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Register a new userUnusual ferroelectric and magnetic phases in multiferroic 2H-BaMnO$_3$ ceramics
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The structural phase transition in hexagonal BaMnO$_3$ occurring at $T_c$=130 K was studied in ceramic samples using electron and X-ray diffraction, second harmonic generation as well as by dielectric and lattice dynamic spectroscopies. The low-temperature phase (space group $P6_{3}cm$) is ferroelectric with a triplicated unit cell. The phase transition is driven by an optical soft mode from the Brillouin-zone boundary [$q = (frac{1}{3},frac{1}{3},0)$]; this mode activates in infrared and Raman spectra below $T_c$ and it hardens according to the Cochran law. Upon cooling below $T_c$, the permittivity exhibits an unusual linear increase with temperature; below 60 K, in turn, a frequency-dependent decrease is observed, which can be explained by slowing-down of ferroelectric domain wall motions. Based on our data we could not distinguish whether the high-temperature phase is paraelectric or polar (space groups $P6_{3}/mmc$ or $P6_{3}mc$, respectively). Both variants of the phase transition to the ferroelectric phase are discussed based on the Landau theory. Electron paramagnetic resonance and magnetic susceptibility measurements reveal an onset of one-dimensional antiferromagnetic ordering below $approx220,rm K$ which develops fully near 140 K and, below $T_{n} approx 59,rm K$, it transforms into a three-dimensional antiferromagnetic order.
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Dielectric and magnetic properties of Eu0.5Ba0.25Sr0.25TiO3 are investigated between 10 K and 300 K in the frequency range from 10 Hz to 100 THz. A peak in permittivity revealed near 130 K and observed ferroelectric hysteresis loops prove the ferroelectric order below thistemperature. The peak in permittivity is given mainly by softening of the lowest frequency polar phonon (soft mode revealed in THz and IR spectra) that demonstrates displacive character of the phase transition. Room-temperature X-ray diffraction analysis reveals cubic structure, but the IR reflectivity spectra give evidence of a lower crystal structure, presumably tetragonal I4/mcm with tilted oxygen octahedra as it has been observed in EuTiO3. The magnetic measurements show that the antiferromagnetic order occurs below 1.8 K. Eu0.5Ba0.25Sr0.25TiO3 has three times lower coercive field than Eu0.5Ba0.5TiO3, therefore we propose this system for measurements of electric dipole moment of electron.
Low-energy magnetic excitations of the easy-axis antiferromagnet TbFe$_3$(BO$_3$)$_4$ are investigated by far-infrared absorption and reflection spectroscopy in high magnetic fields up to 30 T. The observed field dependence of the resonance frequencies and the magnetization are reproduced by a mean-field spin model for magnetic fields applied both along and perpendicular to the easy axis. Based on this model we determined the full set of magnetic interactions, including Fe-Fe and Fe-Tb exchange interactions, single-ion anisotropy for Tb ions and $g$-factors, which describe the ground-state spin texture and the low-energy spin excitations of TbFe$_3$(BO$_3$)$_4$. Compared to earlier studies we allow a small canting of the nearly Ising-like Tb moments to achieve a quantitative agreement with the magnetic susceptibility measurements. The additional high energy magnetic resonance lines observed, besides the two resonances expected for a two-sublattice antiferromagnet, suggest a more complex six-sublattice magnetic ground state for TbFe$_3$(BO$_3$)$_4$.
We report the low-temperature coexistence in NdFe3(BO3)4 of an incommensurate magnetic phase with a strained commensurate magnetic phase that is primarily at the surface of the crystal. Increasing the temperature or magnetic field decreases the incommensurability and stabilizes the commensurate magnetic phase above Tic ~14 K or Hic = 0.9 T. A comparison to published studies indicates the onset of longitudinal magnetostriction and electric polarization at the magnetic-field-induced transition, which may arise due to a basal plane spin-flop and canting of the moments along the field direction.
We have investigated the effects of substituting In for Mn on the antiferromagnetic phase transition in YMnO3 using magnetic, dielectric, and specific heat measurements. We prepared a set of isostructural phase pure hexagonal YMn$_{1-x}$In$_{x}$O$_{3}$ samples having x=0 to x=0.9, which exhibit a systematic decrease of the antiferromagnetic ordering temperature with increasing In content. The multiferroic phase, which develops below TN, appears to be completely suppressed for x$geq$0.5 in the temperature range investigated, which can be attributed solely to the dilution of magnetic interactions as the crystal structure remains hexagonal. Similar to previous reports, we find an enhancement of the magnetocapacitive coupling on dilution with non-magnetic ions.
We investigate the crystal structure in multiferroic tetragonal perovskite Sr$_{1/2}$Ba$_{1/2}$MnO$_3$ with high accuracy of the order of 10$^{-3}$ Angstrom for an atomic displacement. The large atomic displacement for Mn ion from the centerosymmetric position, comparable with the off-centering distortion in the tetragonal ferroelectric BaTiO$_3$, is observed in the ferroelectric phase ($T_mathrm{N}$ $leq$ $T$ $leq$ $T_mathrm{C}$). In stark contrast, in the multiferroic phase ($T$ $leq$ $T_mathrm{N}$), the atomic displacement for Mn ion is suppressed, but those for O ions are enlarged. The atomic displacements in the polar crystal structures are also analyzed in terms of the ferroelectric modes. In the ferroelectric phase, the atomic displacements are decomposed into dominant positive Slater, negative Last, and small positive Axe modes. The suppression of Slater and Last modes, the sign change of Last mode, and the enlargement of Axe mode are found in the multiferroic phase. The ferroelectric distortion is well reproduced by a first-principles calculation based on Berry phase method, providing an additional information on competing mechanisms to induce the polarization, electronic $p$-$d$ hybridization vs. magnetic exchange-striction.
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