No Arabic abstract
We carried out x-ray absorption spectroscopy (XAS) and x-ray magnetic circular dichroism (XMCD) spectroscopy and investigated cation valence states and spin and orbital magnetic moments in the inverse-spinel ferrimagnet Ni$_{1-x}$Co$_{2+y}$O$_{4-z}$ (NCO) epitaxial films with the perpendicular magnetic anisotropy. We show that the oxygen pressure P$_{O2}$ during the film growth by pulsed laser deposition influences not only the cation stoichiometry (site-occupation) but also the cation valence state. Our XAS results show that the Ni in the O$_{h}$-site is in the intermediate valence state between +2 and +3, Ni$^{(2+delta)+}$ (0<$delta$<1), whose nominal valence state (the $delta$ value) varies depending on P$_{O2}$. On the other hand, the Co in the octahedral (O$_{h}$) and tetrahedral (T$_{d}$) sites respectively have the valence state close to +3 and +2. We also find that the XMCD signals originate mainly from the T$_{d}$-site Co$^{2+}$ (Co$_{Td}$) and O$_{h}$-site Ni$^{(2+delta)+}$ (Ni$_{Oh}$), indicating that these cation valence states are the key in determining the magnetic and transport properties of NCO films. Interestingly, the valence state of Ni$^{(2+delta)+}$ that gives rise to the XMCD signal remains unchanged independent of P$_{O2}$. The electronic structure of Ni$^{(2+delta)+}$ that is responsible for the magnetic moment and electrical conduction differs from those of Ni$^{2+}$ and Ni$^{3+}$. In addition, the orbital magnetic moment originating from Co$_{Td}$ is as large as 0.14 $mu_{B}/Co_{Td}$ and parallel to the magnetization while the Ni$_{Oh}$ orbital moment is as small as 0.07 $mu_{B}/Ni_{Oh}$ and is rather isotropic. The Co$_{Td}$ therefore plays the key role in the perpendicular magnetic anisotropy of the films. Our results demonstrate the significance of the site-dependent cations valence states for the magnetic and transport properties of NCO films.
A perpendicularly magnetized ferromagnetic layer is an important building block for recent/future highdensity spintronic memory applications. This paper reports on the fabrication of perpendicularly magnetized Ni / Pt superlattices and the characterization of their structures and magnetic properties. The optimization of film growth conditions allowed us to grow epitaxial Ni / Pt (001) superlattices on SrTiO$_{3}$ (001) single crystal substrates. We investigated their structural parameters and magnetic properties as a function of the Ni layer thickness, and obtained a high uniaxial magnetic anisotropy energy of 1.9 x 10$^{6}$ erg/cm$^{3}$ for a [Ni (4.0 nm) / Pt (1.0 nm)] superlattice. In order to elucidate the detailed mechanism on perpendicular magnetic anisotropy for the Ni / Pt (001) superlattices, the experimental results were compared with the first-principles calculations. It has been found that the strain effect is a prime source of the emergence of perpendicular magnetic anisotropy.
X-ray absorption spectroscopy was used to determine the valence state in La$_2$Co$_{1-x}$Mn$_{1+x}$O$_6$ ($xapprox 0.23$) thin films. We found that in spite of the non-stoichiometry, Co is in a divalent state while Mn ions show a mixed valence state. The relation of this finding with the magnetic properties of the films is discussed. X-ray magnetic circular dichroism measurements prove that magnetic anisotropy originates from Co spin-orbit coupling and it is strain-dependent: a strong increase of the angular contribution to the magnetic moment is found when in-plane (out-of-plane) and cell parameters get expanded (compressed). This behavior is reproduced by first order perturbation theory calculations.
By means of photoemission and x-ray absorption spectroscopy, we have studied the electronic structure of (Ni,Zn,Fe,Ti)$_{3}$O$_{4}$ thin films, which exhibits a cluster glass behavior with a spin-freezing temperature $T_f$ of $sim 230$ K and photo-induced magnetization (PIM) below $T_f$. The Ni and Zn ions were found to be in the divalent states. Most of the Fe and Ti ions in the thin films were trivalent (Fe$^{3+}$) and tetravalent (Ti$^{4+}$), respectively. While Ti doping did not affect the valence states of the Ni and Zn ions, a small amount of Fe$^{2+}$ ions increased with Ti concentration, consistent with the proposed charge-transfer mechanism of PIM.
Mn$_{3-x}$Ga (x = 0.1, 0.4, 0.7) thin films on MgO and SrTiO$_3$ substrates were investigated with magnetic anisotropy perpendicular to the film plane. An anomalous Hall-effect was observed for the tetragonal distorted lattice in the crystallographic D0$_{22}$ phase. The Hall resistivity $varrho_{xy}$ was measured in a temperature range from 20 to 330 K. The determined skew scattering and side jump coefficients are discussed with regard to the film composition and used substrate and compared to the crystallographic and magnetic properties.
The ferrimagnetic spinel oxide Zn(x)Fe(3-x)O(4) combines high Curie temperature and spin polarization with tunable electrical and magnetic properties, making it a promising functional material for spintronic devices. We have grown epitaxial thin films with 0<=x<=0.9 on MgO(001) substrates with excellent structural properties both in pure Ar atmosphere and an Ar/O2 mixture by laser molecular beam epitaxy. We find that the electrical conductivity and the saturation magnetization can be tuned over a wide range during growth. Our extensive characterization of the films provides a clear picture of the underlying physics of this spinel ferrimagnet with antiparallel Fe moments on the A and B sublattice: (i) Zn substitution removes both Fe3+ moments from the A sublattice and itinerant charge carriers from the B sublattice, (ii) growth in finite oxygen partial pressure generates Fe vacancies on the B sublattice also removing itinerant charge carriers, and (iii) application of both Zn substitution and excess oxygen results in a compensation effect as Zn substitution partially removes the Fe vacancies. A decrease (increase) of charge carrier density results in a weakening (strengthening) of double exchange and thereby a decrease (increase) of conductivity and the saturation magnetization. This scenario is confirmed by the observation that the saturation magnetization scales with the longitudinal conductivity. The combination of tailored films with semiconductor materials such as ZnO in multi-functional heterostructures seems to be particularly appealing.