Disorder dependence electron phonon scattering rate of V82Pd18 − xFex alloys at low temperature

We have systematically investigated the disorder dependence electron phonon scattering rate in three dimensional disordered V₈₂Pd_18 ? xFe_x alloys. A minimum in temperature dependence resistivity curve has been observed at low temperature $T=T_{\mathrm{m}}$. In the temperature range $5\text{ K}\le T\le T_{\mathrm{m}}$ the resistivity correction follows ${{\rho }_{\mathrm{o}}}^{5/2}{T}^{1/2}$ law. The dephasing scattering time has been calculated from analysis of magnetoresistivity by weak localization theory. The electron dephasing time is dominated by electron–phonon scattering and follows anomalous temperature (T) and disorder $({\rho }_0)$ dependence behaviour like ${\tau }_{\mathrm{e}\text{-}\mathrm{ph}}^{?1}\propto T^2/{\rho }_0$, where ${\rho }_0$ is the impurity resistivity. The magnitude of the saturated dephasing scattering time $({\tau }_0)$ at zero temperature decreases with increasing disorder of the samples. Such anomalous behaviour of dephasing scattering rate is still unresolved.     

YbNi2: A heavy fermion ferromagnet

Measurements of the magnetization and specific heat of YbNi₂ binary alloy are reported. The DC magnetic susceptibility displays a ferromagnetic behavior with a Curie temperature T_C=10.5 K, one of the highest found in Yb compounds. Moreover, the temperature dependence of the specific heat exhibits a lambda anomaly with a peak of 5.12 J/mol K at 9.4 K. The analysis also shows an additional magnetic contribution around 32 K stemming from the crystalline electric field of a quartet at ${\Delta }_1=72\mathrm{K}$ and a doublet at ${\Delta }_2=126\mathrm{K}$, according to the splitting of the Yb³⁺ ion in cubic symmetry. From the magnetic contribution to the specific heat, a relatively high Kondo temperature $T_K=27\mathrm{K}$ is estimated. Below the magnetic transition, the specific heat shows a huge value of the electronic coefficient ${\gamma }_{\mathit{LT}}=573\mathrm{mJ}/\mathrm{mol}\mathrm{K}$, which is a signature of a heavy fermion behavior. Therefore, this alloy is a fine example of enhanced ferromagnetism and heavy fermion behavior among Yb compounds.     

Pressure behaviour of birefringence in [(CH3)2CHNH3)]4Cd3Cl10 crystal

The studies of birefringence of [(CH₃)₂CHNH₃)]₄Cd₃Cl₁₀ single crystal were carried out in the temperature interval 240–420 K and in the hydrostatic pressure range up to 570 MPa. The shift of temperature of phase transition at T₁ to higher temperature is observed with increase of pressure with the pressure coefficient ${\mathit{dT}}_1/\mathit{dp}=0.233\mathrm{K}/\mathrm{MPa}$. The shift of phase transition at T₂ to higher temperatures with the pressure coefficient ${\mathit{dT}}_2/\mathit{dp}=0.063\mathrm{K}/\mathrm{MPa}$ is observed up to about 250 MPa. At temperature T_PCP=310 K and pressure p_PCP=310 MPa the character of continuous phase transition changes to there first order and it corresponds to the tricritical point existence. Based on the studies of the temperature and pressure dependences of birefringence of [(CH₃)₂CHNH₃)]₄Cd₃Cl₁₀ crystal, its (p,T) phase diagram was constructed and its main features were discussed.     

Triangle for the entropic index q of non-extensive statistical mechanics observed by Voyager 1 in the distant heliosphere

Tsallis [Physica A 340 (2004) 1) identified a set of numbers, the “q-triplet” ≡ {q_stat, q_sen, q_rel}, for a system described by non-extensive statistical mechanics. The deviation of the q's from unity is a measure of the departure from thermodynamic equilibrium. We present observations of the q-triplets derived from two sets of daily averages of the magnetic field strength B observed by Voyager 1 in the solar wind near 40 A.U. during 1989 and near 85 A.U. during 2002, respectively. The results for 1989 do not differ significantly from those for 2002. We find $q_{\mathrm{stat}}=1.75\pm 0.06$, $q_{\mathrm{sen}}=-0.6\pm 0.2$, and $q_{\mathrm{rel}}=3.8\pm 0.3$.     

Orientation relationship between α-Fe precipitate and α-Al2O3 matrix in iron-implanted sapphire

Fe ions were implanted into α-Al₂O₃ single crystals (sapphire) at room temperature and annealed in a reducing atmosphere. The orientation relationships (ORs) between α-Fe particles and sapphire matrix were investigated using transmission electron microscopy (TEM). All the α-Fe particles have the orientation relationship (OR) of (1 1 1)_α-Fe || (0 0 0 1)_sapphire and ${[1\overline{1}0]}_{\alpha \text{-Fe}}\left|\right|{[11\overline{2}0]}_{\text{sapphire}}$ with sapphire. This OR is predicted precisely by the coincidence of reciprocal lattice points (CRLP) method. The other OR of (1 1 0)_α-Fe || (0 0 0 1)_sapphire and ${[111]}_{\alpha \text{-Fe}}\left|\right|{[5\overline{1}\overline{4}0]}_{\text{sapphire}}$ reported before is confirmed by the same method to be one of the secondary preferred orientation relationships in the α-Fe/sapphire system.     

p(x) and Tc(x) characteristics in the Y 1−b(Ca)bBa2Cu3O6+x cuprate family

A model has been proposed to calculate the $p\left(x\right)$ and $T_c\left(x\right)$ dependences in the Y _1?b(Ca)_bBa₂Cu₃O_6+x high-$T_c$ cuprate family and applied to $b=0$, $b=0.1$, and $b=0.2$ cases, for which experimental data exist in the literature. The results obtained imply that the Ca efficiency to provide holes is independent of the basal plane oxygen concentration, which is consistent with a view that electrons from CuO₂ layers would go primarily to Ca since it is twice closer than oxygen (in addition, the chain oxygen is screened by a layer made up of Ba and O(4) ions). It is shown that, in fully oxygenized compounds ($x=1$) the average efficiency, $\chi$, of a chain oxygen to attract an electron from the two nearby layers is reduced by the Ca insertion, though not because the charge transfer mechanism is in itself weakened by Ca, but because a part of electrons that are otherwise available in CuO${}_2$ layers has already been removed by the substitution of Y ³⁺ with Ca²⁺. It has been found that the $b$-dependence of the average oxygen doping efficiency can be fairly accurately described by the following relation: $\chi \left(b\right)=0.39\times (1?0.78b)$. The calculated $p\left(x\right)$ and $T_c\left(x\right)$ dependences are in very good agreement with the available experimental data.     

Examining the fragmentation of 158 A GeV lead ions on copper target: Charge-changing cross sections

A stack of plastic CR-39 Track Detectors were exposed to 158 A GeV ²⁰⁷Pb ions at the CERN-SPS beam facility. The exposure of stack was performed at normal incidence with a fluence of about $1500\mathrm{ions}/{\mathrm{cm}}^2$. The total number of lead ions in each spill was about $7.8\times {10}^4$ with eight spills on each stack. For the stack with the Cu target, the lengths of etched cones on one face of the CR-39 detectors (before and after the target) were measured. Using these measurements and charge identification methodology in CR-39 track detectors, total and partial charge changing cross sections of 158 A GeV ${\mathrm{Pb}}^{82+}$ ions on Cu and CR-39 targets are determined in the charge region $63⩽Z⩽82$. The possibilities of presence and absence of odd–even effect in measured partial charge changing cross sections of 158 A GeV Pb ions for Cu and CR-39 targets are described. The charge resolution $({\sigma }_Z)$ achieved in the present experiment is $\sim 0.18\mathrm{e}$–0.21e. The analysis of discrepancies between our experimental results and other published results for the identical reaction is also presented.