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dc.contributor.authorVullum, Fride
dc.contributor.authorNitsche, Fabian
dc.contributor.authorSelbach, Sverre Magnus
dc.contributor.authorGrande, Tor
dc.date.accessioned2014-12-01T13:05:37Z
dc.date.accessioned2016-05-18T11:12:39Z
dc.date.available2014-12-01T13:05:37Z
dc.date.available2016-05-18T11:12:39Z
dc.date.issued2008
dc.identifier.citationJournal of Solid State Chemistry 2008, 181(10):2580-2585nb_NO
dc.identifier.issn0022-4596
dc.identifier.urihttp://hdl.handle.net/11250/2389570
dc.description.abstractThe solid solubility between LaNbO4 and LaTaO4 was investigated by X-ray diffraction, and a two-phase region was observed in the composition region LaNb1−xTaxO4 where 0.4⩽x⩽0.8. Single-phase LaNb1−xTaxO4 (0⩽x⩽0.4) with the monoclinic Fergusonite structure at ambient temperature, was observed to transform to a tetragonal Scheelite structure by in-situ high-temperature X-ray diffraction, and the phase transition temperature was shown to increase with increasing Ta-content. This ferroelastic to paraelastic second-order phase transition was described by Landau theory using spontaneous strain as an order parameter. The thermal expansion of LaNb1−xTaxO4 (0⩽x0.4) was shown to be significantly higher below the phase transition than above. Single-phase LaNb1−xTaxO4 (0.8⩽x⩽1) with another monoclinic crystal structure at ambient temperature was shown to transform to an orthorhombic crystal structure by X-ray diffraction and differential scanning calorimetry. The phase transition temperature was observed to decrease with decreasing Ta-content. Finally, orthorhombic LaTaO4 could also be transformed to monoclinic LaTaO4 at ambient temperature by applying a uniaxial pressure of 150–170 MPa, reflecting the lower molar volume of monoclinic LaTaO4.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.titleSolid solubility and phase transitions in the system LaNb1-xTaxO4nb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.date.updated2014-12-01T13:05:37Z
dc.source.volume181nb_NO
dc.source.journalJournal of Solid State Chemistrynb_NO
dc.source.issue10nb_NO
dc.identifier.doi10.1016/j.jssc.2008.06.032
dc.identifier.cristin361699
dc.description.localcode(c) 2008 Elsevier Inc. All rights reserved. This is the authors' accepted and refereed maniscript to the article.nb_NO


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