Structural and electrical properties of La2-xSrxMo2O9-δ
Sr-doped La2Mo2O9 were prepared by solid state reaction and characterized by XRD, impedance spectroscopy and Hebb- Wagner polarization method. XRD patterns of the samples indicated that the solubility limit of Sr2+ in La2-xSrxM02O9 -δ was in the range of 7 mol.% to 7.5 tool.%, i.e., the maximum stoi...
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Published in | Journal of rare earths Vol. 31; no. 4; pp. 428 - 434 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.04.2013
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Subjects | |
Online Access | Get full text |
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Summary: | Sr-doped La2Mo2O9 were prepared by solid state reaction and characterized by XRD, impedance spectroscopy and Hebb- Wagner polarization method. XRD patterns of the samples indicated that the solubility limit of Sr2+ in La2-xSrxM02O9 -δ was in the range of 7 mol.% to 7.5 tool.%, i.e., the maximum stoichiometric coefficient x in La2~SrxMo209_a was larger than 0.14 and less than 0.15. The cubic lattice parameter of La2 xSrxM02Og-δ (0〈x〈4) increased linearly with the content of dopant Sr2+ increasing and the relationship could be expressed as: a=0.7154+0.0045 lx (ram). The total conductivities of Sr-doped La2M0209 were measured by im- pedance spectroscopy method in argon and air atmosphere, respectively. The results indicated that substituting Sr2+ fbr La3+ could suppress the first order phase transform ofLa2M02O9 and stabilize the cubic structure to room temperature, and tile conductivities of Sr-doped La2M02O9 were more sensitive to the change of atmosphere than that of undoped La2M02O9. The conductivity variation of Sr-doped La2M02O9 with the dopant content exhibited similar trend in air and argon atmosphere, firstly decreased and then increased with the dopant content increasing, and a minimum value appeared at x=0.1. The electronic conductivities of Sr-doped La2M02O9 were measured using Hebb-Wagner polarization method in argon atmosphere. It could be found that Sr-doping caused the increase in electronic conductivity and decrease in oxide-ion transport numbers, but the conducting species were predominantly oxide ions. And the oxide-ion transport numbers of some St-doped La2Mo2O9 samples could also reach 0.99. |
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Bibliography: | YAN Baijun , LI Ming , ZHANG Jiayun (State Key Laboratory of Advanced Metallurgy, School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083, China) 11-2788/TF Sr-doped La2Mo2O9 were prepared by solid state reaction and characterized by XRD, impedance spectroscopy and Hebb- Wagner polarization method. XRD patterns of the samples indicated that the solubility limit of Sr2+ in La2-xSrxM02O9 -δ was in the range of 7 mol.% to 7.5 tool.%, i.e., the maximum stoichiometric coefficient x in La2~SrxMo209_a was larger than 0.14 and less than 0.15. The cubic lattice parameter of La2 xSrxM02Og-δ (0〈x〈4) increased linearly with the content of dopant Sr2+ increasing and the relationship could be expressed as: a=0.7154+0.0045 lx (ram). The total conductivities of Sr-doped La2M0209 were measured by im- pedance spectroscopy method in argon and air atmosphere, respectively. The results indicated that substituting Sr2+ fbr La3+ could suppress the first order phase transform ofLa2M02O9 and stabilize the cubic structure to room temperature, and tile conductivities of Sr-doped La2M02O9 were more sensitive to the change of atmosphere than that of undoped La2M02O9. The conductivity variation of Sr-doped La2M02O9 with the dopant content exhibited similar trend in air and argon atmosphere, firstly decreased and then increased with the dopant content increasing, and a minimum value appeared at x=0.1. The electronic conductivities of Sr-doped La2M02O9 were measured using Hebb-Wagner polarization method in argon atmosphere. It could be found that Sr-doping caused the increase in electronic conductivity and decrease in oxide-ion transport numbers, but the conducting species were predominantly oxide ions. And the oxide-ion transport numbers of some St-doped La2Mo2O9 samples could also reach 0.99. inorganic compounds; ionic conduction; X-ray diffraction; impedance spectroscopy; rare earths ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1002-0721 2509-4963 |
DOI: | 10.1016/S1002-0721(12)60299-3 |