High-field magnetoresistance of polycrystalline ZrZn2

We report magnetoresistance measurements of polycrystalline ZrZn₂ as a function of temperature (4.2–48K) and magnetic field up to 19 T. The results indicate the presence of both positive and negative contributions to the magnetoresistance. The latter is due to spin fluctuations. Below T_c the resistivity varies with temperature like T² over the entire field range (0–19 T). The coefficient of the T² -term decreases with increasing field and fits a $\text{H}{}^{\mathrm{<mtext>?</mtext><mtext>1</mtext><mtext>3</mtext>}}$ dependence above ～ 10 T, in accordance with theoretical predictions. Complex behaviour of the magnetoresistance is found in the paramagnetic regime above ～ 5 T.     

Electrical transport properties of a quasi-one-dimensional Nb3Te4 single crystal

The electrical resistance of a linear chain metal Nb₃Te₄ were measured from 1.3 to 320 K. The residual resistance ratio $\text{R(300}\text{K}\text{)}\text{R(4.2}\text{K}\text{)}$ is about 3. Nb₃Te₄ shows an anomaly in the resistivity vs temperature at about 80 K, suggesting an occurrence of a charge-density-wave transition. The transverse and longitudinal magnetoresistance at 4.2 K are proportional to the magnetic field in the range of 2–58 kOe. In the superconducting region close to the transition temperature T_c, the critical magnetic field H_c2 is proportional to δT=T_c?T. The angular dependence of H_c2 fits well with the fluxoid model of the Ginzburg-Landau theory. The ratio of the critical fields parallel and perpendicular to the chain direction is 4.8.     

Electrical resistivity and magnetoresistance of CeB6

Electrical resistivity and magnetoresistance of CeB₆ single crystal have been measured in the temperature range from 1.3 to 300 K under the magnetic field up to 85 kOe. Three characteristic phases are distinguished consistently with other measurements. The Kondo like behaviour in the resistivity observed in the high temperature phase is fitted by the conventional form for the dilute Kondo state with the Kondo temperature T_K = 5 ～ 10K and the unitarity limit resistivity $\text{?}{}_{\mathrm{u}}\text{? 110 μΩ}$ cm/Ce-atom. The negative magnetoresistance in the middle phase is stronger with increasing magnetic field and with decreasing temperature suggesting rapid destruction of the Kondo state. The magnetoresistance in the low temperature phase exhibits some anomalies suggesting sub-phases corresponding to several kinds of spin ordering.     

The relaxation time study by Shubnikov-De Haas effect in Pb0.82Sn0.18 Te narrow band-gap semiconductors

The nature of broadening of the Landau levels in Pb_0.82Sn_0.18Te on the basis of recent experimental data is discussed. One needs to take into account the dependence of the monotonic part of magnetoresistance on the magnetic field H to determine the Dingle temperature on the Shubnikov-de Haas data. The Dingle temperature in solid solutions of Pb_0.82Sn_0.18Te is large (T_D=2.2?24.8 K) and depends on H. The T_D(H) dependence is explained of the transition to quantum limit. In this case the relaxation time _D=?(πkT_D)^?1 is increased with rising of the magnetic field, which is in accordance with the theory of Abrikosov. The _D/₀ dependence on carriers concentration can explain scattering on short range potential supposing the total scattering cross-section to be $\text{S}{}_{\mathrm{T}}\text{～?}{}^{\mathrm{<mtext>?1</mtext><mtext>2</mtext>}}$. It was shown that the presence of random fluctuations of crystal potential in the solid solution is the most possible reason of broadening of the quantum levels. The experiment supports the dependence T_D ～ √n obtaining theoretically. cally.     

Crystal fields and the Kondo properties of CeAl3

Crystal fields are included in a model calculation of the magnetization of the Kondo compound CeAl₃. Using parameters taken from experiment, the predicted magnetization at T=1.4 and 4.2K for applied magnetic fields H less than 10T is in good agreement with experiment. Using this magnetization, the model also correctly predicts the decrease in the specific heat C as a function of H for 0.35 ?T?0.9K. In particular, it correctly predicts that this decrease is approximately linear in H and that $\text{(}\text{?H}\text{?H}\text{)}{}_{\mathrm{T}}$ is approximately temperature independent.     

Longitudinal magnetoresistance in zero-gap CdxHg1−xTe at low temperatures

The longitudinal magnetoresistance Δ?₆(H)/?₀ is studied experimentally in gapless solid solutions Cd_xHg_1?xTe (0 < x < 0.15) for temperatures 1.3–15 K and the electron concentrations n ～ 10¹⁵ cm^?3. The temperature and the magnetic field dependences of the observed negative longitudinal magnetoresistance are explained by the resonant nature of electron scattering by an acceptor level. The quantitative analysis of the $\text{Δ?6(H)}\text{?}{}_0$ field dependence for weak magnetic fields under strong carrier degeneracy makes it possible to evaluate parameters of the acceptor level involved.     

A Mössbauer study of amorphous Fe40Ni40B20

Amorphous Fe₄₀Ni₄₀B₂₀ (VITROVAC 0040) alloy has been investigated using ⁵⁷Fe Mössbauer Spectroscopy. The Curie temperature T_c is found to be well defined and is 695 ± 1 K. The quadrupole splitting just above T_c is 0.64 mm sec^?1. The crystallization temperature is 698 ± 2 K, close to but definitely above T_c. The average hyperfine field H_eff(T) of the glassy state shows a temperature dependence of $\text{H}{}_{\mathrm{<mtext>eff</mtext>}}\text{(0)[1 ? B}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{(T/T}{}_{\mathrm{c}}\text{)}{}^{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{? C}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}\text{(T/T}{}_{\mathrm{c}}\text{)}{}^{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}\text{? …]}$ indicative of the existence of spin wave excitations. The values of $\text{B}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$ and $\text{C}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ are found to be 0.40 and 0.06, respectively, for T/T_c ? 0.72. At temperatures close to T_c, H_eff(T) varies as (1 ? T/T_c)^β where β is one of the critical exponents and its value is found to be 0.29 ± 0.02.     

Thermal changes in the optical properties of SnSxSe2−x crystals

Optical measurements on crystals in the series SnS_xSe_2?x for 0 ? x ? 2, have yielded information on the changes in the ordinary refractive index $\text{Δn}\text{ΔT}$ and the energy gap $\text{ΔEg}\text{ΔT}$ in the temperature range 125–425 K. The coefficient $\text{Δn}\text{ΔT}$ has values +40 to +160 × 10^?6K^?1 and this confirms that covalent bonding predominantly exists in these materials. The coefficient $\text{ΔEg}\text{ΔT}$ remains fairly consistent for all values of x with an average value of -8.0×10^-4eV K^-1.     

Pressure induced phase transition in the highly anisotropic compound: Y2[Pt(CN)4]3·21H2O

For the linear chain system Y₂[Pt(CN)₄]₃·21H₂O a pressure induced phase transition is observed by emission spectroscopy. At p_trans=(5±0.5) kbar and T=295 K the compound undergoes a first order phase transition, in the course of which the intra-chain Pt-Pt distance R shrinks by $\text{ΔR≈}\text{-0.03}\text{A}\text{?}$. An approximate value had already been found at standard pressure for a temperature induced phase transition (T_trans=218 K).     

Magnetic hyperfine interaction and curie temperatures of amorphous (FexNi1−x)80P14B6

Amorphous magnetic glasses (Fe_xNi_1?x)₈₀P₁₄B₆ (0.1 ? x ? 1) have been studied by Mössbauer spectroscopy. At 4.2 K, well-defined and very similar spectra have been observed for samples with different Fe concentration. This suggests that the Fe hyperfine field distribution is insensitive to the amount of dilutant. The value of the average hyperfine field at 4.2 K increases with Fe concentration. A value of 232 kOe is obtained by extrapolating to zero Fe concentration. The relationship $\text{H}{}_{\mathrm{eff}}\text{(O) = (232 + 33}\text{μ}\text{)}\text{kOe}$, similar to that of crystalline Fe-Ni alloys describes the results. The values of T_c = 60 K, 234 K and 425 K have been determined for samples with x = 0.125, 0.25 and 0.375 respectively. The T_C vs. x relation suggests a critical concentration of x_c ? 0.1, above which ferromagnetism exists. By fitting the measured values of T_C to the results of a coherent potential approximation, exchange interaction temperatures of J_FeFe = 617 K, J_FeNi = 800 K and J_NiNi ? 0 K have been obtained.     

Long range interactions and spin wave excitations in FexPd82−xSi18 metallic glasses

The low temperature magnetization of amorphous Fe_xPd_82?xSi₁₈, 2 ? x ? 25, approaches saturation like 1/H. RKKY-type cluster-cluster interactions and single impurity effects are indicated. The effective strength of the RKKY interaction decreases with increasing x. The magnetization of both spin glass-like and weakly ferromagnetic alloys exhibits Bloch's T^{$\text{3}\text{2}$} dependence. The spin wave stiffness constants increase linearly with 2 ? x ? 25. The range of exchange interactions decreases with increasing x.     

Electrical transport and magnetic properties of Nd2(WO4)3

Measurements of the molar magnetic susceptibility (X_m) of a powdered sample of Nd₂(WO₄)₃ in the temperature range 300–900 K, and the electrical conductivity (σ) and dielectric constant (?$\text{)}\text{?}$ of pressed pellets of the compound in the temperature range 4.2–1180 K are reported. X_m obeys the Curie-Weiss law with a Curie constant C= 3.13 K/mole, a paramagnetic Curie temperature θ= ?60 K and a moment of Bohr magnetons, p= 3.49 for the Nd³⁺ ion. The electrical conductivity data can be explained in terms of the usual band model and impurity levels. Both the σ and ?$\text{\$}\text{?}$data indicate some sort of phase transition round 1025 K. The conductivity follows Mott's law $\text{σ = A exp (?B/T}{}^{\mathrm{<mtext>1</mtext><mtext>4</mtext>}}\text{)}$ in the temperature range $\text{200 < T < 3000}\text{K with}\text{B = 45.00 (}\text{K}\text{)}{}^{\mathrm{<mtext>1</mtext><mtext>4</mtext>}}\text{and}\text{A = 1.38 × 10}{}^{\mathrm{?5}}\text{Ω}{}^{\mathrm{?1}}\text{cm}{}^{\mathrm{?1}}$. The dielectric constant increases slowly up to 600 K, as is usual for ionic solids. The increase becomes much faster above 600 K, which is attributed to space-charge polarization of thermally generated charge carriers.     

Structure,vibrational study and conductivity of the trihydrated uranyl bis(dihydrogenophosphate): UO2(H2PO4)2·3H2O

The X-ray structure (293 K) of UO₂(H₂PO₄)₂·3H₂O has been refined (R = 0.062): M_r = 518g, space group: P2₁/c (Z = 4); $\text{a = 10.816(1)}\text{A}\text{?}$, $\text{b = 13.896(2)}\text{A}\text{?}$, $\text{c = 7.481(1)}\text{A}\text{?}$, β = 105.65(1)^°, $\text{V = 1082.7(2)}\text{A}\text{?}{}^3$; D_c = 3.17 Mg m^?3. The structure consists of infinite chains along the (101) axis with U atoms bridged by two H₂PO₄ groups. The U atom is surrounded by a pentagonal bipyramid of oxygen atoms, one of them being an equatorial water molecule. The cohesion between the chains is ensured by hydrogen bonds involving the two last water molecules. An assignment of IR and Raman bands with isotopic substitution spectra is proposed. A phase transition at 128 K was made evident by DSC and spectroscopy. The room-temperature phase is characterized by a high disorder of the OH bond orientation while in the low-temperature phase H₂O and POH species appear well oriented. The conductivity seems to occur by proton transfer and protonic-species rotation at the POH-water molecular interface between the chains. ac conductivity has been determined by means of the complex-impedance method ($\text{σ}{}_{\mathrm{<mtext>RT</mtext>}}\text{～ (3?12) × 10}{}^{\mathrm{?5}}\text{Ω}{}^{\mathrm{?1}}\text{cm}{}^{\mathrm{?1}}$; E ～ 0.20 eV).     

Critical behaviour of a uniaxial ferromagnet,ErCl3·6H2O with predominant dipolar interactions

The parallel magnetic susceptibility χ of a uniaxial ferromagnet ErCl₃·6H₂O has been measured between 0.3 and 4.2K and specially near T_c = 0.353 K. The predominant contribution to the Curie-Weiss temperature is due to the dipolar interactions. χ is proportional to ?^?γ with $\text{? =}\text{T}\text{T}{}_{\mathrm{c}}\text{?1}$ in the range 10^?3 < ? < 5 × 10^?2. The γ value, γ = 1.01 ±0.03 is consistent with the theoretical prediction for a uniaxial dipolar ferromagnet.     

Electronic-excitation transfer collisions in flames—V. Cross sections for quenching and doublet-mixing of K(42P)-doublet by N2, O2, H2 and H2O

Weighted average cross sections for quenching of the K(4²P)-doublet by N₂, H₂, O₂ and H₂O, measured in flames, show no significant temperature dependence in the range from 1500 to 2500K. Doublet mixing cross sections for K(4²P$\text{3}\text{2}$?4²P$\text{1}\text{2}$) transitions were measured at 1720K for N₂, O₂, H₂O. The ratios of both mixing cross sections were measured independently and were found to agree with the detailed balance condition within 2 per cent. It is shown that an ionic intermediate-state model cannot explain the large magnitude of N_2? mixing cross sections.     

Magnetization process and principal magnetic susceptibilities in RbMnF3

The temperature dependence of χ_⊥, initialχ_p (powder), and evaluated χ_∥ for RbMnF₃ are reported for the temperature range of 4.2–106 K. A shallow minimum at $\text{T}\text{T}{}_{\mathrm{N}}\text{? 0.72}$ is observed in χ_⊥. The field dependence of the magnetization shows a smooth rotation of the spins to a normal direction above H_c ? 2.43 kOe at 4.2 K.     

Magnetic structures of PrCO2Si2 and TbCo2Si2 compounds

Neutron diffraction studies of polycrystalline PrCo₂Si₂ and TbCo₂Si₂ compounds were carried out at 4.2 and 293 K. Both samples have collinear antiferromagnetic order below T_N(31(1) and 46(1) K for Pr and Tb compound respectively), with their magnetic moments parallel to the c axis. The ordered magnetic moment values of Pr and Tb at 4.2 K (3.19 and 9.12 μ_B respectively), are close to the saturation value of the free ions. The corresponding magnetic space group P_l4/mnc (Sh⁴¹⁰₁₂₈) is body-anticentered ($\text{k =}\text{111}\text{222}$ refering to P_l cell).     

Large magnetic entropy change near room temperature in the LaFe11.5Si1.5H1.3 interstitial compound

The LaFe_11.5Si_1.5H_1.3 interstitial compound has been prepared. Its Curie temperature T_C (288 K) has been adjusted to around room temperature, and the maximal magnetic entropy change (|ΔS|～17.0 J·kg^-1·K^-1 at T_C) is larger than that of Gd (|ΔS|～9.8 J·kg^-1·K^-1 at T_C=293 K) by ～73.5% under a magnetic change from 0 to 5 T. The origin of the large magnetic entropy change is attributed to the first-order field-induced itinerant-electron metamagnetic transition. Moreover, the magnetic hysteresis of LaFe_11.5Si_1.5H_1.3 under the increase and decrease of the field is very small, which is favourable to magnetic refrigeration application. The present study suggests that the LaFe_11.5Si_1.5H_1.3 compound is a promising candidate as a room-temperature magnetic refrigerant.     

Vibrational spectra and force constants of symmetric tops: High resolution spectra of monoisotopic H3SiCl in the 2200-cm−1 region and rovibrational analysis of the ν1 and ν4 fundamentals

The gas phase infrared spectra of monoisotopic H₃Si³⁵Cl and H₃Si³⁷Cl have been studied in the $\text{ν}{}_1\text{ν}{}_4$ region near 2200 cm^?1 with a resolution of 0.012 and 0.04 cm^?1, respectively, and rotational fine structure for ΔJ = ±1 branches has been resolved. In addition, some information on ν₃ + ν₄ of H₃Si³⁵Cl near 2750 cm^?1 has been obtained. ν₁ and ν₄ are weakly coupled by Coriolis x, y resonance, $\text{B}\text{Ω}{}_{14}\text{ζ}{}_{14}\text{～ 2 × 10}{}^{\mathrm{?3}}\text{cm}{}^{\mathrm{?1}}$, only the upper states K′ = 2, l = 0 and K′ = 1, l = ?1 being substantially affected. Local perturbation due to rotational l(±1, ±1)-type resonance with ν₃ + ν₅⁺¹ + ν₆⁺¹ and ν₃ + ν₅⁺¹ + ν₆^?1 is revealed in the ΔK = +1 and ?1 branches, respectively. From a fit of the experimental line positions, standard deviations of 1.4 and 3.8 × 10^?3 cm^?1, respectively, to a model with five interacting levels conventional excited state parameters and interaction constants have been obtained. In $\text{H}{}_3\text{Si}{}^{35}\text{Cl}\text{H}{}_3\text{Si}{}^{37}\text{Cl}$ the fundamentals are ν₁, $\text{2201.94380(15)}\text{2201.9345(7)}$ and ν₄, $\text{2209.63862(8)}\text{2209.6254(2)}\text{cm}{}^{\mathrm{?1}}$, respectively. Q branches of the “hot” band (ν₃ + ν₄) ? ν₃ and of ν₄ of the ²⁹Si and ³⁰Si species have been detected.     

Critical slowing down of fluctuations in squaric acid (H2C4O4) at the phase transition observed by 13C spin-lattice relaxation

Spin lattice relaxation T₁ of naturally abundant ¹³C nuclei in squaric acid was measured close to the antiferroelectric-paraelectric phase transition temperature T_c = 373 K. A rapid increase in $\text{1}\text{T}{}_1$ is observed close to T_c coming from above, which follows the power law $\text{1}\text{T}{}_1\text{～ ε}{}^{\mathrm{?1.4}}$ where $\text{ε =}\text{(T ? T}{}_{\mathrm{c}}\text{)}\text{T}{}_{\mathrm{c}}$. This behaviour is explained on the basis of the two-dimensional character of the fluctuations.