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Register a new userMagnetoelectric Effect driven by Magnetic Domain Modification in LuFe2O4
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Magneto-capacitance effect was investigated using the impedance spectroscopy on single crystals of LuFe2O4. The intrinsic impedance response could be separated from the interfacial response and showed a clear hysteresis loop below TFerri ~ 240 K under the magnetic field. The neutron diffraction experiment under the magnetic field proves the origin of dielectric property related to the motion of nano-sized ferromagnetic domain boundary. These results imply that the modification of the microscopic domain structure is responsible for the magnetoelectric effect in LuFe2O4.
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We report the discovery of linear magnetoelectric effect in the well-known green phase compound, Sm2BaCuO5, which crystallizes in the centrosymmetric orthorhombic (Pnma) structure. Magnetization and specific heat measurements reveal the long-range antiferromagnetic ordering of Cu2+ and Sm3+-ions moments at TN1 = 23 K and TN2 = 5 K, respectively. Applied magnetic field induces dielectric anomaly at TN1 whose magnitude increases with field, which results in significant (1.7%) magnetocapacitance effect. On the other hand, the dielectric anomaly observed in zero-applied magnetic field at TN2 shows a small (0.4%) magnetocapacitance effect. Interestingly, applied magnetic field induces an electric polarization below TN1 and the polarization varies linearly up to the maximum applied field of 9 T with the magnetoelectric coefficient {alpha} ~ 4.4 ps/m, demonstrating high magnetoelectric coupling. Below TN2, the electric polarization decreases from 35 to 29 {mu}C/m2 at 2 K and 9 T due to ordering of Sm-sublattice. The observed linear magnetoelectricity in Sm2BaCuO5 is explained using symmetry analysis.
Magnetic and magnetoelectric excitations in the multiferroic TbMnO_3 have been investigated at terahertz frequencies. Using different experimental geometries we can clearly separate the electro-active excitations (electromagnons) from the magneto-active modes, i.e. antiferromagnetic resonances (AFMR). Two AFMR resonances were found to coincide with electromagnons. This indicates that both excitations belong to the same mode and the electromagnons can be excited by magnetic ac-field as well. In external magnetic fields and at low temperatures distinct fine structure of the electromagnons appears. In spite of the 90^o rotation of the magnetic structure, the electromagnons are observable for electric ac-fields parallel to the a-axis only. Contrary to simple expectations, the response along the c-axis remains purely magnetic in nature.
The transmission electron microscopy observations of the charge ordering (CO) which governs the electronic polarization in LuFe2O4-x clearly show the presence of a remarkable phase separation at low temperatures. Two CO ground states are found to adopt the charge modulations of Q1 = (1/3, 1/3, 0) and Q2 = (1/3 + y, 1/3 + y, 3/2), respectively. Our structural study demonstrates that the incommensurately Q2-modulated state is chiefly stable in samples with relatively lower oxygen contents. Data from theoretical simulations of the diffraction suggest that both Q1- and Q2-modulated phases have ferroelectric ordering. The effects of oxygen concentration on the phase separation and electric polarization in this layered system are discussed.
We present single-crystal neutron diffraction measurements on multiferroic LuFe2O4 showing phase transitions at 240 and 175 K. Magnetic reflections are observed below each transition indicating that the magnetic interactions in LuFe2O4 are 3-dimensional (3D) in character. The magnetic structure is refined as a ferrimagnetic spin configuration below the 240 K transition. While 3D magnetic correlations persists below 175 K, a significant broadening of the magnetic peaks is observed along with the build up of a diffuse component to the magnetic scattering.
We present a unique example of giant magnetoelectric effect in a conventional multiferroic HoMnO3, where polarization is very large (~56 mC/m2) and the ferroelectric transition temperature is higher than the magnetic ordering temperature by an order. We attribute the uniqueness of the giant magnetoelectric effect to the ferroelectricity induced entirely by the off-center displacement of rare earth ions with large magnetic moments. This finding suggests a new avenue to design multiferroics with large polarization and higher ferroelectric transition temperature as well as large magnetoelectric effects.
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