Quantum rotational scattering of H2 and its isotopologues with He

Quantum close-coupling computations of the rotational quenching of H₂ and its isotopologues due to He impact are performed using a highly accurate potential energy surface. State-to-state cross sections are obtained in a wide range of collision energies between 10^?5 cm^?1 and 10⁴ cm^?1, and the theoretical rate coefficients are reported for temperatures ranging from 10^?4 K to 3000 K. Compared with previous studies, the well depth of the potential adopted in this study is larger, leading to stronger resonance effects in the cross sections of He-HD. The accurate potential was employed to investigate the isotope effects of H₂ in detail. The cross-section resonances shift towards lower collision energies and become stronger with increasing reduced mass. The calculated cross sections and rate coefficients of H₂ and its isotopic variants in collisions with He are provided to study the energy transfer in these systems.     

Electron Transitions during the Capture of an Electron by a He<Superscript>2+</Superscript> Ion at the Argon Atom

We have measured the absolute values of the total cross section of the one-electron capture by He²⁺ ions in the kinetic energy range 2–30 keV at the Ar atoms. The absolute values of the differential scattering cross sections of He⁺ ions formed during the one-electron capture and the electron capture with ionization at energies of 2.2, 5.4, and 30 keV have been determined. The electronic states of the formed ions have been determined using collision spectroscopy based on analysis of the change in the kinetic energy of He⁺ after the interaction. We have measured doubly differential (with respect to the kinetic energy and the scattering angle) cross sections of the formation of free electrons. The free electron formation channels (direct ionization and electron capture with ionization) have been analyzed by calculating the electron terms of the (HeAr)²⁺ system. The calculated cross section of capture with ionization is in conformity with the cross section measured using collision spectroscopy.     

Charge exchange in collisions between heavy low-charged ions

The probabilities and the effective cross sections of collision-induced one-electron charge exchange between singly charged and four-charged heavy Xe, Cs, Ba, Pb, Bi, and U ions at energies E>0.1 keV/u are calculated by a method of multichannel normalization in the impact parameter representation. The cross sections are rather large with a maximum σ_m≈10⁻¹⁵ cm² at relative energies E _m ≈10–30 keV/u. For collision energies E<10 keV/u, the cross sections sharply decrease with growing resonance defect of the reaction. At high energies E>1 MeV/u, the charge exchange proceeds largely by the capture of inner shell electrons of the ionic targets. The charge exchange cross sections calculated for low-charged Xe, Cs, Ba, Pb, Bi, and U ions are compared with available theoretical and experimental data.     

Observation of high-energy electrons from a metal target irradiated by protons with a mean energy of 25 keV

Electrons with abnormally high energies of up to 16 keV are detected from an iron target irradiated by ions (H⁺, Fe⁺, Fe²⁺, Fe³⁺) with energies ranging from 20 to 100 keV from the plasma of a high-power femtosecond laser pulse with an intensity of 10¹⁶ J/(s cm²). These electrons indicate that the energy of an incident ion is almost completely transferred to an electron knocked out of the target. In a range of 6–16 keV, the spectrum of electrons knocked out of the K shell of iron atoms by protons with an energy of 22 ± 2 keV is quasi-exponential with an exponent of 4 keV. For 8-keV electrons, the double differential cross section for ionization by such protons is estimated as 10^?7 b/(eV sr).     

Transitions between the components of the fine structure in He and He-Like ions colliding with protons

The cross sections for the transitions between the components of the fine structure of triplet levels with n = 2 and 3 in He and He-like ions colliding with protons have been considered. The feature of the problem is the presence of a virtual level coupled with the components of the multiplet by dipole-allowed transitions. As a result, the cross section at intermediate collision velocities has a peak, which is sometimes much higher than the cross section for the transition induced by collisions with electrons. The cross sections for He and C⁴⁺ and Fe²⁴⁺ ions have been calculated by the tight-binding method.     

Dissociation of alkane ionized molecules

The subject of investigation is the fragmentation of variously charged molecular ions arising in col-lisions of several kiloelectronvolt H⁺, He²⁺, and Ar⁶⁺ ions with molecules of the simplest alkanes (from methane to butane). Using the method of time-of-flight mass spectrometry, the formation cross sections of dissociation-induced fragment ions are measured. The dissociation takes place when an incident ion captures an electron from a methane, ethane, or propane molecule. The role of additional ionization of the molecule, which accompanies the electron capture by the incident ion, is elucidated. The kinetic energy spectrum for protons resulting from the fragmentation of multiply charged alkane ions is determined. The most plausible kinetic energies of protons depending on the degree of ionization and molecule size fall into the range 1–25 eV. It is shown that, when the molecule loses several electrons, the kinetic energies of protons are governed by Coulomb interaction between all fragment ions and are determined by their flying apart from the relative spatial arrangement of corresponding atoms in a parent molecule.     

State-selective radiative recombination cross sections of argon ions

The n-, (n,l)- and fine-structure level state-selective radiative recombinations (RR) cross sections of argon ions Ar¹⁸⁺,Ar¹³⁺,Ar⁷⁺ and Ar⁺ are obtained with the semi-classical Kramer formula, the relativistic self-consistent field (RSCF) method and the relativistic configuration interaction (RCI) method. It is found that for the highly charged ions with few electrons, the cross sections calculated with these three methods are in good agreement with each other. But as the number of electrons increases, the Kramer formula deviates from the RSCF and RCI results. For instance, when the energy of the incident electron is larger than 100 eV, the n-state selective cross sections of Ar⁷⁺ calculated from the Kramer formula are underestimated for more than 50%. The RSCF results are in general agreement with the RCI results. However, for the low charged ions, a clear distinction appears due to the strong configuration interaction, especially near the Cooper minimum. The n-resolved (n≤10) and total Maxwellian averaged rate coefficients are calculated, and the analytic fitting parameters are also provided.     

Secondary Electron and Negative-Ion Emission from Metal Surface under the Bombardment by Positive Ions (H<Superscript>+</Superscript>, Cl<Superscript>+</Superscript>, HCl<Superscript>+</Superscript>)

A trap for positive ions (H⁺, Cl⁺, HCl⁺) is created within a time-of-flight mass spectrometer. The yields of secondary electrons and negative ions (HCl^?, H^?) formed due to forward and backward scattering of positive ions by steel wire at different kinetic energies (200–750 eV) are measured.     

Interaction of H− ions with foil targets in the charge exchange system of a beam transport channel

The possibility of experimentally modeling the interaction of high energy H⁻ ions with foil targets using beams with more accessible lower energies that have the same dimensionless interaction parameter and similar current characteristics is pointed out. Results are presented from the first stage of a study of the beam-foil stripping of 2 and 7 MeV H⁻ ions. An analysis of the charge composition of the beam after a carbon foil serves as a basis for determining the corresponding cross sections for stripping of the ions and ionization of the product hydrogen atoms. The data from these and other beam-foil experiments are in good agreement with theoretical cross sections on carbon at different energies, as well with calculated values based on the superposition of experimental cross sections for gaseous carbon-containing targets. Zh. Tekh. Fiz. 68, 102–105 (August 1998) Deceased.     

First state selective electron capture measurements with trapped highly charged ions

The first state selective electron capture cross section measurements at eV energies are reported for collisions between C⁴⁺ ions and H₂ molecules. The cross sections are measured in a crossed beam experiment by means of Photon Emission Spectroscopy. The ion beams are decelerated in an octopole ion trap where the trap is used to guide the ion beam through the collision region. The experimental results are in excellent agreement with previous measurements at higher energies. The 3-state atomic orbital calculations of Gargaud and McCarroll generally agree with our measurements although there are some discrepancies at lower energies. However, the results for C⁴⁺ are still on a relative scale. To put our measurements on an absolute scale the N⁴⁺+ H system is investigated at keV energies. These results are in good agreement with the data of previous experiments. This revised version was published online in August 2006 with corrections to the Cover Date.     

H<Superscript>+</Superscript> and He<Superscript>2+</Superscript> impact charge transfer cross sections of magnesium

H⁺ impact single and He²⁺ impact single and double electron capture cross sections of magnesium atoms have been calculated in the modified binary encounter approximation (BEA). The accurate expressions of ion impact s_DE\sigma _{\Delta {E}} (cross section for energy transfer DE\Delta E) and Hartree-Fock momentum distributions of the target electrons have been used throughout the calculations. On the basis of the present work it is concluded that inner shell captures by H⁺ and He²⁺ ions incident on magnesium atoms contribute partly to single electron capture and partly to transfer ionization cross sections. The calculated He²⁺ impact double electron capture cross sections of magnesium are in reasonably good agreement with the experimental observations. This indicates the success of the present theoretical approach in study of charge transfer cross sections of atoms as indirect mechanisms do not interfere with double electron capture processes in this case.     

Single-electron charge transfer and excitations at collisions between Bi<Superscript>4+</Superscript> ions in the kiloelectronvolt energy range

Pioneering theoretical data for single-electron charge transfer and excitations due to collisions between Bi⁴⁺ ions in the ground (6s) and metastable (6p) states are gained in the collision energy interval 5–75 keV in the center-of-mass frame. The cross sections of the processes are calculated in terms of the close-coupling method in the basis of two-electron quasi-molecular states for the Coulomb trajectory of nuclei. It is found that single-electron capture into the singlet 6s ² states of Bi³⁺ ions makes a major contribution to the charge transfer total cross section for Bi⁴⁺(6s) + Bi⁴⁺(6s) collisions (reaction 1), whereas single-electron capture into the singlet 6s6p states is the basic contributor to the total cross section in Bi⁴⁺(6s) + Bi⁴⁺(6p) collisions (reaction 2). In the collision energy interval mentioned above, the collision cross sections vary between 1.2 × 10^?17 and 1.9 × 10^?17 cm² for reaction 1 and between 3.8 × 10^?17 and 5.3 × 10^?17 cm² for reaction 2. In reaction 1, the 6s → 6p excitation cross sections vary from 0.6 × 10^?16 to 0.8 × 10^?16 cm² for the singlet channel and from 2.2 × 10^?16 to 2.8 × 10^?16 cm² for the triplet channel. The calculation results are compared with the data obtained in experiments with crossed ion beams of kiloelectronvolt energy. The fraction of metastable ions in the beams is estimated by comparing the experimental data with the weighted average theoretical results for the cross sections of reactions 1 and 2. From the data for the charge transfer cross sections, one can estimate particle losses in relativistic beams due to a change in the charge state of the ions colliding with each other in the beam because of betatron oscillations.     

Electron capture by slow multiply charged Ar and Ne ions from atomic hydrogen

At collision energies below 15 keV total charge transfer cross sections have been measured for multiply charged Ar^ζ+(2≦ζ≦6) and Ne^ζ+(2≦ζ≦4) ions colliding with atomic hydrogen. A Wood discharge was used to provide a hydrogen target with a sufficiently high degree of dissociation. Results are compared with measurements performed at higher energies and with theoretical calculations. For ζ=2 cross sections in atomic hydrogen are much smaller than in the molecular case, for ζ>2 the ratio of these cross sections varies between 0.7 and 1.6.     

Fragmentation of polyatomic ions produced by electron-loss collisions of butane and isobutane molecules with ions of kiloelectronvolt energy

Fragmentation accompanying the loss of electrons by butane and isobutane (C₄H₁₀) molecules in collisions with energy H⁺, He²⁺, and Ar⁶⁺ ions of kiloelectronvolt energies is studied. The electron density functional technique is applied to C _n H_2n+2 alkane molecules and their respective C _n H _2n+2 ⁺ ions to carry out quantum-chemical calculations of the atomic spacing, electron total energy for the initial configuration of the ionizing molecules and ions in the ground state, and atomic bond breaking energy necessary to produce different ion fragments. The fragmentation energy is correlated with the fragmentation probability. It is shown that the relative cross sections of ion fragmentation depend primarily on the related energy consumption. However, the process cross section is also strongly affected by the initial configuration of C₄H₁₀ isomer molecules, as well as by the amount of dangling and arising atomic bonds involved in the formation of each ion fragment.     

Interaction of <Superscript>3</Superscript>He<Superscript>2+</Superscript> and Ar<Superscript>6+</Superscript> ions with acetylene,ethylene, and ethane molecules

Time-of-flight mass spectroscopy methods are employed for studying processes occurring during capture of electrons by ³He²⁺ and Ar⁶⁺ multiply charged ions with energy 6z keV (z is the ion charge) from C₂H _n molecules (n = 2, 4, 6) with different multiplicities of C-C bonds. Fragmentation schemes of the molecular ions formed in such processes are established from analysis of correlations of recording times for all fragment ions. The absolute values of the cross sections of capture of an electron and capture with ionization are measured, as well as the cross sections of formation of fragment ions in these processes. The absolute values of total capture cross sections for several electrons are determined.     

One-electron capture in collisions of fast ions with atoms

The properties of one-electron charge transfer between ions and atomsB ^Z++A →B ^(Z?1)+ A ⁺ are studied at relative velocities of the colliding particles higher than target electron velocities. Calculations of partial and total cross sections in collisions of protons and multiply-charged ions with neutral atoms are performed and compared with experimental data. The universal curve for the capture of the targetK- andL-electrons is given. In all cases at sufficiently high collision energies the electron capture from outer shells decreases and the capture of electrons from inner shells of the target atom becomes predominant.     

Study of cross sections for the loss of outer 1s, 2s, and 2p electrons by fast ions and atoms of light elements

In the case of light-element ions propagating with velocities V = 1.83 and 3.65 au in H₂, He, N₂, Ne, and Ar, the loss cross sections σ_{i, i+m} for m electrons (m = 1, 2, 3) are considered. The partial loss cross sections σ_i(nl) for one of the outer 1s, 2s, or 2p electrons are determined using the obtained data. It is shown that the experimental cross sections for the loss of the 1s and 2s electrons by positive ions qualitatively agree with the theoretical values calculated in the Born approximation. In the case of the ion velocity V = 1.83 au, the cross sections σ_i for 2p electrons are greater than the cross sections σ_i (1s) and σ_i (2s) by a factor of 1.2–3 for the same binding energies of electrons in the ion (I _nl > 20 eV). It is found experimentally that, at V = 1.83 au, the cross sections σ_i (2p) for I _nl ～ 10–20 eV are less than the cross sections σ_i (1s) by a factor of 2–3, which is probably caused by a decrease in the screening parameter (θ_2p < 1) of the outer shell of atoms.     

Production rates for π+ K −, pK −, and pπ− atoms in inclusive processes

The yields of π⁺ K ^?, pK ^?, and pπ^? atoms in the reaction p + Al → atom + X at energies of 24, 70, 450 GeV and emission angles of θ_lab=1°–6° are calculated from inclusive-production cross sections for p, π⁺, π^?, and K ^?. Estimates of these hadronic-atom yields for a Ta target are also given. The inclusive-production cross sections for p, π⁺, π^?, and K ^? are obtained within the Lund model of string fragmentation. The accuracy of the calculations is estimated by comparing single particle yields calculated by the Lund model and experimental yields of particles in proton-nucleus interactions.     

Absolute cross sections for one electron capture into excited projectile states in collisions between He2+ (15–150 keV) and Li atoms

We have studied the He²⁺-Li collision system at laboratory energies between 15 and 150 keV using optical methods. From the measured emission cross sections we derive state-selective capture cross sections for n = 2,3,4 and n ? 5 states of the He⁺ ions. Our data are consistent with theoretical predictions of Bransden and Ermolaev. The total capture cross sections as evaluated from our emission cross section data, agree very well with the results of McCullough et al. obtained from projectile charge detection measurements. Near 15 keV our emission cross sections for 30.4 nm and 25.6 nm are much larger than those measured previously by Barrett and Leventhal at slightly lower energies.     

Loss of electrons from fast heavy structure ions colliding with atoms

Nonperturbative theory is developed for the multiple ionization of fast heavy structure ions colliding with neutral complex atoms. The cross sections for multiple loss of electrons by structure uranium ions U¹⁰⁺ (loss of up to 82 electrons) and U²⁸⁺ (loss of up to 64 electrons) colliding with argon atoms are calculated. The results are compared with available experimental data.