Specific features of the effect of dopants on the phase formation of YBO3 and ScBO3 during synthesis from the amorphous precursor state

The effect of dopants on the structural states of the YBO₃ and ScBO₃ borates during sequential isothermal annealings of the amorphous precursor state and the batch from a mixture of micropowders of initial rare-earth metal oxides of the same composition has been investigated using X-ray diffraction. It has been demonstrated that, in both cases, the phase sequences of rare-earth metal borates differ substantially from each other. Possible factors responsible for the strong effect of dopants on the structural sequences during the synthesis of the YBO₃ and ScBO₃ borates from the amorphous precursor state have been analyzed.     

In situ electron microscopy investigations of solid-state synthesis in Al/Au thin bilayer films

In situ transmission electron microscopy investigations of solid-state synthesis in Al/Au thin bilayer films are conducted. The samples are heated in the column of a transmission electron microscope. The heating temperature is changed from room temperature to 300°C with a heating rate of up to 120°C min^?1. It is found that solid-phase synthesis starts at ≈100°C. At 140 ± 5°C, two crystal phases, Al₂Au (Fm3m) and AlAu₂ (I4/mmm), are simultaneously observed, while at 235 ± 5°C and higher (up to 300°C) only Al₂Au phase is detected.     

The relation between the electronic and magnetic structures of manganites in the tight-binding approximation

Analytic expressions for the dispersion curves E(k) of RMnO₃ (R=La, Pr, Nd, Sm, and other RE elements) have been obtained in the tight-binding approximation for the main types of magnetic ordering on the Mn sublattice. The first calculation of E(k) taking into account the oxygen subsystem and mutual ordering of the manganese and RE sublattices is reported. The results obtained permit a qualitative interpretation of some features observed in the behavior of the rare-earth manganites. Fiz. Tverd. Tela (St. Petersburg) 41, 2179–2182 (December 1999)     

Spectroscopic study of magnetic phase transitions in Nd<Subscript>x</Subscript>Gd<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Fe<Subscript>3</Subscript>(BO<Subscript>3</Subscript>)<Subscript>4</Subscript>

Magnetic ordering and spin reorientation in iron borates Nd_xGd_1?xFe₃(BO₃)₄ (x = 0.01, 0.04, 0.25, 1.0) are studied using a rare-earth spectroscopic probe.     

Magnetostriction in the rare-earth ferroborates RFe3(BO3)4, R=Pr and Tb

Recent experimental data for magnetostriction in the rare-earth (RE) ferroborates RFe₃(BO₃)₄ with R=Pr and Tb are discussed from a theoretical point of view. Multipole moments of RE ions are calculated in the framework of a crystal-field model for the RE ion and the molecular-field approximation. Quadrupole approximation is shown to be sufficient for interpretation of data for longitudinal magnetostriction at the magnetic field along the trigonal axis. Parameters of PrFe₃(BO₃)₄ are deduced when accounting for the experimental magnetization curves that manifest a spin-flop transition.     

Study of Automatic Transmission Fluid in a Serpentine Minichannel Heat Exchanger: An Experimental Approach

An experimental investigation was conducted on automatic transmission fluid cooling in a minichannel heat exchanger using a closed-loop integrated thermal wind tunnel test facility. Effects of automatic transmission fluid Reynolds number (Re_L) on heat transfer coefficient and Nusselt number were examined within the Re_L of 3–30 for air-flow Re of 1,450–5,200. Effects of serpentine on heat transfer enhancement and flow characteristics were evaluated through Dean number analysis. The analysis of Eckert number and Brinkman number showed a contribution to the viscous heating even for a low Re_L in the minichannel. The study showed enhanced heat transfer characterizations of the multi-port minichannel heat exchanger.     

Synthesis,Characterization, and Antibacterial Activity of RE(III) Complexes with L-Isoleucine and 1,10-Phenanthroline

Six new ternary rare-earth (La, Eu, Sm, Nd, Y, Yb) complexes with L-isoleucine and 1,10-phenanthroline have been synthesized. Their compositions were characterized as RE(Ile)₃PhenCl₃ · 4H₂O (RE = La, Eu, Sm, Nd, Y, Yb; Ile = L-isoleucine; phen = 1,10-phenanthroline) by elemental analysis, EDTA titration, molar conductance measurement, UV spectra, FT-IR spectra, and TG-DTA. The average diameters of growth inhibition area and the minimal inhibitory concentration (MIC) of the complexes were studied by disc diffusion method and dilution method in nutrient broth. The results showed that the ternary rare-earth complexes strongly exhibited the antibacterial activity against Escherichia coli and Staphylococcus aureus and that their antibacterial effects were better than those of rare-earth chlorides, L-isoleucine, and 1,10-phenanthroline.     

Ultrahigh pressure equation of state of tantalum to 310 GPa

ABSTRACT

The isothermal compression of transition metal tantalum (Ta) was studied in a diamond anvil cell by X-ray diffraction utilizing rhenium (Re) and gold (Au) as internal X-ray pressure standards. The Re pressure marker was employed during non-hydrostatic compression to pressures up to 310?GPa while the Au pressure marker was used during quasi-hydrostatic compression in a neon pressure-transmitting medium to 80?GPa. Two ultra-high pressure experiments were conducted on Ta and Re mixtures utilizing focused-ion beam machined toroidal diamond anvils with central flats varying from 8 microns to 16 microns in diameter. The Ta metal was observed to be stable in the body-centered-cubic phase to a volume compression V/V₀?=?0.581. The measured equations of state (EOS) of Ta using two different calibrations of the Re pressure marker are compared with the ambient temperature isotherm derived from shock compression data. We provide a detailed analysis of EOS fit parameters for Ta under quasi-hydrostatic and non-hydrostatic conditions.     

Fine sructure of Na5Lu9F32 nanocrystallites formed at the initial stages of crystallization

X-ray diffraction investigations have demonstrated that the initial stages of the formation and growth of Na₅Lu₉F₃₂ nanocrystallites from a powder mixture of lutetium fluoride, ammonium fluoride, and sodium fluoride during the solid-phase synthesis are accompanied by complex structural transformations, among which a cyclic transformation of the type single-phase → two-phase → single-phase state can be distinguished. It is shown that the two-phase state consists of two isomorphous phases with a small misfit of the lattice parameters. The isomorphous phases have common extended interphase boundaries, along which a continuous change of the lattice parameters occurs as one phase transforms into the other. A long-term annealing of the two-phase state leads to the final single-phase state, which is characterized by the growth of nanocrystallites to the scale of microcrystallites.     

GdFeCo磁光薄膜中RE-TM反铁磁耦合与激光感应超快磁化翻转动力学研究

使用飞秒时间分辨抽运-探测磁光克尔光谱技术,研究了激光加热GdFeCo磁光薄膜跨越铁磁补偿温度时稀土-过渡金属(RE-TM)反铁磁交换耦合行为和超快磁化翻转动力学. 实验观察到由于跨越铁磁补偿温度、净磁矩携带者交换而引起的磁化翻转反常克尔磁滞回线以及在同向外磁场下,反常回线上大于和小于矫顽力部分的饱和磁化强度不同,显示出GdFeCo中RE与TM之间的非完全刚性反铁磁耦合. 在含有Al导热底层的GdFeCo薄膜上观测到饱和磁场下激光感应磁化态翻转及再恢复的完整超快动力学过程. 与剩磁态的激光感应超快退磁化过 关键词： 补偿温度 磁化翻转 反铁磁耦合 GdFeCo     

Magneto-optical Faraday and Kerr effect of orthoferrite thin films at high temperatures

Orthoferrites present, as bulk materials, reorientation transitions of their magnetic moment alignment at temperatures depending on the rare-earth (RE) ion. In particular, orthoferrites (REFeO₃) with RE = Sm, Dy, present this transition at T _SRT = 443 K and 36 K, respectively. The spectra of the complex Kerr and Faraday angle have been measured on orthoferrite thin films (RE = Sm, Dy, Y), which were prepared by pulsed laser deposition on amorphous quartz substrates. The obtained spectra exhibit contributions of both surfaces and interfaces. Propagation effects of the polarized light in the magneto-optical medium which is interpreted in terms of a simplified theoretical formalism, is also observed. For selected photon energies, temperature dependent Faraday rotation measurements, , on orthoferrite thin films (RE = Sm, Dy, Y) have been performed. A quite different thermal variation compared to the bulk magnetization has been observed. Curie temperatures are found to be close to the bulk values or slightly larger by 10 K to 20 K as in the case of DyFeO₃ and YFeO₃. For RE = Sm and Dy, increases with increasing temperature contrary to the saturation magnetization, passes through a maximum at about 460 K and vanishes with a T _C of 647±18 K, 695 K for RE = Sm and Dy respectively. Received 28 July 2000     

Divalent rare-earth ions Pr,Sm, Нo,Er, Tm,and Yb in crystals of alkaline-earth fluorides

The absorption spectra of radiation-colored CaF₂, SrF₂, and BaF₂ crystals activated by trivalent Pr, Sm, Нo, Er, Tm, and Yb (rare-earth, RE) ions are studied. It is shown that ionizing radiation reduces the impurity ions to the divalent state. The temperature resistance of divalent RE ions of radiation-colored CaF₂ crystals correlates with the chemical stability of the compounds with divalent RE ions. The photochromic centers are produced in CaF₂-Pr crystal colored by radiation at room temperature and heated to 200°C.     

Magnetic studies of rare-earth tungstates

Measurement of magnetic susceptibility (χ_m) of rare-earth tungstates RE₂(WO₄)₃ with RE = Gd, Tb, Dy, Ho, Er, Tm and Yb have been reported in the temperature range 3–300 K at a magnetic field of 3.2 × 10⁵ Am^-1. All the tungstates are found to be ferrimagnetic with a ferrimagnetic Curie-temperature lying in the range 15–27 K. Evaluated magneton numbers agree fairly well with free tripositive rare-earth ions. The results are discussed on the basis of a new proposed model. Except for Tb all the evaluated parameters have systematic variation over the entire rare-earth series.     

Fluoreszenzlebensdauern einiger wasserhaltiger Salze des Europiums und des Terbiums

At 300°K the fluorescent lifetimes of the levels⁵D₀ of Eu³⁺ and⁵D₄ of Tb³⁺ were measured in the RE(C₂H₅SO₄)₃·9H₂O, RE(BrO₃)₃·9H₂O, RECl₃·6H₂O, RE(NO₃)₃·6H₂O and (RE)₂(SO₄)₃·8H₂O. The fluorescent lifetimes of the above mentioned hydrated crystals are preliminary determined by radiationless transitions. An empirical relation can be obtained for the probabilityw for the radiationless transitions of the formw=const·α _RE·α _Lattice. The factorsα _RE andα _Lattice depend only on the rare-earth ion or the lattice respectively. A structure of the interaction Hamiltonian between the rare-earth ion and the lattice is proposed, which leads to the empirically found relation. The influence of electron- andX-irradiation on the lifetime of the level⁵D₄ in TbCl₃·6H₂O was investigated at 77°K. A decrease of the lifetime and a nonexponential decay of the fluorescence were found. By heating up the crystal to room temperature thermoluminescence and annealing of the irradiation defects are observed.     

Crystal fields of hexameric rare-earth clusters in fluorites

In solid solutions of alkaline-and rare-earth fluorides with a fluorite structure, ions of most elements of the rare-earth (RE) row form hexameric clusters that assimilate the minor component of the solid solutions (fluorine) and build it into the cubic fluorite lattice without changing its shape. An analysis of the EPR spectra of paramagnetic RE ions (Er³⁺, Tm³⁺, Yb³⁺) in clusters of diamagnetic ions (Lu³⁺, Y³⁺) confirms their hexagonal structure, which was established when studying the superstructures of the compounds under study. In such a cluster, a RE ion is in a nearly tetragonal crystal field, with the parameters of this field differing radically from those of single cubic and tetragonal RE centers in crystals with a fluorite structure. In particular, this field causes high (close to limiting) values of the g_∥ factors of the ground states of the paramagnetic RE ions. Computer simulation is used to determine the atomic structure of a hexameric cluster in MF₂ crystals (M = Ca, Sr, Ba). The crystal field and energy spectrum of Er³⁺, Tm³⁺, and Yb³⁺ ions in such clusters are calculated, and the spectroscopic parameters of the ground states of these ions are determined. The calculations confirm the earlier assumption that the unusual EPR spectra of nonstoichiometric fluorite phases are related to RE ions in hexameric clusters.     

Features of the doping effect on YAlO3 phase sequences during synthesis from an amorphous precursor state

Using X-ray diffraction methods, it has been shown that small lanthanum (La) dopants during solid-phase synthesis of YAlO₃ from an amorphous precursor state initiate the formation of the high-temperature hexagonal modification of yttrium aluminate in the first crystallization stages, whereas the equilibrium perovskite phase has an orthorhombic cell. At the same time, during YAlO₃ synthesis without dopants, yttrium-aluminum garnet Y₃Al₅O₁₂ is formed in the first crystallization stages, rather than the perovskite modification, as it follows from the precursor stoichiometry. The effect of lanthanum dopants on YAlO₃ phase sequences during synthesis from the amorphous precursor state is qualitatively explained.     

NMR studies of singlet-ground-state rare-earth ions in high-T c superconductors

Many of presently known high-T _c superconductors contain rare-earth (RE) ions with an even number of electrons in an unfilled 4f-shell (Pr³⁺, Tb³⁺, Ho³⁺, Tm³⁺). If the ground state of 4f-electrons is non-degenerate and separated from excited states by high enough energy intervals, one can observe the so-called “enhanced NMR” of RE nuclei at low temperatures. In the present paper some aspects of the enhanced NMR are analyzed in applications to the crystal and electron structure of high-T _c superconductors.     

Synthesis under ambient pressure and tri-axial magnetic orientation in REBa2Cu4O8 (RE = Y,Sm, Eu,Gd, Dy,Ho, Er)

We report the rare-earth (RE)-dependent magnetization axes of REBa₂Cu₄O₈, which was synthesized by a flux method under ambient pressure, using powder samples tri-axially oriented in a modulated rotating magnetic field of 10 T. By optimizing the growth temperature and cooling rate, RE124 crystals were successfully grown for RE = Y, Sm, Eu, Gd, Dy, Ho, and Er. From the X-ray diffraction measurement, the magnetically oriented directions were largely dependent on the type of RE ions of RE124. However, the tri-axial magnetic anisotropies of RE124 could be qualitatively understood in terms of the magnitude relation between the single-ion magnetic anisotropy of RE³⁺ ions and the magnetic anisotropy generated by the CuO₂ plane and Cu–O chain. For the practical use of this magneto-scientific process, the control of magnetization axes and tri-axial magnetic anisotropies through crystallochemical control is indispensable.     

On the prospects for technical applications of BiFeO<Subscript>3</Subscript> compounds substituted with rare-earth elements

Solid solutions of Bi_1-x Re _x FeO₃ (Re=La, Nd; x=0-0.2) compounds were synthesized, and their room-temperature magnetoelectric and magnetodielectric properties were studied. Amplification of magnetoelectric and magnetodielectric effects with increasing the rare-earth doping level was detected in the concentration range x under study. The results obtained confirm the prospects for applications of bismuth ferrite-based compounds as magnetoelectric converters and magnetic field sensors.     

Magnetic properties of rare earth iron borates: Spectroscopic investigation by the method of rare earth probe

The magnetic phase transitions and magnetic structures in RFe₃(BO₃)₄ (R = Y, Gd-Er) iron borates have been investigated by the method of erbium spectroscopic probe. The magnetic ordering temperatures have been determined. On the basis of the comparison of the character of splitting of the spectral lines of the probe Er³⁺ ion in RFe₃(BO₃)₄(R = Y, Dy-Er) iron borates and in GdFe₃(BO₃)₄, a complicated whose magnetic structure is known, a conclusion is drawn about the orientation of the magnetic moments of iron: in dysprosium and terbium iron borates, an easy-axis magnetic structure is implemented, whereas an easy-plane structure occurs in holmium, erbium, and yttrium iron borates.