Preferential sputtering of TIC under keV Ar+ ion bombardment: Simultaneous sputtering-ISS measurement with He+ and Ar+ ions

The composition change of the outermost atom layer of TiC(110) under ion bombardment with 1.5–3 keV He⁺ and He⁺ + Ar⁺ ions has been measured by ion scattering spectroscopy with He⁺ ions at different sample temperatures. It has been found that the preferential sputtering of C atoms takes place for both the He⁺ and Ar⁺ ion bombardment, however the preferred sputtering is more pronounced for Ar⁺ ions than for He⁺ ions. The ion bombardment with He⁺ ions at elevated sample temperatures hardly results in any change in surface composition below ～800°C, while Ar⁺ ion bombardment results in C enrichment for elevated temperatures as reported so far.     

Theory of Isotope Effects on He+ Trapping in Solid Hydrogen

We are currently investigating the influence of vibrational effects on the strength of trapping of He⁺ in solid hydrogen. Such effects can lead to an isotope dependence of the trapping energy associated with the hydrogen molecules and He⁺ ion. At the present time, our focus is on the isotope effect for ³He⁺ and ⁴He⁺, which we are studying through the vibrational motions of the trapped He⁺ ions in the potential they experience as they move about their equilibrium positions. The potential governing the vibrations has been obtained from Hartree–Fock cluster calculations of the total energy of the cluster composed of the He⁺ ion and up to the third nearest neighbor hydrogen molecules as a function of the displacement of the He⁺ ion from its trapped position. The energy eigenvalues for the ground vibrational states of ³He⁺ and ⁴He⁺ in this potential come out as 1.29 and 0.96 meV, respectively, leading to corresponding reductions by these amounts in the binding energy of 8.6 eV for both ions without vibrational effects. The difference of these reductions can be considered as an isotope shift, its value for this case being 0.33 meV. From the analysis for these results, it is suggested that isotope shift effects for deuteron and triton in solid D–T would have the same order of magnitude. A procedure for more accurate investigations of the isotope shifts is discussed. This revised version was published online in August 2006 with corrections to the Cover Date.     

Exit angle dependence of charge-state distribution of backscattered He ions

Exit angle and energy dependences of the charge-state distribution of backscattered He ions were investigated when 500 keV He⁺ ions were incident on SiO₂. The energy dependence of the He⁺ fraction was estimated by comparing the measured He⁺ spectra with the simulated spectra of He ions in all charge states at the exit angles of 5-25° with respect to the SiO₂ surface. We found that the He⁺ fraction is almost independent of the exit angle at energies higher than 250 keV and the observed energy dependence of the He⁺ fraction is in good agreement with that for the carbon-foil-transmission experiment. In the low energy region (<250 keV), however, the He⁺ fraction decreases as the exit angle decreases.     

A new channel of the concentration decay of doubly charged helium ions in a plasma

A model describing the decay of concentrations of excited helium atoms and ions taking into account doubly ionized helium is constructed on the basis of experimental data on excitation of a helium plasma by a pulsed electron beam. From this model, the rate constant of reaction He⁺⁺+He_m→He⁺+He ₀ ⁺ is estimated. It is found to agree in order of magnitude with theoretical estimates made in the framework of a model of polarization capture.     

Electronic absorption spectrum of CO+ in an ion beam

The He+He⁺¹ interactions have been studied, as a function of the internuclear separation R, in terms of the electronic forces acting on the nuclei and the change in the charge distribution. The analysis reveals that at large R the atomic densities are polarized inwards, causing an attractive force on each nucleus, while at small R the difference in the nature of the interactions in the ²Σ_u and ²Σ_g systems is noted. It is seen that the He+He⁺¹ (²Σ_u) interaction is less attractive than the He⁺¹+He⁺¹ interaction at lower values of R.     

He+离子和Ar原子碰撞过程中激发态的研究

在He⁺离子和Ar原子碰撞过程中,同样存在着电子俘获激发和直接激发两种过程。本文把实验结果同He⁺离子和Ne原子碰撞体系进行了比较,发现:在入射离子速度较小时,实验所得到的Hel三重态发射截面要大得多;当入射离子He⁺的速度大于一个原子单位(2.2×10⁸cm/s)时,情况则相反。因此,在俘获电子过程中,势能亏损同He⁺离子的入射速度是两个非常重要的因素,而且它们之间存在一个竞争过程。入射离子He 关键词：     

Specific features of the excitation spectrum of helium II in a plasma initiated by an electron beam

The emission of a low-pressure helium plasma (P≤2 Torr) initiated by a monochromatic electron beam is investigated. It is found that an increase in the current leads to a drastic increase in the rate of charge exchange of doubly charged helium ions. The assumption is made that inelastic collisions of He⁺⁺ ions with metastable helium atoms provide the main channel of charge exchange of these ions due to the reaction He⁺⁺+Hem→ He⁺*+He ₀ ⁺ .     

Electron-spin-dependent 4He+ ion scattering on Bi surfaces

We studied low-energy (～ 1.55 keV) electron-spin-polarized ⁴He⁺ ion scattering on a Bi(111) ultrathin film epitaxially grown on a Si(111) substrate. We observed that the scattered ion intensity differed between the incident He⁺ ions with up and down spins even though Bi is a non-magnetic element. To analyze the origin of this spin-dependent ion scattering (the spin asymmetry), we investigated the detailed relationship between the spin asymmetry and the incident angle, the azimuthal angle, the scattering angle, and the incident energy. All the data indicate that the spin asymmetry originates from the scattering cross section owing to the non-central force in the He⁺–Bi atom binary collision. The non-central force is most likely attributed to the spin–orbit coupling that acts transiently on the He⁺ 1s electron spin in the binary collision.     

Exchange and nuclear symmetry interference in He+-He scattering

A method is described to determine the potential difference, V _g-V _u, that will accurately reproduce the exchange and nuclear symmetry oscillations observed by Aberth et al. in their experimental work on He⁺-He differential scattering. It is demonstrated that at higher energies and angles the experimental results for ⁴He⁺-⁴He, ⁴He⁺-³He and ³He⁺-³He appear incompatible with one another when investigated in terms of a two-state scattering theory. This is an indication that at these energies and angles the theory may require modification to include the effects of coupling to higher states.     

Ab Initio Investigation of Helium Bubble Formation from Trapped He+ Ions in Solid Hydrogen

We are involved in a program aimed at a first-principles examination of the possibility of helium bubble formation in solid hydrogen. Our procedure is based on an extension of the Hartree–Fock cluster approach that we have been using for study of individual He⁺ ions in solid hydrogen. The preliminary results of our cluster investigations of a particular configuration of two He⁺ ions in neighboring tetrahedral interstitial positions are presented here. It has been found that the hydrogen molecules common to the two He⁺ ions lead to a substantial attractive force between the ions that almost overcomes their inherent repulsion, leading to a binding energy for this configuration only slightly less than the binding energy for two well separated trapped He⁺ ions. The analysis of our results have suggested future investigations of different pairs of trapping sites which appear to be more favorable for providing higher binding energies for the He⁺ pairs. This revised version was published online in August 2006 with corrections to the Cover Date.     

Screening effects in secondary electron production by equal velocity H+, H+2, He+, He++ions

Electron spectra produced by equal velocity (0.75 MeV/amu) H⁺, H⁺₂, He⁺ and He ⁺⁺ ions are shown. Screening effects are observed for He⁺ ions but not for H⁺₂. He⁺⁺ cross sections scale like Z² = 4 when compared to H⁺ cross sections.     

Surface composition modification of tungsten higher oxide under He<Superscript>+</Superscript> ion bombardment

The surface reduction of higher oxide WO₃ under irradiation by He⁺ ions with the energies 1 and 3 keV in a high vacuum is investigated by X-ray photoelectron spectroscopy. It is found that lower WO₂ and intermediate WO _x (2 < x < 3) oxides form first in WO₃ surface layers under He⁺ ion bombardment, and with an increase in the irradiation dose metallic tungsten forms. It is shown that the degree of irradiated oxide surface metallization increases with an increase in the energy of the bombarding He⁺ ions. A comparison of WO₃ oxide surface composition modification under He⁺ and Ar⁺ ion irradiation is presented.     

Ion beam induced reaction of carbon films on Si(1 0 0)

The irradiation effects of 2 MeV He⁺ and Ar⁺ ions on the film structure of the C–Si system were investigated with RHEED and XPS. The formation of SiC phase and/or the growth of epitaxial SiC were possible by He⁺ irradiation for the carbon films up to 0.7 nm in thickness, which was thinner than that by Ar⁺ irradiation. The He⁺ irradiation could not grow the turbostratic graphite which could be grown by Ar⁺ irradiation. The mechanism of the formation and the epitaxial growth of SiC by ion irradiation was discussed from the view point of the energy transfer from the irradiated ions.     

Oscillations in scattered 4He+ ion yield curves from HgCdTe

Ion scattering spectra using ⁴He⁺ from Te and from epitaxial HgCdTe on CdTe were measured. A nearly smooth featureless curve was obtained for ⁴He⁺ → Te in the metal, but in the HgCdTe the ⁴He⁺ → Te curve showed oscillatory fine structure similar to that obtained from Sn. Apparently the Te molecular orbital energies have changed allowing quasiresonant interactions between ion and atom. Ion scattering spectrometry may provide bonding information as well as elemental analysis capability.     

Effect of helium/argon gas ratio in a He-Ar-Cu<Superscript>+</Superscript> IR hollow-cathode discharge laser: modeling study and comparison with experiments

The He-Ar-Cu⁺ IR laser operates in a hollow-cathode discharge, typically in a mixture of helium with a few-% Ar. The population inversion of the Cu⁺ ion levels, responsible for laser action, is attributed to asymmetric charge transfer between He⁺ ions and sputtered Cu atoms. The Ar gas is added to promote sputtering of the Cu cathode. In this paper, a hybrid modeling network consisting of several different models for the various plasma species present in a He-Ar-Cu hollow-cathode discharge is applied to investigate the effect of Ar concentration in the gas mixture on the discharge behavior, and to find the optimum He/Ar gas ratio for laser operation. It is found that the densities of electrons, Ar⁺ ions, Ar_m ^* metastable atoms, sputtered Cu atoms and Cu⁺ ions increase upon the addition of more Ar gas, whereas the densities of He⁺ ions, He₂ ⁺ ions and He_m ^* metastable atoms drop considerably. The product of the calculated Cu atom and He⁺ ion densities, which determines the production rate of the upper laser levels, and hence probably also the laser output power, is found to reach a maximum around 1–5 % Ar addition. This calculation result is compared to experimental measurements, and reasonable agreement has been reached. Received: 14 October 2002 / Revised version: 28 November 2002 / Published online: 19 March 2003 RID="*" ID="*"Corresponding author. Fax: +32-3/820-23-76, E-mail: annemie.bogaerts@ua.ac.be     

Charge exchange in He++Li collisions

A two-state model, based on atomic wave functions and allowing for momentum transfer factors, is employed to calculate cross sections for the formation of excited states of He⁺ in collisions of He⁺⁺ ions with Li in the ground state, for energies in the range 5–64 keV. It is shown that the selective capture into the n=3 levels of He⁺, predicted at low energies by Shipsey et al., persists up to energies of ≈30 keV.     

Enhanced photoemission and ionization of He+ by simultaneous irradiation of fundamental laser and high-order harmonic pulses

We simulate the response of He⁺ exposed simultaneously to fundamental and 27th harmonic pulses from an intense Ti:sapphire laser. High-order harmonic emission from He⁺ is enhanced by 17 orders of magnitude compared with the case of the fundamental pulse alone. Moreover, while an individual 10 fs laser with a fundamental wavelength of 800 nm and a peak intensity of 3×10¹⁴ W/cm², or its 27th harmonic pulse with a peak intensity of 10¹³ W/cm², ionizes no more than 5×10^-6 of He⁺, their combined pulses lead to a surprisingly high He²⁺ yield of 17%. The underlying mechanism is either harmonic generation from a coherent superposition of states or two-color frequency mixing, depending on the laser wavelength. PACS 32.80.Rm; 42.50.Hz; 42.65.Ky     

Theory for Relative Strengths of Trapping of He+ Ions in Solid, Liquid and Gaseous Hydrogen

The study of trapping of He⁺ ion in solid hydrogen is important both as a problem in solid state physics and also as an applied physics problem in the field of muon catalyzed fusion (μCF). In μCF, He⁺ ion acts as a trap for μ⁻, interrupting the chain reaction aspect of the catalytic role of μ⁻ in producing fusion of deuteron and triton and of triton and triton in solid hydrogen composed of ²H–³H and ³H–³H molecules, respectively. Using the Hartree–Fock procedure, combined with procedures for including many-body effects, as well as relaxation effects associated with the He⁺–H₂ distances and the adjustment of the H–H separation, we have investigated the trapping of He⁺ in gaseous and solid state environments. For the former, the environment of He⁺ is simulated by a single hydrogen molecule and for the solid by clusters appropriately chosen to represent the hexagonal close-packed structure. Our results for the gaseous state indicate that the trapping is rather strong with a binding energy of 8.5 eV, with almost equal binding energy in the linear and triangular configurations with respect to the H–H direction. For the solid, both the likely sites for He⁺ trapping, namely the tetrahedral and octahedral interstitial sites, are also found to provide deep traps (8.6 eV) of almost equal strength, independent of the orientations of the neighboring molecules, showing that the trapping is not influenced by the orientational disorder in the surrounding hydrogen molecules. Further, the influence of next nearest neighbor hydrogen molecules is found to enhance the trapping energy for He⁺ substantially, by 0.6 eV, with the incorporation of the third nearest neighbors having a much smaller added effect, demonstrating the convergence of our results with respect to the size of the cluster chosen to simulate the solid. The substantial influence on the He⁺ trapping energy found for the neighbors beyond the nearest ones provides an explanation of the greater accumulation of helium in the solid state of hydrogen in μCF experiments as compared to the liquid. Suggestions are made regarding the possible reasons for the almost negligible accumulation of helium in the liquid state. This revised version was published online in August 2006 with corrections to the Cover Date.     

Use of a diabatic molecular expansion in studies on electron capture by He2+ ions in helium at keV energies

In this preliminary work, using a 3-state diabatic molecular expansion without any excited channels, we have studied within the semiclassical impact parameter approximation the single charge transfer process He²⁺+He(1s ²)→He⁺(1s)+He⁺(1s). Our results agree very well with experiment, which demonstrates the usefulness of this type of diabatic molecular basis in doubly charged ion-atom collision systems.