Direct and indirect dipole-dipole coupling between111Cd,113Cd and125Te in solid CdTe

In nuclear magnetic resonance spectra of¹¹³Cd and¹²⁵Te in solid CdTe a splitting has been found. The intensity of the satellites is proportional to the natural abundance of¹¹¹Cd,¹¹³Cd and¹²⁵Te. From a NMR rotation pattern of¹²⁵Te in a CdTe single crystal in addition to a direct dipole-dipole coupling between¹²⁵Te and¹¹¹Cd,¹¹³Cd an indirect anisotropic dipole-dipole interaction has been observed. If the direct dipoledipole coupling is calculated from crystal geometry and from the gyromagnetic ratios of¹¹³Cd and¹²⁵Te, the indirect dipole-dipole interaction isJ (¹¹³Cd–¹²⁵Te)=(765±90)Hz perpendicular andJ (¹¹³Cd–¹²⁵Te)=(435±120)Hz parallel to the internuclear axis.     

Fluctuating Electric Field Gradients at 111Cd in Ice

¹¹¹Cd–PAC measurements have been made using the high specific activity of ¹¹¹In in the methanol–water mixtures of various concentrations at the room temperature. These experiments revealed that the perturbation factors 〈A ₂ G ₂〉 (integrated over two mean lives τ_N) do not follow the dependence of the macroscopic viscosity η. The observed dynamic character of the PAC spectra in ice is explained by the mobility of orientational and ionic defects. The activation energy for the diffusion process was determined to be E _a =0.35(1) eV. This revised version was published online in September 2006 with corrections to the Cover Date.     

An NMR quantum computer of the semiconductor CdTe

We propose a method to implement a quantum computer by solid-state NMR. We can use the J-coupling for the quantum gate in CdTe. Both Cd and Te have two isotopes with spin 1/2, then we can have 4-qubits. The decoherence by dipole interaction may be minimized by preparing the isotope superlattice grown in the order of—¹¹¹Cd–¹²³Te–¹¹³Cd–¹²⁵Te—in the [111] direction and by applying the magnetic field in the direction of [100], the magic angle of the dipole interaction. The optical pumping technique can be used in CdTe to make the initialization of the qubits.     

Physical properties of the doped manganites Ln0.5M0.5Mno3 (Ln = Pr,La; M = Sr,Ca, Ba)

We present the structural, magnetic and electrical properties of some manganese oxides such as Ln_0.5M_0.5MnO₃ (Ln = La, Pr and M = Ca, Sr, Ba) in which the average ionic radius <r_A> of the A site cation is varied while keeping the Mn³⁺/Mn⁴⁺ ratio fixed to 1. All the studied samples have a perovskite structure with rhombohedral or orthorhombic distortion. This distortion was related to the A cation size. The lattice volume increases lineraly with ( r _A) in all the range 1.179–1.3264 Å. The magnetic investigation shows that the magnetic transition temperature T _t, and magnetisation saturation M _s have similar behaviour by increasing and decreasing with (r _A). The electrical measurements show conduction by small polarons attributed to a large canting angle 9 in all the range 4–300 K in the two ferromagnetic compounds La_0.5Sr_0.5MnO₃ and La_0.5Sr_0.5MnO₃.     

Structural,magnetic, and physical properties of La(1–x)MnO3±δ nano-manganite

A detailed structural, magnetic and physics properties of La_1?xMnO_3±δ (LMO) nanomanganites were investigated to find out the role of cationic vacancies (La vacancy with Mn³⁺/Mn⁴⁺) in grain size modulation. Crystal structure and phase analysis of all samples were carried out by Rietveld refinement of high-resolution XRD and neutron diffraction data. We report here, the oxygen content in studied LMO compound decreases with increase in La vacancies in parent site and a parasitic Mn₃O₄ phase has been evolved in the range of 0.9 ≥ La/Mn ≥ 0.7. Para to ferro magnetic transition temperature (T_C) of all nanometric samples (La/Mn < 0.9) was found at high temperature side (≥260 K) whereas, the same for bulk one (La/Mn ≥ 0.9) was around 160 K. The enhancement of T_C (~70 K) with size reduction is attributed to broadening of bandwidth due to compaction of MnO₆ octahedra in system unit cell. In bulk sample, a secondary cluster/spin glassy phase is found below 50 K, whereas the glassy phase has been suppressed in nanoscale. Field-dependent magneto-resistance measurements are also carried out for all samples at different temperatures to get a profound insight of magneto-transport dynamics of the present system.     

The electric field gradient at111Cd in vanadium oxides

The electric field gradient (efg) of¹¹¹Cd in polycrystalline V₂O₅ was studied using perturbed angular correlation (PAC) spectroscopy, with the¹¹¹In activity ion-implanted at 400 keV. Between the individual steps of an isochronal annealing program, a distinct efg (v _Q 1=88.1(3) MHz, ₁=0.62(2)) was recorded the contribution of which increased with annealing temperature up to 74% at 870 K. Corresponding X-ray analysis of inactive V₂O₅ samples, which underwent the same annealing treatment, proved that the sample always stayed as V₂O₅. Since V₂O₅ has only one equivalent cation site, it is concluded that this efg belongs to¹¹¹Cd at this site. Oxidation of a vanadium foil atT=675 and 800 K at =200 mbar also yielded this efg. From PAC measurements in VO₂, two well-defined efg's were found above and below the metal-semiconductor transition at 340 K, which are tentatively attributed to the monoclinic and the tetragonal phase.Supported by Deutsche Forschungsgemeinschaft and DAAD.On leave from the University of Durban-Westville, South Africa.     

Structure and chemical bond characteristics of LaB6

The structure and chemical bond characteristics of LaB₆ have been achieved by means of the density functional theory using the state-of-the-art full-potential linearized augmented plane wave (FPLAPW) method, which are implemented within the EXCITING code. The results show our optimized lattice constant a (4.158 Å), parameter z (0.1981) and bulk modulus B (170.4 GPa) are in good agreement with the corresponding experimental data. Electron localization function (ELF) shows the La–La bond mainly is ionic bond, La–B bond is between ionic and covalent bond while the covalent bond between the nearest neighbor B atoms (B2 and B3) is a little stronger than that between the nearer neighbor B atoms (B1 and B4).     

Hyperfine interaction of111Cd in antiferromagnetic cobalt oxide

The temperature dependence of the hyperfine field of substitutional¹¹¹Cd in antiferromagnetic CoO has been measured by means of the perturbed angular correlation technique. The Larmor frequency ω_L is found to obey a power law ω_L(t=ω₀ t ^β) up tot _max=0.4 wheret=1−T/T _N is the reduced temperature withT _N=291.2(3) K and β=0.393 (5) the critical exponent. The results are discussed and compared with PAC experiments on¹¹¹Cd in NiO and Ni and with results obtained by other methods.     

Electrical resistivity and superconductivity of amorphous La−Ag alloys

We report on measurements of the electrical resistivity and the superconducting transition temperature of amorphous La–Ag alloys (60–74 at % La) obtained by liquid quenching. The temperature coefficient of the resistivity is always slightly negativ, its value cannot be described well by existing theories.T _c depends linearly on the La content and seems to be not very sensitive to the second alloy constituent.Dedicated to Prof. Dr. W. Buckel on the occasion of his 60th birthday     

Pressure dependence of the electric field gradient in Sb and Sb1−x M x (M=ln,Zn, Ge,Pb, Cd,Sn) at the site of111Cd

Using the¹¹¹Cd-TDPAC (time differential perturbated angular correlation) method, the pressure dependence of the electric field gradient (EFG) in Sb and Sb_1–x M _x (M=ln, Zn, Ge, Pb, Cd, Sn) was investigated. The application of a phenomenological ansatz for the parametrisation of the pressure and temperature dependence of the EFG made it possible to combine temperature data gained in former studies [1], [2] with the pressure dependent data presented in this paper. The resulting pressure dependence of –2±0.2 MHz/kbar is shown to be independent of concentration and element of admixture. Results for the volume and explicit temperature dependence agree with existing information on the mixed system Sb_1–x M _x (M=ln, Zn, Ge, Pb, Cd, Sn); the investigation of the EFG in Sb_1–x–y M _x Pb _y showed that the resulting EFG may be interpreted as the weighted sum of the individual contributions of the two metals.This paper is dedicated to Prof. Dr. W. Kreische on the occasion of his 60th aniversary on 02.02.1995     

Roles of the blocking layer in high temperature copper-oxide superconductors

Roles of the blocking layer that we named the layer which separates Cu–O₂ layers more than 6Å have been studied by comparing two kinds of highT _c copperoxide superconductors such as Bi(2212) and La(2126) compound. These following results have been obtained. The hole concentration decreases when Sr is substituted by La and increases when Bi is substituted by Pb in Bi(2212), and it can be optimized by these substitution. In La(2126)T _c becomes up to 43K and the hole concentration (p;[Cu–O]^+p) increases to 0.09 by the substitution of Ca for La and heat treatment under high oxygen partial pressure. The distance between Cu–O₂ layers in both Bi(2212) and La(2126) are not changed by these substitution and heat treatment. We have found that the blocking layer has not direct roles for the maximumT _c value of the material though by supplying carriers to Cu–O₂ layers, it affects the actualT _c value.     

Superconductivity at 40 K in La1.8Sr0.2CuO4

High-T _c superconductivity withT _c onsets up to 42 K (midpoint: 37 K, zero resistance: 34 K) is observed in X-rays homogeneous single phase La_1.8Sr_0.2CuO₄. The quarternary compounds La_2–x Ba _x CuO₄ and La_2–x Sr _x CuO₄ (0x0.3 for Ba and 0x<1 for Sr, depending on the heating conditions) are mixed-valence oxygen defect oxides, characterized by the presence of Cu²⁺ and Cu³⁺ simultaneously. These oxides have a tetragonal symmetry (space group:I 4/mmm) similar to that of K₂NiF₄. We report the synthesis, characterization, and superconducting properties of various high-temperature superconducting La–Ba–Cu–O and La–Sr–Cu–O compounds. Through the substitution of Sr for Ba in these oxygen defect compounds an increasing superconducting transition temperature onset from 28 K to 35 K for La_1.8Sr_0.1Ba_0.1CuO₄ was observed. A positive initial pressure coefficient ofdTc/dp=290 (mK/kbar) has been found for La_1.8Sr_0.2CuO₄ with a magnetic susceptibility change consistent with the 100% diamagnetic expectation value.     

The Magnetic Hyperfine Field of 111Cd in the Rare Earth–Nickel Laves Phases RNi2

The magnetic hyperfine field of ¹¹¹Cd in the C15 Laves phases RNi₂ has been investigated by perturbed angular correlation (PAC) spectroscopy as a function of temperature for the rare earth constituents R = Nd, Sm, Gd, Tb, Dy, Ho, Er, and Tm.     

The electric quadrupole interaction of 111Cd in ZrZn2 and Zn in the samples prepared at 8 GPa

The perturbed angular correlation (PAC) measurements with the ¹¹¹In-¹¹¹Cd nuclear probe embedded into the lattice of the cubic (C15) Laves compound ZrZn₂ showed that ¹¹¹Cd nuclei experienced an axially symmetric electric quadrupole interaction with a frequency ν _Q  = 132.4 MHz at room temperature. The samples were synthesized and doped with the probe at a pressure 8 GPa. The temperature dependence of ν _Q was shown to be linear: ν _Q (T) = 147(1 − 0.033 T) MHz. Since the value of ν _Q is very close to that known for ¹¹¹Cd in the lattice of Zn, we have checked if it could be assigned to residual Zn metal in the sample. For the Zn sample melted and doped with ¹¹¹In at 8 GPa we have obtained ν _Q  = 117.3 MHz at 300 K and 127 MHz at 80 K – both values considerably lower than that for ¹¹¹In doped Zn samples prepared at an ambient pressure. These data, and the fact that ν _Q (T) in Zn is known to follow the T ^3/2 law, allow to attribute the ν _Q value quoted above to ¹¹¹Cd nuclei at the substitutional sites with tetrahedral symmetry in the Zn sublattice of ZrZn₂.     

Ab initio study of the EFG tensor at Cd impurities in Sc2O3 semiconductor

We present an ab initio study of diluted Cd impurities localized at both cation sites of the semiconductor Sc₂O₃. The electric-field-gradient (EFG) tensor at Cd impurities located at both cationic sites of the host structure was determined from the calculation of the electronic structure of the doped system. Calculations were performed with the full-potential augmented-plane wave plus local orbitals (APW+lo) method within the framework of the density functional theory. We studied the atomic structural relaxations and the perturbation of the electronic charge density induced by the impurities in the host system in a fully self-consistent way. We showed that the Cd impurity introduces an increase of 8% in the nearest oxygen neighbors bond-lengths, changing the EFG sign for probes located at the asymmetric cation site. The APW+lo predictions for the charged state of the Cd impurity were compared with EFG results existent in the literature, coming from time-differential γ–γ perturbed-angular-correlations experiments performed on ¹¹¹Cd-implanted Sc₂O₃ powder samples. From the excellent agreement between theory and experiment, we can strongly suggest that the Cd acceptor impurities are ionized at room temperature. Finally, we showed that simple calculations like those performed within the point-charge model with antishielding factors do not correctly describe the problem of a Cd impurity in Sc₂O₃.     

Nd crystal-field study of weakly doped Nd1−xCaxMnO3

Nd³⁺ crystal-field excitations in Nd_1−xCa_xMnO₃ (x=0.025, 0.05 and 0.1) single crystals are studied via infrared transmission as a function of temperature and external magnetic field. We report excitations associated with Nd³⁺ sites as detected in NdMnO₃ and excitations due to Ca doping. The latter reveal phase separation between the usual A-type antiferromagnetic states and the insulating canted (ferromagnetic) spin states in the vicinity of doped Ca²⁺ ions. Both Nd³⁺ crystal-field levels could be described using calculated parameters for NdMnO₃. Also, while oxygen stoichiometry and coherent Jahn–Teller distortions seem not to be affected by Ca doping, increased absorption bandwidths characterize the doped crystals.     

TDPAC measurement of quadrupole interaction at111Cd in the nearly heavy fermion system USn2.9

Quadrupole interaction at¹¹¹Cd probe has been studied in the nearly heavy fermion system USn_3– using the TDPAC method. We observe a large quadrupole interaction frequency withv _Q =89.9(10) MHz at 300 K which is much higher than the earlier reported result. The observed frequency shows a linear temperature dependence in the range 25–300 K.     

On the Cd III spectrum in a pulsed helium discharge

On the basis of the spectral line intensity relaxation during the plasma decay, fifty six spectral lines between 219 nm and 330 nm in the cadmium (Cd) spectrum were identified as Cd III (doubly ionized) or Cd IV (triply ionized) lines. The measured Stark widths of twelve, the most intense spectral lines around 315±15 nm with well defined profiles, are presented. Investigated spectral lines originate from the high lying energy levels, not classified up to now. A linear low-pressure pulsed arc was used as an optically thin plasma source. A pulsed discharge was produced in a pyrex discharge tube. Helium was chosen as the carrier gas. The cadmium atoms were sputtered from the thin cadmium cylindrical plates located in the homogeneous axial part of the discharge tube. The helium plasma was operated at electron temperatures up to 19 000 K and 1.1 × 10²³ m^-3 electron density. The stepwise ionization processes via the high lying singly ionized (Cd II) energy levels, populated well due to the Penning and charge exchange effects, provide high density of the Cd III (and Cd IV) ions in our helium plasma. The temporal evolutions of the spectral line intensities were monitored using a spectrograph and an ICCD camera as a highly sensitive detection system.     

Magnetic and magnetotransport properties of Co-doped manganites with perovskite structure

A systematic study of the doping of the Mn-sites by cobalt in three series of manganites — La_0.76Ba_0.24(Mn_1−xCo_x)O₃ single crystals, La_2/3Ba_1/3(Mn_1−xCo_x)O₃ and La(Mn_1−xCo_x)O₃ ceramics has been performed. It was found that La(Mn_1−xCo_x)O₃ annealed at 800°C in the range 0.4x0.9 is a mixture of ferromagnetic domains with ordered Mn and Co ions and ionically disordered spin-glass domains. In the quenched samples the fraction of spin-glass-type component increases strongly. The La_2/3Ba_1/3(Mn_1−xCo_x)O₃ solid solutions exhibit also an evidence for phase separation in the range 0.5x0.8. All the La(Mn_1−xCo_x)O₃ samples show an insulating behavior, however, magnetoresistance reduces strongly when the cobalt content rises to x=0.5. The La_0.76Ba_0.24(Mn_1−xCo_x)O₃ single crystals show first-order phase transition below their Curie points associated with a change of ground state of the Co²⁺ ions. The magnetic phase diagrams are depicted. The results are discussed in terms of positive Mn³⁺–O–Mn⁴⁺, Mn³⁺–O–Mn³⁺, Mn⁴⁺–O–Co²⁺ and negative Mn⁴⁺–O–Mn⁴⁺, Co²⁺–O–Co²⁺, Co²⁺–O–Mn³⁺ superexchange interactions as well as Co²⁺ and Mn⁴⁺ ionic ordering.