Stabilization of E-type antiferromagnetic ordering in La and Y substituted orthorhombic LuMnO3: A first-principles study

We carry out first principles density functional theory calculations of non-lone pairs, namely, La and Y substituted orthorhombic LuMnO₃, to verify the generality of symmetry breaking effects observed in the lone pair cations substituted orthorhombic rare earth manganites. Our calculations revealed that similar to lone pair cations ordering at the A-site of LuMnO₃, non-lone pair cations ordering also results in the lowering of the symmetry thereby proving that the symmetry breaking with A-site ordering is a generic effect. Interestingly, we were able to stabilize the large radius La substituted LuMnO₃ into an E-type antiferromagnetic (E-AFM) phase, in contrast to the normally expected A-type antiferromagnetic (A-AFM) phase of large radius rare earth manganites such as LaMnO₃.     

Synthesis and structural determination of the new oxide fluoride BaFeO2F

Low temperature fluorination of BaFeO_3−x using poly(vinylidene fluoride) leads to the formation of the oxide fluoride BaFeO₂F. Mössbauer spectroscopy shows that this phase exhibits magnetic ordering at room temperature due to interactions between the Fe³⁺ ions, with an ordering temperature of 645 (±5) K. Neutron diffraction studies show that the phase has cubic symmetry and confirm the presence of magnetic ordering (G-type antiferromagnetic) at room temperature.     

Magnetic ordering temperatures in rare earth metal dysprosium under ultrahigh pressures

Magnetic ordering temperatures in heavy rare earth metal dysprosium (Dy) have been studied using an ultrasensitive electrical transport measurement technique in a designer diamond anvil cell to a pressure of 69 GPa and a temperature of 10 K. Previous studies using magnetic susceptibility measurements at high pressures were able to track magnetic ordering temperature only till 7 GPa in the hexagonal close packed (hcp) phase of Dy. Our studies indicate that the magnetic ordering temperature shows an abrupt drop of 80 K at the hcp-Sm phase transition followed by a gradual decrease that continues till 17 GPa. This is followed by a rapid increase in the magnetic ordering temperatures in the double hcp phase and finally leveling off in the distorted face centered cubic phase of Dy. Our studies reaffirm that 4f-shell remains localized in Dy and there is no loss of magnetic moment or 4f-shell delocalization for pressures up to 69 GPa.     

Magnetic dimensionality of Y(2−x)DyxBaCuO5

In this communication, we report the effect that doping Y₂BaCuO₅ with Dy has on its two-dimensional (2D) magnetic structure. Pure samples at both ends of the series, as well as samples doped with 1, 5, 10 and 25% dysprosium, have been characterised using X-ray diffraction, and AC susceptibility together with neutron diffraction studies on the 1 and 5% samples, which were used to measure the magnetic ordering at low temperatures. The results show that 1% Dy is enough to disrupt the 2D magnetic ordering turning it into a 3D array. The low dysprosium concentration indicates that the 3D ordering is achieved without the existence of a rare earth magnetic sublattice. The change in the ordering temperature from 27 K for the pure Y₂BaCuO₅ to 16 K for the 1 and 5% Dy compounds, together with the parameters from the AC susceptibility fittings, reveal that the effect of the Dy doping affects the electronic structure of the Cu ions that become involved in the superexchange pathways. The discrepancy between the parameters obtained by the Curie-Weiss fittings of the real part of the AC susceptibility and the neutron diffraction results, shows that the exchange mechanism deviates from the mean field model for all dysprosium concentrations.     

Magnetic properties of R3Rh2 compounds with R=Gd, Tb,Dy, Ho and Er

Bulk magnetic measurements performed on polycrystalline samples of the tetragonal compounds R₃Rh₂ with R=Gd, Tb, Dy, Ho and Er are presented. All the compounds are ferromagnetic at low temperature. However in Tb₃Rh₂ an antiferromagnetic behaviour is observed between 14 and 24 K. In Gd₃Rh₂, where the magnetocrystalline anisotropy must be negligible, it seems that the magnetic structure is not collinear. In the other compounds the observed properties essentially result from indirect exchange interactions and crystal field effects acting on the rare earth ions which lie in low symmetry sites.     

Magnetic interactions in Pr1−xTbxMn2Ge2

The magnetic moments in the rare earth and Mn sublattices of RMn₂Ge₂, where R is a rare earth element, feature a variety of ordering configurations. In PrMn₂Ge₂ and TbMn₂Ge₂, the interlayer magnetic coupling in the Mn sublattice is, respectively, ferromagnetic and antiferromagnetic below about 350 K. At low temperatures, the rare earth sublattice also orders and reconfigures the ordering in the Mn sublattice. In this study, we investigate the variations in the magnetic properties of Pr_1−xTb_xMn₂Ge₂ as a function of rare earth concentration by examining the evolution of the features in the temperature dependence of the magnetization. The results of earlier neutron diffraction and Mössbauer studies on samples with x=0 and 1 are also used for interpreting the magnetization data and to give an account of the competing effects between various magnetic structures in the Mn and rare earth sublattices. The results are summarized in the Pr_1−xTb_xMn₂Ge₂ magnetic phase diagram.     

Paramagnetic properties of cubic RbSm3F10 and KHo3F10

The title compounds crystallize in the cubic KY₃F₁₀ structure, with the rare earth ion occupying a site of tetragonal symmetry. Paramagnetic susceptibilities are compared with predictions based on experimental crystal field parameters, down to temperatures of ∼10 mK.     

Magnetic properties of RNi2Si2 compounds (R= rre earth)

We report an extensive study of the magnetic properties of tetragonal RNi₂Si₂ compounds (R=Pr, Nd, Gd, Tb, Dy, Ho, Er, Tm), through resistivity, neutron diffraction, susceptibility and magnetization experiments. All compounds exhibit complex incommensurate antiferromagnetic structures, while a transition occurs in TbNi₂Si₂ between a modulated phase and a simple antiferromagnetic structure, stable at low temperature. The magnitude of the bilinear exchange interactions deviates from the Gennes law and the direction of the ordered magnetic moments presents anomalies across the series, including the probable existence of other types of interactions between the rare earth ions.     

A comparative Raman study of 0.65(PbMg<Subscript>1/3</Subscript>Nb<Subscript>2/3</Subscript>O<Subscript>3</Subscript>) -0.35(PbTiO<Subscript>3</Subscript>) single crystal and thin film

We report a comparative Raman study of 0.65(PbMg_1/3Nb_2/3O₃)-0.35(PbTiO₃) (PMN-0.35PT) single crystal and thin film. Raman spectra investigation indicates a change in bulk from the high temperature cubic to the tetragonal phase and then to the low temperature Mc monoclinic phase. The transition temperatures are in good agreement with the ones previously observed by dielectric measurements on the same sample. In contrast, we observe no phase transition to the monoclinic phase in the PMN-0.35PT 4000 Å thick film and only a cubic to tetragonal diffuse transition has been determined at high temperature. The enhanced stability of the tetragonal phase and the absence of low temperature monoclinic phase have been attributed to the in plane strain.     

Structural and magnetic phase transitions in rare-earth-cadmium equiatomic compounds

The tendency to structural instability and the nature of the magnetic ordering are investigated in all the cubic rare-earth-cadmium equiatomic compounds from measurements of resistivity and magnetic susceptibility. The CsCl-type structure is stable at room temperature in all the compounds. However, LaCd exhibits a lattice change at 61 K, while CeCd and PrCd undergo two transitions at 107 and 216 K, and 125 and 190 K, respectively. The low-temperature phases are unknown, but seem to have a symmetry lower than tetragonal. Other compounds are cubic at least in their paramagnetic phase. In connection with the change in the lattice symmetry, a change of the magnetic ordering is observed from ferromagnetism towards antiferromagnetism. Among the heavy rare-earth compounds, cubic thus ferromagnetic, DyCd plays a peculiar role since it undergoes a structural transition in its ordered range, the magnetoelastically stressed lattice becoming unstable again. The strength of bilinear interactions and the occurrence of quadrupolar pair coupling are then discussed.     

Jahn-Teller distortion and magnetoresistance in electron doped Sr1-xCexMnO3 (x = 0.1, 0.2, 0.3 and 0.4)

Neutron and electron diffraction, electrical transport and magnetic measurements have been carried out on a newly synthesized electron doped Sr_1-xCe _x MnO₃ (x = 0.1, 0.2, 0.3 and 0.4) system. For x=0.1, while cooling, it undergoes a first-order metal-insulator transition at 315 K which is associated with a structural transition from cubic (Pm3m) to tetragonal (I4/mcm) due to Jahn-Teller ordering () which stabilizes a chain like (C-type) antiferromagnetic ground state with . The antiferromagnetic insulator state is insensitive to an applied magnetic field of 7 T. With increase of x, while the nuclear structure at room temperature for x=0.2 and 0.3 remains tetragonal, for x=0.4 it becomes orthorhombic (Imma) where the doping electrons seem to occupy mainly the d _x2-y2 symmetry. Further, the JT distortion and the antiferromagnetic interactions decrease with doping and a small negative magnetoresistance appears for . Magnetic measurements show that the dilution of antiferromagnetic interaction results into a spin glass like behaviour at low temperature for the samples with x=0.3 and 0.4. This behaviour is in contrast with the CMR properties of calcium based electron doped systems and hole doped manganites. The stability of C-type antiferromagnetic ordering in the electron doped system with large A-site cationic size may be responsible for the absence of double exchange ferromagnetism and CMR effect. Received 10 September 1999     

Phase transitions in the ferromagnetic alloys Ni2+x Mn1−x Ga

The phase diagram of the cubic ferromagnetic shape-memory alloy Ni_2+x Mn_1−x Ga is constructed theoretically for the case when the Curie temperature is close to the structural transition temperature. This diagram agrees well with the experimental data obtained from resistance and magnetic susceptibility measurements. It is shown that the transition from the paramagnetic cubic phase to the ferromagnetic tetragonal phase can be second-order or first-order. Pis’ma Zh. éksp. Teor. Fiz. 67, No. 3, 212–216 (10 February 1998)     

Magnetic behavior of Dy3+ Ion in Dy2(SeO4)3 · 8H2O. Experimental and theoretical study including the effects of J-J mixing

Single crystals of dysprosium selenate octahydrate were grown and magnetic measurements carried out on the principal anisotropies and the principal susceptibility χ₁ at room temperature and their thermal variation down to 90 K. The magnetic moment is found to be slightly lower than the free-ion value, although the anisotropy is quite high. The variation of the average moment with temperature is very small and a least squares fit to a Curie-Weiss law yielded ?0.97 K as the paramagnetic Curie temperature. An analysis of the data was undertaken on the basis of interaction of the rare earth ion with its immediate neighbors. A crystal field (CF) of tetragonal symmetry which is the approximate site symmetry of the RE³⁺ ion, gave an excellent simulation of the observed behavior. Considerable effects of J-J mixing of the first three J-multiplets with the ground one were noticed. g-factors and the Schottky anomalies in the heat capacity were determined theoretically. Various hyperfine properties, including the thermal variation of the Mössbauer spectra, were computed for both isotopes of dysprosium in the light of the proposed CF.     

Abnormal magnetic properties of the Ce24Co11 hexagonal phase

The lighter rare earth-cobalt and thorium-cobalt binary systems were revised on the rare earth or thorium side, by metallographic, electron microprobe and X-ray methods. In agreement with previous works, it is confirmed that, in these systems, the first intermetallic compound corresponds to the following stoichiometry: 3:1 for trivalent La, Pr and Nd; 7:3 for tetravalent Th; 24:11 for Ce. The electronic structure of Ce in the hexagonal (P6₃mc) Ce₂₄Co₁₁ phase was investigated via magnetic susceptibility measurements in the 4.2–1300 K temperature range. The results show that the Curie-Weiss law is not followed, no magnetic order occurs down to 4.2 K and a very small change in the thermal behaviour of the magnetic susceptibility appears above the melting point of the phase (750 K). The abnormally low values of the magnetic susceptibility of Ce₂₄Co₁₁ could be understood by assuming Co is a non-magnetic state and Ce in a temperature dependent mixed valence state.     

Magnetization and heat capacity studies of double perovskite compounds Ba2SmRuO6 and Ba2DyRuO6

Here we report the magnetic and heat capacity studies of the double perovskite compounds Ba₂SmRuO₆ and Ba₂DyRuO₆. Antiferromagnetic transitions are inferred at 54 and 47 K in Ba₂SmRuO₆ and Ba₂DyRuO₆, respectively, in the magnetization measurements. Heat capacity measurements show large jumps at the corresponding temperatures and confirm the bulk magnetic ordering. Both the measurements provide clear indication of the ordering of the rare earth moments also along with the Ruthenium moments. However, the heat capacity results suggest that the ordering of rare earth magnetic moments is spread over a large temperature range. An anomaly observed in the magnetization measurements at 42 K (below the magnetic ordering) in Ba₂SmRuO₆ is discerned as a reorientation of Sm³⁺ moments.     

Ce掺杂SrMnO3的电子结构和磁性的第一性原理研究

用含超软赝势平面波方法的广义梯度近似第一性原理对Ce掺杂SrMnO₃的电子结构和磁性进行了相关研究. 不同的Mn-O键长说明MnO₆八面体发生了强的Jahn-Teller扭曲, 并伴随着晶体构型由立方体(Pm3m)转变为四方晶系(I4/mcm), 同时,Jahn-Teller扭曲也稳定了C型反铁磁基态构型. 电子结构结果表明SrMnO₃和Sr_1-xCe_xMnO₃(x=0.12     

Field induced phase transitions on NdRhIn5 and Nd2RhIn8 antiferromagnetic compounds

In this work, we have investigated the low temperature magnetic phase diagram of the tetragonal NdRhIn₅ and Nd₂RhIn₈ single crystals by means of temperature and field dependent heat capacity and magnetic susceptibility measurements. These compounds order antiferromagnetically with a Néel temperature (T_N) of 11 and 10.7 K for NdRhIn₅ and Nd₂RhIn₈, respectively. The constructed magnetic phase of both compounds are anisotropic and show, as expected, a decrease of T_N as a function of the magnetic field for c crystallographic direction. However when the magnetic field is applied along of the c-axis, which is the magnetic easy axis, first-order-like field induced transitions are observed within the antiferromagnetic state. We compare the phase diagrams obtained for NdRhIn₅ and Nd₂RhIn₈ with those for their cubic relative NdIn₃.     

Magnetic and EPR studies of the EuFe<Subscript>3</Subscript>(BO<Subscript>3</Subscript>)<Subscript>4</Subscript> single crystal

Magnetic and electron paramagnetic resonance (EPR) properties of EuFe₃(BO₃)₄ single crystals have been studied over the temperature range of 300–4.2 K and in a magnetic field up to 5 T. The temperature, field and orientation dependences of susceptibility, magnetization and EPR spectra are presented. An antiferromagnetic ordering of the Fe subsystem occurs at about 37 K. The easy direction of magnetization perpendicular to the c axis is determined by magnetic measurements. Below 10 K, we observe an increase of susceptibility connected with the polarization of the Eu sublattice by an effective exchange field of the ordered Fe magnetic subsystem. In a magnetic field perpendicular to the c axis, we have observed an increase of magnetization at T < 10 K in the applied magnetic field, which can be attributed to the appearance of the magnetic moment induced by the magnetic field applied in the basal plane. According to EPR measurements, the distance between the maximum and minimum of derivative of absorption line of the Lorentz type is equal to 319 Gs. The anisotropy of g-factor and linewidth is due to the influence of crystalline field of trigonal symmetry. The peculiarities of temperature dependence of both intensity and linewidth are caused by the influence of excited states of europium ion (Eu³⁺). It is supposed that the difference between the g-factors from EPR and the magnetic measurements is caused by exchange interaction between rare earth and Fe subsystems via anomalous Zeeman effect.     

Evidence of glassy ferromagnetic phase and kinetic arrest of electronic phase in Sm0.35Pr0.15Sr0.5MnO3 manganites

The effect of doping of rare earth Pr³⁺ ion as a replacement of Sm³⁺ in Sm_0.5Sr_0.5MnO₃ is investigated. Temperature dependent dc and ac magnetic susceptibility, resistivity, magnetoresistance measurements on chemically synthesized (Sm_0.5−xPr_x)Sr_0.5MnO₃ show various unusual features with doping level x=0.15. The frequency independent ferromagnetic to paramagnetic transition at higher temperature (∼191 K) followed by a frequency dependent reentrant magnetic transition at lower temperature (∼31 K) has been observed. The nature of this frequency dependent reentrant magnetic transition is described by a critical slowing down model of spin glasses. From non-linear ac susceptibility measurements it has been confirmed that the finite size ferromagnetic clusters are formed as a consequence of intrinsic phase separation, and undergo spin glass-like freezing below a certain temperature. There is an unusual observation of a 2nd harmonic peak in the non-linear ac susceptibility around this reentrant magnetic transition at low temperature (∼31 K). Arrott plots at 10 and 30 K confirm the existence of glassy ferromagnetism below this low temperature reentrant transition. Electronic- and magneto-transport measurements show a strong magnetic field—temperature history dependence and strong irreversibility with respect to the sweeping of magnetic field. These results are attributed to the effect of phase separation and kinetic arrest of the electronic phase in this phase separated manganite at low temperatures.