Anisotropic magnetic susceptibility and phase transitions in intercalated graphite: KC24

We measured the magnetic susceptibility of KC₂₄ from 4.2 to 300 K and found no anomalies near the phase transitions at 95 and 123 K as observed in the resistivity. We conclude that the transitions must be due to order- disorder transitions of the K atoms and not charge density wave formation. The susceptibility is anisotropic; at room temperature $\text{χ}{}_{\mathrm{g}}\text{(}\text{H}\text{6}\text{c}\text{)= + 1.50 × 10}{}^{-6}\text{emu g}{}^{-1}\text{± 2\%}$ and $\text{χ}{}_{\mathrm{g}}\text{(}\text{H}\text{⊥}\text{c}\text{)= + 0.045 × 10}{}^{-6}\text{emu g}{}^{-1}\text{± 50\%}$. This anisotropy is not understood in terms of simple rigid band extensions of the band structure of graphite.     

X-ray diffraction, Raman spectrum and magnetic susceptibility of the magnetic semiconductor Cu2FeSnS4

In an attempt to resolve the crystal structure and the corresponding space group of the magnetic semiconductor Cu₂FeSnS₄, samples of this compound were studied by X-ray diffraction, differential thermal analysis, Raman scattering and magnetic susceptibility. It was found that at room temperature this compound prepared by a careful crystal growth process, including annealing to equilibrium at a suitable temperature followed by slow cooling of the samples to 300 K, crystallizes in a tetragonal structure with space group .     

Anisotropic resistivity and anisotropic magnetoresistance of the magnetic semiconductor FeCr2S4

Transport measurements were performed on FeCr₂S₄ parallelepipeds with {100} faces, cut from vapour grown crystals. This made possible the separation of the spontaneous effect from the field dependent effect. The anisotropy of the latter effect only depends on the direction of B relative to the crystallographic axes. The anisotropy of the magnetoresistance has been analysed in terms of spin disorder scattering.     

Cooperative emission study in ytterbium doped NdVO4

The infrared and visible cooperative emissions of ytterbium ions are studied in Yb-doped NdVO₄ single crystals. The absorption of optical phonons allows the emissions at room temperature when a Nd:YAG laser is used. Low temperature emissions are observed due to the Nd³⁺→Yb³⁺ energy transfer following an argon ion laser excitation of the Nd³⁺ ions. Analysis of the cooperative emission at low doping concentration (1%) indicates that it is generated by distant pair forming Yb³⁺ ions while at high doping concentration (≥ 5%) close ions magnetically coupled and superexchange mechanisms prevail in the emitting process.     

Anisotropic magnetic susceptibility of single crystal Ca2Y2Cu5O10 with edge-sharing CuO2 chain

We report a successful crystal growth of Ca₂Y₂Cu₅O₁₀ and anisotropic behavior of magnetic susceptibility associated with an antiferromagnetic phase transition. Single crystals were obtained by the floating-zone method using an infrared radiation furnace. Composition and structural characterization shows that the grown crystals are qualified for physical measurements. The magnetic susceptibility along each crystallographic axis shows a typical behavior of antiferromagnetic phase transition at T_N=31 K, and the ordered magnetic moments are found to lie along the b-axis.     

Bulk and local magnetic susceptibility in CeAl2 and CeB6

A comprehensive and high-precision magnetoresistance (MR) Δρ/ρ(H,T)$\mathrm{\Delta }\rho /\rho (H,T)$ and magnetization M(H,T) measurements have been carried out for two well known and archetypal magnetic strongly correlated electron systems—CeAl₂ and CeB₆. It was shown that the main Brillouin-type component of MR in these magnetic heavy fermion compounds can be consistently interpreted in the frameworks of a simple relation between resistivity and magnetization—Δρ/ρ∼M²$\mathrm{\Delta }\rho /\rho \sim M^2$ obtained by Yosida [Phys. Rev. 107 (1957) 396]. A local magnetic susceptibility _χloc(T,H)=(1/H^*(d(Δρ/ρ)/dH))^1/2${\chi }_{\mathrm{loc}}(T,H)=(1/H^{*}(\mathrm{d}(\mathrm{\Delta }\rho /\rho )/\mathrm{d}H){)}^{1/2}$ was deduced directly from this part of MR and compared in details with the data of bulk susceptibility χ(T,H) measurements. Two additional contributions to MR have been also deduced for CeAl₂ ((i) linear (∼H) and (ii) nanoscale ferromagnetic components) and applied for a characterization of spin polarons in this magnetic material. The dependencies χ_loc(T,H) and χ(T,H) obtained in this study for CeB₆ and CeAl₂ allow us to analyze the H–T magnetic phase diagram in these magnetic heavy fermion compounds.     

Infrared-excited bright green and red luminescence in La3Ga5.5Ta0.5O14 doped with erbium and ytterbium

Bright green (at 525 and 550 nm) and red (at 660 nm) luminescence in Er:Yb:La₃Ga_5.5Ta_0.5O₁₄ (LGT) powder synthesized by solid state reaction was obtained by pumping at 936 nm. Yb³⁺-Er³⁺ energy transfer processes accounting for population of the ²H2_11/2, ⁴S_3/2 and ⁴F_9/2 Er³⁺ levels are discussed. The dependence of ratio between the intensities of the green and red luminescence on pump intensity is analyzed. The rather high quantum efficiency (58%) of the (⁴S_3/2, ²H2_11/2) Er³⁺ emitting level recommends LGT doped with erbium and ytterbium for upconversion applications.     

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.     

NMR,magnetic susceptibility and specific heat of CrAl7

The temperature dependence of the magnetic susceptibility, Knight shift and specific heat for the compound CrAl₇ have been measured. These measurements point out that, at the temperature around T_N ≈220 K the compound CrAl₇ presents a second order phase transition from the electron itinerant antiferromagnetism state to the paramagnetic state. The NMR and magnetic susceptibility measurements are correlated and the results are discussed in terms of the electron itinerant antifer-romagnetism and rigid band models. For the temperature independent-term of the susceptibility all the contributions are given.     

Anisotropic polarons in lightly doped La2CuO4

The unusual anisotropy of an activation energy for the conductivity of highly pure La₂CuO₄ is explained in terms of disk-like polarons with large in-plane radius and small interplane one. For such a polaron the anisotropy of the mobility mechanism appears in a wide range of T: the in-plane hops are thermoactivated, while the interplane ones are due to the quantum tunneling. The T-dependence of Hall effect and the possibilities for the microscopic structure of a polaron in La₂CuO₄ are briefly discussed.     

Anisotropic domain-wall dynamics in proton-irradiated KH2PO4

KH₂PO₄ single crystals have been studied by employing complex impedance measurements in view of the domain freezing effect. As a result, distinct behaviors of the anisotropic domain-wall dynamics in the activation energy of domain freezing and the Vogel–Fulcher temperature before and after proton irradiation have been identified in the anisotropic crystal structure.     

Structural, microstructural and magnetic properties of NiFe2O4, CoFe2O4 and MnFe2O4 nanoferrite thin films

The structural, microstructural and magnetic properties of nanoferrite NiFe₂O₄ (NF), CoFe₂O₄ (CF) and MnFe₂O₄ (MF) thin films have been studied. The coating solution of these ferrite films was prepared by a chemical synthesis route called sol-gel combined metallo-organic decomposition method. The solution was coated on Si substrate by spin coating and annealed at 700 °C for 3 h. X-ray diffraction pattern has been used to analyze the phase structure and lattice parameters. The scanning electron microscopy (SEM) and atomic force microscopy (AFM) have been used to show the nanostructural behavior of these ferrites. The values of average grain's size from SEM are 44, 60 and 74 nm, and from AFM are 46, 61 and 75 nm, respectively, measured for NF, CF and MF ferrites. At room temperature, the values of saturation magnetization, M_s∼50.60, 33.52 and 5.40 emu/cc, and remanent magnetization, M_r∼14.33, 15.50 and 1.10 emu/cc, respectively, are observed for NF, CF and MF. At low temperature measurements of 10 K, the anisotropy of ferromagnetism is observed in these ferrite films. The superparamagnetic/paramagnetic behavior is also confirmed by χ′(T) curves of AC susceptibility by applying DC magnetizing field of 3 Oe. The temperature dependent magnetization measurements show the magnetic phase transition temperature.     

Anomalous magnetic behaviour and susceptibility maximum in CeSn3

Anomalous magnetic behaviour observed in one of cerium intermetallic compound, CeSn₃, is analysed in the spirit of the Fermi liquid model, by regarding even the 4f-electrons of cerium as itinerant. It is shown that the appearance of the broad peak of the susceptibility at about 150°K can be attributed to the T²1nT dependence of the susceptibility on temperature.     

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.     

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.     

Anharmonicity in silicate crystals: Temperature dependence of Au type vibrational modes in ZrSiO4 and LiAlSi2O6

Infrared reflection spectra for the extraordinary ray of zircon and spondumene have been obtained in the frequency range from 270 to 1500 cm^?1 and from room temperature up to 1300°K. Using a combination of Kramers-Kronig analysis and a classical dispersion theory, the oscillator parameters of the A_2u modes in zircon and A_u modes in spodumene were determined. The temperature dependence of observed mode damping is analysed on the basis of quantum theoreticall results involving both cubic and quartic anharmonic contributions. The comparison of the present results with other data reported in previously studied silicate crystals, shows that the observed anharmonic behavior of internal and external modes is consistent with simple considerations based on the site vicinity of each ion.     

Spectroscopic and magnetic properties of Fe3Fe4(AsO4)6

The infrared (IR) and ⁵⁷Fe-Mössbauer spectra of Fe₃^IIFe₄^III(AsO₄)₆ were recorded and analyzed on the basis of its structural characteristics. The IR spectrum presents a high complexity, showing an important number of bands and splittings, as a consequence of the presence of three structurally independent AsO₄³⁻ groups. The analysis of the four quadrupole signals shown by the Mössbauer spectrum allowed to attain a detailed insight into the cation distribution over the available crystallographic sites. The alternating current susceptibility measurements indicate a paramagnetic to ferrimagnetic transition in the material at about 59 K.     

Anisotropy in the magnetic susceptibility of 2H-TaSe2

The magnetic susceptibility of 2H-TaSe₂ is temperature dependent and anisotropic. The susceptibility with H parallel to the c axis is approximately 2.5 times that perpendicular. The decrease in susceptibility below the charge density wave transition at 122 K is also anisotropic with [χ₆(122 K) ? χ₆(4.2 K]?[χ_⊥(122 K) ? χ_⊥(4.2 K)] ≈ 4. Consequently, this change cannot be simply interpreted as a change in the density of states at the Fermi level, unless very anisotropic electron g values are assumed.     

Spectroscopic and magnetic susceptibility analyses of the FJ and D4 energy levels of Tb(4f) in TbAlO3

Detailed analyses of spectroscopic and temperature-dependent magnetic susceptibility data are reported for the crystal-field split energy levels of the ⁷F_J and ⁵D₄ of Tb³⁺ in stoichiometric single crystals of ortho-aluminate TbAlO₃. The spectroscopic data include absorption spectra obtained between 2940 and 480 nm from 8 to 300 K. High resolution fluorescence spectra are reported, representing transitions from ⁵D₄ to ⁷F_6,5,4, at a sample temperature of 85 K. Using crystal-field modeling techniques recently adapted for low symmetry systems, we have assigned all 58 experimental Stark levels within the ⁷F_J and ⁵D₄ manifolds, with a fitting standard deviation of 4.5 cm⁻¹ (3.8 cm⁻¹ rms error). As a further test, the theoretical Stark levels and calculated wavefunctions were used to determine the temperature dependence of the magnetic susceptibility along the c-axis of the TbAlO₃ crystal. Good agreement is obtained between the calculated susceptibility and temperature-dependent magnetic data reported earlier, including a prediction of a 0.2 cm⁻¹ splitting of the ground-state quasi-doublet. The susceptibility calculation also confirms the predicted ordering of states within the ⁷F₆ multiplet manifold.