High-field magnetization study of aTm2Co17single crystal (original) (raw)
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Physical Review B, 2010
Magnetocaloric effect (MCE) in TbCo2-xFex has been studied by dc magnetization measurements.On substituting Fe in TbCo2, not only the magnetic transition temperature is tuned to room temperature, but also the operating temperature range for MCE is increased from 50 K for TbCo2 to 95 K for TbCo1.9Fe0.1. The maximum magnetic entropy change (-{\Delta}SM) for TbCo1.9Fe0.1 is found to be 3.7 J kg-1 K-1 for a 5 T field change, making it a promising candidate for magnetic refrigeration near room temperature. The temperature dependent neutron diffraction study shows a structural phase transition (from cubic to rhombohedral phase with lowering of temperature) which is associated with the magnetic phase transition and these transitions broaden on Fe substitution. To investigate the nature of the paramagnetic to ferrimagnetic phase transition, we performed a critical exponent study. From the derived values of critical exponents, we conclude that TbCo2 belongs to the 3D Heisenberg class with short-range interaction, while on Fe substitution it tends towards mean-field with long-range interaction. The derived values of critical exponents represent the phenomenological universal curve for the field dependence of {\Delta}SM, indicating that TbCo2 and TbCo1.9Fe0.1 belong to two different universality classes.
2008
Single crystals of R$_2$CoGa$_8$ series of compounds were grown, for the first time, by high temperature solution growth (flux) method. These compounds crystallize in a tetragonal crystal structure with the space group P4/mmmP4/mmmP4/mmm. It has been found that R$_2$CoGa$_8$ phase forms only with the heavier rare earths, starting from Gd with a relatively large c/ac/ac/a ratio of approx\approxapprox 2.6. The resultant anisotropic magnetic properties of the compounds were investigated along the two principal crystallographic directions of the crystal viz., along [100] and [001]. The nonmagnetic compounds Y$_2$CoGa$_8$ and Lu$_2$CoGa$_8$ show diamagnetic behavior down to the lowest temperature (1.8 K) pointing out the non-magnetic nature of Co in these compounds and a relatively low density of electronic states at the Fermi level. Compounds with the magnetic rare earths order antiferromagnetically at temperatures lower than 30 K. The easy axis of magnetization for R$_2$CoGa$_8$ (R = Tb, Dy and Ho) is found to be along the [001] direction and it changes to [100] direction for Er$_2$CoGa$_8$ and Tm$_2$CoGa$_8$. The magnetization behavior is analyzed on the basis of crystalline electric field (CEF) model. The estimated crystal field parameters explains the magnetocrystalline anisotropy in this series of compounds.