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Y掺杂BaZrO3 质子导体的常压和高压合成及表征
引用本文:薛燕峰,王野,许大鹏,李莉萍,郭星原,苏文辉. Y掺杂BaZrO3 质子导体的常压和高压合成及表征[J]. 吉林大学学报(理学版), 2007, 45(5): 827-830
作者姓名:薛燕峰  王野  许大鹏  李莉萍  郭星原  苏文辉
作者单位:吉林大学,物理学院,长春,130021;长春理工大学,理学院大学物理基础教学部,长春,130022;中国科学院,福建物质结构研究所,福州,350002;吉林大学,物理学院,长春,130021;哈尔滨工业大学,凝聚态科学与技术研究中心,哈尔滨,150001;中国科学院,国际材料物理中心,沈阳,110015
摘    要:利用固相反应法和高压高温法研究BaZr1-xYxO3(x=0,0.05,0.10,0.15,0.20)的合成. XRD和Raman谱结果表明, 在常压和1 300 ℃进行固相反应不能得到纯立方钙钛矿相BaZr1-xYxO3. 对上述样品进行高压(3.6 GPa)再处理, 低掺杂量样品(x=0,0.05)在500 ℃时得到较纯的立方钙钛矿相, 表明增加压力可促进固相反应; 在高掺杂量样品(x≥0.1)中出现少量BaCO3和m-ZrO2相, 表明增加压力不利于固相反应. 高压合成样品的晶格常数和晶胞体积均小于常压合成的样品. 保持压力不变, 当温度为1 000 ℃时, 各样品均出现明显的BaO杂相. 表明在500 ℃时, 高压处理可提高BaZr1-xYxO3
关 键 词:高压高温合成  立方钙钛矿  Raman光谱  结构
文章编号:1671-5489(2007)05-0827-04
收稿时间:2007-01-02
修稿时间:2007-01-02

Synthesis and Characterization of Y Doped BaZrO3 Protonic Conductors under Common and High Pressure
XUE Yan-feng,WANG Ye,XU Da-peng,LI Li-ping,GUO Xing-yuan,SU Wen-hui. Synthesis and Characterization of Y Doped BaZrO3 Protonic Conductors under Common and High Pressure[J]. Journal of Jilin University: Sci Ed, 2007, 45(5): 827-830
Authors:XUE Yan-feng  WANG Ye  XU Da-peng  LI Li-ping  GUO Xing-yuan  SU Wen-hui
Affiliation:1. College of Physics, Jilin University, Changchun 130021, China; 2. Department of Foundation Teaching of College Physics, School of Science, Changchun University of Science and Technology, Changchun 130022, China;3. Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China; 4. Center for the Condensed|matter Science and Technology, Harbin Institute of Techology, Harbin 150001, China;
Abstract:Samples BaZr1-xYxO3(x=0,0.05,0.10,0.15,0.20) were prepared by solid-state reaction method under high-pressure and high-temperature. XRD and Raman measurements show that the products obtained by solid state reaction method at 1 300 ℃ belonged to cubic perovskite structure, but part of high degree diffract peaks split slightly. The samples (x=0,0.05) were in pure cubic perovskite structure under high pressure (3.6 GPa) and temperature (500 ℃), which shows that press can accelerate the reaction. But some BaCO3 and m-ZrO2 appeared in other samples (x≥0.1), which shows that press baffled the reaction. Under 3.6 GPa at1 000 ℃, the peaks of BaO appeared clearly and increased with the content of Y3+. Therefore, to synthesis cubic perovskite structure BaZr1-xYxO3 under high-pressure and high-temperature, the temperature should be below 500 ℃.
Keywords:high-pressure and high-temperature synthesis   cubic perovskite   Raman spectrum   structure
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