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Register a new userSimulations of magnetic and magnetoelastic properties of Tb2Ti2O7 in paramagnetic phase
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Magnetic and magnetoelastic properties of terbium titanate pyrochlore in paramagnetic phase are simulated. The magnetic field and temperature dependences of magnetization and forced magnetostriction in Tb2Ti2O7 single crystals and polycrystalline samples are calculated in the framework of exchange charge model of crystal field theory and a mean field approximation. The set of electron-deformation coupling constants has been determined. Variations of elastic constants with temperature and applied magnetic field are discussed. Additional strong softening of the crystal lattice at liquid helium temperatures in the magnetic field directed along the rhombic symmetry axis is predicted.
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In terms of a semi-phenomenological exchange charge model, we have obtained estimates of parameters of the crystal field and parameters of the electron-deformation interaction in terbium titanate Tb2Ti2O7 with a pyrochlore structure. The obtained set of parameters has been refined based on the analysis of spectra of neutron inelastic scattering and Raman light scattering, field dependences of the forced magnetostriction, and temperature dependences of elastic constants.
Recent experimental results have emphasized two aspects of Tb2Ti2O7 which have not been taken into account in previous attempts to construct theories of Tb2Ti2O7: the role of small levels of structural disorder, which appears to control the formation of a long-range ordered state of as yet unknown nature; and the importance of strong coupling between spin and lattice degrees of freedom, which results in the hybridization of crystal field excitons and transverse acoustic phonons. In this work we examine the juncture of these two phenomena and show that samples with strongly contrasting behavior vis-a-vis the structural disorder (i.e. with and without the transition to the ordered state), develop identical magnetoelastic coupling. We also show that the comparison between single crystal and powder samples is more complicated than previously thought - the correlation between lattice parameter (as a measure of superstoichiometric Tb$^{3+}$) and the existence of a specific heat peak, as observed in powder samples, does not hold for single crystals.
High-quality single crystals of CoTiO$_3$ are grown and used to elucidate in detail structural and magnetostructural effects by means of high-resolution capacitance dilatometry studies in fields up to 15 T which are complemented by specific heat and magnetization measurements. In addition, we refine the single-crystal structure of the ilmenite ($Rbar{3}$) phase. At the antiferromagnetic ordering temperature $T_mathrm{N}$, pronounced $lambda$-shaped anomaly in the thermal expansion coefficients signals shrinking of both the $c$ and $b$ axes, indicating strong magnetoelastic coupling with uniaxial pressure along $c$ yielding six times larger effect on $T_mathrm{N}$ than the pressure applied in-plane. The hydrostatic pressure dependency derived by means of Gruneisen analysis amounts to $partial T_mathrm{N}/ partial papprox 2.7(4)$~K/GPa. The high-field magnetization studies in static and pulsed magnetic fields up to 60~T along with high-field thermal expansion measurements facilitate in constructing the complete anisotropic magnetic phase diagram of CoTiO$_3$. While the results confirm the presence of significant magnetodielectric coupling, our data show that magnetism drives the observed structural, dielectric, and magnetic changes both in the short-range ordered regime well-above $T_mathrm{N}$ as well as in the long-range magnetically ordered phase.
We carried out detailed studies of the magnetic structure, magnetoelastic coupling, and thermal properties of EuCrO$_3$ nano-powders from room temperature to liquid helium temperature. Our neutron powder diffraction and X-ray powder diffraction measurements provide precise atomic positions of all atoms in the cell, especially for the light oxygen atoms. The low-temperature neutron powder diffraction data revealed extra Bragg peaks of magnetic origin which can be attributed to a $G_x$ antiferromagnetic structure with an ordered moment of $sim$ 2.4 $mu_{rm B}$ consistent with the $3d^3$ electronic configuration of the Cr$^{3+}$ cations. Apart from previously reported antiferromagnetic and ferromagnetic transitions in EuCrO$_3$ at low temperatures, we also observed an anomaly at about 100 K. This anomaly was observed in temperature dependence of samples, lattice parameters, thermal expansion, Raman spectroscopy, permittivity and conductance measurements. This anomaly is attributed to the magnetoelastic distortion in the EuCrO$_3$ crystal.
The series of intermetallic compounds $R$NiSi$_3$ ($R$ = rare earth) shows interesting magnetic properties evolving with $R$ and metamagnetic transitions under applied magnetic field for some of the compounds. The microscopic magnetic structures must be determined to rationalize such rich behavior. Here, resonant x-ray magnetic diffraction experiments are performed on single crystals of GdNiSi$_{3}$ and TbNiSi$_{3}$ at zero field. The primitive magnetic unit cell matches the chemical cell below the Neel temperatures $T_{N}$ = 22.2 and 33.2 K, respectively. The magnetic structure is determined to be the same for both compounds (magnetic space group $Cmmm$). It features ferromagnetic {it ac} planes that are stacked in an antiferromagnetic $+-+-$ pattern, with the rare-earth magnetic moments pointing along the $vec{a}$ direction, which contrasts with the $+--+$ stacking and moment direction along the $vec{b}$ axis previously reported for YbNiSi$_3$. This indicates a sign reversal of the coupling constant between second-neighbor $R$ planes as $R$ is varied from Gd and Tb to Yb. The long {it b} lattice parameter of GdNiSi$_{3}$ and TbNiSi$_{3}$ shows a magnetoelastic expansion upon cooling below $T_N$, pointing to the conclusion that the $+-+-$ stacking is stabilized under lattice expansion. A competition between distinct magnetic stacking patterns with similar exchange energies tuned by the size of $R$ sets the stage for the magnetic ground state instability observed along this series.
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