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At least 811 records · Page 45

Structural and magnetic properties of CoTeMo⁢O 6

Here, we have conducted a comprehensive investigation into the magnetic properties of the chiral multiferroic material CoTeMo⁢O 6 . In contrast with the previous claim of canted antiferromagnetic order with ferromagnetic components [Y. Doi et al., J. Solid State Chem. 182, 3232 (2009)], our investigation reveals an antiferromagnetic ground state with compensated moments, providing an interesting platform for exploring exotic material properties. Through careful measurements of magnetization under a series of applied fields, we demonstrate that there exist two sequential field-induced magnetic transitions in CoTeMo⁢O 6 , with one occurring at 𝐻 𝑐⁢1 =460 Oe along the 𝑎 axis, and the other at 𝐻 𝑐⁢2 =1.16 T with the field along the 𝑏 axis. The values of 𝐻 𝑐⁢1 and 𝐻 𝑐⁢2 exhibit strong angular dependence and diverge with different rates as the applied field is rotated 90 ° within the 𝑎⁢𝑏 plane. This reflects the distinct nature of these transitions, which is further supported by the different critical behavior of 𝐻 𝑐⁢1 and 𝐻 𝑐⁢2 , characterized by the values of 𝛾, in the function of 𝐻 𝑐 =𝐻 0 ⁡(1−𝑇/𝑇 𝑐 ) 𝛾 . Furthermore, we have demonstrated that there exist structural and magnetic twin domains in CoTeMo⁢O 6 that strongly affect the experimental measurement of their macroscopic properties. Intriguingly, these twin domains can be related to the orthorhombicity/chirality of the crystal structure with the space group 𝑃⁢2 1 ⁢2 1⁢ 2. We further explored the magnetic and structural domains with uniaxial pressure and polarized light microscopy. Our results suggest that CoTeMo⁢O 6 could be used as a unique platform for investigating the intriguing physics involving intertwined degrees of freedom. The tunability of the underlying domain distribution and its strong anisotropy could also be useful for developing functional devices and applications.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Spin-orbit coupling and electronic charge effects in Mott insulators

We derive the effective charge- and current-density operators for the strong-coupling limit of a single-band Mott insulator in the presence of spin-orbit coupling and show that the spin-orbit contribution to the effective charge density leads to novel mechanisms for multiferroic behavior. In some sense, these mechanisms are the electronic counterpart of the ionic-based mechanisms, which have been proposed for explaining the electric polarization induced by spiral spin orderings. In addition, the new electronic mechanisms are illustrated by considering cycloidal and proper-screw magnetic orderings on sawtooth and kagome lattices. As for the isotropic case, geometric frustration is crucial for achieving this purely electronic coupling between spin and charge degrees of freedom.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

General microscopic model of magnetoelastic coupling from first principles

Magnetoelastic coupling, i.e., the change of crystal lattice induced by a spin order, is not only scientifically interesting, but also technically important. In this work, we propose a general microscopic model from firstprinciples calculations to describe the magnetoelastic coupling and provide a way to construct the microscopic model from density functional theory calculations. Based on this model, we reveal that there exists a previously unexpected contribution to the electric polarization induced by the spin order in multiferroics due to the combined effects of magnetoelastic coupling and piezoelectric effect. Interestingly and surprisingly, we find that this latticedeformation contribution to the polarization is even larger than that from the pure electronic and ion-displacement contributions in BiFeO 3 . We conclude this model of magnetoelastic coupling can be generally applied to investigate the other magnetoelastic phenomena.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Ultrafast relaxation dynamics in BiFeO 3 /YBa 2 Cu 3 O 7 bilayers

The temperature dependence of the relaxation dynamics in the bilayer thin film heterostructure composed of multiferroic BiFeO 3 (BFO) and superconducting YBa 2 Cu 3 O 7 (YBCO) grown on (001) SrTiO 3 substrate is studied by time-resolved pump-probe technique, and compared with that of pure YBCO thin film grown under the same growth conditions. The superconductivity of YBCO is found to be retained in the heterostructure. We observe a speeding up of the YBCO recombination dynamics in the superconducting state of the heterostructure, and attribute it to the presence of weak ferromagnetism at the BFO/YBCOinterface as observed inmagnetization data. An extension of the Rothwarf-Taylor model is used to fit the ultrafast dynamics of BFO/YBCO, that models an increased quasiparticle occupation of the ferromagnetic interfacial layer in the superconducting state of YBCO.

36 MATERIALS SCIENCE↗

Magnetoelectric phase diagrams of multiferroicGdMn2O5

Electric and magnetic properties of multiferroic GdMn 2 O 5 in external magnetic fields were investigated to map out the magnetoelectric phases in this material. Due to strong magnetoelectric coupling, the dielectric permittivity is highly sensitive to phase boundaries in GdMn 2 O 5 , which allowed us to construct the field-temperature phase diagrams. Several phase transitions are observed which are strongly field dependent with respect to field orientation and strength. The phase diagram for a magnetic field along the crystallographic a axis corresponds well to a polarization step, as induced by 90° rotation of Gd magnetic moments. Our results support the model of two ferroelectric sublattices, Mn-Mn and Gd-Mn, with strong R -Mn (4f - 3d) interaction for the polarization in R Mn 2 O 5 .

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Directly probing spin dynamics in insulating antiferromagnets using ultrashort terahertz pulses

We investigate spin dynamics in the antiferromagnetic (AFM) multiferroic TbMnO3 using opticalpump, terahertz (THz)-probe spectroscopy. Photoexcitation results in a broadband THz transmission change, with an onset time of 25 ps at 6 K that becomes faster at higher temperatures. We attribute this time constant to spin-lattice thermalization. The excellent agreement between our measurements and previous ultrafast resonant x-ray diffraction measurements on the same material confirms that our THz pulse directly probes spin order. We suggest that this could be the case in general for insulating AFM materials, if the origin of the static absorption in the THz spectral range is magnetic.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Helical magnetism in Sr-doped CaM n 7 O 12 films

Noncollinear magnetism can play an important role in multiferroic materials but is relatively understudied in oxide heterostructures compared to their bulk counterparts. Using variable temperature magnetometry and neutron diffraction, we demonstrate the presence of helical magnetic ordering in CaMn 7 O 12 and Ca 1-x Sr x Mn 7 O 12 (for x up to 0.51) thin films. Consistent with bulk Ca 1-x Sr x Mn 7 O 12 , the net magnetization increases with Sr doping. Neutron diffraction confirms that the helical magnetic structure remains incommensurate at all values of x, while the fundamental magnetic wavevector increases upon Sr substitution. Lastly, this result demonstrates a chemical-based approach for tuning helical magnetism in quadruple perovskite films and enables future studies of strain and interfacial effects on helimagnetism in oxide heterostructures.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Nontrivial topology and localization in the double exchange model with possible applications to perovskite manganites

The double exchange model describing the coupling between conduction electrons and localized magnetic moments is relevant for a large family of physical systems including manganites. Here we reveal that the one-dimensional double exchange model with an incommensurate magnetic elliptical spiral is a topological insulator with a Chern number 2Z in the two-dimensional space with one physical dimension and one ancillary dimension spanned by the Goldstone mode of the spiral. Moreover, the electronic states can be localized for a strong local exchange coupling. The topological protected edge states are responsible for the pumping of electron charge, and give rise to multiferroic response. Furthermore, our work uncovers hitherto undiscovered nontrivial topology and Anderson localization in the double exchange model with possible applications to perovskite manganites.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Intrinsic structural instabilities of domain walls driven by gradient coupling: Meandering antiferrodistortive-ferroelectric domain walls in BiFeO 3

Using the Landau-Ginzburg-Devonshire approach, we predict the intrinsic instability of the ferroelectric-ferroelastic domain walls in the multiferroic BiFeO 3 emerging from the interplay between the gradient terms of the antiferrodistortive and ferroelectric order parameters at the walls. These instabilities are the interface analog of the structural instabilities in the vicinity of phase coexistence in the bulk, and so they do not stem from incomplete polarization screening in thin films or its spatial confinement, electrostrictive or flexoelectric coupling. The effect of BiFeO 3 material parameters on the 71°, 109°, and 180° walls is explored, and it is shown that the meandering instability appears at 109° and 180° walls for small gradient energies, and the walls become straight and broaden for higher gradients. In contrast to the 180° and 109° domain walls, uncharged 71° walls are always straight, and their width increases with increasing the tilt gradient coefficient. As a result, the wall instability and associated intrinsic meandering provide insight into the behavior of morphotropic and relaxor materials, wall pinning, and mechanisms of interactions between order parameter fields and local microstructure.

36 MATERIALS SCIENCE↗

Magnetic interactions in BiFeO 3 : A first-principles study

First-principles calculations, in combination with the four-state energy mapping method, are performed to extract the magnetic interaction parameters of multiferroic BiFeO 3 . Such parameters include the symmetric exchange (SE) couplings and the Dzyaloshinskii-Moriya (DM) interactions up to second-nearest neighbors, as well as the single-ion anisotropy (SIA). Here, all magnetic parameters are obtained not only for the R3c structural ground state, but also for the R3m and R¯3c phases in order to determine the effects of ferroelectricity and antiferrodistortion distortions, respectively, on these magnetic parameters. In particular, two different second-nearest-neighbor couplings are identified and their origins are discussed in details. Moreover, Monte Carlo (MC) simulations using a magnetic Hamiltonian incorporating these first-principles-derived interaction parameters are further performed. They result (i) not only in the accurate prediction of the spin-canted G-type antiferromagnetic structure and of the known magnetic cycloid propagating along a < 1¯10 > direction, as well as their unusual characteristics (such as a weak magnetization and spin-density-waves, respectively), (ii) but also in the finding of another cycloidal state of low-energy and that awaits to be experimentally confirmed. Turning on and off the different magnetic interaction parameters in the MC simulations also reveal the precise role of each of them on magnetism.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Giant Spin-Driven Ferroelectric Polarization in BiFeO 3 at Room Temperature

Although BiFeO 3 is the most extensively investigated multiferroic material, its magnetoelectic couplings are barely understood. Here we report a thorough study of the magentoelectric (ME) couplings in spin-cycloidal buk BiFeO 3 using first-principles calculations and microscopic spin-wave models compared with neutron-scattering measurements. We find that huge exchange-striction (ES) polarizations, i.e. the electric response of the magnetic exchange through ferroelectric and antiferrodistortive distortions, is giant enough to dominate over all other ME couplings. We show that BiFeO 3 has a hidden record-high spin-driven polarization ( 3 C/cm 2 ) at room-temperature. The huge ES polarizations can be tuned by coupling to the antiferrodistortive rotations.

36 MATERIALS SCIENCE↗

Inversion of ferrimagnetic magnetization by ferroelectric switching via a novel magnetoelectric coupling

Although several multiferroic materials or heterostructures have been extensively studied, finding strong magnetoelectric couplings for the electric field control of the magnetization remains challenging. Here, a novel interfacial magnetoelectric coupling based on three components (ferroelectric dipole, magnetic moment, and antiferromagnetic order) is analytically formulated. As an extension of carrier-mediated magnetoelectricity, the new coupling is shown to induce an electric-magnetic hysteresis loop. In addition, realizations employing BiFeO 3 bilayers grown along the [111] axis are proposed. Without involving magnetic phase transitions, the magnetization orientation can be switched by the carrier modulation driven by the field effect, as confirmed using first-principles calculations.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Intrinsic Two-Dimensional Ferroelectricity with Dipole Locking

Out-of-plane ferroelectricity with a high transition temperature in ultrathin films is important for the exploration of new domain physics and scaling down of memory devices. However, depolarizing electrostatic fields and interfacial chemical bonds can destroy this long-range polar order at two-dimensional (2D) limit. In this paper we report the experimental discovery of the locking between out-of-plane dipoles and in-plane lattice asymmetry in atomically thin In 2 Se 3 crystals, a new stabilization mechanism leading to our observation of intrinsic 2D out-of-plane ferroelectricity. Through second harmonic generation spectroscopy and piezoresponse force microscopy, we found switching of out-of-plane electric polarization requires a flip of nonlinear optical polarization that corresponds to the inversion of in-plane lattice orientation. The polar order shows a very high transition temperature (~700Κ) without the assistance of extrinsic screening. This finding of intrinsic 2D ferroelectricity resulting from dipole locking opens up possibilities to explore 2D multiferroic physics and develop ultrahigh density memory devices.

2-dimensional systems↗

Evidence for Electronically Driven Ferroelectricity in a Strongly Correlated Dimerized BEDT-TTF Molecular Conductor

By applying measurements of the dielectric constants and relative length changes to the dimerized molecular conductor kappa-(BEDT-TTF)(2)Hg(SCN)(2)Cl, we provide evidence for order-disorder type electronic ferroelectricity that is driven by the charge order within the (BEDT-TTF)(2) dimers and stabilized by a coupling to the anions. According to our density functional theory calculations, this material is characterized by a moderate strength of dimerization. This system thus bridges the gap between strongly dimerized materials, often approximated as (imer-Mott systems at 1/2 filling, and nondimerized or weakly dimerized systems at 1/4 filling, exhibiting a charge order. Our results indicate that intradimer charge degrees of freedom are of particular importance in correlated kappa-(BEDT-TTF)(2)X salts and can create novel states, such as electronically driven multiferroicity or charge-order-induced quasi-one-dimensional spin liquids.

Gati, Elena↗

Tuning the Néel Temperature of Hexagonal Ferrites by Structural Distortion

To tune the magnetic properties of hexagonal ferrites, a family of magnetoelectric multiferroic materials, by atomic-scale structural engineering, we studied the effect of structural distortion on the magnetic ordering temperature ( T N ) in these materials. Using the symmetry analysis, we show that unlike most antiferromagnetic rare-earth transition-metal perovskites, a larger structural distortion leads to a higher T N in hexagonal ferrites and manganites, because the K 3 structural distortion induces the three-dimensional magnetic ordering, which is forbidden in the undistorted structure by symmetry. We also revealed a near-linear relation between T N and the tolerance factor and a power-law relation between T N and the K 3 distortion amplitude. Following the analysis, a record-high T N (185 K) among hexagonal ferrites was predicted in hexagonal ScFeO 3 and experimentally verified in epitaxially stabilized films. Furthermore these results add to the paradigm of spin-lattice coupling in antiferromagnetic oxides and suggests further tunability of hexagonal ferrites if more lattice distortion can be achieved.

36 MATERIALS SCIENCE↗

Electric-Field Control of Magnetization, Jahn-Teller Distortion, and Orbital Ordering in Ferroelectric Ferromagnets

Controlling the direction of the magnetization by an electric field in multiferroics that are both ferroelectric and strongly ferromagnetic will open the door to the design of the next generation of spintronics and memory devices. Using first-principles simulations, we report that the discovery that the PbTiO 3 /LaTiO 3 (PTO/LTO) superlattice possesses such highly desired control, as evidenced by the electric-field-induced rotation of 90° and even a possible full reversal of its magnetization in some cases. Moreover, such systems also exhibit Jahn-Teller distortions, as well as orbital orderings, that are switchable by the electric field, therefore making PTO/LTO of importance for the tuning of electronic properties too. Here, the origin for such striking electric-field controls of magnetization, Jahn-Teller deformations, and orbital orderings resides in the existence of three different types of energetic coupling: one coupling polarization with antiphase and in-phase oxygen octahedral tiltings, a second one coupling polarization with antiphase oxygen octahedra tilting and Jahn-Teller distortions, and finally a biquadratic coupling between antiphase oxygen octahedral tilting and magnetization.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Nanosecond Optically Induced Phase Transformation in Compressively Strained BiFeO 3 on LaAlO 3

Above-band-gap optical illumination of compressively strained BiFeO 3 induces a transient reversible transformation from a state of coexisting tilted tetragonal-like and rhombohedral-like phases to an untilted tetragonal-like phase. Time-resolved synchrotron x-ray diffraction reveals that the transformation is induced by an ultrafast optically induced lattice expansion that shifts the relative free energies of the tetragonal-like and rhombohedral-like phases. The transformation proceeds at interfaces between regions of the tetragonal-like phase and regions of a mixture of tilted phases, consistent with the motion of a phase boundary. The optically induced transformation demonstrates that there are new optically driven routes towards nanosecond-scale control of phase transformations in ferroelectrics and multiferroics.

36 MATERIALS SCIENCE↗