SrTb2Fe2O7 studied by mössbauer spectra of 57Fe

The temperature dependence of the hyperfine parameters of ⁵⁷Fe in SrTb₂Fe₂O₇ gave a magnetic ordering temperature T_N=542 K, saturation effective magnetic fieldH_eff(0)=552 kGand Debye temperature θ_D=330 K. The princip al axis of the PFG tensorV_zzis angled at 9° to the crystallographic c axis. Mössbauer spectra at 4.2 K reveal reorientation of iron spin.     

Electron-phonon scattering in potassium at high magnetic fields

We have measured the temperature dependence of both the zero-field resistivity and the transverse magnetoresistance of polycrystalline potassium wires (?(300 K)/?(4.2 K)=140 to 6000) in fieldsH?35 kG and at temperaturesT?4.2 K. Our principal findings are: 1) The presence of a large magnetic fieldH=35 kG does not alter the temperature dependence of ? from that observed atH=0; below 4.2 K theT-dependent part of the resistivities,_?T (H=0) and_?T (H=35 kG), fit well to the function exp (?Θ*/T) with the same Θ*=23K. 2) Deviations from Matthiessen's rule are significantly reduced in a strong field so that the magnitude of_?T (H=0) approaches that of_?T (H=35 kG) as sample purity decreases. 3) The slope of the high-field linear magnetoresistance increases slightly (?8%) from 1.5 K to 4.2 K. We attribute the exponential temperature dependence of_?T (H) to the freezing out of electron-phonon umklapp processes as has been shown for the zero-field resistivity. The reduction in deviations from Matthiessen's rule at high fields can be understood within semiclassical theory, but the latter cannot explain the failure of_?T (H) to saturate at high fields. A proposal by Young that electron-phonon umklapp scattering may contribute aT-dependent high-field linear magnetoresistance in potassium is considered.     

Mössbauer effect study of SrEu2Fe2O7

The antiferromagnetic ferrite SrEu₂Fe₂O₇ was studied by Mössbauer effect of⁵⁷Fe in the range 77–650 K. Analysis of the data gives a Neel temperature of 544 K±2 K and an extrapolated effective magnetic fieldH(OK) of 545 kG. Good fit to the spectrum at 290 K is obtained withH _eff=475 kG, δ=0.37 mm/s, 1/2e ² qQ(1+η ²/3)=0.70mm/s, θ and ?=90°. The Brillouin function forS=5/2 poorly fits the experimental data of hyperfine magnetic fields. In the critical rangeH _eff can be described byH(T)=H(0)D(1?T/T _N )^β, where β nearly 0.29. The quadrupole interaction parameter is quite temperature independent, of the order of 0.69 mm/s in the paramagnetic state. Agreement with the value obtained by a point charge calculation is good. The largest axis of the EFG tensor,V _zz , lies in the plane (110), making an angle of 22.6° with thec axis. The direction of magnetization is nearly perpendicular toV _zz in [110] direction.     

Study of quasi two-body final states in K−n reactions at 8.25 GeV/c

Cross sections for various channels in 3 prong + V₀ final states of K^?n interactions are obtained at 8.25 GeV/c. An energy dependence study of the quasi two-body reactions Σ^?(1385) + vector meson and ΛB^? seem to imply the presence of cuts in the Regge exchange formalism, whereas the reaction Δ(1236) $\text{K}$¹ (890) does not require such cuts. Upper limits of 1 and 2 μb are found for the reactions K^?n → ΛA₁ and K^?n → ΛA₂.     

Magnetic and electric hyperfine interactions of181Ta implanted in thulium

The magnetic and electric hyperfine interaction at the site of dilute¹⁸¹Ta impurities in the rare earth metal Tm has been investigated as a function of temperature by TDPAC measurements. The samples were prepared by ion implantation of radioactive¹⁸¹Hf. In the paramagnetic phase between 100 K and 700 K the electric fieldgradient is a linear function of temperature: V_zz(T)=V_zz(O)·(1-A·T) with A=4.6·10^?4K^?1 and V_zz(293K)=6.4 (4)·10¹⁷v/cm². The TDPAC spectrum observed at 4.2 K reflects the 4 magnetically non-equivalent sites for an impurity in magnetically ordered Tm. The relative values and amplitudes of the corresponding 4 magnetic hyperfine fields are consistent with the predictions of the RKKY theory.     

Magnetic properties of the compounds N(CH3)4MnIIMIII(CN)6 ·8 H2O(MIII = Mn,Fe)

In the isostructural cyanobridged chain compounds N(CH₃)₄Mn^IIM^III(CN)₆ · 8H₂O high spin Mn(II) ions couple antiferromagnetically to low spin Mn(III) of Fe(III) ions. The Mn^II–Mn^III compound orders ferrimagnetically below T_N = 28.5 ± 1 K. The tetragonal a and b axes are easy ones for the magnetic moments. In the Mn^II–Fe^III compound antiferromagnetic order occurs below T_N = 9.3 K, with spins aligned along the tetragonal c axis. The compound undergoes a meta-magnetic transition from the antiferromagnetic to a ferrimagnetic phase. This occurs at 2 K for a field H_crit ≈ 1.2 T. The temperature dependence of H_crit, which vanishes at T_N, is followed. The tricritical temperature T¹ is ～ 5 K.     

Magnetoresistance of La<Subscript>0.67</Subscript>Sr<Subscript>0.33</Subscript>MnO<Subscript>3</Subscript> epitaxial films grown on a substrate with low lattice mismatch

The structure, electrical resistivity, and magnetoresistance of La_0.67Sr_0.33MnO₃ heteroepitaxial films (120-nm thick) practically unstrained by lattice mismatch with the substrate were studied. A strong maximum of negative magnetoresistance of ≈27% (for μ₀H = 4 T) was observed at T ≈360 K. While the magnetoresistance decreased monotonically in magnitude with decreasing temperature, it was still in excess of 2% at 150 K. For T < 250 K, the temperature dependence of the electrical resistivity ρ of La_0.67Sr_0.33MnO₃ films is fitted well by the relation ρ = ρ₀ + ρ ₁(H)T^2.3, where ρ₀ = 1.1×10^?4 Ω cm, ρ₁(H = 0) = 1.8×10^?9 Ω cm/K^2.3, and ρ₁(μ₀H = 4 T)/ρ₁(H = 0) ≈0.96. The temperature dependence of a parameter γ characterizing the extent to which the electrical resistivity of the ferromagnetic phase of La_0.67Sr_0.33MnO₃ films is suppressed by a magnetic field (μ ₀H = 5 T) was determined.     

Magnetic and Transport Properties of Tm2Co7B3 Compound

Magnetic and transport properties of Tm₂Co₇B₃ compound have been studied. This compound crystallizes in the hexagonal Ce₂Co₇B₃ type structure. The coercivity (H _c) of the compound was determined from hysteresis measurements in fields up to 4 T. The temperature dependence of coercivity has been explained by a thermally activated process of domain wall motion. The resistivity at low temperatures shows a T ² dependence. At higher temperatures the resistivity is not a linear function of temperature, which indicates an electron-phonon interaction in the presence of a small s-d scattering.     

Spin-lattice relaxation of the Vk-center in LiF

The angular and temperature dependences of the spin-lattice relaxation (SLR) rate of V_k-centers in LiF doped with Mg or Ag have been investigated. In the temperature interval 4.2–100 K the results can be fitted by the formula $\text{τ}{}^{\mathrm{?1}}\text{= A(θ)T + Be}{}^{\mathrm{<mtext>?\Delta </mtext><mtext>T</mtext>}}$ with A(0°) = 0.11 sec^?1K^?1, A(90°) = 1.3 sec^?1K^?1, B = 3 × 10⁵sec^?1 and Δ = (175 ± 15)K.A mechanism for the SLR is considered, assuming the modulation of the hyperfine interaction by phononinduced transitions between the ground and excited states of the resonant molecular vibrations of the V_k-center. This mechanism is found to explain the value, the temperature dependence and the isotropy of τ^?1 in the interval T = 20–100 K.The one-phonon SLR mechanisms of the V_k-center in the T < 10 K region are discussed.     

Anisotropy of Hc2 in superconducting Pb-1.8 at% Tl

The temperature dependence of the H_c2 anisotropy has been measured on Pb-1.8 at% Tl alloys. The experiments indicate that the anisotropy does not vanish when the Ginsburg-Landau parameter K₁(T) approaches 2^{$\text{?1}\text{2}$}.     

Microfabrication and magnetoelectric properties of amorphous magnetic-tunnel-junctions with Co–Fe–B/Al–O/Co–Fe–B hardcore structure

Both single-barrier magnetic tunnel junctions (SBMTJs) and double-barrier magnetic tunnel junctions (DBMTJs) with an amorphous hardcore structure of Co₆₀Fe₂₀B₂₀/Al–O/Co₆₀Fe₂₀B₂₀ were microfabricated. A high TMR ratio of 102.2% at 4.2 K was observed in the SBMTJs after annealing at 265 °C for 1 h. High TMR ratio of 56.2%, low junction resistance-area product RS of 4.6 kΩ μm², small coercivity H_C=25 Oe, and relatively large bias-voltage-at-half-maximum TMR with the value V_1/2 greater than 500 mV at room temperature (RT) had been achieved in such Co–Fe–B SBMTJs. Whereas, high TMR ratio of 60% at RT and 89% at 30 K, low junction resistance-area product RS of 7.8 kΩ μm² at RT and 8.3 kΩ μm² at 30 K, low coercivity H_C=8.5 Oe at RT and H_C=14 Oe at 30 K, and relatively large bias-voltage-at-half-maximum TMR with the value V_1/2 greater than 1150 mV at RT had been achieved in the Co–Fe–B DBMTJs. Temperature dependence of the TMR ratio, resistance, and coercivity from 4.2 K to RT, and applied voltage dependence of the TMR ratio and resistance at RT for such amorphous MTJs were also investigated.     

Relaxation phenomena and nuclear magnetic resonance of116In(T 1/2=14s) produced by capture of polarized neutrons in the indium III–V compounds

Polarized¹¹⁶In nuclei have been produced by capture of polarized thermal neutrons in several In compounds. At temperaturesT below 77 °K and magnetic field strengthsH ₀ of several kOe, asymmetries of a few percent of the β^? decay of the¹¹⁶In ground state could be observed in polycrystalline InP, InAs and InSb, thus indicating the nuclear polarization. Nuclear magnetic resonance signals have been measured with the result for the magnetic moment μ _i (¹¹⁶In)=2.7723 (10) nm (uncorrected). β^? decay asymmetry and spin lattice relaxation timeT ₁ have been studied as a function ofH ₀ andT. The effect ofH ₀ is to decouple the hyperfine interaction caused by the capture-γ recoil process. However,H ₀ has no influence uponT ₁, which demonstrates the absence of nuclear relaxation due to paramagnetic impurities.T ₁ is determined by quadrupolar relaxation. A quadrupole momentQ(¹¹⁶In)=0.09 (2) b was calculated by comparison of the¹¹⁶In relaxation rates with those of the stable¹¹⁵In isotope in the same compounds. Above 30 °K the temperature dependence of 1/T ₁ agrees with a recent theoretical investigation. Below 30 °K the relaxation rate shows an anomalous behaviour, which can be explained by resonance modes due to recoil lattice defects.     

Equation of state and thermal expansivity of LiF and NaF

The high-pressure and high-temperature behaviors of LiF and NaF have been studied up to 37 GPa and 1000 K. No phase transformations have been observed for LiF up to the maximum pressure reached. The B1 to B2 transition of NaF at room temperature was observed at ～28 GPa, this transition pressure decreases with temperature. Unit-cell volumes of LiF and NaF B1 phase measured at various pressures and temperatures were fitted using a P–V–T Birch–Murnaghan equation of state. For LiF, the determined parameters are: α₀ = 1.05 (3)×10^?4 K^?1, dK/dT = ?0.025 (2) GPa/K, V ₀ = 65.7 (1) Å³, K ₀ = 73 (2) GPa, and K′ = 3.9 (2). For NaF, α₀ = 1.34 (4)×10^?4 K^?1, dK/dT = ?0.020 (1) GPa/K, V ₀ = 100.2 (2) Å³, K ₀ = 46 (1) GPa, and K′ = 4.5 (1).     

Evolution of domain walls and reversal mechanism in exchange-coupled nanolayers

The demagnetization process for an exchange-coupled double-nanolayer system with perpendicular easy axes has been investigated within a micromagnetic model. The nucleation field, coercivity and angular distribution of the magnetization, have been obtained as functions of the thickness L of the misaligned layer, the layer with the easy axis perpendicular to the applied field. It is found that the coercivity is identical to the nucleation field only for very small L. For larger L (larger than a quarter of its Bloch wall width), the nucleation field is negative while the coercivity saturates at 0.414H_K, where H_K is the anisotropy field. Thus for larger L, the coercivity mechanism is self-pinning rather than pure nucleation. This self-pinning has both attributes of traditional nucleation and pinning.     

Large deviations and Lifshitz singularity of the integrated density of states of random Hamiltonians

We consider the integrated density of states (IDS) ρ_∞(λ) of random Hamiltonian H_ω=?Δ+V_ω, V_ω being a random field on ? ^d which satisfies a mixing condition. We prove that the probability of large fluctuations of the finite volume IDS |Λ|^?1ρ(λ, H_Λ(ω)), Λ ? ? ^d , around the thermodynamic limit ρ_∞(λ) is bounded from above by exp {?k|Λ|},k>0. In this case ρ_∞(λ) can be recovered from a variational principle. Furthermore we show the existence of a Lifshitztype of singularity of ρ_∞(λ) as λ → 0⁺ in the case where V_ω is non-negative. More precisely we prove the following bound: ρ_∞(λ)≦exp(?kλ^?d/2) as λ → 0⁺ k>0. This last result is then discussed in some examples.     

Structural, vibrational and dielectric properties of new potassium hydrogen sulfate arsenate: K4(SO4)(HSO4)2(H3AsO4)

A new compound, K₄(SO₄)(HSO₄)₂(H₃AsO₄) was synthesized from water solution of KHSO₄/K₃H(SO₄)₂/H₃AsO₄. This compound crystallizes in the triclinic system with space group P1¯ and cell parameters: a=8.9076(2) Å, b=10.1258(2) Å, c=10.6785(3) Å; α=72.5250(14)°, β=66.3990(13)°, γ=65.5159(13)°, V=792.74(3) Å³, Z=2 and ρ_cal=2.466 g cm⁻³. The refinement of 3760 observed reflections (I>2σ(I)) leads to R₁=0.0394 and wR₂=0.0755. The structure is characterized by SO₄²⁻, HSO₄⁻ and H₃AsO₄ tetrahedra connected by hydrogen bridge to form two types of dimer (H(16)S(3)O₄⁻?S(1)O₄²⁻ and H(12)S(2)O₄⁻?H₃AsO₄). These dimers are interconnected along the [1¯ 1 0] direction by the hydrogen bonds O(3)-H(3)?O(6). They are also linked by the hydrogen bridge assured by the hydrogen atoms H(2), H(3) and H(4) of the H₃AsO₄ group to build the chain S(1)O₄?H₃AsO₄ which are parallel to the “a” direction. The potassium cations are coordinated by eight oxygen atoms with K-O distance ranging from 2.678(2) to 3.354(2) Å.Crystals of K₄(SO₄)(HSO₄)₂(H₃AsO₄) undergo one endothermic peak at 436 K. This transition detected by differential scanning calorimetry (DSC) is also analyzed by dielectric and conductivity measurements using the impedance spectroscopy techniques. The obtained results show that this transition is protonic by nature.     

Magnetic susceptibility of (CH3NH3)2FeCl3Br: An example of a canted spin system

Magnetic susceptibility of (CH₃NH₃)₂FeCl₃Br is measured in the temperature range 80–200°K. A sharp peak characteristic of a spin canted system is found at T_N(H=0)=98° K. Magnetic field dependence of the susceptibility and the effect of the halide ion size on the canted spin is discussed.     

Inclusive cross sections in the central region and the supercritical pomeron

Using the double-Regge formalism and a supercritical pomeron with α_P(0)=1+Δ, we analyse the energy dependence of inclusive cross sections for negatively charged particles (c⁻) and K_s⁰ at CM rapidity y=0 in the CERN PS-Sp̄pS collider energy range. The values of Δ(c⁻)=0.170±0.008 and Δ(K_s⁰)=0.167±0.024 are found to be very close to each other and compatible with estimates of Δ derived from the total cross sections.     

Anomalous pressure dependence of the Lamb-Mössbauerf-factor in the spin crossover system [Fe(2-pic-ND2)3]Cl2·EtOD

The pressure dependence of the Lamb-Mössbauer factor of the spin crossover compound [Fe(2-pic-ND₂)₃]Cl₂·EtOD(2-pic-ND₂=2-picolylamine, deuterated at the^?NH₂ group) has been measured at pressures up to 1500 bar and at three temperatures (115.7, 146.7, 185.6 K) around the transition temperatureT _t=135 K. The temperature dependence of the unit cell volume has been determined by X-ray diffraction. In the transition region (T=146.7 K), the pressure dependence of thef-factor shows an anomalous increase as compared to the dependence below and above the transition. The behaviour off(p, T), its anomaly and absolute value, can be consistently explained within a theoretical model which treats the compound as an isotropic elastic medium. The Poisson ratio of σ=0.4, the bulk modulusK (185.6 K)=1.26·10¹⁰ Nm^?2, and the Grüneisen constant γ^G=3.1 were determined.     

Magnetoelastic properties of ErMn6Sn6 intermetallic compound

The thermal expansion and magnetostriction of polycrystalline sample of the ErMn₆Sn₆ intermetallic compound with hexagonal HfFe₆Ge₆-type structure are investigated in the temperature range of 77 K to above 400 K. The thermal expansion measurement of the sample shows anomalous behavior around its T_N=340 K. The isofield curves of volume magnetostriction also reveal anomalies at paramagnetic-antiferromagnetic and antiferromagnetic-ferrimagnetic phase transitions. In the antiferromagnetic state, the transition to ferrimagnetism can be induced by an applied magnetic field. The threshold field for the metamagnetic transition H_th increases from 0.18 T at 84 K to about 1 T around 220 K, and then decreases monotonously to T_N. This behavior is well consistent with that observed earlier on magnetization curves attributed to exchange-related metamagnetic transition rather than the anisotropy-related one. Furthermore, the low H_th values suggest that the Mn-Mn coupling in ErMn₆Sn₆ is not so strong. The experimental results obtained are discussed in the framework of two-magnetic sublattice by bearing in mind the lattice parameter dependence of the interlayer Mn-Mn exchange interaction in this layered compound. From the temperature dependence of magnetostriction values and considering the magnetostriction relation of a hexagonal structure, we attempt to determine the signs of some of the magnetostriction constants for this compound.