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Register a new userMagnetoelectric coupling in a ferroelectric/ferromagnetic chain revealed by ferromagnetic resonance
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Understanding the multiferroic coupling is one of the key issues in the feld of multiferroics. As shown here theoretically, the ferromagnetic resonance (FMR) renders possible an access to the magnetoelectric coupling coefficient in composite multiferroics. This we evidence by a detailed analysis and numerical calculations of FMR in an unstrained chain of BaTiO3 in the tetragonal phase in contact with Fe, including the effect of depolarizing field. The spectra of the absorbed power in FMR are found to be sensitive to the orientation of the interface electric polarization and to an applied static electric field. Here we propose a method for measuring the magnetoelectric coupling coefficient by means of FMR.
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The magnetization characteristic in a permalloy thin strip is investigated by electrically measuring the anisotropic magnetoresistance and ferromagnetic resonance in in-plane and out-of-plane configurations. Our results indicate that the magnetization vector can rotate in the film plane as well as out of the film plane by changing the intensity of external magnetic field of certain direction. The magnetization characteristic can be explained by considering demagnetization and magnetic anisotropy. Our method can be used to obtain the demagnetization factor, saturated magnetic moment and the magnetic anisotropy.
Ferromagnetic resonance (FMR) was used to investigate the static and dynamic magnetic properties of carbon-doped Mn5Ge3 (C$_{0.1}$ and C$_{0.2}$) thin films grown on Ge(111). The temperature dependence of magnetic anisotropy shows an increased perpendicular magneto-crystalline contribution at 80K with an in-plane easy axis due to the large shape contribution. We find that our samples show a small FMR linewidth (corresponding to an intrinsic magnetic damping parameter $alpha$=0.005), which is a measure of the spin relaxation and directly related with the magnetic and structural quality of the material. In the perpendicular-to-plane geometry, the FMR linewidth shows a minimum at around 200K for all the samples, which seems to be not correlated to the C-doping. The magnetic relaxation parameters have been determined and indicate the two-magnon scattering as the main extrinsic contribution. We observe a change in the main contribution from scattering centres in Mn5Ge3C0.2 at low temperatures, which could be related to the minimum in linewidth.
Contribution of d-electron to ferroelectricity of type-II multiferroics causes strong magneto-electric coupling and distinguishes them from the conventional type-I multiferroics. However, their therein polarization is too small because the ferroelectricity is merely a derivative from the magnetic order. Here we report a new class of multiferroic materials, monolayer VOX2 (X = Cl, Br, and I), which combine the advantages of type-I and type-II multiferroics. Both ferroelectricity and magnetism arise from the same V cation, where the filled d-orbital is perpendicular to an a priori ferroelectric polarization and thus poses no hindrance to ferroelectricity, indicating a violation of the usual d0 rule. This makes the combination of large polarizations and strong magneto-electric coupling possible. Our findings not only add new ferromagnetic-ferroelectric multiferroics, but also point to a unique mechanism to engineer multiferroics.
The broadband ferromagnetic resonance measurement using the rectifying effect of Ni81Fe19 wire has been investigated. One wire is deposited on the center strip line of the coplanar waveguide (CPW) and the other one deposited between two strip lines of CPW. The method is based on the detection of the magnetoresistance oscillation due to the magnetization dynamics induced by the radio frequency field. The magnetic field dependences of the resonance frequency and the rectification spectrum are presented and analytically interpreted on the standpoint of a uniform magnetization precession model.
The direct magnetoelectric (ME) effect resulting from the polarization changes induced in a ferroelectric film by the application of a magnetic field to a ferromagnetic substrate is described using the nonlinear thermodynamic theory. It is shown that the ME response strongly depends on the initial strain state of the film. The ME polarization coefficient of the heterostructures involving Terfenol-D substrates and compressively strained lead zirconate titanate (PZT) films, which stabilize in the out-of-plane polarization state, is found to be comparable to that of bulk PZT/Terfenol-D laminate composites. At the same time, the ME voltage coefficient reaches a giant value of 50 V/(cm Oe), which greatly exceeds the maximum observed static ME coefficients of bulk composites. This remarkable feature is explained by a favorable combination of considerable strain sensitivity of polarization and a low electric permittivity in compressively strained PZT films. The theory also predicts a further dramatic increase of ME coefficients at the strain-induced transitions between different ferroelectric phases.
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