Magnetic phase transition in the Fe60Al40 transition metal aluminide from the ferromagnetic disordered A2-phase to the paramagnetic ordered B2-phase as a function of annealing up to 1000 °C has been investigated by means of magneto-optical and spectroscopy techniques, i.e., Kerr effect, positron annihilation, and Mössbauer spectroscopy. The positron annihilation spectroscopy has been performed in-situ sequentially after each annealing step at the Apparatus for In-situ Defect Analysis that is a unique tool combining positron annihilation spectroscopy with temperature treatment, material evaporation, ion irradiation, and sheet resistance measurement techniques. The overall goal was to investigate the importance of the open volume defects onto the magnetic phase transition. No evidence of variation in the vacancy concentration in matching the magnetic phase transition temperature range (400–600 °C) has been found, whereas higher temperatures showed an increase in the vacancy concentration.
Hard x-ray absorption and magnetic circular dichroism spectroscopy have been applied to study the consequential changes of the local environment around Fe atoms and their orbital polarizations in 40 nm thick Fe 60 Al 40 thin films along the order-disorder (B2 → A2) phase transition initiated by 20-keV Ne + ion irradiation with fluences of (0.75-6) ×10 14 ions cm −2. The analysis of the extended x-ray absorption fine structure spectra measured at the Fe K edge at room temperature revealed an increased number of Fe-Fe nearest neighbors from 3.47(7) to 5.0(1) and ∼1% of volume expansion through the transition. The visualization of the Fe and Al nearest-neighbor rearrangement in the first coordination shell of Fe absorbers via the transition was carried out by wavelet transformations. The obtained changes in Fe coordination are evidently reflected in the x-ray magnetic circular dichroism spectra which show an increased orbital magnetic moment of Fe atoms and a pronounced magnetic multielectronic excitations peak at ∼60 eV above the edge. The amplitudes of both peaks demonstrated similar dependencies on the irradiation fluence. The results of self-consistent density functional calculations on relaxed Fe 60 Al 40 model structures for the ordered (B2) and the disordered (A2) phases are consistent with the experimental findings and point to the formation of Fe-rich regions in the films studied.
The influence of Co-doping in off-stoichiometric Ni–Mn–Ga and Ni–Mn–Ga–Co thin films on the magnetic coupling of the atoms is investigated with x-ray magnetic circular dichroism in both the martensitic as well as austenitic phase, respectively. Additionally, first principles calculations were performed to compare the experimentally obtained absorption spectra with theoretical predictions. Calculated exchange constants and density of states for the different atomic sites underline the large influence of chemical and magnetic order on the magnetocaloric properties of the material.
Materials with high volume magnetization are perpetually needed for the generation of sufficiently large magnetic fields by writer pole of magnetic hard disks, especially for achieving increased areal density in storage media. In search of suitable materials combinations for this purpose, we have employed density functional theory to predict the magnetic coupling between iron and gadolinium layers separated by one to several monolayers of 3d transition metals (Sc-Zn). We demonstrate that it is possible to find ferromagnetic coupling for many of them and in particular for the early transition metals giving rise to high moment. Cr and Mn are the only elements able to produce a significant ferromagnetic coupling for thicker spacer layers. We also present experimental results on two trilayer systems Fe/Sc/Gd and Fe/Mn/Gd. From the experiments, we confirm a ferromagnetic coupling between Fe and Gd across a 3 monolayers Sc spacer or a Mn spacer thicker than 1 monolayer. In addition, we observe a peculiar dependence of Fe/Gd magnetic coupling on the Mn spacer thickness.
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