• DocumentCode
    1152224
  • Title

    The role of f electrons in rare-earth and uranium intermetallics

  • Author

    Radwanski, R.J.

  • Author_Institution
    Centre for Solid State Phys., Krakow
  • Volume
    30
  • Issue
    2
  • fYear
    1994
  • fDate
    3/1/1994 12:00:00 AM
  • Firstpage
    1136
  • Lastpage
    1138
  • Abstract
    Electronic structures of Nd3+ and U3+ ions in NdNi5 and UPd2Al3 intermetallic compounds have been discussed. The strong correlation between the charge distribution at the vicinity of the f-shell electrons and the magnetic state of the f electron subsystem of these Kramers ions has been underlined. The formation of the local magnetic moment, of the ordered magnetic state, of the singlet ground state and of the energy gap in the ordered state is evaluated in conjugation with the temperature dependence of the energy level scheme. It is argued that as a function of the charge distribution and the spin-dependent interactions many exotic properties are expected resembling those found in heavy-fermion compounds
  • Keywords
    aluminium alloys; antiferromagnetic properties of substances; band model of magnetism; charge-ordered states; crystal field interactions; energy gap; ferromagnetic properties of substances; localised electron states; magnetic moments; neodymium alloys; nickel alloys; palladium alloys; uranium alloys; Kramers ions; Nd3+ ions; NdNi5; U3+ ions; UPd2Al3; antiferromagnet; charge distribution; electronic structure; energy gap; energy level scheme temperature dependence; f electron localization; f electron subsystem; f-shell electrons; ferromagnet; hexagonal CEF interactions; local magnetic moment; magnetic state; ordered state; singlet ground state; spin-dependent interactions; Electrons; Energy states; Intermetallic; Magnetic moments; Magnetic properties; Neodymium; Physics; Solid state circuits; Stationary state; Temperature dependence;
  • fLanguage
    English
  • Journal_Title
    Magnetics, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0018-9464
  • Type

    jour

  • DOI
    10.1109/20.312212
  • Filename
    312212