Magnetization and magnetic susceptibility of GdH3

Magnetic susceptibility measurement in the range 1.4 to 4.2 K reveal a maximum in χ at 3.65 K, and two maxima in Δχ/ΔT, one at 3.32 K (assumed to be T_N), and another at 1.8 K. High field magnetization measurements indicate a saturation moment of 7 μ_B.     

Heat capacity of RbMnF3 and EuO near the magnetic phase transitions

Precision measurements of C_p near the antiferromagnetic transition in RbMnF₃ and near the ferromagnetic transition in EuO yield critical exponents α = α′ = ?0.14 and α = α′ = ?0.04 respectively.     

Magnetization and magnetic susceptibility of single crystals of HoTiO3 and ErTiO3

Bulk magnetization measurements have been performed on single crystals of HoTiO₃ and ErTiO₃. The easy direction of magnetization is along the b-axis for HoTiO₃ and along the c-axis for ErTiO₃ with respect to the Pbnm chemical cell. These findings are in qualitative agreement with the results of two independent powder neutron diffraction studies. The saturation magnetic moments at 4.2 K along the easy axes are 7.3(2)μ_B per formula unit for HoTiO₃ and 6.9(2)μ_B for ErTiO₃. In addition, single crystal susceptibility data were analyzed using the theory of Boutron to yield values for the Heisenberg exchange coupling and the second-order crystal field terms B⁰₂ and B²₂.     

Critical behaviour of the linear birefringence in 3d-Heisenberg antiferromagnets : RbMnF3, KNiF3 and KCoF3

The linear birefringence of stress induced single antiferromagnetic T-domains of RbMnF₃, KNiF₃ and KCoF₃ has been measured in the vicinity of T_N. We deduce the critical behaviour in such 3d-Heisenberg systems, showing a symmetry breaking at the transition involving a unique wave vector of the order parameter in the Brillouin zone. The critical exponent $\text{β}$ of the linear birefringence has been found to be larger than 2β, in agreement with the theoretical predictions of G. Gehring.     

Magnetization process of Hf0.8Ta0.2Fe2 in strong pulsed magnetic fields

The magnetization process of an itinerant-electron magnet Hf_0.8Ta_0.2Fe₂ has been measured in pulsed magnetic fields up to 300 kOe at 4–330 K. The magnetic phase boundary in the high-field region has been determined and the temperature dependence of the high-field susceptibility in the ferromagnetic or saturated paramagnetic state is reported.     

Magnetization studies of TbFeO3

The spontaneous magnetization and principal magnetic susceptibilities of TbFeO₃ were measured from 4.2 to 300 K. The weak ferromagnetic moment is along the c crystallographic axis in the entire temperature range. The field dependence of the magnetization at 4.2 K was also studied. The magnetic behavior is interpreted in terms of an interaction between the ordered Fe³⁺ spin system and the electrons occupying the lowest lying “accidental” doublet of the Tb³⁺ ions. The FeTb interaction and the Tb³⁺ Van Vl eck susceptibility along the c axis play significant roles in determining the magnetic configuration of the Fe³⁺ spin system. No indication was found that the TbTb interaction plays a significant role in the magnetic behavior of TbFeO₃ at temperature above 4.2 K.     

Magnetization reversal in Fe48Pt34B34 magnetic foils

Exchange-spring magnet L1-FePt/(Fe₂B+α-Fe) is fabricated by flash annealing a melt-spun Fe₄₈Pt₃₄B₃₄ foil. A coercivity of 8500 Oe (1 Oe = 79.5775 A/m), squareness (M_r/M_s) of 0.70, saturation magnetization of 10.2 kGs (1 Gs = 10^-4 T) and an effective anisotropy K_eff =2.0 × 10⁷ ergs/cm³ are obtained. A two-step magnetization reversal feature is characterized in this paper. An exchange bias phenomenon is also observed in a low saturation field.     

Observation of ultrasonic interaction with field independent NMR modes in RbMnF3

Field independent nuclear magnetic resonance modes have been observed in the antiferromagnet RbMnF₃ by detecting their interaction with a longitudinal ultrasonic wave propagating along the direction of the equilibrium sublattice magnetizations.     

Bilinear and biquadratic exchange interactions and their effect on magnetic susceptibilities of KMgF3: Mn and KZnF3: Mn

Exchange interaction constants of nearest (J₁) and next-nearest-neighbor (J₂) Mn²⁺ in KMgF₃: Mn and KZnF₃: Mn have been evaluated from the magnetic susceptibilities. For KZnF₃: Mn, J₁ = 8.2 ± 0.5 K; this is consistent with the ESR value if biquadratic exchange is present.     

Knight shifts and magnetic susceptibilities of the intermetallic compounds CeCu4 and CeCu5

The magnetic susceptibility and Knight shift of the compounds CeCu₄ and CeCu₅ have been measured over the temperature ranges 80–800 and 140–400 K, respectively. The most important contributions to the magnetic susceptibility are the Curie-Weiss term, expressing the paramagnetism of the localized ?-electrons, and a temperature independent term, which have both been determined. The phenomenological exchange integral F_s? between the 4?-electron spins and conduction electron spins was found to be ?10.43× 10^?3 eV for CeCu₄ and 3.9 × 10^?3 eV for CeCu₅. A reversal in the sign of the s?? coupling for CeCu₅ is noted.     

The magnetic structures of LaTiO3 and CeTiO3

The basic features of the magnetic structures of LaTiO₃ and CeTiO₃ were determined by powder neutron diffraction. LaTiO₃ (T_N = 125 K) is a type G antiferromagnet with a moment on Ti (III) of 0.45(5)μ_B at 10 K. As bulk magnetic measurements indicate a weak ferromagnetic moment, a G_zF_x or G_xF_z configuration is implied. CeTiO₃ (T_N) = 116 K) shows more complex behaviour. At 81 K only G and F type reflections are observed. The most consistent interpretation is to assign G-type configuration to Ti(III) and an induced F_z on Ce(III). Moments are 0.36μ_B on Ti(III) and 0.4(1)μ_B on Ce(III). It is also possible to assign both G and F components to Ti(III). This demands a “canting angle” of 34° to explain the F moment. Below 80 K a C-type component develops. A model assuming a G_zF_x configuration for Ti(III) and a C_yF_x configuration for Ce(III) provides a good fit to the data. This assignment is consistent with Bertaut's symmetry considerations. Other models which violate Bertaut's rules also fit the data.     

The magnetic structures of HoTiO3 and ErTiO3

The magnetic structures of rare-earth titanium perovskites, ErTiO₃ and HoTiO₃, have been determined at 4.2 K by neutron diffraction. The Er³⁺ moment of (8.5 ± 0.5) μ_B lies along [001] and is colinear with the titanium moment of (-0.7 ± 0.3) μ_B. The Ho³⁺ moment of (8.1 ± 0.5) μ_B is inclined at an angle of 24° to the bc plane and 32° to the ab pla so as to produce an antiferromagnetic ordering of the x component and a ferromagnetic ordering of the y and the z components. The titanium moment of (-0.55 ± 0.3) μ_B lies in the bc plane but its precise direction has not been determined.     

Magnetism without magnetic ions in non-magnetic perovskites SrTiO3, SrZrO3 and SrSnO3

Using the full-potential linearized augmented plane-wave (FP-LAPW) method with the generalized gradient approximation (GGA) for the exchange-correlation potential, we studied spin polarization induced by replacement of oxygen atoms by non-magnetic 2p impurities (B, C and N) in non-magnetic cubic SrMO₃ perovskites, where M=Ti, Zr and Sn. The results show that the magnetization may appear because of the spin–split impurity bands inside the energy gap of the insulating SrMO₃ matrix. Large magnetic moments are found for the impurity centers. Smaller magnetic moments are induced on the oxygen atoms around impurities. It is shown that SrTiO₃:C and SrSnO₃:C should be magnetic semiconductors while other compounds in this series (SrTiO₃:B, SrTiO₃:N and SrZrO₃:C) are expected to exhibit magnetic half-metallic or pseudo-half-metallic properties.     

Magnetization reorientation in HoCo2

In order to confirm the magnetization reorientation in HoCo₂, torque measurements have been performed at various temperatures on a spherical single crystal, in the (001) and (011) planes. The easy magnetization direction is the [110] axis at 4.2 K and the [100] axis above 16 K. Furthermore, between 11 K and 16 K, the easy magnetization direction rotates progressively within the (001) plane. These results agree with the magnetization measurements and can be interpreted by a crystal field model.     

Structure,electrical and magnetic properties of CaAs3, SrAs3, BaAs3 and EuAs3

The crystal structures and electrical properties of CaAs₃, SrAs₃, BaAs₃ and EuAs₃ have been studied by single crystal X-ray investigations, temperature dependent resistivity measurements and optical measurements. The structures of the triclinic CaAs₃ and monoclinic SrAs₃, BaAs₃ and EuAs₃ are closely related. The two-dimensional infinite polyanionic AS₃^2? nets are derivatives of the black phosphorus structure. CaAs₃ and BaAs₃ are semiconducting, while SrAs₃ and EuAs₃ show semimetallic behavior. The paramagnetic EuAs₃ undergoes a magnetic phase transition at 10.5 K.     

Determination of zone-boundary magnon energy and damping in RbMnF3 by means of light scattering experiments

New experimental data of two-magnon Raman scattering on the cubic antiferromagnet RbMnF₃ are used to obtain information on the single spin dynamics in all the ordered phase. The comparisons with the existing second order theory and with the neutron scattering data shows that the light scattering gives correct values for energy and lifetime of the zone boundary magnetic excitations.     

Understanding the magnetic ground state of rare-earth intermetallic compound Ce4Sb3: Magnetization and neutron diffraction studies

Magnetization and neutron diffraction studies have been performed on Ce₄Sb₃ compound (cubic Th₃P₄-type, space group I4¯3d, no. 220). Magnetization of Ce₄Sb₃ reveals a ferromagnetic transition at ∼5 K, the temperature below which the zero-field-cooled and field-cooled magnetization bifurcate in low applied fields. However, a saturation magnetization (M_S) value of only ∼0.93μ_B/Ce³⁺ is observed at 1.8 K, suggesting possible presence of crystal field effects and a paramagnetic/antiferromagnetic Ce³⁺ moment. Magnetocaloric effect in this compound has been computed using the magnetization vs. field data obtained in the vicinity of the magnetic transition, and a maximum magnetic entropy change, −ΔS_M, of ∼8.9 J/kg/K is obtained at 5 K for a field change of 5 T. Inverse magnetocaloric effect occurs at ∼2 K in 5 T indicating the presence of antiferromagnetic component. This has been further confirmed by the neutron diffraction study that evidences commensurate antiferromagnetic ordering at 2 K in zero magnetic field. A magnetic moment of ∼1.24μ_B/Ce³⁺ is obtained at 2 K and the magnetic moments are directed along Z-axis.     

Non-colinear magnetic structure of U3P4 and U3As4

Neutron diffraction experiments have been performed on single crystal samples of U₃P₄ and U₃As₄. The magnetic ordering is found to be a non-collinear three axial structure in which magnetic moments of U⁴⁺ ions are tilted from the [111] axis by an angle of about twenty degrees within (110) planes.     

Raman scattering in magnetic US3

A Raman scattering investigation of magnetic US₃ has been made from 7 to 300 K. Comparison of room temperature spectra with those of the non magnetic isostructural sulfide HfS₃ allowed the assignment of most of the lines to $\textcolor{red}{}\text{=}\text{0}$ optical phonons. Drastic changes take place in the 10?150 cm^?1 range when lowering the temperature down to 7 K : four equally spaced lines appear at 54, 72.5, 91 and 109.5 cm^?1. Three of them broaden significantly with increasing temperature and disappear near 50 K, at which previous measurements indicate a maximum in the magnetic susceptibility and suggest a magnetic phase transition. The stronger fourth line is still observed at 100 K and merges into a phonon line at higher temperature. These four lines are attributed to electronic transitions within the 5f² configuration of U⁴⁺. Their temperature dependences appear to involve a spin-dependent scattering mechanism and are consistent with antiferromagnetic ordering.