFE ceramics showed a peculiar diffuse phase transition and dielectric relaxation at the low temperature (down to −100 °C) due to a frustration between AFE and FE state. With an increase in composition x, electrically field-induced AFE-FE switching field (E_AFE-FE) and AFE-paraelectric (PE) phase transition temperature (T_c) are depressed in the temperature (T)-Ti composition (x) phase diagram, a FE-AFE-PE triple phase point (T_tr) with the lowest transition temperature occurred at x=0.09. The pyroelectric currents under an application of various external electric field (E) were measured to identify a T-E phase diagram of the PLBZST compound.     

Dielectric behaviour of La substituted BPZT ceramics

Here, we report dielectric behaviour of lanthanum substituted Ba_0.80Pb_0.20Ti_0.90Zr_0.10O₃ (BPZT) ceramics. The material series with compositional formula Ba_0.80−xLa_xPb_0.20Ti_0.90Zr_0.10O₃ (BLPZT) with x varying from 0 to 0.01 in the steps of 0.0025 was chosen for investigations. The material was synthesized by solid state reaction method. Reacted powder compacted in form of circular discs were sintered at 1325 °C. All the samples were subjected to X-ray diffraction (XRD) analysis and found to be single phase. Dielectric behaviour was studied as a function of frequency and temperature and Curie temperature (T_c) was determined. T_c was found to decrease with increasing x. The details are discussed and presented in this paper.     

High-frequency ultrasonic transducer based on lead-free BSZT piezoceramics

This paper describes the fabrication and evaluation of a high-frequency (40 MHz) transducer based on lead-free piezoceramics for ultrasonic imaging. The transducer with an aperture size of 0.9 mm has been fabricated using barium strontium zirconate titanate ((Ba_0.95Sr_0.05)(Zr_0.05Ti_0.95)O₃, abbreviated as BSZT) ceramics. The lead-free BSZT has a piezoelectric d₃₃ coefficient of 300 pC/N and an electromechanical coupling factor k_t of 0.45. High-frequency ultrasound transducers were fabricated and a bandwidth of 76.4% has been achieved with an insertion loss of −26 dB. Applications in high resolution biological and medical imaging could be possible with this lead-free material.     

Release of charges under external fields of PbLa（Zr,Sn,Ti）O3 ceramic

This paper investigates the pyroelectric of poled antiferroelectric (AFE) ceramic Pb 0.97 La 0.02 (Zr 0.69 Sn 0.196 Ti 0.114)O 3 and its remnant polarization dependence of hydrostatic pressure.The results show that the bound charges of poled sample can be released in short time by temperature field or pressure field.The released charge abruptly forms a large pulse current.The phenomena of released charge under external fields result in the ferroelectric-AFE phase transition induced by temperature or hydrostatic pressure.     

(Bi,La)4Ti3O12-Sr(Bi,La)4Ti4O15共生结构铁电材料性能研究

采用固相烧结工艺，制备了不同La掺杂量(x=0.00，0.25，0.50，0.75，1.00，1.25和1.50) 的(Bi, La)₄Ti₃O₁₂-Sr(Bi, La)₄Ti4O₁₅ (SrBi_8-xLa_xT i₇O₂₇)共生结构铁电陶瓷样品.用x射线衍射对其进行微结构分析 ，并测量铁 关键词： 4Ti₃O₁₂-SrBi₄Ti₄O₁₅')" href="#">Bi₄Ti₃O₁₂-SrBi₄Ti_{4O15 La掺杂 铁电性能 居里温度 弛豫铁电}     

Electromechanical-induced antiferroelectricben ferroelectric phase transition in PbLa(Zr,Sn,Ti)O3 ceramic

Antiferroelectric—ferroelectric (AFE—FE) phase transition in ceramic Pb_0.97La_0.02(Zr_0.75Sn_0.136Ti_0.114)O₃ (PLZST) was studied by dielectric spectroscopy as functions of frequency (10²—10⁵ Hz) and pressure (0—500 MPa) under a DC electric field. The hydrostatic pressure-dependent remnant polarization and dielectric constant were measured. The results show that remnant polarization of the metastable rhombohedral ferroelectric PLZST poled ceramic decreases sharply and depoles completely at phase transition under hydrostatic pressure. The dielectric constant undergoes an abrupt jump twice during a load and unload cycle under an electric field. The two abrupt jumps correspond to two phase transitions, FE—AFE and AFE—FE.