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Synthesis of Er2Ir2O7 pyrochlore iridate by solid-state-reaction and CsCl flux method

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F21%3A10419183" target="_blank" >RIV/00216208:11320/21:10419183 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=ZHevvpn_WZ" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=ZHevvpn_WZ</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.matchemphys.2020.123868" target="_blank" >10.1016/j.matchemphys.2020.123868</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis of Er2Ir2O7 pyrochlore iridate by solid-state-reaction and CsCl flux method

  • Original language description

    The solid-state reaction, hydrothermal synthesis and CsCl flux methods were employed preparing Er2Ir2O7 pyrochlore iridate. A mixture of initial Er2O3 and IrO2 oxides was thermally treated, following the temperature evolution of individual phases by means of x-ray diffraction and energy dispersive x-ray spectroscopy. Reactions by hydrothermal synthesis, using various commonly used mineralising agents, showed negligible increase in the pyrochlore phase fraction. The solid-state reaction method allowed a preparation of Er2Ir2O7, however the reacted mixture contained a high percentage (60%) of initial unreacted Er2O3. Adding an excess of IrO2 to the initial content improved the composition of the reacted sample (50% of Er2Ir2O7 for initial Er2O3:IrO2 ratio 0.9:2.1). Nevertheless, a secondary Er-Ir-O phase with slightly larger crystallographic unit cell was also created as an additional product. An optimised flux synthesis, consisting of repeated heating and regrinding cycles at 800 degrees C and using CsCl as a flux, provided the best conditions for single phase pyrochlore preparation. A sample with 94% Er2Ir2O7 was further improved by repeated reaction with additional excess IrO2 oxide. A successful preparation route for (at least) the heavy-rare earth pyrochlore iridates is established.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Materials Chemistry and Physics

  • ISSN

    0254-0584

  • e-ISSN

  • Volume of the periodical

    258

  • Issue of the periodical within the volume

    leden

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    7

  • Pages from-to

    123868

  • UT code for WoS article

    000595353900004

  • EID of the result in the Scopus database

    2-s2.0-85092405278