A theoretical study of the non-adiabatic charge transfer process Ar2+ (3 P) + He(1 S) → Ar+(2 P) + He+(2 S)

CI calculation with a large basis have been used to calculate the two lowest ³Π adiabatic potential energy curves for the title reaction. These potentials have been transformed to diabatic potentials by employing a recipe based on the CI coefficients. Quantum mechanical close coupling calculations in the diabatic basis have produced total and differential cross sections which are in good agreement with experimental data. Full quantum mechanical and Landau-Zener calculations of the total cross section are in fair agreement with recent experimental measures and by small changes to the diabatic potentials can be brought into essentially exact agreement.     

Gas-discharge XeF* (B→X) laser with high specific output energy

The discharge characteristics of the XeF* (BX) laser are investigated. The NF₃ and Xe partial pressure of the laser gas mixture and the total gas pressure have been varied. A highest specific output energy of 4.7 J/l with an efficiency of 0.5% was obtained from a X-ray preionized Ne/Xe/NF₃ gas mixture at 6 bar with single-pulse excitation through a multichannel spark gap.     

Excitation and Quencing of Rotational Energy Levels of the О3 Ozone Molecule by Collisions with Noble Gas Atoms (Ar and He)

Russian Physics Journal - The scattering cross sections of rotational excitations of O3 by collisions with noble gas atoms (Ar and He) have been calculated using the two-body scheme implemented in...     

Time-resolved spectroscopy and energy transfer in Pr3+-doped Gd2(SO4)3·8H2O

The luminescence of Pr³⁺ in gadolinium sulfate hydrate is reported for 195 nm laser excitation. the Pr³⁺ ion acts as a sensitizer of the host lattice emission. The Pr³⁺Gd³⁺ energy transfer occurs in two different ways. In the octahydrate the transfer occurs from the lowest component of the 4f5d configuration of Pr³⁺, but in the samples with less water there is energy transfer from the¹ S _o level of Pr³⁺ to several Gd³⁺ levels. The Pr³⁺ emission in the two modifications is, of course, also strikingly different.Deceased 24 December 1994     

Resonant Raman scattering in organic conductors α and β-(BEDT-TTF)2X (X=I3 and IBr2)

Molecular vibrations in the crystals of organic conductors α and β-(BEDT-TTF)₂X, (X=I₃, IBr₂), a neutral donor BEDT-TTF, and acceptors n-Bu₄N·I₃ and n-Bu₄N·IBr₂ are investigated by Raman scattering. Strong Resonant effects are observed in the I₃ compounds, when the incident laser wavelength approaches the optical transition energy of the I₃ anion. More than ten overtones of the symmetric stretching mode of anions appear. For the modes related to the C=C vibrations the decrease of peak energies and their broadening are observed in the charge-transfer salts.     

High-Resolution Spectroscopy of Jet-Cooled (32)SO(2) and (34)SO(2): The ã(3)B(1)-;X(1)A(1), 2(1)(0) and 1(1)(0) Bands

Laser-induced excitation spectra of the two bands ?(3)B(1)-;X(1)A(1), 2(1)(0) and 1(1)(0) of (32)SO(2) and (34)SO(2) have been recorded in a supersonic jet at a resolution of 0.015 cm(-1). The rotational and electron-spin fine structure has been analyzed for both isotopic species. Analysis of the rotational and electron-spin fine structure yields precise values of the rotational constants A, B, and C and the spin constants alpha and beta for both (32)SO(2) and (34)SO(2) in the states ?(3)B(1) (010) and (100). No interaction between these two vibrational states with any nearby triplet state is observed for rotational levels with J 相似文献   

State-to-state rotational energy transfer in OH (A 2Σ+, υ′=1)

State-to-state rotational energy transfer (RET) coefficients for thermal collisions of OH (A ²⁺, =1) with He, Ar, N₂, CO₂, and H₂O at 300K were determined from time-resolved laser-induced fluorescence (LIF) measurements. The RET coefficients are very similar in both qualitative behaviour and absolute magnitude to those measured previously for OH (A ²⁺, =0).     

Luminescence and energy transfer in La2O3–Nb2O5–B2O3:M3+ (M=Bi,Eu, Dy) glasses

The luminescence and energy transfer processes in La₂O₃–Nb₂O₅–B₂O₃:M³⁺ (M=Bi, Eu, Dy) glasses were investigated using luminescence spectroscopy (excitation and emission, down to 4.2 K) and decay time measurements at room temperature. The observation of niobate luminescence implies a considerable degree of short- and intermediate-range order in these glasses. Energy transfer from the niobate groups to the lanthanide ions was observed for Eu³⁺, but not for Dy³⁺, suggesting that the energy transfer process occurs to the charge-transfer state of the Eu³⁺ ion, rather than to its f-levels. Inter-Eu³⁺ energy transfer was negligible in the concentration range investigated (up to 3 mol%). In contrast, cross-relaxation processes between Dy³⁺ ions were active at concentrations as low as 0.5 mol%. In the Bi³⁺ doped glasses the energy transfer was observed from the Bi³⁺ excited levels to the oxygen deficient niobate groups.     

Single-electron charge transfer in collisions of CF 2 ++ with Ar and Ne at collision energies 3–5 eV

Non-dissociative, single-electron charge transfer processes between the dication CF ₂ ⁺⁺ and Ar and Ne were investigated in crossed beam scattering experiments at collision energies of 3.0 and 4.55eV (c.m.). The reaction with Ar produces CF ₂ ⁺ in its ground state and, to a smaller extent, in the excited CF ₂ ⁺ (²_u) state. The reaction with Ne occurs only with an excited state of CF ₂ ⁺⁺ lying about 4.4 eV above the ground state and present in a small amount in the reactant dication beam; its molecular product is CF ₂ ⁺ in the ground state.     

Electron-vibrational energy exchange in collisions of electronically excited N2(A 3Σ u + ) molecules with Zn(X 1 S) atoms

The interaction matrix between the N₂ molecule in the X ¹Σ _g ⁺ and A ³Σ _u ⁺ states and the Zn atom in the ¹ S and ³ P states calculated earlier by the asymptotic method was used to find the rate constants for the electron-vibrational energy exchange N₂(A ³Σ _u ⁺ , v) + Zn(¹ S) → N₂(X ¹Σ ₈ ⁺ , v′) + Zn(³ P). The calculations were performed by the transition state method, and the probabilities of transitions between intersecting electron-vibrational terms of the system in motion along the reaction coordinate were determined by the Landau-Zener equation. The calculated electron excitation transfer constants between N₂(A ³Σ _u ⁺ , v = 1, 0) and Zn(¹ S) over the temperature range 300–900 K were on the order of 10^?11?10^?12 cm³/s.     

Fusion and transfer cross sections of 3He induced reaction on Pt and Au in energy range 10–24.5 MeV

In experiments performed by accelerated ion ³He-beam irradiated gold and platinum targets on the cyclotron U-120M of the Nuclear Physics Institute of the Czech Academy of Sciences, ?e?, reactions of complete and incomplete fusion and nucleon transfer reactions in the ³He energy range from 10 to 24.5 MeV have been investigated. To determine the yield of the nuclides resulting from the nuclear reaction, the activation technique has been used. The obtained data are analyzed using models based on statistical calculations and compared with similar results for other light stable particles. Transfer reactions with positive Q values have relatively high cross sections in the energy range below the Coulomb barrier. These cross sections continue to grow with increasing ³He energy, and, in the case of capturing neutron from target nucleus by a nucleus of ³He, the excitation functions of these reactions reach their maximum almost at the Coulomb barrier of the reactions.     

The differential interference angle of ^2∏[Case（a）] diatom on rotational energy transfer in NO（X^2∏） collision with He,Ne and Ar system

To study theoretically the relationship between the differential interference angle and the scattering angle in collisional quantum interference （CQI）, we have investigated the differential interference angle of the atom-diatomic [case（a）] molecule system in detail. For the 2∏ electronic state in Hund＇s case （a）, the degree of the differential interference is also discussed. The differential interference angles of NO（X^2∏） are calculated quantitatively for the rotational energy transfer in Hund＇s case （a） induced by collision with He, Ne and Ar atoms. The method to calculate the differential interference angle is presented. Several factors that affect the differential interference angle are investigated. Finally the variation of the differential interference angle with the impact parameter and relative velocity is discussed.     

Differential elastic and quenching cross sections for Ar*(3P) and CO2(X1 ∑ g +)

The energy dependence of the differential scattering of metastable Ar*(³P) by ground-state CO₂(X¹ ∑ _g ⁺) has been studied at relative kinetic energies from 58 to 126 meV over an angular range of 5–160° c.m. using crossed molecular beams. The position and curvature of rainbow maxima, which are observed at each energy, are used to obtain parameters for a Lennard-Jones (12, 6) spherically symmetric potential. The position of the minimum, r _m = 5·02 ± 0·65 Å, is identical to that for K + CO₂ and the well depth, ε = 16·3 ± 0·8 meV, is about 10 per cent greater. The scattered intensity shows a distinct fall-off on the dark side of the rainbow compared to that expected for elastically scattered Ar*. This depletion, caused primarily by the quenching of Ar*, is analysed in terms of the optical-shadow model to determine the energy dependence of the observed quenching cross section, which is predicted to have a maximum of 67 Ų at 193 meV.     

Production of high energy deuterons in the reaction:3He+3He→4He+2H+e ++v

Experiments on the reaction:³He+³He→⁴He+²He using a single four detector telescope have shown evidence for the production of deuteron pulses, consistent with the²He→²H+e⁺+v fusion reaction in the final state. New measurements on the same reaction using improved techniques viz.A) a windowless³He gas target andB) α- d correlation detection with 5 ns resolving time and antipileup circuitry have been performed. Calibrations were obtained from the⁷Li+³He→²H+⁴He+⁴He reaction spectra. The correlation angles were 30° and 97° for the alphas and deuterons respectively. Deuteron pulses have been observed, correlated with alpha particles. A cross section of (1.7 ±0.5)nbsr^?1MeV^?1 was obtained consistent with previous measurements using a single telescope.     

A theoretical study of energy transfer in the quenching of O(1 D 2) by CO(1Σ+)

Energy transfer processes occurring during the collisional quenching of O(¹ D) by CO(¹Σ⁺) are studied using a classical collision complex model together with potentials previously derived for the C(³ P) + O₂(³Σ _g ^-) reaction. Room temperature quenching rate constants, electronic-vibrational transfer efficiencies and product vibrational state distributions are in good agreement with experiment. The calculated and experimental temperature dependences of the electronic-vibrational transfer efficiencies and vibrational populations, however, disagree. The effect of using vibrationally excited CO as a quenching partner is studied and shown to result in a lowering of the quenching rate constant by a factor of 4 at room temperature. Enhancement of initial translational energy by the equivalent of a vibrational quantum of energy leads to an even larger decrease in the rate constant. This difference between vibrational and translational energy enhancement is interpreted in terms of an increased centrifugal barrier in the latter case.     

Discharged generator of singlet oxygen for oxygen-iodine laser. Transport kinetics of O2(a 1δg) and O2(b 1σ g + ) molecules and O(3 P) atoms in Ar:O2 and He:O2 flows excited by a 13.56-MHz discharge

To understand and reveal the basic physical factors providing the possibility of scaling of a discharged singlet oxygen generator (DSOG) in an oxygen-iodine laser, the production, and transport kinetics of metastable O₂(a ¹δ_g) and O₂(b ¹σ _g ⁺ ) molecules, as well as O(³ P) atoms, were investigated in Ar:O₂ and He:O₂ gas flows excited by a 13.56-MHz discharge in a wide range of pressures (4–40 Torr) and oxygen percentages. It is shown that the densities and transport kinetics of O₂(a ¹δ_g), O₂(b ¹σ _g ⁺ ), and O(³ P) appear similar for oxygen mixtures with argon and helium in the same conditions independent of discharge mode. Compared to pure O₂, the dilution of oxygen with an inert gas allows higher energy inputs per an oxygen molecule to achieved, especially under conditions of the homogeneous discharge mode (α-mode), which gives a higher efficiency of O₂(a ¹δ_g) excitation in Ar:O₂ and He:O₂ mixtures. But the maximum attainable yield of singlet oxygen in Ar:O₂ and He:O₂ at fixed partial O₂ pressure is found to be comparable with the O₂(a ¹δ_g) yield in pure oxygen at the same pressure. The reason for this is the increased three-body deactivation of O₂(a ¹δ_g) by atomic oxygen in the mixtures because of the greater total pressure. The estimation of the rate constant of O₂(a ¹δ_g) three-body quenching by O(³ P) in Ar:O₂ and He:O₂ mixtures as (1.5 ± 0.5) × 10^?32 cm⁶/s was carried out from the analysis of transport kinetics of singlet and atomic oxygen in the discharge afterglow at high pressures exceeding ～10 Torr. A similar analysis for the lower pressures has revealed that losses both of metastable O₂(a ¹δ_g) and O₂(b ¹σ _g ⁺ ) molecules, and of O(³ P) atoms on the surface of the discharge tube, are determined by the density of each of the components. The obtained loss probabilities of O₂(a ¹δ_g), O₂(b ¹σ _g ⁺ ), and O(³ P) on the silica surface show that the surface loss probabilities of all the species can increase noticeably under the discharge exposure. Thus, the key parameters determining the maximal O₂(a ¹δ_g) yield in the DSOG are a homogeneous volumetric mode of the discharge, energy input per oxygen molecule in this mode, and a low rate of O₂(a ¹δ_g) quenching. Just three-body quenching of O₂(a ¹δ_g) by O(³ P) limits the singlet oxygen yield with increasing pressure. The fast removal of atomic oxygen both in discharge and in the earlier afterglow could provide DSOG scaling with pressure.     

New states and γ-transitions in 209Bi observed in the (3He, d*γγ)-subcoulomb-reaction

High-spin states in ¹⁴³Pm have been investigated via the ¹²⁸Te(¹⁹F,4nγ)¹⁴³Pm reaction using techniques of in-beam γ-spectroscopy. γ-ray singles, γ-γ coincidences, γ-ray anisotropies and DCO ratios have been measured. Based on these measurements, the level scheme of ¹⁴³Pm has been extended up to an excitation energy of 10535.4 keV, including 48 new γ-rays deexciting 28 new levels. The yrast levels in ¹⁴³Pm can be understood qualitatively in the framework of a weak-coupling model. Received: 10 July 2000 / Accepted: 12 October 2000     

Nuclear structure studies of 125Te with (n,γ), (d,p) and (3He,α) reactions

Levels in ¹²⁵Te were investigated in the range up to 3.3 MeV excitation energy by the (n,γ), (d,p) and (³He,α) reactions. Over 160 levels and about 360 γ-transitions were established, most for the first time. The states below 2.3 MeV with the most complete spectroscopic information were interpreted in terms of the interacting boson-fermion model (IBFM). Unitary treatment of both positive- and negative-parity states is achieved with the same model parameter close to the intermediate case between O(6) and U(5) limits. Excitation energies, electromagnetic transition rates, γ-branchings and spectroscopic factors are discussed in connection with the possible structures. A family of low-spin negative-parity states has been identified and understood by the IBFM proving their antialigned origin.