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Register a new userCoupled magnetic and electric hysteresis in the multiferroic double perovskite Lu2MnCoO6
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We investigate a magnetic hysteresis loop with a remanent moment that couples to electric polarization to create coupled hysteretic multiferroic behavior in Lu2MnCoO6. Measurements of elastic neutron diffraction, muon spin relaxation, and micro-Hall magnetometry demonstrate an unusual mechanism for the magnetic hysteresis, namely the hysteretic evolution of a microscopic magnetic order, and not classic ferromagnetic domain effects. We show how the frustrated spin system evolves from antiferromagnetism with an incommensurate long-wavelength modulation and strong fluctuations towards a net magnetism. We also clarify the different temperature scales for the onset of ordering, dynamics, and hysteresis.
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We report electric polarization and magnetization measurements in single crystals of double perovskite Lu2MnCoO6 using pulsed magnetic fields and optical second harmonic generation (SHG) in DC magnetic fields. we observe well-resolved magnetic field-induced changes in the electric polarization in single crystals and thereby resolve the question about whether multiferroic behavior is intrinsic to these materials or an extrinsic feature of polycrystals. We find electric polarization along the crystalline b-axis, that is suppressed by applying a magnetic fields along c-axis and advance a model for the origin of magnetoelectric coupling. We furthermore map the phase diagram using both capacitance and electric polarization to identify regions of ordering and regions of magnetoelectric hysteresis. This compound is a rare example of coupled hysteretic behavior in the magnetic and electric properties. The ferromagnetic-like magnetic hysteresis loop that couples to hysteretic polarization can be attributed not to ordinary ferromagnetic domains, but to the rich physics of magnetic frustration of Ising-like spins in the axial next-nearest neighbor interaction model.
We present a new member of the multiferroic oxides, Lu$_2$MnCoO$_6$, which we have investigated using X-ray diffraction, neutron diffraction, specific heat, magnetization, electric polarization, and dielectric constant measurements. This material possesses an electric polarization strongly coupled to a net magnetization below 35 K, despite the antiferromagnetic ordering of the $S = 3/2$ Mn$^{4+}$ and Co$^{2+}$ spins in an $uparrow uparrow downarrow downarrow$ configuration along the c-direction. We discuss the magnetic order in terms of a condensation of domain boundaries between $uparrow uparrow$ and $downarrow downarrow$ ferromagnetic domains, with each domain boundary producing a net electric polarization due to spatial inversion symmetry breaking. In an applied magnetic field the domain boundaries slide, controlling the size of the net magnetization, electric polarization, and magnetoelectric coupling.
Electric manipulation of magnetic properties is a key problem of materials research. To fulfil the requirements of modern electronics, these processes must be shifted to high frequencies. In multiferroic materials this may be achieved by electric and magnetic control of their fundamental excitations. Here we identify magnetic vibrations in multiferroic iron-borates which are simultaneously sensitive to external electric and magnetic fields. Nearly 100% modulation of the terahertz radiation in an external field is demonstrated for SmFe3(BO3)4. High sensitivity can be explained by a modification of the spin orientation which controls the excitation conditions in multiferroic borates. These experiments demonstrate the possibility to alter terahertz magnetic properties of materials independently by external electric and magnetic fields.
The paper deals with the hyperfine interactions observed on the 57Fe nucleus in multiferroic BiFeO3 by means of the 14.41-keV resonant transition in 57Fe, and for transmission geometry applied to the random powder sample. Spectra were obtained at 80 K, 190 K and at room temperature. It was found that iron occurs in the high spin trivalent state. Hyperfine magnetic field follows distribution due to the elliptic-like distortion of the magnetic cycloid. The long axis of the ellipse is oriented along <111> direction of the rhombohedral unit cell. The hyperfine magnetic field in this direction is about 1.013 of the field in the perpendicular direction at room temperature. This ratio diminishes to 1.010 at 80 K. Axially symmetric electric field gradient (EFG) on the iron atoms has the principal axis oriented in the same direction and the main component of the EFG is positive. Our results are consistent with the finding that iron magnetic moments are confined to the [1-21] crystal plane.
Many multiferroic materials, with various chemical compositions and crystal structures, have been discovered in the past years. Among these multiferroics, some perovskite manganites with ferroelectricity driven by magnetic orders are of particular interest. In these multiferroic perovskite manganites, not only their multiferroic properties are quite prominent, but also the involved physical mechanisms are very plenty and representative. In this Brief Review, we will introduce some recent theoretical and experimental progress on multiferroic manganites.
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