Photoproduction of πmesons off protons from the Δ(1232) region to Eγ = 3 GeV

Photoproduction of π⁰-mesons was studied with the Crystal-Barrel detector at ELSA for incident energies from 300MeV to 3GeV. Differential cross-sections dσ/dΩ, dσ/dt, and the total cross-section are presented. For E _γ < 3GeV, the angular distributions agree well with the SAID parametrization. At photon energies above 1.5GeV, a strong forward peaking indicates t-channel exchange to be the dominant process. The rapid variations of the cross-section with energy and angle indicate production of resonances. An interpretation of the data within the Bonn-Gatchina partial-wave analysis is briefly discussed.     

Independent electron theory of multiple ionization of xenon by intense laser pulses

The intensity dependence of the multiphoton ionization spectra of Xe atoms has been investigated with an improved accuracy and well-controlled laser parameters. In particular, we have examined the ionization rates for X³⁺, X²⁻, X⁺ as functions of the laser intensity and the pressure in the target chamber. The apparatus used for these measurements is characterized by a high-energy resolution (better than 200 meV) and a completely digital acquisition system. The time-of-flight spectra clearly show the contributions of the different isotopes present in Xe gas. The laser pulses have been characterized with great accuracy by monitoring the energy, pulse width and divergence shot by shot. The ionization rates of the different ions have been used for testing the basic assumption of the Geltman theory of multiple ionization based on the single electron ionization model. We have found that for the small intensity range investigated the quantity (dXe ⁺/dI)·(dXe ³⁺/dI)/(dXe ²⁺/dI)² appears to be quite close to the value 0.5 predicted by this model.     

Correlation and polarization characteristics of the nuclear quasi-free (p,dπ<Superscript>+</Superscript>) reaction

An extended set of observables of the nuclear quasi-free (p, dπ⁺) reaction including the triple differential cross-section for coincidence measurements, its analyzing power in case of polarized proton beams and, also, the parameters of the polarization of the excited recoil nucleus and the produced deuteron are considered in the framework of the distorted-wave impulse approximation using the reaction ¹⁶O(p, dπ⁺)¹⁵N at a proton energy of 650 MeV as an example. The calculations show a high sensitivity of the differential cross-section and, especially, of the polarization transfer characteristics of the reaction to the spin-multipole decomposition of the amplitude of the basic two-body pp → dπ⁺ process.     

Doping and temperature dependence of the spin susceptibility in the p-d model

The spin magnetic susceptibility of the p-d model is calculated by means of a perturbation theory in the hybridization term V through a generalized cumulant expansion (GCE). The analysis is approached from the paramagnetic metallic phase. The results qualitatively reproduce some unusual magnetic properties in the normal state of the hole-doped cuprates, supporting the scenario of a Van Hove singularity near the Fermi level. Received 15 October 1998 and Received in final form 24 March 1999     

Production of secondaries in high-energy <Emphasis Type="Italic">d</Emphasis>+Au collisions

In the framework of the quark–gluon string model we calculate the inclusive spectra of secondaries produced in d+Au collisions at intermediate (CERN SPS) and at much higher (RHIC) energies. The results of numerical calculations at intermediate energies are in reasonable agreement with the data. At RHIC energies numerically large inelastic screening corrections (percolation effects) should be accounted for in the calculations. We extract these effects from the existing experimental data of RHIC on minimum-bias and central d+Au collisions. The predictions for p+Au interactions at LHC energy are also given.     

Elastic cross sections of 1s-muonic atoms at low energies in non-adiabatic approach

The low-energy elastic cross-section in collisions of a muonic atom with the hydrogen isotope is investigated, employing a new wave function (trial) and using the coordinate-space Faddeev–Hahn model. The wave function includes non-adiabatic terms. Our results of s–wave cross-sections are given, at the tμ(1s) + d scattering. Calculated cross-sections are in good accord with the results published by Chiccoli et al., while having no good agreement with other recent reports.     

Fine-structure energy levels, oscillator strengths and lifetimes in Co XV

Excitation energies from ground state for 97 fine-structure levels as well as oscillator strengths and radiative decay rates for all electric-dipole-allowed and intercombination transitions among the fine-structure levels of the terms belonging to the (1s ²2s ²2p ⁶)3s ²3p, 3s ³ p ², 3s ²3d, 3p ³, 3s3p3d, 3p ²3d, 3s3d ², 3s ²4s, 3s ²4p, 3s ²4d, 3s ²4f, and 3s3p4s configurations of Co XV are calculated, using extensive configuration-interaction (CI) wave functions, obtained with the CIV3 computer code of Hibbert. The important relativistic effects in intermediate coupling are included through the Breit-Pauli approximation via spin-orbit, spin-other-orbit, spin-spin, Darwin and mass correction terms. Small adjustments to the diagonal elements of the Hamiltonian matrices have been made. Our calculated excitation energies, including their ordering, are in excellent agreement with the experimental results and the experimentally compiled energy values of the National Institute for Standards and Technology (NIST) wherever available. The mixing among several fine-structure levels is found to be very strong, with most of the strongly mixed levels belonging to the (1s ²2s ²2p ⁶)3p ²3d and 3s3d ² configurations. The strong mixing among several fine-structure levels makes it very difficult to identify them uniquely. Perhaps, that may be the reason for the lack of both experimental and theoretical results for these levels. We believe that our extensive calculated values can guide experimentalists in identifying the fine-structure levels in their future work. From our radiative decay rates we have also calculated radiative lifetimes of some fine-structure levels. In this calculation we also predict new data for several fine-structure levels where no other theoretical and/or experimental results are available.     

Frustration of antiferromagnetism in the t-t′-Hubbard model at weak coupling

The perfect-nesting instability towards antiferromagnetism of the Hubbard model is suppressed by next-nearest neighbor hopping t′. The asymptotic behavior of the critical coupling U_c(t′) at small t′ is calculated in dimensions d = 2,3, ∞ using Hartree theory; this yields the exact result at least in d > 2. The order of the transition is also determined. A region of stability of a metallic antiferromagnetic phase in d = 3 is identified.     

Recent charm measurements through hadronic decay channels with STAR at RHIC in 200 GeV Cu+Cu collisions

We report on the measurements of D ⁰ and D _s meson production in 200 GeV Cu+Cu collisions at the STAR at RHIC experiment. Results are discussed with reference to pQCD predictions of the open charm cross-section as well as the statistical hadronization model.     

Ab initio calculation of the 4He(e, e'd )d reaction

The two-body knock-out reaction ⁴He(e, e'd )d is calculated at various momentum transfers. The full four-nucleon dynamics is taken into account microscopically both in the initial and the final states. As NN interaction the central MT-I/III potential is used. The calculation shows a strong reduction of the coincidence cross-section due to the final-state interaction. Nonetheless, the theoretical results exhibit a considerable overestimation of the experimental cross-section at lower momentum transfer. Comparisons with other, less complete, calculations suggest that consideration of a more realistic ground state might not be sufficient for a good agreement with experiment, rather a more realistic final-state interaction could play an essential role.     

The linkage between macroscopic gettering mechanisms and electronic configuration of 3d-elements in p/p+ epitaxial silicon wafers

We have measured the gettering efficiencies for Cr, Mn, Fe, Co, Ni and Cu in p/p+ epitaxial wafers. The gettering test started with a reproducible spin-on contamination on the front side of the wafers in the 10¹²–10¹⁴ atoms/cm² range, followed by thermal treatment to redistribute the metallic impurities in the wafer. The gettering efficiencies were measured by a novel wet chemical stratigraphic etching technique in combination with inductively-coupled plasma mass spectrometry. The residual bulk metal contamination was also measured by this method. This procedure led to global distributions of the 3d elements on the wafer’s front side, in the bulk of the wafer and on the wafer’s back side. Recovery rates were found to be 34%, 2.3%, 100%, 85%, 100% and 100% for Cr, Mn, Fe, Co, Ni and Cu, respectively. An impurity segregation effect in the wafer bulk was measured for Cu (100%) and Cr (34%), while no detectable segregation-induced gettering mechanisms were detected for the other elements in the applied concentration range. The segregation-induced gettering mechanisms were interpreted from the electronic structure of the metallic impurities. For segregation gettering by increased solubility in p+ silicon, the metallic species must form donors. Only Cu⁺ (3d ¹⁰) and Cr⁺ (3d ⁵) can form singly positively charged species that exhibit a spherical electronic distribution. It is well known from spinell structures that 3d ¹⁰ and, to a smaller extent 3d ⁵, are stable configurations in tetrahedral structures like the silicon lattice. Thus, we link the segregation-induced gettering mechanism in p/p+ epitaxial wafer to the electronic configuration of the 3d elements. Received: 19 January 2001 / Accepted: 31 January 2001 / Published online: 20 June 2001     

Antiferromagnetism and superconductivity in a model with extended pairing interactions

The competition between antiferromagnetism and the d + id superconducting state is studied in a model with near and next near neighbour interactions in the absence of any on-site repulsion. A mean field study shows that it is possible to have simultaneous occurrence of an antiferromagnetic and a singlet d + id superconducting state in this model. In addition, such a coexistence generates a triplet d + id superconducting order parameter with centre of mass momentum Q = (π,π) dynamically having the same orbital symmetry as the singlet superconductor. Inclusion of next nearest neighbour hopping in the band stabilises the d_xy superconducting state away from half filling, the topology of the phase diagram, though, remains similar to the near neighbour model. In view of the very recent observation of a broad region of coexistence of antiferromagnetic and unconventional superconducting states in organic superconductors, the possibility of observation of the triplet state has been outlined. Received 30 November 2000 and Received in final form 27 March 2001     

Chemical analysis of semiconducting and metallic SmS thin films by X-ray photoelectron spectroscopy

We studied the chemical state of semiconducting and metallic SmS thin films by X-ray photoelectron spectroscopy (XPS), which were fabricated using dual-target magnetron sputtering by controlling the power applied to both metal and chalcogenide targets. On the basis of the valence band spectra obtained, it was suggested that semiconducting SmS has the final state corresponding to the Sm²⁺(4f⁶) configuration below the Fermi level, and metallic SmS has mainly the Sm³⁺(4f⁵) final state and a virtual band state in the Sm 5d band, contributing to the delocalization of 4f electrons and the emergence of metallic conductivity (4f⁶d⁰-4f⁵d¹). Thus, the spectra of our fabricated SmS thin films correspond to the band structure obtained from the dielectric property. This is the first work performed on the intrinsically prepared metallic SmS while the former works done for the sample transformed from semiconductor to metal phase by hard polishing.     

Improved piezoelectric properties of cellular polypropylene ferroelectrets by chemical modification

To improve the thermal stability of piezoelectricity of polypropylene (PP) ferroelectrets, chemical modification of the cellular PP film was performed via chromic acid oxidation and then hydrofluoric acid treatment. Deep chemical modification is achieved as indicated by the energy-dispersive X-ray analyses on the cross-section of the modified cellular PP film. The results of the isothermal decay for piezoelectric d ₃₃-coefficient at 70°C indicate the improved thermal stability of piezoelectricity and the enhanced piezoelectric activity of the modified PP ferroelectrets. The former is attributed to the improvement of thermal stability of the charges trapped in the internal void surface layers as indicated by the thermally stimulated discharge measurements, while the latter results not only from the improved thermal stability of the charges but also from the reduction in Young’s modulus of the PP ferroelectrets due to the chemical modification as revealed by the dielectric resonance analyses.     

Quantum rotors with regular frustration and the quantum Lifshitz point

We have discussed the zero-temperature quantum phase transition in n-component quantum rotor Hamiltonian in the presence of regular frustration in the interaction. The phase diagram consists of ferromagnetic, helical and quantum paramagnetic phase, where the ferro-para and the helical-para phase boundary meets at a multicritical point called a (d,m) quantum Lifshitz point where (d,m) indicates that the m of the d spatial dimensions incorporate frustration. We have studied the Hamiltonian in the vicinity of the quantum Lifshitz point in the spherical limit and also studied the renormalisation group flow behaviour using standard momentum space renormalisation technique (for finite n). In the spherical limit ()one finds that the helical phase does not exist in the presence of any nonvanishing quantum fluctuation for m =d though the quantum Lifshitz point exists for all d > 1+m/2, and the upper critical dimensionality is given by d _u = 3 +m/2. The scaling behaviour in the neighbourhood of a quantum Lifshitz point in d dimensions is consistent with the behaviour near the classical Lifshitz point in (d+z) dimensions. The dynamical exponent of the quantum Hamiltonian z is unity in the case of anisotropic Lifshitz point (d>m) whereas z=2 in the case of isotropic Lifshitz point (d=m). We have evaluated all the exponents using the renormalisation flow equations along-with the scaling relations near the quantum Lifshitz point. We have also obtained the exponents in the spherical limit (). It has also been shown that the exponents in the spherical model are all related to those of the corresponding Gaussian model by Fisher renormalisation. Received: 23 December 1997 / Received in final form: 6 January 1998 / Accepted: 7 January 1998     

Thermal lens spectrometry in pyroelectric lithium niobate crystals

In this work, the light-induced lens effect due to thermal and/or photorefractive processes was studied in pyroelectric (undoped and Fe²⁺-doped) lithium niobate crystals (LiNbO₃) using thermal lens spectrometry with a two-beam (pump–probe) mode-mismatched configuration. The measurements were carried out at two pump beam wavelengths (514.5 and 750 nm) to establish a full understanding of the present effects in this material (thermal and/or photorefractive). We present an easy-to-implement method to determine quantitative values of the pyroelectric coefficient (dP _s/dT), its contribution to the thermal effect and other thermo-optical parameters like thermal diffusivity (D), thermal conductivity (K) and temperature coefficient of the optical path length change (ds/dT). These measurements were performed in LiNbO₃ and LiNbO₃:Fe (0.1 ppm Fe²⁺) crystals with c axis along the direction of laser propagation.     

Unified calculations of the optical band positions and spin-Hamiltonian parameters for V2+ ions in CdCl2 crystal

The eight optical spectral band positions and three spin-Hamiltonian parameters (g factors g_//, g_⊥ and zero-field splitting D) of V²⁺ ions in trigonal CdCl₂ crystal are calculated together from the complete diagonalisation (of energy matrix) method (CDM) based on the two-spin-orbit-parameter model (also called the cluster approach). In the model, differing from the usual one-spin-orbit-parameter model in the conventional crystal-field theory (where only the contribution to spin-Hamiltonian parameters due to the spin-orbit parameter of central dⁿ ion is considered), both the contributions from the spin-orbit parameter of central dⁿ ion and that of ligand ions are taken into account. The calculated results show reasonable agreement with the experimental values. The local lattice relaxation in the vicinity of V²⁺ ion due to the introduction of V²⁺ impurity is acquired from the calculations. The calculations of spin-Hamiltonian parameters from the CDM based on the one-spin-orbit-parameter and those from the perturbation theory method based on the two-spin-orbit-parameter model are also made for comparison. The results are discussed.     

The conductor-insulator transition as a result of antiferromagnetic ordering in monosulfides of 3<Emphasis Type="Italic">d</Emphasis> metals

The electron-energy structure of the structure of monosulfides of 3d metals is calculated using a modified LAPW + lo technique that allows for the antiferromagnetic ordering in different crystallographic layers. It is shown that the splitting of d-states of the transition metal with regard to the antiferromagnetic ordering in layers leads to a transition of VS, MnS, CoS, NiS, and FeS monosulfides in the troilite structure from metallic to semiconducting state.