Browse
Submit Data
Databases
API
Help

Dataset Information

26 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

A three-order-parameter bistable magnetoelectric multiferroic metal.

ABSTRACT: Using first-principles calculations we predict that the layered-perovskite metal Bi₅Mn₅O₁₇ is a ferromagnet, ferroelectric, and ferrotoroid which may realize the long sought-after goal of a room-temperature ferromagnetic single-phase multiferroic with large, strongly coupled, primary-order polarization and magnetization. Bi₅Mn₅O₁₇ has two nearly energy-degenerate ground states with mutually orthogonal vector order parameters (polarization, magnetization, ferrotoroidicity), which can be rotated globally by switching between ground states. Giant cross-coupling magnetoelectric and magnetotoroidic effects, as well as optical non-reciprocity, are thus expected. Importantly, Bi₅Mn₅O₁₇ should be thermodynamically stable in O-rich growth conditions, and hence experimentally accessible.

SUBMITTER: Urru A

PROVIDER: S-EPMC7530708 | biostudies-literature | 2020 Oct

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

A three-order-parameter bistable magnetoelectric multiferroic metal.

Urru Andrea A Ricci Francesco F Filippetti Alessio A Íñiguez Jorge J Fiorentini Vincenzo V

Nature communications 20201001 1

Using first-principles calculations we predict that the layered-perovskite metal Bi5Mn5O17 is a ferromagnet, ferroelectric, and ferrotoroid which may realize the long sought-after goal of a room-temperature ferromagnetic single-phase multiferroic with large, strongly coupled, primary-order polarization and magnetization. Bi5Mn5O17 has two nearly energy-degenerate ground states with mutually orthogonal vector order parameters (pola ...[more]

PMID: 33004814

Similar Datasets

Magnetoelectric interaction in molecular multiferroic nanocomposites.

Project description:Incorporation of magnetic and electric orders in a form of multiferroics is an interesting topic in materials science. Making a molecular heterogeneous composite by incorporating the molecular magnet vanadium-chromium Prussian blue analogue (V-Cr PBA) and a molecular ferroelectric imidazolium chloride C3N2H5-ClO4 (ImClO4) provides a pathway towards achieving the room temperature magnetoelectric effect. The change of magnetization of about 6% is shown as a result of applying an electric field (21 kV cm-1) to the composite made of the aforementioned molecular crystals at room temperature. In the ferromagnetic resonance measurement (FMR) under the effect of an applied electric field, a shift of the resonance magnetic field is also observed in the nanocomposites. This work provides a pathway towards molecular multiferroic nanocomposites with magnetoelectric coupling interactions at room temperature.

| S-EPMC9400656 | biostudies-literature

Magnetoelectric Response in Multiferroic SrFe12O19 Ceramics.

Project description:We report here realization of ferroelectricity, ferromagnetism and magnetocapacitance effect in singleSrFe12O19ceramic at room temperature. The ceramics demonstrate a saturated polarization hysteresis loop, two nonlinear I-V peaks and large anomaly of dielectric constant near Curie temperature, which confirm the intrinsic ferroelectricity of SrFe12O19 ceramicswith subsequent heat-treatment in O2atmosphere. The remnant polarization of the SrFe12O19 ceramic is estimated to be 103μC/cm2. The ceramic also exhibits strong ferromagnetic characterization, the coercive field and remnant magnetic moment are 6192Oe and 35.8emu/g, respectively. Subsequent annealing SrFe12O19 ceramics in O2 plays a key role on revealing its intrinsic ferroelectricity and improving the ferromagnetism through transforming Fe2+ into Fe3+. By applying a magnetic field, the capacitance demonstrates remarkable change along with B field, the maximum rate of change in ε (Δε(B)/ε(0)) is 1174%, which reflects a giant magnetocapacitance effect in SrFe12O19. XPS and molecular magnetic moment measurements confirmed the transformation of Fe2+ into Fe3+ and removal of oxygen vacancies upon O2 heat treatment. These combined functional responses in SrFe12O19 ceramics opens substantial possibilities for applications in novel electric devices.

| S-EPMC5147852 | biostudies-literature

Magnetoelectric coupling of domains, domain walls and vortices in a multiferroic with independent magnetic and electric order.

Project description:Magnetically induced ferroelectrics exhibit rigidly coupled magnetic and electric order. The ordering temperatures and spontaneous polarization of these multiferroics are notoriously low, however. Both properties can be much larger if magnetic and ferroelectric order occur independently, but the cost of this independence is that pronounced magnetoelectric interaction is no longer obvious. Using spatially resolved images of domains and density-functional theory, we show that in multiferroics with separately emerging magnetic and ferroelectric order, the microscopic magnetoelectric coupling can be intrinsically strong even though the macroscopic leading-order magnetoelectric effect is forbidden by symmetry. We show, taking hexagonal ErMnO3 as an example, that a strong bulk coupling between the ferroelectric and antiferromagnetic order is realized because the structural distortions that lead to the ferroelectric polarization also break the balance of the competing superexchange contributions. We observe the manifestation of this coupling in uncommon types of topological defects like magnetoelectric domain walls and vortex-like singularities.

| S-EPMC8149668 | biostudies-literature

Directed synthesis of a hybrid improper magnetoelectric multiferroic material.

Project description:Preparing materials which simultaneously exhibit spontaneous magnetic and electrical polarisations is challenging as the electronic features which are typically used to stabilise each of these two polarisations in materials are contradictory. Here we show that by performing low-temperature cation-exchange reactions on a hybrid improper ferroelectric material, Li2SrTa2O7, which adopts a polar structure due to a cooperative tilting of its constituent TaO6 octahedra rather than an electronically driven atom displacement, a paramagnetic polar phase, MnSrTa2O7, can be prepared. On cooling below 43 K the Mn2+ centres in MnSrTa2O7 adopt a canted antiferromagnetic state, with a small spontaneous magnetic moment. On further cooling to 38 K there is a further transition in which the size of the ferromagnetic moment increases coincident with a decrease in magnitude of the polar distortion, consistent with a coupling between the two polarisations.

| S-EPMC8368162 | biostudies-literature

Large Magnetoelectric Coupling in the Thin Film of Multiferroic CuO.

Project description:We report observation of large magnetoelectric coupling in an epitaxial thin film of multiferroic CuO grown on the (100)MgO substrate by the pulsed laser deposition technique. The film is characterized by X-ray diffraction, transmission electron microscopy, and Raman spectrometry. The crystallographic structure of the film turns out to be monoclinic (space group C2/c) with [111]CuO||[100]MgO "out-of-plane" epitaxy and "in-plane" domain structure. The lattice misfit strain is found to vary within ±1-3%. The dc resistivity, magnetization, dielectric spectroscopy, and remanent ferroeletric polarization have been measured across 80-300 K. The dielectric constant is found to decrease by >20% under a moderate magnetic field of ∼18 kOe while the remanent ferroelectric polarization, emerging at the onset of magnetic transition (T N ∼ 175 K), decreases by nearly 50% under ∼18 kOe field. These results could assume importance as the strain-free bulk CuO does not exhibit magnetoelectric coupling within such magnetic field regime. The strain-induced large magnetoelectric coupling in the CuO thin film would generate new possibility of further strain tuning to observe room-temperature magnetoelectric multiferroicity suitable for scores of applications such as memories, sensors, energy-harvesting devices, generators, amplifiers, and so forth.

| S-EPMC7496646 | biostudies-literature

Strain-Mediated Giant Magnetoelectric Coupling in a Crystalline Multiferroic Heterostructure.

Project description:Multiferroic heterostructures based on the strain-mediated mechanism present ultralow heat dissipation and large magnetoelectric coupling coefficient, two conditions that require endless improvement for the design of fast nonvolatile random access memories with reduced power consumption. This work shows that a structure consisting of a [Pb(Mg1/3Nb2/3)O3]0.7-[PbTiO3]0.3 (001) substrate on which a crystalline FeGa(001)/MgO(001) bilayer is deposited exhibits a giant magnetoelectric coupling coefficient of order 15 × 10-6 s m-1 at room temperature. That result is a 2-fold increment over the previous highest value. The spatial orientation of the magnetization vector in the epitaxial FeGa film is switched 90° with the application of electric field. The symmetry of the magnetic anisotropy is studied by the angular dependence of the remanent magnetization, demonstrating that poling the sample generates a switchable uniaxial magnetoelastic anisotropy in the film that overcomes the native low 4-fold magnetocrystalline anisotropy energy. Magnetic force microscopy shows that the switch of the easy axis activates the displacement of domain walls and the domain structures remain stable after that point. This result highlights the interest in single-crystalline structures including materials with large magnetoelastic coupling and small magnetocrystalline anisotropy for low-energy-consuming spintronic applications.

| S-EPMC8483440 | biostudies-literature

Giant chiral magnetoelectric oscillations in a van der Waals multiferroic.

Project description:Helical spin structures are expressions of magnetically induced chirality, entangling the dipolar and magnetic orders in materials1-4. The recent discovery of helical van der Waals multiferroics down to the ultrathin limit raises prospects of large chiral magnetoelectric correlations in two dimensions5,6. However, the exact nature and magnitude of these couplings have remained unknown so far. Here we perform a precision measurement of the dynamical magnetoelectric coupling for an enantiopure domain in an exfoliated van der Waals multiferroic. We evaluate this interaction in resonance with a collective electromagnon mode, capturing the impact of its oscillations on the dipolar and magnetic orders of the material with a suite of ultrafast optical probes. Our data show a giant natural optical activity at terahertz frequencies, characterized by quadrature modulations between the electric polarization and magnetization components. First-principles calculations further show that these chiral couplings originate from the synergy between the non-collinear spin texture and relativistic spin-orbit interactions, resulting in substantial enhancements over lattice-mediated effects. Our findings highlight the potential for intertwined orders to enable unique functionalities in the two-dimensional limit and pave the way for the development of van der Waals magnetoelectric devices operating at terahertz speeds.

| S-EPMC11306099 | biostudies-literature

Electric-field control of skyrmions in multiferroic heterostructure via magnetoelectric coupling.

Project description:Room-temperature skyrmions in magnetic multilayers are considered to be promising candidates for the next-generation spintronic devices. Several approaches have been developed to control skyrmions, but they either cause significant heat dissipation or require ultrahigh electric fields near the breakdown threshold. Here, we demonstrate electric-field control of skyrmions through strain-mediated magnetoelectric coupling in ferromagnetic/ferroelectric multiferroic heterostructures. We show the process of non-volatile creation of multiple skyrmions, reversible deformation and annihilation of a single skyrmion by performing magnetic force microscopy with in situ electric fields. Strain-induced changes in perpendicular magnetic anisotropy and interfacial Dzyaloshinskii-Moriya interaction strength are characterized experimentally. These experimental results, together with micromagnetic simulations, demonstrate that strain-mediated magnetoelectric coupling (via strain-induced changes in both the perpendicular magnetic anisotropy and interfacial Dzyaloshinskii-Moriya interaction is responsible for the observed electric-field control of skyrmions. Our work provides a platform to investigate electric-field control of skyrmions in multiferroic heterostructures and paves the way towards more energy-efficient skyrmion-based spintronics.

| S-EPMC7803786 | biostudies-literature

Solutions for maximum coupling in multiferroic magnetoelectric composites by material design.

Project description:Electrical control of magnetization offers an extra degree of freedom in materials possessing both electric and magnetic dipole moments. A stochastic optimization combined with homogenization is applied for the solution for maximum magnetoelectric (ME) coupling coefficient α of a laminar ME composite with the thickness and orientation of ferroelectric phase as design variables. Simulated annealing with a generalized Monte Carlo scheme is used for optimization problem. Optimal microstructure with single and poly-crystalline configurations that enhances the overall α is identified. It is found that juxtaposing a preferentially oriented ferroelectric material with a ferromagnetic ferrite into a composite would result in manifold increase in magnetoelectric coupling. The interface shear strains are found to be richly contributing to the ME coupling. The preferential orientation of the ferroelectric phase in the optimal ME composite laminate is demonstrated using the optimal pole figure analyses.

| S-EPMC5861126 | biostudies-literature

Synthetic magnetoelectric coupling in a nanocomposite multiferroic.

Project description:Given the paucity of single phase multiferroic materials (with large ferromagnetic moment), composite systems seem an attractive solution to realize magnetoelectric coupling between ferromagnetic and ferroelectric order parameters. Despite having antiferromagnetic order, BiFeO3 (BFO) has nevertheless been a key material due to excellent ferroelectric properties at room temperature. We studied a superlattice composed of 8 repetitions of 6 unit cells of La0.7Sr0.3MnO3 (LSMO) grown on 5 unit cells of BFO. Significant net uncompensated magnetization in BFO, an insulating superlattice, is demonstrated using polarized neutron reflectometry. Remarkably, the magnetization enables magnetic field to change the dielectric properties of the superlattice, which we cite as an example of synthetic magnetoelectric coupling. Importantly, controlled creation of magnetic moment in BFO is a much needed path toward design and implementation of integrated oxide devices for next generation magnetoelectric data storage platforms.

| S-EPMC4357856 | biostudies-other

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data