Rémi Arras

Interface Magnetoelectric Coupling in Co/Pb(Zr,Ti)O3

Magnetoelectric coupling at multiferroic interfaces is a promising route toward the nonvolatile electric-field control of magnetization. Here, we use optical measurements to study the static and dynamic variations of the interface magnetization induced by an electric field in Co/PbZr0.2Ti0.8O3 (Co/PZT) bilayers at room temperature. The measurements allow us to identify different coupling mechanisms. We further investigate the local electronic and magnetic structure of the interface by means of transmission electron microscopy, soft X-ray magnetic circular dichroism, and density functional theory to corroborate the coupling mechanism. The measurements demonstrate a mixed linear and quadratic optical response to the electric field, which results from a magneto-electro-optical effect. We propose a decomposition method of the optical signal to discriminate between different components involved in the electric field-induced polarization rotation of the reflected light. This allows us to extract a signal that we can ascribe to interface magnetoelectric coupling. The associated surface magnetization exhibits a clear hysteretic variation of odd symmetry with respect to the electric field and nonzero remanence. The interface coupling is remarkably stable over a wide frequency range (1-50 kHz), and the application of a bias magnetic field is not necessary for the coupling to occur. These results show the potential of exploiting interface coupling with the prospect of optimizing the performance of magnetoelectric memory devices in terms of stability, as well as fast and dissipationless operation.

Evolution of magnetic properties and damping coefficient of Co2MnSi Heusler alloy with Mn/Si and Co/Mn atomic disorder

Ferromagnetic resonance has been used to investigate the effect of Mn/Si and Co/Mn atomic disorder on the magnetic properties and dynamic relaxation of Co 2 MnSi Heusler alloy. He + ion irradiation at 150 KeV is used to induce Co/Mn and Mn/Si swap in the initial structure of the material. While Mn/Si disorder is found to show similar magnetic behavior as compared to the L2 1 order, we observe a strong impact of Co/Mn swap on the static and dynamic properties of the alloy. These results are explained with regard to electronic band structure and damping coefficient first-principles calculations showing the modification of the minority-spin density of states at the Fermi energy and local magnetic orbital moment with Co/Mn swap.

First-principles electronic structure calculations for the whole spinel oxide solid solution range MnxCo3−xO4 (0 ≤ x ≤ 3) and their comparison with experimental data

Transition metal spinel oxides have recently been suggested for the creation of efficient photovoltaic cells or photocatalysts. These compounds can be easily tuned by doping to adapt their electronic or magnetic properties. However, their cation distribution is very complex and band structures are still a subject of controversy. We propose a complete density functional theory investigation of MnxCo3-xO4 compounds, using different approximations in order to explain the variation of these properties as a function of composition (for 0 ≤ x ≤ 3) and determine the electronic structure over the whole solid solution range. A detailed study of their atomic structure, magnetic properties and electronic structure is given and compared with experimental data. The unit cell volume calculated for each composition is in agreement with the volume obtained experimentally in ceramics, while a cubic-to-tetragonal structural transition is predicted at x = 2.0. An antiferromagnetic to ferrimagnetic behavior is observed at the lowest ordering temperature depending on the composition. The band gap, deduced from our band structure calculations, strongly decreases upon doping of the end members Co3O4 and Mn3O4, but is partly restored by the tetragonal distortion. A direct band gap, close to 0.5-0.8 eV, is calculated for 0.25 ≤ x ≤ 2.25, justified by inter-metal transitions from Mn ions on octahedral sites.

Noble Metal Nanocluster Formation in Epitaxial Perovskite Thin Films

We studied the synthesis of nanocomposite materials consisting of noble metal clusters embedded in an oxide semiconductor matrix. The embedded nanostructures form in a simple self-organized single-step growth process. The primary interest is in developing materials for photo-electrochemical energy conversion where spatially inhomogeneous band structures can enhance photogenerated charge separation and carrier extraction from a semiconductor. We show that spontaneous segregation of metallic Ir occurs during the initial growth of an Ir:SrTiO3 thin film. Cross-sectional transmission electron microscopy suggests that the nanoscale Ir clusters are epitaxial with the host lattice, and their presence is not detectable by surface morphology measurements.

First-principles calculation of the effects of tetragonal distortions on the Gilbert damping parameter of Co2MnSi

We present an ab initio study of the influence of the tetragonal distortion, on the static and dynamic (Gilbert damping parameter) magnetic properties of a Co2MnSi crystal. This tetragonal distortion can for instance be due to strain, when Co2MnSi is grown on a substrate with a small lattice mismatch. Using fully relativistic Korringa-Kohn-Rostoker (KKR) calculations, in conjunction with the coherent potential approximation (CPA) to describe atomic disorder and the linear response formalism to compute the Gilbert damping parameter, we show that a tetragonal distortion can substantially change the properties of Co2MnSi, in a way which depends on the kind of atomic disorder.