Number of the records: 1  

Low-temperature phase transition and magnetic properties of K.sub.3./sub.YbSi.sub.2./sub.O.sub.7./sub.

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    SYSNO ASEP0545145
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleLow-temperature phase transition and magnetic properties of K3YbSi2O7
    Author(s) Dabić, P. (RS)
    Kahlenberg, V. (AT)
    Krüger, B. (AT)
    Rodić, M. (RS)
    Kovač, S. (RS)
    Blanuša, J. (RS)
    Jagličić, Z. (SI)
    Karanović, L. (RS)
    Petříček, Václav (FZU-D) RID, ORCID, SAI
    Kremenović, A. (RS)
    Number of authors10
    Source TitleActa Crystallographica Section B-Structural Science Crystal Engineering and Materials. - : Wiley
    Roč. 77, č. 4 (2021), s. 584-593
    Number of pages10 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsalkali rare-earth silicates ; phase transition ; magnetic properties ; crystal field splitting ; lanthanide silicates
    Subject RIVBM - Solid Matter Physics ; Magnetism
    OECD categoryCondensed matter physics (including formerly solid state physics, supercond.)
    R&D ProjectsGA18-10504S GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportFZU-D - RVO:68378271
    UT WOS000683554100014
    EID SCOPUS85112075570
    DOI10.1107/S2052520621006077
    AnnotationThe new ambient-temperature hexagonal (space group P63/mmc) polymorph of tripotassium ytterbium(III) disilicate (β-K3YbSi2O7) has been synthesized by the high-temperature flux method and subsequently structurally characterized. In the course of the temperature-dependent single-crystal diffraction experiments, a phase transformation of β-K3YbSi2O7 to a novel low-temperature orthorhombic phase (β'-K3YbSi2O7, space group Cmcm) has been observed at about 210 K. β-K3YbSi2O7 is isostructural with K3ErSi2O7, whereas β'-K3YbSi2O7 adopts a new type of structure.
    WorkplaceInstitute of Physics
    ContactKristina Potocká, potocka@fzu.cz, Tel.: 220 318 579
    Year of Publishing2022
    Electronic addresshttps://doi.org/10.1107/S2052520621006077
Number of the records: 1  

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