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作 者:林晓敏[1] 朱丽丽[1] 韩健[1] 刘晓梅[2]
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130021
出 处:《高等学校化学学报》2015年第1期61-66,共6页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:51272087);吉林省教育厅科学技术研究项目(批准号:2014181)资助~~
摘 要:采用柠檬酸溶胶-凝胶法制备了固体电解质Ce0.9Er0.1-xPrxO1.95+δ(x=0.02-0.08),利用X射线粉末衍射(XRD)、原子力显微镜(AFM)、拉曼光谱(Raman)、X射线光电子能谱(XPS)和交流阻抗谱研究了样品的微观结构和电性能.XRD结果表明,800℃煅烧的所有样品均形成了单相立方萤石结构;Raman光谱结果表明,Ce0.9Er0.05Pr0.05O1.95+δ具有氧缺位的立方萤石结构;XPS分析表明,Ce0.9Er0.05Pr0.05O1.95+δ存在氧缺位,Pr3+离子和Pr4+离子共存;AFM观测结果表明,1300℃下烧结的样品比1400℃下烧结的样品致密;交流阻抗谱结果表明,Pr掺杂量x=0.05时,Ce0.9Er0.05Pr0.05O1.95+δ的电导率最高(σ600℃=1.34×10-2S/cm,Ea=0.90 e V),比未掺杂Pr的Ce0.9Er0.1O1.95(σ600℃=8.81×10-3S/cm,Ea=0.92 e V)提高了52%,说明在Ce0.9Er0.1O1.95中适量掺杂Pr可提高材料的电导率,降低活化能.The microstructure and electrical conductivity of Ce0.9Er0.1-xPrxO1.95+δ(x=0—0. 08) solid electro- lytes synthesized by citric sol-gel method were characterized by means of X-ray diffraction ( XRD ) , atomic force microscopy( AFM) , Raman, X-ray photoelectron spectroscopy and impedance spectroscopy. XRD meas- urements show that all the samples calcined at 800 ℃ crystallize in single cubic fluorite structure. The Raman spectra indicate that the Ce0. 9 Er0. 05 Pr0. 05 O1. 95+δis cubic fluorite structure with oxygen vacancies. X-ray photoe- lectron spectroscopy analysis suggest that oxygen vacancies and the mixed valence Pr3+ and Pr4+ ions exist in Ce0. 9 Er0. 05 Pr0. 05 O1. 95+δ. AFM results show that sample Ce0. 9 Er0. 05 Pr0. 05 O1. 95+δsintered at 1300℃ is denser than that sintered at 1400 ℃. The maximum conductivity of Ce0. 9 Er0. 05 Pr0. 05 O1. 95+δ is found at x=0. 05 (σ600 ℃=1. 34 ×10-2 S/cm, Ea=0. 90 eV) . The conductivity of Ce0. 9 Er0. 05 Pr0. 05 O1. 95+δincreases by 52% in comparison with that of Ce0.9Er0.1O1.95 without Pr(σ600 ℃ =8. 81×10-3 S/cm, Ea=0. 92 eV), which suggests that co- doping with appropriate ratio of Pr can further improve the electrical performance of Ce0. 9 Er0. 1 O1. 95 .
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