20 research outputs found
Octupolar ordering of Gamma8 ions in magnetic field
We study f-electron lattice models which are capable of supporting octupolar,
as well dipolar and quadrupolar, order. Analyzing the properties of the Gamma8
ground state quartet, we find that (111)-type combinations of the Gamma5
octupoles Tbeta(111)=Tbeta(x)+Tbeta(y)+Tbeta(z) are the best candidates for
octupolar order parameters. Octupolar ordering induces Gamma5-type quadrupoles
as secondary order parameter. Octupolar order is to some extent assisted, but
in its basic nature unchanged, by allowing for the presence of quadrupolar
interactions. In the absence of an external magnetic field, equivalent results
hold antiferro-octupolar ordering on the fcc lattice. In this sense, the choice
of our model is motivated by the recent suggestion of octupolar ordering in
NpO2.
The bulk of our paper is devoted to a study of the effect of an external
magnetic field on ferro-octupolar ordering. We found that octupolar order
survives up to a critical magnetic field if the field is lying in specific
directions, while for general field directions, the underlying symmetry of the
model is destroyed and therefore the phase transition suppressed even in weak
fields. Field-induced multipoles and field-induced couplings between various
order parameters are discussed on the basis of a group theoretical analysis of
the Helmholtz potential. We also studied the effect of octupolar ordering on
the non-linear magnetic susceptibility which satisfies Ehrenfest-type relations
at continuous octupolar transitions.Comment: 29 pages, 10 figures LaTeX In its contents, the present version
agrees with the published one (see Journal Reference below). Essential
additions to the text in Sec. III, otherwise some change of wording, and
minor correction
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THE MELTING POINT AND THE DENSITY OF NEPTUNIUM METAL A MICRO MELTING POINT APPARATUS FOR METALS
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THERMODYNAMIC PROPERTIES OF THORIUM TETRAFLUORIDE FROM 5 TO 300 K, AND THE MAGNETIC ENTROPY OF URANIUM TETRAFLUORIDE
Thermophysics of thallium alkanoates IV. Heat capacity and thermodynamic functions of thallium(I) n-dodecanoate from 7 to 470 K,
The thermal behavior of thallium(I) n-dodecanoate was studied by adiabatic calorimetry from 6 to 350 K and by d.s.c. from 230 through 470 K. The agreement between the results (temperature and thermal functions of transitions and heat capacity) from both methods was within the experimental error over the common temperature range. Several phases were observed in the sample. Four of the five solid-to-solid transitions appeared in the common temperature range of both techniques. The two lowest-temperature transitions appear as a bifurcated pair (at 282.65 and 284.8 K) with (Cp,m/R) [approximate] 250 and 450, respectively. The third and fourth occur at 293.1 and 312.1 K with (Cpm/R) [approximate] 250 and 14000. Above 350 K three more transitions were measured by d.s.c.: solid-to-solid, solid-to-mesophase, and mesophase, and mesophase-to-isotropic-liquid transformations at 356.6, 400.1, and 471.5 K. The corresponding values of [Delta]trsSmo/R for the seven transitionswere 0.910, 1.111, 0.710, 2.075, 0.69, 1.64, and 0.50. Smoothed thermodynamic values are tabulated at selected temperatures through the "clearing" point.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/27004/3/0000571.pd