10 research outputs found
Magnetoresistance, specific heat and magnetocaloric effect of equiatomic rare-earth transition-metal magnesium compounds
We present a study of the magnetoresistance, the specific heat and the
magnetocaloric effect of equiatomic Mg intermetallics with , Eu, Gd, Yb and , Au and of GdAuIn. Depending on the
composition these compounds are paramagnetic (, Yb) or they
order either ferro- or antiferromagnetically with transition temperatures
ranging from about 13 to 81 K. All of them are metallic, but the resistivity
varies over 3 orders of magnitude. The magnetic order causes a strong decrease
of the resistivity and around the ordering temperature we find pronounced
magnetoresistance effects. The magnetic ordering also leads to well-defined
anomalies in the specific heat. An analysis of the entropy change leads to the
conclusions that generally the magnetic transition can be described by an
ordering of localized moments arising from the half-filled
shells of Eu or Gd. However, for GdAgMg we find clear evidence
for two phase transitions indicating that the magnetic ordering sets in
partially below about 125 K and is completed via an almost first-order
transition at 39 K. The magnetocaloric effect is weak for the antiferromagnets
and rather pronounced for the ferromagnets for low magnetic fields around the
zero-field Curie temperature.Comment: 12 pages, 7 figures include
Electronic structure of AuMg and AgMg ( = Eu, Gd, Yb)
We have investigated the electronic structure of the equiatomic EuAuMg,
GdAuMg, YbAuMg and GdAgMg intermetallics using x-ray photoelectron
spectroscopy. The spectra revealed that the Yb and Eu are divalent while the Gd
is trivalent. The spectral weight in the vicinity of the Fermi level is
dominated by the mix of Mg , Au/Ag and bands, and not by the
. We also found that the Au and Ag bands are extraordinarily
narrow, as if the noble metal atoms were impurities submerged in a low density
metal host. The experimental results were compared with band structure
calculations, and we found good agreement provided that the spin-orbit
interaction in the Au an Ag bands is included and correlation effects in an
open shell are accounted for using the local density approximation +
Hubbard scheme. Nevertheless, limitations of such a mean-field scheme to
explain excitation spectra are also evident.Comment: 4 pages, 3 figures, Brief Repor