Magnetic structure of the Sm5Ge4-type Tb2Ti3Ge4

The orthorhombic Sm₅Ge₄-type Tb₂Ti₃Ge₄ shows square modulated non-collinear magnetic ordering with wave vector K=[±1/3, 1/2, 1/2] at 2 K. The terbium magnetic moments lie in the bc plane and magnetic moment value of 7.5(2) μ_B/Tb is obtained at 2 K.     

The influence of gallium on magnetocaloric effect in Gd60Tb40 alloys

The influences of gallium substitution for terbium in Gd₆₀Tb₄₀ on the phase formation, Curie temperature and magnetic entropy change have been investigated. A series of Gd₆₀Tb_40−xGa_x with x=0, 1, 3 and 5 alloys were prepared by arc-melting method. The X-ray diffraction (XRD) analysis reveals that a small amount of Ga substitution for terbium in Gd₆₀Tb₄₀ can form the solid solution (Gd, Tb). The Curie temperature (T_c) increases from 270 K for Gd₆₀Tb₄₀ to 297 K for Gd₆₀Tb₃₇Ga₃, while the maximum magnetic entropy changes ΔS_{M, max} decreases from 5.15 J/K kg for Gd₆₀Tb₄₀ to 3.32 J/K kg for Gd₆₀Tb₃₇Ga₃ with increasing the Ga content.     

Neutron diffraction studies of Tb2Rh3Si5 compound

In this work neutron diffraction studies of Tb₂Rh₃Si₅ compound are reported. The compound crystallizes in the monoclinic crystal structure of Lu₂Co₃Si₅-type. At 1.5 K an antiferromagnetic ordering with a propagation vector k=(1/2;1/2;1/2) was observed. The Tb magnetic moments of 9.8(2) μ_B form a non-collinear magnetic structure. In the vicinity of Néel temperature of 8 K a change of the magnetic ordering is evidenced. The change seems to be connected with phase transition from commensurate to incommensurate sine-wave modulation of the Tb magnetic moments.     

Giant forced volume magnetostriction in polycrystalline Tb0.3Dy0.7Fe1.95 alloys under magnetomechanical loading

The axial and transversal linear magnetostrictions (λ_∥ and λ_⊥) in [1 1 0] oriented polycrystalline Tb_0.3Dy_0.7Fe_1.95 alloys were measured simultaneously under uniaxial magnetomechanical loading to get the forced volume magnetostriction (ω=λ_∥+2λ_⊥). Despite the almost zero ω observed in Terfenol-D single crystals, it reaches up to 1000×10⁻⁶ in polycrystalline Tb_0.3Dy_0.7Fe_1.95 alloys near the saturation magnetic field under a stress above 50 MPa.     

Synthesis and luminescence properties of Tb:NaGd(WO4)2 novel green phosphors

Tb³⁺:NaGd(WO₄)₂ (Tb:NGW) phosphors with different Tb³⁺ concentrations have been synthesized by a mild hydrothermal process directly without further sintering treatment. X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence excitation and emission spectra and decay curve were used to characterize the Tb:NGW phosphors. XRD analysis confirmed the formation of NGW with scheelite structure. SEM study showed that the obtained Tb:NGW phosphors appeared to be nearly spherical and their sizes ranged from 1 to 1.5 μm. The excitation spectra of these systems showed an intense broad band with maximum at 270 nm related to the O→W ligand-to-metal charge-transfer state. Photoluminescence spectra indicated the phosphors emitted strong green light centered at 545 nm under UV light excitation. Analysis of the photoluminescence spectra with different Tb³⁺ concentrations revealed that the optimum dopant concentration for Tb³⁺ is about 15 at% of Tb³⁺ ions in Tb:NGW phosphors.     

Magnetic and crystallographic study of Tb0.75Y0.25Co3B2

Tb_0.75Y_0.25Co₃B₂ was studied as a function of temperature by neutron powder diffraction, ac susceptibility and SQUID magnetization measurements. The solid solution, which is of hexagonal symmetry and is paramagnetic at 300 K, undergoes a magnetic Co–Co ordering transition at ∼150 K, and a second magnetic Tb–Tb ordering transition at ∼17 K. The latter induces a spin-reorientation transition, in which the magnetic axis rotates from the c-axis toward the basal plane. The component of the magnetic axis, which is perpendicular to c, leads to a crystal symmetry reduction from hexagonal to monoclinic. The observed magnitude of the magnetic moment of the Tb ion is 1.5 μ_B, unusually small relative to the free ion and parent compound (TbCo₃B₂) values. These magnetic and crystal properties are discussed and compared with what was previously published for the parent compound.     

The antiferromagnetic structure of TbB4

The magnetic structure of the rare earth tetraboride TbB₄ (crystallographic space group P4/mbm) has been determined by neutron diffraction on a polycrystalline sample. Below the experimentally determined Néel temperature of T_N = (43±1) K TbB₄ is ordered antiferromagnetically. The data refinement yielded a magnetic moment value of (7.7 ± 0.2) μ_B/Tb ion at 4.2 K which we interpret as Tb⁴⁺. The magnetic structure is antiferromagnetic collinear with the moments perpendicular to the tetragonal axis.     

Magnetic order of Mn5Si3-type Tb5Sb3 and Tb5Si1.5Sb1.5

Neutron diffraction study has been performed on the Tb₅Sb₃ and Tb₅Si_1.5Sb_1.5 compounds (hexagonal Mn₅Si₃-type, hP16, P6₃/mcm) to understand their magnetic structures. The temperature dependence of neutron diffraction results proves that these intermetallics show a complex magnetic ordering. The Tb₅Sb₃ presents five subsequent changes in magnetic structure at ∼150, 119, 85, 70 and 54 K on cooling: paramagnet→antiferromagnetic flat spiral→ferromagnetic cone→antiferromagnetically canted ferromagnetic cone→canted AF→sine modulated AF. The Tb₅Si_1.5Sb_1.5 shows two subsequent changes in magnetic structure at 123 and 66 K: paramagnet→sine modulated antiferromagnet I→sine modulated antiferromagnet II. The Tb₅Si₃, Tb₅Sb₃ and Tb₅Si_1.5Sb_1.5 have the different magnetic structure in the full temperature range.     

Magnetotransport properties and magnetocaloric effect in La0.67Ca0.33Mn1−xTMxO3 (TM=Cu,Zn) perovskite manganites

The magnetic and transport properties of the perovskites La_0.67Ca_0.33Mn_1-xTM_xO₃ were found to be sufficiently changed with the substitution of Mn-sites by other 3d transition-metal cations (TM=Cu,Zn; x=0.15). The values of T_C, T_M−I, and T_CMR were surveyed when Mn was replaced by Cu and Zn. The magnetic field induced resistivity and magnetic entropy change of these samples showed abrupt changes near T_C (194.2 and 201.5 K for Cu and Zn-doped case respectively) and attained the highest values among the doped cases (up to 20% Cu). The maximum values (obtained at H=4 kOe) of magnetoresistance ratio (CMR) were 27.8%, and 24.5% and of magnetic entropy change (−ΔS_M) were 3.9 and 3.2 J/kg K for Cu and Zn-doped, respectively.     

Structure and magnetic properties of melt-spun Tb0.27Dy0.73Fex ribbons

The structure and magnetic properties of the melt-spun ribbons of Tb_0.27Dy_0.73Fe_x alloy are investigated as a function of various wheel speeds during melt-quenching using a single-roll technique. It is found that Tb_0.27Dy_0.73Fe_x alloy is difficult to be fabricated as amorphous state by using the melt-quenching method. X-ray diffractions show that all these ribbons for x=1.7−2.0 are the MgCu₂-type phase at the wheel speed of 45 m s⁻¹. For Tb_0.27Dy_0.73Fe_x alloy, the high wheel speed is beneficial to eliminate the RFe₃ phase and form the perfect MgCu₂-type phase. Compared with the bulk of Tb_0.27Dy_0.73Fe_1.95, these ribbons exhibit higher intrinsic coercivity value and their saturation magnetizations increase as well. The magnetostriction of Tb_0.27Dy_0.73Fe_1.95 composite with 4% epoxy resin is 640×10⁻⁶ at 900 kA m⁻¹.     

Structural and magnetic properties of Mn3−xCdxTeO6 (x=0, 1, 1.5 and 2)

Mn₃TeO₆ exhibits a corundum-related A₃TeO₆ structure and a complex magnetic structure involving two magnetic orbits for the Mn atoms [Ivanov et al., 2011 [3]]. Mn_3−xCd_xTeO₆ (x=0, 1, 1.5, and 2) ceramics were synthesized by solid state reaction and investigated using X-ray powder diffraction, electron microscopy, and calorimetric and magnetic measurements. Cd²⁺ replaces Mn²⁺ cations without greatly affecting the structure of the compound. The Mn and Cd cations were found to be randomly distributed over the A-site. Magnetization measurements indicated that the samples order antiferromagnetically at low temperature with a transition temperature that decreases with increasing Cd doping. The nuclear and magnetic structure of one specially prepared ¹¹⁴Cd containing sample: Mn_1.5¹¹⁴Cd_1.5TeO₆, was studied using neutron powder diffraction over the temperature range 2-295 K. Mn_1.5¹¹⁴Cd_1.5TeO₆ was found to order in an incommensurate helical magnetic structure, very similar to that of Mn₃TeO₆ [Ivanov et al., 2011 [3]]. However, with a lower transition temperature and the extension of the ordered structure confined to order 240(10) Å.     

Anti-Invar properties and magnetic order in fcc Fe-Ni-C alloy

Anti-Invar effect was revealed in the fcc Fe-25.3%Ni-0.73%C (wt%) alloy, which demonstrates high values of thermal expansion coefficient (TEC) (15-21)×10⁻⁶ K⁻¹ accompanied by almost temperature-insensitive behavior in temperature range of 122-525 K. Alloying with carbon considerably expanded the low temperature range of anti-Invar behavior in fcc Fe-Ni-based alloy. The Curie temperature of the alloy T_C=195 K was determined on measurements of temperature dependences of magnetic susceptibility and saturation magnetization. The Mössbauer and small-angle neutron scattering (SANS) experiments on the fcc Fe-25.3%Ni-(0.73-0.78)%C alloys with the varying temperatures below and above the Curie point and in external magnetic field of 1.5-5 T were conducted. Low value of the Debye temperature Θ_D=180 K was estimated using the temperature dependence of the integral intensity of Mössbauer spectra for specified temperature range. The inequality B_eff=(0.7-0.9)B_ext was obtained in external field Mössbauer measurement that points to antiferromagnetically coupled Fe atoms, which have a tendency to align their spins perpendicular to B_ext. Nano length scale magnetic inhomogeneities nearby and far above T_C were revealed, which assumed that it is caused by mixed antiferromagnetically and ferromagnetically coupled Fe atom spins. The anti-Invar behavior of Fe-Ni-C alloy is explained in terms of evolution of magnetic order with changing temperature resulting from thermally varied interspin interaction and decreasing stiffness of interatomic bond.     

Magnetic Structures and Magnetic Phase Transitions in Rare-Earth <Emphasis Type="Italic">R</Emphasis>Mn<Subscript>2</Subscript>Si<Subscript>2</Subscript> Intermetallic Compounds (<Emphasis Type="Italic">R</Emphasis> = Sm,Tb)

The magnetic structures that form in La_1–xR_xMn₂Si₂ (R = Sm, Tb) layered compounds with various concentrations x have been determined by magnetic neutron diffraction and magnetic measurements, and the magnetic phase diagrams have been built. It is shown that the formation of the magnetic structures is dependent not only on exchange interactions, but also on the type of the magnetic anisotropy of a rare-earth atom. It is found that, in La_1–xTb_xMn₂Si₂ compounds with 0.2 < x < 0.5, the competition of the Tb–Mn and Mn–Mn interlayer exchange interactions and the existence of a strong uniaxial magnetic anisotropy in the Mn and Tb sublattices leads to the frustrated magnetic state and prevents the formation of the long-range magnetic order in the Tb sublattice.     

Magnetostriction of TbxHo0.75−xPr0.25(Fe0.9B0.1)2 (x=0–0.3) compounds

The Tb_xHo_0.75−xPr_0.25(Fe_0.9B_0.1)₂ (x=0, 0.1, 0.15, 0.2, 0.25, and 0.3) compounds are found to stabilize in a cubic Laves phase structure. The lattice parameter, magnetostriction (at 10 kOe), and Curie temperature are found to increase with increasing Tb content. The compound with x=0.15 exhibits a possible anisotropy compensation between the Tb and (Ho/Pr) sublattices. The easy magnetization direction rotates towards the 〈1 1 1〉 from the 〈1 0 0〉 direction, with increasing Tb content. The splitting of the (4 4 0) peak accompanied by the spontaneous magnetostriction-induced rhombohedral distortion is observed for compounds with x?0.15 and the spontaneous magnetostriction (λ_1 1 1) is found to increase with Tb content.     

Photoluminescence properties and effects of dopant concentration in Bi2ZnB2O7:Tb phosphor

A novel green phosphor, Tb³⁺ doped Bi₂ZnB₂O₇ was synthesized by conventional solid state reaction method. The phase of synthesized materials was determined using the XRD, DTA/TG and FTIR. The photoluminescence characteristics were investigated using spectrofluorometer at room temperature. Bi₂ZnB₂O₇:Tb³⁺ phosphors excited by 270 nm and 485 nm wavelengths. The emission spectra were composed of three bands, in which the dominated emission of green luminescence Bi₂ZnB₂O₇:Tb³⁺ attributed to the transition ⁵D₄ → ⁷F₅ is centered at 546 nm. The dependence of the emission intensity on the Tb³⁺ concentration for the Bi_2−xTb_xZnB₂O₇ (0.01 ≤ x ≤ 0.15) was studied and observed that the optimum concentration of Tb³⁺ in phosphor was 13 mol% for the highest emission intensity at 546 nm.     

Influence of Tb substitution for La on the structure,magnetic and magneto-transport properties of La1.2Sr1.8Mn2O7

The physical properties of Tb³⁺ ions substitution at A-site are investigated in the layered manganite La_1.2Sr_1.8Mn₂O₇. A series of La_1.2−xTb_xSr_1.8Mn₂O₇ (x=0, 0.05, 0.15, and 0.20) shows that doping with a Tb ion of smaller radius in La_1.2Sr_1.8Mn₂O₇ caused diffraction peaks to shift to high angle. Some samples have an impure diffraction at about 30°, but all samples form single-phase. Samples can be well indexed on a Sr₃Ti₂O7-type tetragonal structure with the space group I4/mmm. According to the M-T curves, when x≤0.05, the series of samples shows ferromagnetism at low temperatures. With increasing temperature, they have two magnetic transitions at different temperatures. When x≥0.15, the magnetizations dramatically decrease. The ρ–T curves of samples show the metal–insulator transition for x=0, 0.05, and the maximum MR values in magnetic field 5 T are 74% at about 73 K and 94% at about 86 K. When x≥0.15, the samples remain in the insulator state in the whole observed temperature range, and the maximum MR values of 86% and 69% appeared at 74 K and 42 K.     

First-principles study of the structural, magnetic, and electronic properties of LiMBO3 (M = Mn, Fe, Co)

We present a first-principles calculation for the structural, magnetic, and electronic properties of LiMBO₃ (M = Mn, Fe, Co). Along the [0 0 1] direction, transition metals shows antiferromagnetic coupling in LiMBO₃ of both hexagonal and monoclinic lattices. The calculated magnetic moment of 5μB per formula unit is close to the experimental value. These compounds are semiconductors with band gap of 0.4-2 eV, and with average intercalation voltages of 2-4.8 V.     

Physical properties of the cubic spinel LiMn2O4

We have performed an ab initio study of structural, electronic, magnetic, vibrational and thermal properties of the cubic spinel LiMn₂O₄ by employing the density functional theory, the linear-response formalism, and the plane-wave pseudopotential method. An analysis of the electronic structure with the help of electronic density of states shows that the density of states at the Fermi level (N (E_F)) is found to be governed by the Mn 3d electrons with some contributions from the 2p states of O atoms. It is important to note that the contribution of Mn 3d states to N(_EF)$N\left(E_F\right)$ is as much as 85%. From our phonon calculations, we have obtained that the main contribution to phonon density of states (below 250 cm⁻¹) comes from the coupled motion of Mn and O atoms while phonon modes between 250 cm⁻¹ and 375 cm⁻¹ are characterized by the vibrations of all the three types of atoms. The contribution from Li increases rapidly at higher frequency (above 375 cm⁻¹) due to the light mass of this atom. Finally, the specific heat and the Debye temperature at 300 K are calculated to be 249.29 J/mol K and 820.80 K respectively.     

Synthesis, microstructure and photoluminescence of Eu/Tb activated Y2SiO5 nanophosphors by new silicate sources

Y_2−xTb_xSiO₅ and Y_2−xEu_xSiO₅ nanophosphors with seven different kinds of silicate sources were synthesized by sol-gel method. The structures have been investigated to be composed of nanometer-size grains of 30-60 nm through X-ray diffraction (XRD) and scanning electron microscopy (SEM) was used to compare the different morphology of patterns from seven different silicon sources. The photoluminescence of Y_2−xTb_xSiO₅ was investigated as a function of silicate sources and the results revealed that these nanometer materials showed the characteristic emission ⁵D₄ → ⁷F_J (J = 6, 5, 4, 3) of Tb ions. The characteristic emission ⁵D₀ → ⁷F_J (J = 1, 2, 4) of Eu ions was also found in the materials of Y_2−xEu_xSiO₅.