Magnetic properties of R2Pt compounds with R = Gd,Tb, Dy,Ho, Er and Tm

Magnetic properties of polycrystalline samples of R₂Pt compounds (R = Gd, Tb, Dy, Ho, Er and Tm) are presented. The Gd, Td, Dy, Ho based compounds are ferromagnetic with Curie temperatures ranging between 155 and 17 K. Er₂Pt and Tm₂Pt are antiferromagnetic with Néel temperatures of 9 and 5 K respectively. The observed properties are discussed considering indirect exchange interactions and crystal field effects acting on the rare earth ions which lies in very low symmetry sites.     

Spin and temperature dependence of the magnetic hyperfine field of Cd in the rare earth-aluminum Lavesphase compounds RAl2

Perturbed angular correlation spectroscopy has been used to investigate the combined magnetic and electric hyperfine interaction of the probe nucleus ¹¹¹Cd in ferromagnetically ordered rare earth (R)-dialuminides RAl₂ as a function of temperature for the rare earth constituents R=Pr, Nd, Sm, Eu, Tb, Dy, Ho and Er. In compounds with two magnetically non-equivalent Al sites (R=Sm, Tb, Ho, Er), the magnetic hyperfine field was found to be strongly anisotropic. This anisotropy is much greater than the anisotropic dipolar fields, suggesting a contribution of the anisotropic 4f-electron density to magnetic hyperfine field at the closed-shell probe nucleus. The spin dependence of the magnetic hyperfine field reflects a decrease of the effective exchange parameter of the indirect coupling with increasing R atomic number. For the compounds with the R constituents R=Pr, Nd, Tb, Dy and Ho the parameters B₄, B₆ of the interaction of the crystal field interaction have been determined from the temperature dependence of the magnetic hyperfine field. The ¹¹¹Cd PAC spectrum of EuAl₂ at 9 K confirms the antiferromagnetic structure of this compound.     

The magnetic hyperfine field at Cd nuclei in the rare earth ferromagnets Gd,Tb, Dy,Ho, Er and Tm

The time differential perturbed angular correlation technique has been used to study the combined magnetic and electric hyperfine interactions at the site of a¹¹¹Cd impurity in the rare earth ferromagnets Gd, Tb, Dy, Ho, Er, and Tm at 4.2 °K. The following magnetic hyperfine fields at the site of¹¹¹Cd have been found: ¦H _hf ¦=340(7) kG in Gd, 275 (5) kG in Tb, 221 (4) kG in Dy, 116 (3) kG in Er and 60 (6) kG in Tm. In Ho two magnetically different sites were observed with magnetic fields of 159 (3) and 139 (3) kG. Both sites are equally populated. The coupling constantJ _5f of the conduction electron-4f interaction has been calculated for the different rare earth metals from the measured hyperfine fields by means of the RKKY theory.     

The Magnetic Hyperfine Field of 111Cd in the Rare Earth–Nickel Laves Phases RNi2

The magnetic hyperfine field of ¹¹¹Cd in the C15 Laves phases RNi₂ has been investigated by perturbed angular correlation (PAC) spectroscopy as a function of temperature for the rare earth constituents R = Nd, Sm, Gd, Tb, Dy, Ho, Er, and Tm.     

Anomalous hyperfine field and orbital moment of cobalt in RCo2; R = Pr,Nd, Sm,Gd, Tb,Dy, Ho,Er and Tm

⁵⁹Co spin echo NMR spectra in the magnetically ordered phase of the MgCu₂ type RCo₂ compounds (R = Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er and Tm) have been observed. For the RCo₂ with the easy direction of magnetication parallel to the 〈011〉 or 〈111〉 direction, the ⁵⁹Co hyperfine fields at two magnetically inequivalent Co sites are found to be antiparallel, revealing a large anisotropy in the ⁵⁹Co hyperfine field. The results are discussed in terms of a large and anisotropic orbital moment of Co. The transferred hyperfine field due to rare earth spins is estimated from well resolved satellite lines observed in Tb_1?xY_xCo₂. The nuclear quadrupole splitting in the magnetically ordered phase is found to be always larger than that in the paramagnetic phase.     

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.     

Magnetic properties of RE2Au compounds (RE = Pr,Nd, Gd,Tb, Dy,Ho, Er,Tm and Y)

Magnetic properties of nine RE₂Au compounds have been studied in fields of up to 19 kOe in the temperature range 4.2K–300K. It has been found that all compounds are paramagnetic at room temperature except Gd₂Au. The compounds with Pr, Nd, Ho, Er and Tm exhibit Curie-Weiss behaviour with paramagnetic moments in close agreement with those expected for the free RE³⁺ ion. The moment of gold was found to be zero. The compounds with Pr, Nd, Tb, Dy, Er and Tm are antiferromagnetic at low temperatures. It appears that Ho₂Au is ferromagnetically ordered below 4.5 K. No evidence for magnetic ordering was found for Y₂Au. The compound with Tb exhibits metamagnetic behaviour.     

Magnetic properties of ternary gallides of type RNi4Ga (R=rare earths)

The magnetic properties of RNi₄Ga (R=La, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm and Lu) compounds have been investigated. These compounds form in a hexagonal CaCu₅ type structure with a space group P6/mmm. Compounds with the magnetic rare earths, R= Nd, Sm, Gd, Tb, Dy, Ho, Er and Tm, undergo a ferromagnetic transition at 5, 17, 20, 19, 12, 3.5, 8 and 6.5 K, respectively. The transition temperatures are smaller compared to their respective parent compounds RNi₅. PrNi₄Ga is paramagnetic down to 2 K. LaNi₄Ga and LuNi₄Ga are Pauli paramagnets. All the compounds show thermomagnetic irreversibility in the magnetically ordered state except GdNi₄Ga.     

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.     

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.     

Neutron diffraction study of the magnetic ordering in the series R 2 BaNiO 5 (R = Rare Earth)

A neutron diffraction study, as a function of temperature, of the title compounds is presented. The whole family (space group Immm, a ≈ 3.8?, b ≈ 5.8?, c ≈ 11.3?) is structurally characterised by the presence of flattened NiO₆ octahedra that form chains along the a-axis, giving rise to a strong Ni-O-Ni antiferromagnetic interaction. Whereas for Y-compound only strong 1D correlations exist above 1.5 K, presenting the Haldane gap characteristic of 1D AF chain with integer spin, 3D AF ordering is established simultaneously for both R and Ni sublattices at temperatures depending on the rare earth size and magnetic moment. The magnetic structures of R₂BaNiO₅ ( R = Nd, Tb, Dy, Ho, Er and Tm) have been determined and refined as a function of temperature. The whole family orders with a magnetic structure characterised by the temperature-independent propagation vector = (1/2, 0, 1/2). At 1.5 K the directions of the magnetic moments differ because of the different anisotropy of the rare earth ions. Except for Tm and Yb (which does not order above 1.5 K), the magnetic moment of the R³⁺ cations are close to the free-ion value. The magnetic moment of Ni²⁺ is around 1.4 , the strong reduction with respect to the free-ion value is probably due to a combination of low-dimensional quantum effects and covalency. The thermal evolution of the magnetic structures from T _N down to 1.5 K is studied in detail. A smooth re-orientation, governed by the magnetic anisotropy of R³⁺, seems to occur below and very close to T _N in some of these compounds: the Ni moment rotates from nearly parallel to the a-axis toward the c-axis following the R moments. We demonstrate that for setting up the 3D magnetic ordering the R-R exchange interactions cannot be neglected. Received 19 July 2001     

Magnetic structures and related properties of some rare-earth intermetallic compounds, RCu2

The magnetic structures and some relevant bulk magnetic properties of R(Cu, Ni)₂ (R = Tb, Tb_zY_1−z, Dy, Ho, Er and Tm) are summarized. Basically, the magnetic structures are antiferromagnetically modulated with propagation vector a^*. For R = Tb, Dy, Ho the a-axis anisotropy dominates and the structures are longitudinally modulated. For R = Tm, Er (probably) the b-axis anisotropy dominates and this results in transversely modulated structures. For R = Tb, Dy the structures are collinear, For R = Ho, Er, Tm (probably) an incommensurate modulation coexists with the commensurate a^*-axis modulation at the lowest temperature.     

Susceptibility measurements on some R5In3 compounds

The magnetic susceptibility of some rare earth-indium compounds has been measured in the temperature range 4.2–300 K under a constant field of 1 kOe. The compounds with R = Gd, Tb and Dy are antiferromagnetic, having Néel temperatures between 4.2 and 78 K ; those with R = Ho, Er and Tm seem to be ferromagnetic with ordering temperatures probably below 4.2 K. Y₅In₃ presents a temperature independent susceptibility.     

Magnetic and structural studies of the alloy system REIn0.5Ag0.5

The structural and magnetic properties of the alloy system REIn_0.5Ag_0.5 [RE = Gd, Tb, Dy, Ho, Er, Tm and Yb] are reported. All these alloys (except that of Yb) crystallize in a cubic CsCl type structure at room temperature. Low temperature X-ray diffraction data does not reveal any structural phase transformation down to 8 K. On the basis of magnetic susceptibility data at a different temperature (3–300 K) and applied magnetic field (2 × 10⁵ to 8 × 10⁶ A m^-1, it has been concluded that GdIn_0.5Ag_0.5 is ferromagnetic (T_c = 118 K), TbIn_0.5Ag_0.5 and DyIn_0.5Ag_0.5 are meta magnetic (T_N = 66 and 30 K, respectively) and alloys involving Ho, Er, Tm and Yb are ferrimagnetic with Néel temperatures (T_N) equal to 24, 22, 21 and 20 K, respectively. The evaluated effective magneton number (p) is found to be slightly larger compared to theoretical values for tripositive ions of Gd, Tb and Dy and a bit smaller for Ho, Er, Tm and Yb. The results have been qualitatively explained using appropriate theories.     

Magnetic properties of RNi5−xCux intermetallics

The magnetic properties have been studied for the series of RNi_5−xCu_x intermetallics with R=Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Lu; x  ?2.5. Compositional dependences of magnetic susceptibility for the Pauli paramagnets (R=Y, La, Ce, Lu) and the Curie temperature for ferromagnets (R=Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm) have maximum at x=0.2–0.4$x=0.2–0.4$ and 1, respectively. The substitution of Cu for Ni is accompanied by decreasing spontaneous magnetic moment and increasing coercive force of all ferromagnetic RNi_5−xCu_x but GdNi_5−xCu_x. These results are explained in the frame of band magnetism, random local crystal field, and domain wall pinning theories.     

A study of the magnetic susceptibility of R3Au3Sb4 (R = Tb,Ho, Er,Tm)

The magnetic susceptibilities of the new cubic intermetallic compounds R₃Au₃Sb₄ (R = Tb, Ho, Er, and Tm) have been measured between 4 and 300 K. The compounds are paramagnetic down to 4 K. The experimental effective magnetic moment of the erbium compound is in agreement with the free-ion value, whereas the effective moments of the other three compounds are lower than the corresponding free-ion values. This discrepancy is interpreted in terms of quenching by the crystalline electric field.     

Magnetic structures of the rare earth orthotitanites RTiO3; R = Tb,Dy, Tm and Yb

The magnetic structures of the rare earth orthotitanites, RTiO₃, R = Tb, Dy, Tm and Yb, have been solved using neutron powder diffraction techniques.Two different types of magnetic structure have been found. One has the titanium and rare earth moments antiparallel along the c axis. The other structure has the rare earth moments in the ab plane with both ferromagnetic and antiferromagnetic components. In TbTiO₃, the terbium moment of (8.1 ± 0.4)μ_β has ferromagnetic and antiferromagnetic components along the [100] and [010] directions, respectively, with the moments lying at an angle of (36 ± 3)° to the [100] direction. In DyTiO₃, the dysprosium moment of (9.7 ± 0.7)μ_β has ferromagnetic and antiferromagnetic components along the [010] and [100] directions, respectively, with the moments making an angle of (31 ± 5)° to the [010] direction. TmTiO₃ has a thulium moment of (6.0 ± 0.4)μ_β in a ferromagnetic array along the [001] direction. The average titanium moment in the orthotitanites is (0.7 ± 0.3)μ_β in a direction antiparallel to the ferromagnetic component of the rare earth moment. The ytterbium moment in YbTiO₃ is quenched. It is found to be (1.7 ± 0.2)μ_β assuming a moment direction along [001]. The rare earth moment directions are found to be remarkably consistent in the series RMO₃, M = Ti, Cr, Fe and Al.     

An57Fe Mössbauer study of rare-earth intermetallic compounds R(Fe11Ti)

⁵⁷Fe Mössbauer spectra are reported for the ThMn₁₂ structure series of intermetallic compounds R(Fe₁₁Ti) (R=Y, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Lu). The Mössbauer spectroscopy of oriented absorbers has been used to study the spin reorientation transitions exhibited by the members of the series where the second-order Stevens coefficient α_J of the rare-earth (Nd, Tb and Dy) is negative. A simple model has been established to deduce the canting angle from the Mössbauer spectra of oriented absorbers. The results are analyzed in terms of a crystal-field model. The crystal field parameters must be increased significantly to account for the observed large anisotropy in the Sm(Fe₁₁Ti) compound, which may find applications as a permanent magnet.     

Magnetic susceptibility and electrical resistivity of some Th2Zn17-type rare-earth zinc phases

We report measurements of the magnetic susceptibility and electrical resistivity of the iostructural compounds RE₂Zn₁₇ (RE=La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu). The composition dependence of the lattice parameter and effective moment indicate that all the RE ions are trivalent except Yb which is divalent. Magnetic order is observed in compounds where RE=Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho and Er. A second transition is seen for RE=Pr, Ho, Sm and Tb. Superzone boundary effects are observed in the electrical resistivity of these four alloys as well as in Er₂Zn₁₇. Resistivity measurements reveal concentrated Kondo behavior (or 4f instability) of Ce in Ce₂Zn₁₇.     

Magnetic anisotropy in Fe/rare‐earth multilayers

Magnetic anisotropy of Fe/RE multilayers (RE=Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) was studied using ⁵⁷Fe Mössbauer spectroscopy. Perpendicular magnetic anisotropy was observed in Fe/Pr, Fe/Nd, Fe/Tb, and Fe/Dy multilayers. The external field dependence of the direction of magnetic moments was also examined for Fe/Tb multilayers. The results imply that the perpendicular magnetic anisotropy originates from the single ionic anisotropy of RE at the interfaces.