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Effect of hydrogen doping in UTX compounds

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F09%3A00342557" target="_blank" >RIV/68378271:_____/09:00342557 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Effect of hydrogen doping in UTX compounds

  • Original language description

    Magnetic measurements on the hydrogenated systems U(Co,Fe)Sn and (U,Th)CoSn were performed as part of our investigation of UTX compounds (T-transitional metal and X-p-metal). Both series studied crystallize in the hexagonal structure of ZrNiAl type, space group P (6) over bar 2m symmetry. The crystal-structure type is not changed upon the hydrogenation. In all the cases it leads to a unit-cell expansion (ranging between 3.0% and 3.6%). The Curie temperature T-C increases in the hydrides. This incrementis reduced with increasing Fe concentration. In the compounds with the Th substitution, the Th concentration at which the ferromagnetism vanishes (similar to 60%) remains practically unchanged in the hydrides.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    BM - Solid-state physics and magnetism

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2009

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Applied Physics

  • ISSN

    0021-8979

  • e-ISSN

  • Volume of the periodical

    105

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    3

  • Pages from-to

  • UT code for WoS article

    000266633500658

  • EID of the result in the Scopus database