arXiv subjects

L. N. Bezmaternykh

Publications and source records attributed to L. N. Bezmaternykh.

25 records · Page 2Linked to original sources

arXiv2010

Magnetoelectricity and Magnetostriction due to the Rare Earth Moment in TmAl$_3$(BO$_3$)$_4$

The magnetic properties, the magnetostriction, and the magnetoelectric effect in the d-electron free rare-earth aluminum borate TmAl$_3$(BO$_3$)$_4$ are investigated between room temperature and 2 K. The magnetic susceptibility reveals a strong anisotropy with the hexagonal c-axis as the hard magnetic axis. Magnetostriction measurements show a large effect of an in-plane field reducing both, the a- and c-axis lattice parameters. The magnetoelectric polarization change in a- and c-directions reaches up to 300 $μ$C/m$^2$ at 70 kOe with the field applied along the a-axis. The magnetoelectric polarization is proportional to the lattice contraction in magnetic field. The results of this investigation prove the existence of a significant coupling between the rare earth magnetic moment and the lattice in $R$Al$_3$(BO$_3$)$_4$ compounds ($R$ = rare earth). They further show that the rare earth moment itself will generate a large magnetoelectric effect which makes it easier to study and to understand the origin of the magnetoelectric interaction in this class of materials.

cond-mat.str-el↗

arXiv2009

Magnetoelectric Effect and Spontaneous Polarization in HoFe$_3$(BO$_3$)$_4$ and Ho$_{0.5}$Nd$_{0.5}$Fe$_3$(BO$_3$)$_4$

The thermodynamic, magnetic, dielectric, and magnetoelectric properties of HoFe$_3$(BO$_3$)$_4$ and Ho$_{0.5}$Nd$_{0.5}$Fe$_3$(BO$_3$)$_4$ are investigated. Both compounds show a second order Neél transition above 30 K and a first order spin reorientation transition below 10 K. HoFe$_3$(BO$_3$)$_4$ develops a spontaneous electrical polarization below the Neél temperature (T$_N$) which is diminished in external magnetic fields. No magnetoelectric effect could be observed in HoFe$_3$(BO$_3$)$_4$. In contrast, the solid solution Ho$_{0.5}$Nd$_{0.5}$Fe$_3$(BO$_3$)$_4$ exhibits both, a spontaneous polarization below T$_N$ and a magnetoelectric effect at higher fields that extends to high temperatures. The superposition of spontaneous polarization, induced by the internal magnetic field in the ordered state, and the magnetoelectric polarizations due to the external field results in a complex behavior of the total polarization measured as a function of temperature and field.

cond-mat.str-el↗

arXiv2007

Magnetization and specific heat of TbFe3(BO3)4: Experiment and crystal field calculations

We have studied the thermodynamic properties of single-crystalline TbFe3(BO3)4. Magnetization measurements have been carried out as a function of magnetic field (up to 50 T) and temperature up to 350K with the magnetic field both parallel and perpendicular to the trigonal c-axis of the crystal. The specific heat has been measured in the temperature range 2-300K with a magnetic field up to 9 T applied parallel to the c-axis. The data indicate a structural phase transition at 192 K and antiferromagnetic spin ordering at 40 K. A Schottky anomaly is present in the specific heat data around 20 K, arising due to two low-lying energy levels of the Tb3+ ions being split by f-d coupling. Below TN magnetic fields parallel to the c-axis drive a spin-flop phase transition, which is associated with a large magnetization jump. The highly anisotropic character of the magnetic susceptibility is ascribed mainly to the Ising-like behavior of the Tb3+ ions in the trigonal crystal field. We describe our results in the framework of an unified approach which is based on mean-field approximation and crystal-field calculations.

cond-mat.other↗

arXiv2007

Optical spectra, crystal-field parameters, and magnetic susceptibility of the new multiferroic NdFe3(BO3)4

We report high-resolution optical absorption spectra for NdFe3(BO3)4 trigonal single crystal which is known to exhibit a giant magnetoelectric effect below the temperature of magnetic ordering TN = 33 K. The analysis of the temperature-dependent polarized spectra reveals the energies and, in some cases, symmetries and exchange splittings of Nd3+ 84 Kramers doublets. We perform crystal-field calculations starting from the exchange-charge model, obtain a set of six real crystal-field parameters, and calculate wave functions and magnetic g-factors. In particular, the values g(perpendicular) = 2.385, g(parallel) = 1.376 were found for the Nd3+ ground-state doublet. We obtain Bloc=7.88 T and |JFN|= 0.48 K for the values of the local effective magnetic field at liquid helium temperatures at the Nd3+ site and the Nd - Fe exchange integral, respectively, using the experimentally measured Nd3+ ground-state splitting of 8.8 cm-1. To check reliability of our set of crystal field parameters we model the magnetic susceptibility data from literature. A dimer containing two nearest-neighbor iron ions in the spiral chain is considered to partly account for quasi-one-dimensional properties of iron borates, and then the mean-field approximation is used. The results of calculations with the exchange parameters for Fe3+ ions Jnn = -6.25 K (intra-chain interactions) and Jnnn = -1.92 K (inter-chain interactions) obtained from fitting agree well with the experimental data.

cond-mat.str-el↗

arXiv2006

Magnetic Magnetoelectric and Magnetoelastic Properties of new multiferroic material NdFe3(BO3)4

Complex experimental and theoretical study of the magnetic, magnetoelectric, and magnetoelastic properties of neodymium iron borate NdFe3(BO3)4 along various crystallographic directions have been carried out in strong pulsed magnetic fields up to 230 kOe in a temperature range of 4.2-50 K. It has been found that neodymium iron borate, as well as gadolinium iron borate, is a multiferroic. It has much larger (above 3 10^(-4) C/m^2) electric polarization controlled by the magnetic field and giant quadratic magnetoelectric effect. The exchange field between the rare-earth and iron subsystems (~50 kOe) has been determined for the first time from experimental data. The theoretical analysis based on the magnetic symmetry and quantum properties of the Nd ion in the crystal provides an explanation of an unusual behavior of the magnetoelectric and magnetoelastic properties of neodymium iron borate in strong magnetic fields and correlation observed between them.

cond-mat.mtrl-sci↗

arXiv2006

Magnetic Field Effect and Dielectric Anomalies at the Spin Reorientation Phase Transition of GdFe3(BO3)4

GdFe3(BO3)4 exhibits a structural phase transition at 156 K, antiferromagnetic order of the Fe3+ moments at 36 K followed by a spin reorientation phase transition at 9 K. The reorientation phase transition is studied through dielectric, magnetic and heat capacity measurements under the application of external magnetic fields of up to 7 kOe. The dielectric constant indicates the existence of two distinct anomalies at T_SR = 9 K that separate in temperature under external magnetic fields. The spin rotation phase transition is proven to be of the first-order nature through the magnetic analogue of the Clausius-Clapeyron equation. Magneto-dielectric effect of up to 1% is observed at 8 K and 7 kOe. The uniaxial magnetocaloric effect along the c axis is observed below the spin reorientation phase transition of 9 K.

cond-mat.str-el↗

arXiv2005

Evidence for differentiation in the iron-helicoidal-chain in GdFe$_{3}$(BO$_{3}$)$_{4}$

We report on a single-crystal X-ray structure study of $GdFe_{3}(BO_{3})_{4}$ at room temperature and at T=90 K. At room temperature $GdFe_{3}(BO_{3})_{4}$ crystallizes in a trigonal space group R32 (No. 155), the same as found for other members of iron-borate family $RFe_{3}(BO_{3})_{4}$. At 90 K the structure of $GdFe_{3}(BO_{3})_{4}$ has transformed to the space group $P3_{1}2_{1}$ (No. 152). The low-temperature structure determination gives new insight into the weakly first-order structural phase transition at 156 K and into the related Raman phonon anomalies. The discovery of two inequivalent iron chains in the low temperature structure provide new point of view on the low-temperature magnetic properties.

cond-mat.str-el↗