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作 者:林晓敏[1,2] 闫石[1] 朱丽丽[1] 李莉萍[2] 苏文辉[2,3,4]
机构地区:[1]北华大学物理学院,吉林132013 [2]吉林大学物理学院,长春130023 [3]哈尔滨工业大学凝聚态科学与技术中心,哈尔滨150001 [4]中国科学院国际材料物理中心,沈阳110015
出 处:《化学学报》2009年第12期1389-1394,共6页Acta Chimica Sinica
基 金:国家自然科学基金(No.10374022);吉林省教育厅科研基金资助项目
摘 要:利用溶胶-凝胶法合成了固溶体Ce1-xPrxO2-δ(x=0.05~0.30).X射线衍射(XRD)分析表明,在x≤0.30的范围内形成了单相萤石结构固溶体Ce1-xPrxO2-δ;X射线光电子能谱(XPS)结果表明,样品中氧缺位浓度随掺杂量增大而增大,铈离子主要为Ce4+离子,镨离子以混合价态Pr3+和Pr4+存在;拉曼光谱(Raman)观察到两个峰,458cm-1峰为特征F2g振动谱带,较宽的570cm-1峰与样品中氧离子缺位有关;交流阻抗谱测试表明,固溶体Ce1-xPrxO2-δ的电导率随掺杂量增加而增大,x=0.2时,电导率达到最大,活化能较低,σ600℃=3.28×10-2S/cm,σ700℃=6.06×10-2S/cm,Ea=0.54eV(250~650℃),Ea=0.49eV(650~800℃).Solid solutions Ce1-xPrxO2-δ(x=0.05-0.30) were synthesized by a sol-gel method. The X-ray diffraction analysis showed that solid solutions Ce1-xPrxO2-δ were crystallized in a single fluorite structure in the range of x≤0.30. XPS analysis suggested that the oxygen vacancy concentration increased with increasing the dopant content x, and the mixed valence Pr^3+/Pr^4+ ions and major Ce^4+ ions existed in the solid solutions. The Raman spectra exhibited two peaks. The 458 cm^-1 peak was attributed to Raman active F2g mode that was assigned to a symmetric breathing mode of oxygen atoms around cerium ions. The broad 570 cm^-1 peak was attributed to oxygen vacancies. Impedance spectra showed conductivity values of Ce1-xPrxO2-δ (x=0.05-0.30) which were increased with the dopant content x and reached the maximum at x=0.20, and the relatively low activation energy data, σ600 ℃=3.28× 10^-2 S·cm^-1, σ700℃ =6.06× 10^-2 S·cm^-1, Ea=0.54 eV (250-650 ℃), and Ea=0.49 eV (650-800 ℃).
关 键 词:溶胶-凝胶法 Ce1-xPrxO2-δ X射线光电子能谱 拉曼光谱 电导率
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