X-ray magnetic circular dichroism ͑XMCD͒ measured at T = 6 K and 0 H = 5 T on the ␣-phase Fephthalocyanine ͑FePc͒ textured thin films shows that the Fe 2+ ions present an unusually large, highly unquenched m L = 0.53Ϯ 0.04 B orbital component, with planar anisotropy. The spin m S = 0.64Ϯ 0.05 B and the intra-atomic magnetic dipolar m T components were also obtained. The m L / m S = 0.83 ratio is the largest measured in 3d complexes and compounds. The origin of this unusually high orbital moment is the incompletely filled e g level lying close to the Fermi energy. This explains the unusually large and positive hyperfine field detected by Mössbauer spectroscopy in FePc. The FePc film strong planar anisotropy inferred from XMCD experiments is fully confirmed by magnetization measurements.
We study the magnetic properties of spherical Co clusters with diameters between 0.8 nm and 5.4 nm (25 to 7500 atoms) prepared by sequential sputtering of Co and Al2O3. The particle size distribution has been determined from the equilibrium susceptibility and magnetization data and it is compared to previous structural characterizations. The distribution of activation energies was independently obtained from a scaling plot of the ac susceptibility. Combining these two distributions we have accurately determined the effective anisotropy constant K ef f . We find that K ef f is enhanced with respect to the bulk value and that it is dominated by a strong anisotropy induced at the surface of the clusters. Interactions between the magnetic moments of adjacent layers are shown to increase the effective activation energy barrier for the reversal of the magnetic moments. Finally, this reversal is shown to proceed classically down to the lowest temperature investigated (1.8 K).
A universal curve for the change in the magnetic entropy has been recently proposed for materials with second-order phase transitions. In this work we have studied the universal behavior of the magnetocaloric effect in the family of cobalt Laves phases, RCo 2 , and mixed manganites, La 2/3 ͑Ca x Sr ͑1−x͒ ͒ 1/3 MnO 3 , which exhibit first-and second-order phase transitions. The rescaled magnetic entropy change curves for different applied fields collapse onto a single curve for materials with second-order phase transition as opposed to the first-order phase transition compounds, for which this collapse does not hold. This result suggests that the universal curve may be used as a further criterion to distinguish the order of the phase transition.
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