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

ABSTRACT: 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(Mg_1/3Nb_2/3)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.

SUBMITTER: Begue A

PROVIDER: S-EPMC8483440 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Giant magnetoelectric coupling is a very rare phenomenon that has gained much attention in the past few decades due to fundamental interest as well as practical applications. Here, we have successfully achieved giant magnetoelectric coupling in PbTi1-x V x O3 (x = 0-1) using a series of generalized gradient-corrected GGA (generalized gradient approximation), including on-site Coulomb repulsion (U)-corrected spin-polarized calculations based on accurate density functional theory. Our total energy calculations show that PbTi1-x V x O3 stabilizes in C-type antiferromagnetic ground state for x > 0.123. With the substitution of V into PbTiO3, the tetragonal distortion is highly enhanced accompanied by a linear increase in polarization. In addition, our band structure analysis shows that for lower x values, the tendency to form two-dimensional magnetism of PbTi1-x V x O3 decreases. The orbital magnetic polarization was calculated with self-consistent field method by including orbital polarization correction in the calculation as well as from the computed X-ray magnetic dichroism spectra. A nonmagnetic metallic ground state is observed for the paraelectric phase for V concentration (x) = 1 competing with a volume change of 10% showing a large magnetovolume effect. Our orbital-projected density of states as well as orbital ordering analysis suggest that the orbital ordering plays a major role in the magnetic-to-nonmagnetic transition when going from ferroelectric to paraelectric phase. The calculated magnetic anisotropic energy shows that the direction [110] is the easy axis of magnetization for x = 1 composition. The partial polarization analysis shows that the Ti/V-O hybridization majorly contributes to the total electrical polarization. The present study adds a new series of compounds to the magnetoelectric family with rarely existing giant coupling between electric- and magnetic-order parameters. These results show that such kind of materials can be used for novel practical applications where one can change the magnetic properties drastically (magnetic to nonmagnetic, as shown here) with external electric field and vice versa.

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

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