No Arabic abstract
Polarized neutron reflectometry measurements are presented exploring the evolution of ferrimagnetism in GdTiO$_3$ films as they are confined between SrTiO$_3$ layers of variable thicknesses. As GdTiO$_3$ films approach the thin layer limit and are confined within a substantially thicker SrTiO$_3$ matrix, the TiO$_6$ octahedral tilts endemic to GdTiO$_3$ coherently relax toward the undistorted, cubic phase of SrTiO$_3$. Our measurements reveal that the ferrimagnetic state within the GdTiO$_3$ layers survives as the TiO$_6$ octahedral tilts in the GdTiO$_3$ layers are suppressed. Furthermore, our data suggest that a magnetic dead layer develops within the GdTiO$_3$ layer at each GdTiO$_3$/ SrTiO$_3$ interface. The ferrimagnetic moment inherent to the core GdTiO$_3$ layers is negligibly (in models with dead layers) or only weakly (in models without dead layers) impacted as the octahedral tilt angles are suppressed by more than 50$%$ and the $t_{2g}$ bandwidth is dramatically renormalized.
Bonding geometry engineering of metal-oxygen octahedra is a facile way of tailoring various functional properties of transition metal oxides. Several approaches, including epitaxial strain, thickness, and stoichiometry control, have been proposed to efficiently tune the rotation and tilting of the octahedra, but these approaches are inevitably accompanied by unnecessary structural modifications such as changes in thin-film lattice parameters. In this study, we propose a method to selectively engineer the octahedral bonding geometries, while maintaining other parameters that might implicitly influence the functional properties. A concept of octahedral tilt propagation engineering has been developed using atomically designed SrRuO3/SrTiO3 superlattices. In particular, the propagation of RuO6 octahedral tilting within the SrRuO3 layers having identical thicknesses was systematically controlled by varying the thickness of adjacent SrTiO3 layers. This led to a substantial modification in the electromagnetic properties of the SrRuO3 layer, significantly enhancing the magnetic moment of Ru. Our approach provides a method to selectively manipulate the bonding geometry of strongly correlated oxides, thereby enabling a better understanding and greater controllability of their functional properties.
Dynamic manipulation of magnetism in topological materials is demonstrated here via a Floquet engineering approach using circularly polarized light. Increasing the strength of the laser field, besides the expected topological phase transition, the magnetically doped topological insulator thin film also undergoes a magnetic phase transition from ferromagnetism to paramagnetism, whose critical behavior strongly depends on the quantum quenching. In sharp contrast to the equilibrium case, the non-equilibrium Curie temperatures vary for different time scale and experimental setup, not all relying on change of topology. Our discoveries deepen the understanding of the relationship between topology and magnetism in the non-equilibrium regime and extend optoelectronic device applications to topological materials.
Distortions of the oxygen octahedra influence the fundamental electronic structure of perovskite oxides, such as their bandwidth and exchange interactions. Utilizing a fully ab-initio methodology based on density functional theory plus dynamical mean field theory (DFT+DMFT), we study the crystal and magnetic structure of SrMoO$_3$. Comparing our results with DFT+$U$ performed on the same footing, we find that DFT+$U$ overestimates the propensity for magnetic ordering, as well as the octahedral rotations, leading to a different ground state structure. This demonstrates that structural distortions can be highly sensitive to electronic correlation effects, and to the considered magnetic state, even in a moderately correlated metal such as SrMoO$_3$. Moreover, by comparing different downfolding schemes, we demonstrate the robustness of the DFT+DMFT method for obtaining structural properties, highlighting its versatility for applications to a broad range of materials.
The spatial distribution of the differential conductance for ultrathin Pb films grown on Si(111)7x7 substrate is studied by means of low-temperature scanning tunneling microscopy and spectroscopy. The formation of the quantum--confined states for conduction electrons and, correspondingly, the appearance of local maxima of the differential tunneling conductance are typical for Pb films; the energy of such states is determined mainly by the local thickness of Pb film. We demonstrate that the magnitude of the tunneling conductivity within atomically flat terraces can be spatially nonuniform and the period of the small-scale modulation coincides with the period of Si(111)7x7 reconstruction. For relatively thick Pb films we observe large-scale inhomogeneities of the tunneling conductance, which reveal itself as a gradual shift of the quantized levels at a value of the order of 50 meV at distances of the order of 100 nm. We believe that such large-scale variations of the tunneling conductance and, respectively, local density of states in Pb films can be related to presence of internal defects of crystalline structure, for instance, local electrical potentials and stresses.
Epitaxial strain and chemical substitution have been the workhorses of functional materials design. These static techniques have shown immense success in controlling properties in complex oxides through the tuning of subtle structural distortions. Recently, an approach based on the excitation of an infrared active phonon with intense mid-infrared light has created an opportunity for dynamical control of structure through special nonlinear coupling to Raman phonons. We use first-principles techniques to show that this approach can dynamically induce a magnetic phase transition from the ferromagnetic ground state to a hidden antiferromagnetic phase in the rare earth titanate GdTiO$_3$ for realistic experimental parameters. We show that a combination of a Jahn-Teller distortion, Gd displacement, and infrared phonon motion dominate this phase transition with little effect from the octahedral rotations, contrary to conventional wisdom.