Magnetic properties of R2WO6 (where R=Nd, Sm, Eu, Gd, Dy and Ho)

The magnetic and electrical measurements carried out on the R₂WO₆ tungstates showed a paramagnetic behaviour for samples with R=Nd, Gd, Dy and Ho and more complex one for samples with R=Sm and Eu in the temperature range 4.2-280 K and an insulating state at room temperature. With increasing atomic number of the R element the Curie-Weiss temperature increases from −43.5 K for Nd₂WO₆ to −2.7 K for Ho₂WO₆, excluding Sm₂WO₆ and Eu₂WO₆ compounds for that the Curie-Weiss region is not observed and the imaginary part of susceptibility is close to zero. The effective magnetic moment is close to the theoretical one for the free R ion and the magnetic moment measured in magnetic field of 14 T and at temperature of 4.2 K, generally, does not reach the saturation state. The temperature independent residual susceptibility is negative for Nd₂WO₆ and positive for the remaining compounds suggesting different proportions of the Landau, Pauli and van Vleck contributions to the total susceptibility. An increase of the orbital magnetic contribution to the total magnetic moment is suggested from the fitting of the Landé factor in the compounds under study.     

Susceptibilite magnetique des composes ternaires TCu2Ge2(T = Gd,Tb,Dy,Ho,Er,Tm)

Susceptibility measurements are performed on the tetragonal TCu₂Ge₂ ternary compounds in the temperature range 4.2–200 K under a constant magnetic field of 5 KOe. The compounds with T = Gd,Tb,Dy and Ho are antiferromagnetic with Néel temperatures 12,15,8 and 6.4 K respectively. The compounds with T=Er and Tm do not show any ordering temperature down to 4.2 K. The temperature dependence of the reciprocal susceptibility of all compounds follows a Curie-Weiss law. The paramagnetic Curie temperatures for all compounds are negative.     

Magnetic properties of RCoSi2 compounds (R=rare earth)

New ternary silicides of composition RCoSi₂ (R=rare earth and Y) have been prepared and found to crystallize in the orthorhombic CeNiSi₂-type structure. Their magnetic properties have been studied by means of susceptibility measurements between 2 and 250 K. The Ce and Y compounds show essentially temperature independent Pauli paramagnetism. The compounds with R=Nd, Sm, Gd, Tb, Dy, Ho, Er and Tm show antiferromagnetic ordering below 20 K. The effective rare earh moments in the paramagnetic state agree well with the free ion values, and, for the heavy rare earths, the Néel temperatures vary with the De Gennes factor. There is no indication for a magnetic contribution from the Co sublattice.     

The spin-glass state in Y2Co2/3Mo4/3O7 and Y2Fe2/3Mo4/3O7 complex oxides

The magnetic properties of Y₂ B _2/3Mo_4/3O₇ complex oxides (B = Co, Fe) were studied in the temperature range 2–300 K. At low temperatures, these compounds exhibit spin-glass properties with freezing temperatures T _f=26 and 33 K, respectively, and typical features in the magnetic hysteresis and in the dependences of the real part of the dynamic magnetic susceptibility on temperature and ac magnetic field frequency. Above T _f, the static magnetic susceptibility of the samples studied depends on the applied magnetic field, which is tentatively assigned to the presence of metallic cobalt and/or yttrium orthoferrite YFeO₃ introduced in the course of sample preparation. __________ Translated from Fizika Tverdogo Tela, Vol. 47, No. 12, 2005, pp. 2182–2188. Original Russian Text Copyright ? 2005 by Bazuev, Korolev.     

Magnetic and structural characteristics of the RInCu2 compounds in the Heusler L21 structure

Magnetic and structural behaviour of materials of composition RInCu₂ (R = rare earth) were investigated. All the compounds (R = La-Lu) were found to be isotypic and to crystallize with the Heusler L2₁ type structure. The magnetic behaviour of the compounds was studied in the temperature range 2–300 K. The RInCu₂ (R = Sm, Gd, Tb, Dy) compounds are antiferromagnetically ordered at low temperatures T_N = 12 K for GdInCu₂, Ce in CeInCu₂ is in a pure trivalent state. LaInCu₂ is Pauli paramagnetic and LuInCu₂ is diamagnetic. No superconductivity was observed for temperatures as low as 1.8 K. The observed magnetic properties result from indirect exchange interaction and crystal field effects and compared to the isomorphous MnInCu₂.     

Magnetic properties of RAuNi4 rare earth compounds

Magnetization studies of new f.c.c. RAuNi₄ intermetallic compounds were performed. The compounds with R = Gd, Tb, Dy, Ho and Er are ferromagnetically ordered at temperatures ranging from 14 to 38K. Two ferromagnetic transitions were observed in the magnetization curves. TmAuNi₄ and YbAuNi₄ exhibit paramagnetic behaviour for temperatures as low as 4.2 K.     

Magnetic properties of ternary rare-earth compounds of the type R2Fe14B

Ternary tetragonal compounds of the composition R₂Fe₁₄B were observed for R = Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, and Lu. The lattice constants and the X-ray density of these compounds were determined. Also determined were the magnetic properties, comprising the temperature dependence of the magnetization in the range 4.2–700 K and the field dependence of the magnetization at 4.2 K in fields up to 20 T. These latter measurements were made in two mutually perpendicular directions, making it possible to determine the anisotropy fields. The magnetocrystalline anisotropy was found to consist of contributions due to the Fe and rare-earth sublattice, respectively.     

Magnetocrystalline anisotropy of MnF2 deduced from static torque

The first anisotropy constant K₁ as well as the differential susceptibility ΔX = Xχ - X∥ of MnF₂ has been determined from static torque measurements. The temperature range was for K₁ 4.2 K to 66 K and for ΔX 4.2 K to 300 K. The result for K₁ is in good agreement with values obtained from antiferromagnetic resonance experiments. In order to explain the differential susceptibility in the paramagnetic region, it was found necessary to take the g-factor anisotropy into account.     

Magnetic properties of PrCo2 and its ternary hydride PrCo2H4

Magnetization and susceptibility data on PrCo₂ and PrCo₂H₄ are presented. The ac susceptibility of PrCo₂ measured in zero dc field displays a sharp and high peak at T_c = (39.9 ± 0.2) K. The magnetization versus temperature curves show ferromagnetic behaviour for B >1 T, but display a maximum at lower values of the applied field. These results, together with the behaviour of the hysteresis loops at different temperatures below T_c, indicate that PrCo₂ orders ferromagnetically, the magnetic hardness increasing strongly for T → 0. The saturation moment at 4.2 K equals 3.9 μ_B per formula unit, as found from the magnetization curve measured in a pulsed-field magnet up to B = 30 T.Similar experiments on PrCo₂H₄ provide evidence that the introduction of hydrogen in PrCo₂ not only destroys the long-range atomic order, but also considerably reduces the ferromagnetic interactions. Such an effect of the hydrogen is commonly observed in cobalt intermetallics. Part of the PrCo₂H₄ is found to have decomposed into PrH₂ and free Co. The clusters of free Co atoms give rise to a maximum in the zero-field ac susceptibility versus temperature curves, similar as observed in spin glasses or magnetic glasses. By increasing the ac frequency, the maximum shifts to higher temperatures. The behavior can be explained in terms of the Néel model for superparamagnetic particles with randomly oriented local anisotropy axes.     

Magnetic properties of R3Co29Si4B10 (R=La, Ce, Pr, Nd, Sm, Gd and Dy) borides

The crystal structure and magnetic properties of quaternary rare-earth intermetallic borides R₃Co₂₉Si₄B₁₀ with R=La, Ce, Pr, Nd, Sm, Gd and Dy have been studied by X-ray powder diffraction and magnetization measurements. All compounds crystallize in a tetragonal crystal structure with the space group P4/nmm. Compounds with R=La, Ce, Pr, Nd and Sm are ferromagnets, while ferrimagnetic behavior is observed for R=Gd and Dy. The Curie temperatures vary between 149 K and 210 K. The Curie temperatures in R₃Co₂₉Si₄B₁₀ (R=Ce, Pr, Nd, Sm, Gd, Dy) compounds are roughly proportional to the de Gennes factors.     

Magnetic properties of Fe1−xCoxO

Measurements are reported for the magnetic susceptibility of solid solutions Fe_1-xCo_xO for compositions with x =0.10 to 0.95 and for the temperature range 4.2 to 600 K. It is found that the Curie-Weiss law is obeyed at high temperatures while the dependence of the susceptibility and transition temperature on composition appear to be in good agreement with the “virtual crystal” approximation.     

Superconductivity in the neptunium Chevrel phase Np1+xMo6Se8

The neptunium based Chevrel phases Np_1.0Mo₆Se₈ have been synthesized and their magnetic susceptibility and electrical resistivity have been measured from 3 K to room temperature. These compounds are superconductors with a critical temperature T_c = 5.6 (0.1) K. The magnetic susceptibility shows large crystal field effects with probably an important non-cubic component.     

Temperature dependence of the electrical resistivity of R6(Fe1-xMnx)23 compounds in the temperature range 4.2 to 300 K

The temperature dependence of the electrical resistivity of binary R₆Mn₂₃, R₆Fe₂₃ (R = Y, Dy, Ho, Er, Tm) and pseudobinary R₆(Fe_1-xMn_x)₂₃ (R = Y, Er, Ho) compounds has been determined by a four-probe measuring technique in the temperature range 4 to 400 K.The binary compounds exhibit a prop. T² dependence at low temperatures, while above 100 K a negative curvature of the -T-curves is observed.These experimental results are discussed on the basis of electron-spin wave scattering in the low temperature range and on the basis of s-d scattering in the high temperature range, taking explicitly into account the temperature dependence of the chemical potential.The pseudobinary compounds generally exhibit a decreasing resitivity with increasing temperature, combined with a high residual resistivity. These facts are explained by the so-called strong scattering mechanism and the appearance of “quasilocalized” states.     

Superconducting effects in Hg3-δAsF6

Superconducting properties of Hg_3-δAsF₆ have been investigated by a.c. magnetic susceptibility measurements in the temperature range 1.25–4.2 K and magnetic field range 0–0.05 T and by resistivity measurements in the temperature range 1.25–4.2 K. The properties are attributed to mercury dispersed in isolated regions throughout the sample.     

Low temperature phase transition in the chain-like compounds NbSe3 and TaSe3

New transitions have been observed at low temperature by electrical measurements on the linear trichalcogenides NbSe₃ and TaSe₃. The resistivity of TaSe₃ drops near zero below 1.5 K which may indicate a superconducting transition. The resistivity of NbSe₃ drops below 2.2 K by 30 to 75% of its residual value at 4.2 K. However for TaSe₃ and NbSe₃ initial susceptibility measurements do not show any increase in diamagnetism indicating a flux expulsion. In addition the transitions below the critical temperatures are strongly non-linear with current density higher than 10^-3 A mm^-2.     

Electrical resistivity and magnetic susceptibility studies of the system Mn5Si3-Fe5Si3

Electrical resistivity measurements have been performed on the system Mn_5?x,Fe_xSi₃ for the compounds x = 0,1,2,3,4 and 5 from 4.2 K to above room temperature. From the shape of the ρ(T) curves it can be inferred that the transition from antiferromagnetic to ferromagnetic ordering occurs in the concentration range 3 ? x ? 4; for Fe₅Si₃ and MnFe₄Si₃ the ρ(T) curves are characterized by a break in their slope, whereas for x = 1,2 and 3 a large minimum appears. Mn₅Si₃ exhibits two successive minima at 74 and 105 K. Magnetic susceptibility measurements for x = 1, 2 and 3 give confirmation of the Néel temperature for x = 1 and 2, whereas for x = 3 the behaviour is more complex.     

Magnetic ordering in NdRh2Si2 and ErRH2Si2

Neutron diffraction and magnetization study of polycrystalline NdRh₂Si₂ and ErRh₂Si₂ was performed in the temperature range from 4.2 to 293 K. Both compounds are of ThCr₂Si₂ type crystal structure and exhibit antiferromagnetic ordering below T_N = 53 K and T_N = 12.8 K respectively. The magnetic structure wave vector is τ = [0, 0, 1].     

Magnetic properties of RAu2Si2 rare earth compounds

The magnetic properties of the R Au₂Si₂ compounds with R = Ce-Er have been investigated. It was found that the compounds for which R = Ce, Sm, Gd, Tb and Dy are antiferromagnetically ordered at temperatures ranging from 5.7 to 15.9°K. PrAu₂Si₂ and NdAu₂Si₂ exhibit paramagnetic behavior for temperatures as low as 4.2°K. The magnetic structure is ferrimagnetic for the compounds in which R = Eu, Ho, and Er. The Eu compound is in the divalent state. The Néel and Curie points for this system do not follow the De-Gemnes function. Curie-Weiss Behavior is exhibited by all the compounds with effective moments in good agreement with that of a free tripositive lanthanide ion. The difference in magnetic properties between R Au₂Si₂ and the isomorphous R Fe₂Si₂ series is discussed.     

Possible observation of the coexistence of superconductivity and long-range magnetic order in NdRh4B4

The ternary rare earth compound NdRh₄B₄ has been studied by means of critical field, low temperature heat capacity, and static magnetic susceptibility measurements. Features in the upper critical field and heat capacity data at 1.31 K and 0.89 K suggest the occurrence of long-range magnetic order in the superconducting state. The temperature dependence of the static magnetic susceptibility follows a Curie-Weiss law with an effective magnetic moment μ_eff = 3.58 ± 0.05 μ_B and a Curie-Weiss temperature θ_p = ?6.2 ± 1.0 K between 20 K and room temperature. However,, magnetization vs. applied magnetic field isotherms suggest the development of a ferromagnetic component in the Nd³⁺ magnetization at low temperatures.     

Tunneling study of the charge-density-wave state in 1T-TaS2 and 1T-TaSe2

The charge density wave induced energy gaps of 1T-TaS₂ and 1T-TaSe₂ have been investigated by tunneling measurements at temperatures between 4.2 and 320 K. For 1T-TaS₂, the energy gap 2Δ is about 0.4 eV in the nearly-commensurate phase, and the gap becomes as large as 1.0 eV in the commensurate phase. On the other hand, for 1T-TaSe₂, the energy gap is about 0.5 eV and almost unchanged in the whole temperature range studied. In addition, the two compounds show cusp-like zero bias anomaly at 4.2 K, which might be related to the Coulomb effects in a disordered system