The magnetic proximity effect in top and bottom Pt layers induced by Co in Ta/Pt/Co/Pt multilayers has been studied by interface-sensitive, element-specific x-ray resonant magnetic reflectivity. The asymmetry ratio for circularly polarized x-rays of left and right helicity has been measured at the Pt L 3 absorption edge (11 567 eV) with an in-plane magnetic field (±158 mT) to verify its magnetic origin. The proximity-induced magnetic moment in the bottom Pt layer decreases with the thickness of the Ta buffer layer. Grazing incidence x-ray diffraction has been carried out to show that the Ta buffer layer induces the growth of Pt(011) rather than Pt(111), which in turn reduces the induced moment. A detailed density functional theory study shows that an adjacent Co layer induces more magnetic moments in Pt(111) than in Pt(011). The manipulation of the magnetism in Pt by the insertion of a Ta buffer layer provides a way to control the magnetic proximity effect, which is of huge importance in spin-transport experiments across similar kinds of interfaces.
The metastable iron oxide ϵ-FeO is rare but known for its magnetoelectric properties. While the more common alpha phase has been recognized for a long time as a suitable material for photoelectrochemical cells, its use is limited because of the electron-hole recombination problem when exposed to light. The indirect bandgap of the epsilon phase with its spontaneous polarization may offer a better potential for the application in photoelectrochemistry. Here, we report a detailed study of the electronic and structural features of the epsilon phase of iron oxide, its stability in thin films, and possible water dissociation reactions. Our studies are performed using density functional theory with a Hubbard-U correction. We observe that the stable ϵ-FeO surfaces favor the dissociation of water. The average difference in the energies of the states when water is adsorbed and when it is dissociated is roughly found to be -0.40 eV. Our results compare with the available experimental results where the epsilon phase is reported to be more efficient for the release of hydrogen from renewable oxygenates when exposed to sunlight.
The epsilon Fe2O3 phase of iron oxide has been studied to understand the spin structure and the magnetocrystalline anisotropy in the bulk and in thin films of ε-Fe2O3 and Co-doped ε-Fe2O3. The preferential magnetization direction in the nanoparticles of ε-Fe2O3 is along the a-axis [M. Gich et al., Chem. Mater. 18, 3889 (2006)]. Compared to the bulk band gap of 1.9 eV, the thin-film band gap is reduced to 1.3 eV in the Co-free films and to 0.7 eV in the film with partial Co substitution. The easy magnetization direction of the bulk and Co-free ε-Fe2O3 is along the c-axis, but it switches to the a-axis on Co substitution. All three systems exhibit in-plane anisotropies associated with the orthorhombic crystal structure of the oxide.
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