Ion survival probabilities for 3 keV Ar+ scattering from La,Yb, and chemisorbed H2, O2, and H2O on La surfaces

TOF spectra of scattered primary and surface recoiled neutrals and ions for 3 keV Ar⁺ bombardment of clean La and Yb and H₂, O₂, and H₂O saturated La surfaces are presented. The spectra are analyzed in terms of single (SS) and multiple (MS) scattering of the primary ions and surface recoiling (SR) of adsorbate atoms. Measurement of spectra of neutrals + ions and neutrals alone allows determination of scattered ion fractions Y. The Y values for the SS event are high for clean La (37%) and lower for adsorbate covered La (32% for H₂, 13% for O₂, and 8% for H₂O); Yb exhibits a similar behavior, i.e. 16% for clean Yb and 5% for O₂ + H₂O covered Yb. Photon emission accompanying the scattering collision has been observed from clean La and Yb and adsorbate covered La. A preferential inelastic energy loss of 15 ± 3 eV for the SS event has been observed for scattered neutrals as opposed to ions for La and H₂ saturated La at 135°. These results are interpreted within the models for Auger and resonant electronic charge exchange transitions during approach or departure of an ion with a surface and the electron promotions occuring during close atomic encounters where the electron shells are interpenetrating.     

kinetic energy reflection from polycrystals bombarded with Ar+, Kr+, and Xe+ ions

When the surface of a solid is bombarded with ions a fraction of the primary energy is reemitted by ion reflection and sputtering. The contribution of ion reflection or sputtering to energy reflection is determined by the mass ratio of the bombarding ions to the target atoms.^1,2 In the case of light ions the contribution of reflected ions is dominant. Results for He⁺ and Ne⁺ bombardment were described in a previous paper.³ The present paper deals with results for Ar⁺, Kr⁺, and Xe⁺ bombardment of the same targets as investigated before.³ The energies of the mass selected bombarding ions range from 9 to 16 keV. The measurements were carried out by means of the thermic detector described in a separate paper.⁴ For the given mass ratios most of the reemitted energy is related to sputtering.     

Differential cross sections for charge transfer in collisions of He+, Ne+ and Ar+ with Kr

Differential charge transfer cross sections for collisions of He⁺, Ne⁺ and Ar⁺ with Kr were measured at collision energies below 500 eV. A remarkable fraction of these collisions (2–30 %) occurs with large momentum transfer and small impact parameters. These close collisions lead to an excitation of the product particles, the measured reaction channels are strongly endothermic. In the system Ar⁺+Kr one reaction channel may be described in terms of a curve crossing.     

Sodium halide sputtering by H+, He+, Ar+ ions

Sputtering experiments were performed with 70 to 300 keV H⁺, He⁺ and Ar⁺ ions impinging on KC1, KBr and Kl. The alkali halide samples are prepared as polycrystalline layers of about 2500 Å thickness, deposited on carbon-aluminium backings. During the ion bombardment the targets are kept at elevated temperatures between 50 and 300°C, in order to study the temperature dependence of sputtering. During the irradiation the removal of halogen and sodium is simultaneously observed by Rutherford backscattering.

The present results are (i) preferential sputtering of the halogen atoms, (ii) temperature dependent sputtering yields with 0.2 eV activation energy, (iii) sputtering yields proportional to the electronic stopping power, rather than the nuclear stopping power, and (iv) sputtering yields orders of magnitude higher than estimated by elastic collision cascade theories. These findings can be interpreted by a Pooley process with subsequent migration of the interstitial halogen atom to the surface.     

Molecular adsorbate detection using hyperthermal Cs+ surface scattering: chemisorbed water on Si(111)

Cs⁺ ion beams are scattered from an Si(111) surface chemisorbed with water. Scattering of Cs⁺ ions from the surface at the incidence energies of 10–;15 eV gives rise to reaction products CsOH⁺, CsOH⁺₂ and CsSiO⁺. We interpret that these cluster ions are formed by desorption of X (X = OH, H₂O and SiO), followed by Cs⁺X association and energy quenching near the surface. The Cs⁺ scattering method has potential advantages for adsorbate detection over desorption techniques, in particular for identification of molecular and thermally unstable species.     

The lowest electronic states of Ne2 +, Ar2 + and Kr2 +: comparison of theory and experiment

Non-relativistic configuration interaction (CI) ab initio calculations using large basis sets have been carried out to determine the potential curves of the first electronic states of Ne₂ ⁺, Ar₂ ⁺ and Kr₂ ⁺. The spin—orbit interaction was treated assuming that the spin—orbit coupling constant is independent of the internuclear separation (R). For Ar₂ ⁺, calculated dissociation energies and equilibrium separations are in good agreement with experimental results. The calculations for Ne₂ ⁺ suggest that the lowest vibrational level of the I(1/2u) ground state observed by threshold photoelectron spectroscopy by Hall et al. [1995, J. Phys. B: At. molec. opt. Phys., 28, 2435] and assigned to either ν = 0 or ν = 2 actually corresponds to ν = 4. The calculations also predict the I(1/2g) state of Ne₂ ⁺ and Ar₂ ⁺ to possess a double-well potential and that of Kr₂ ⁺ to be repulsive at short range and to only possess a single shallow well at large internuclear separation. The ab initio calculations provide an explanation for the observation made by Yoshii et al. [2002, J. chem. Phys., 117, 1517] that Kr₂ ⁺ and Xe₂ ⁺ dissociate after photoemission from the II(1/2u) state to the I(1/2g) state whereas Ar₂ ⁺ does not.     

Synthesis and Spectral Study of Several Solid M3[Eu(2,6-Pyridinedicarboxylate)3] Salts (M=Li+, Na+, K+, Rb+, Cs+, NH4 +, and Pyridinium+)

Abstract

Salts of the [Eu(2,6-pyridinedicarboxylate)₃]^3- complex anion and various monovalent inorganic and organic counterions (Li⁺, Na⁺, K⁺, Rb⁺, Cs⁺, NH₄ ⁺, and pyridinium⁺) have been synthesized and studied by emission spectroscopy. The Eu³⁺ ion emission spectra exhibited by these salts have been observed with high resolution (less than 1.0 cm^?1) and at low temperature (77 K). The emission spectra of these compounds indicate that changing the attached counterion does not affect the site symmetry observed by the europium ion beyond slight distortions indicated by small shifts in the energies of the Eu³⁺ electronic levels.     

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.     

Production of high circular polarization by ion surface scattering of ferromagnets

From a theoretical analysis we predict large fractions of circular polarization of light emitted by ions scattered from surfaces of ferromagnetic single crystals. Maximum enhancement of circular polarization as compared to surface ion scattering from non-magnetic materials is again expected at grazing incidence. A circular polarization of 89% was estimated for the case of Ar⁺ ions scattered from the (110) plane of a Ni single crystal.     

Formation of the ion fraction of keV-Energy argon ions upon double scattering by al, Ge, and in targets

The charge fraction of Ar⁺ ions singly or doubly scattered by Al, Ge, and In targets is studied by means of low-energy ion scattering spectroscopy. It is shown that the behavior of the ion fraction is not described by the electron tunneling model in the case of forward scattering by an Al target. The characteristic velocities of ions singly and doubly forward and back scattered by Ge and In targets are found.     

Ion bombardment of ordered Zr3Al

The behaviour of the ordered alloy Zr₃Al was investigated by transmission electron microscopy following ion bombardments at temperatures ranging from 30 to 850 K. Utilizing high energy(0.5–2.0 MeV) C⁺, N⁺ and Ar⁺ ion bombardments, observations were made of the irradiation-induced transformation from the ordered → disordered → amorphous states. Information about individual damage cascades was also obtained using both high energy (C⁺. N⁺ and Ar⁺) and low energy (15–120 keV Cu⁺) ion bombardments.     

Li+ neutralization as a probe of the local electronic potential in Li+-alkali covered metal surface collisions

A theoretical study of Li⁺ neutralization by collision on an alkali covered Al surface is presented. The neutralization probability is computed for Li atoms back scattered from Al sites and from alkali sites on the surface. The calculations are performed with a model representation using lithium as a representative for alkali adsorption. The results reproduce the very large difference in neutralization probability for Li scattered from substrate and adsorbate sites experimentally observed by Weare and Yarmoff [Surf. Sci. 348 (1996) 359] and thus confirm the importance of local effects in atom-surface charge transfer. For scattering from adsorbate sites, the neutralization is shown to be associated with a very large excitation probability of the scattered Li atom.     

Die amorphisierung von kristallen durch ionenbeschuss und mechanismen von sekundärprozessen

Results of an experimental study of the ion-electron-emission coefficient of monocrystalline and amorphous germanium as a function of the angle of incidence for 10–30 keV Ne⁺, Ar⁺, Kr⁺ ions are presented. Using the concept of ion channeling in crystals the energy dependence of anisotropy of the ion-electron-emission coefficient is explained.     

Field ion and scanning tunnel microscopy studies of surface and bulk defects in carbon and silicon

Complex study of surface and bulk defects was performed by field ion and scanning tunnel microscopy. Specimens were irradiated by 20-to 50-keV He⁺, Ar⁺, and Bi⁺ ions at room temperature. The irradiation fluences were between 10¹⁸ and 10²⁰ ion m⁻². Calculated parameters of depletion zones and atomic displacement cascades were compared with theoretical estimates. It was shown that controlled ion bombardment of material surface is an effective tool for fabricating field-emission cathodes for vacuum microelectronics.     

Static sims studies of adsorbate structure: II. CO adsorption on Pd(111); adsorbate-adsorbate interactions on Ru(001), Ni(111) and Pd(111)

In a study of CO adsorption on Pd(111) it is shown that the secondary ion mass spectrum contains information on both adsorbate site geometry and adsorbate coverage. The fractional yields of PdCO⁺, Pd₂CO⁺ and Pd₃CO⁺, as a function of CO coverage are correlated with the changing site geometries suggested by reflection IR data. A relationship between secondary ion emission and the adsorbate-adsorbate interactions revealed by IR and EELS is also demonstrated for CO adsorption on Ru(001), Ni(111) and Pd(111).     

The structure of a stepped copper (410) surface determined by ion scattering spectroscopy

Ion Scattering Spectroscopy applied in the multiple scattering mode is used to determine the structure of a stepped Cu(410) surface. The energy of singly scattered ions is influenced by the presence of neighbour surface atoms. This effect can be used to determine interatomic distances up to about 10Å, as is shown by the results of 8 keV Ar⁺ and 11 keV Ne⁺ scattered through θ = 50°. The edge-edge distance of the stepped copper surface appears to be in accordance with the results of LEED experiments obtained by other investigators. The experiments show a good agreement with the results of the analytical 3-atom model of Poelsema. The energy of the so-called “plateau collision” appears to depend on the effective plateau length l as measured in the plane of incidence. Lengths l between 15 and 60 Å can be determined with an accuracy of 5 Å. Results are shown for 8 and 12 keV Ar⁺, θ = 40° and 60°, and 8 keV Kr⁺ θ = 40°. The experimental dependence of the energy on lis described correctly by a phenomenological model.     

Photon emission from rare gas ion bombardment of metal surfaces

Metal surfaces (Mg, Cu, Zr, Mo) are bombarded with He⁺, Ne⁺ and Ar⁺ in the energy range of 400 eV to 8 keV. Radiation from scattered projectiles and sputtered target particles is observed between 200 and 700 nm. It is shown that most of the radiating particles originate from surface collisions. Auger neutralization, resonance tunneling and direct electron transitions are the important electronic processes involved.     

Interaction studies of cysteine with Li+, Na+, K+, Be2+, Mg2+, and Ca2+ metal cation complexes

The coordination geometries, electronic features, metal ion affinities, entropies, and the energetics of Li⁺, Na⁺, K⁺, Be²⁺, Mg²⁺, and Ca²⁺ metal cations with different possible conformations of cysteine complexes were studied. The complexes were optimized using density functional theory (B3LYP) and second order Moller–Plesset Perturbation (MP2) theory methods using 6‐311 + +G** basis set. The interactions of the metal cations at different nucleophilic sites of cysteine conformations were considered after a careful selection among several binding sites. All the metal cations coordinate with cysteine in a tridentate manner and also the most preferred position for the interaction. It is found that, the overall structural parameters of cysteine are not altered by metal ion substitution, but, the metal ion‐binding site has undergone a noticeable change. All the complexes were characterized by an electrostatic interaction between ligand and metal ions that appears slightly more pronounced for lithium and beryllium metal complexes. The metal ion affinity (MIA) and basis set superposition error (BSSE) corrected interaction energy were also computed for all the complexes. The effect of metal cations on the infrared (IR) stretching vibrational modes of amino N? H bond, side chain thiol group S? H bond, hydroxyl O? H bond, and Carbonyl C?O bond in cysteine molecules have also been studied. The nature of the metal ion‐ligand bond and the coordination properties were examined using natural bond order (NBO) at bond critical point (electron density and their Laplacian of electron density) through Atoms in Molecules (AIM) analyses. Copyright © 2010 John Wiley & Sons, Ltd.     

Ion-enhanced gas-surface chemistry: The influence of the mass of the incident ion

There are many examples of situations in which a gas-surface reaction rate is increased when the surface is simultaneously subjected to energetic particle bombardment. There are several possible mechanisms which could be involved in this radiation-enhanced gas-surface chemistry. In this study, the reaction rate of silicon, as determined from the etch yield, is measured during irradiation of the Si surface with 1 keV He⁺, Ne⁺, and Ar⁺ ions while the surface is simultaneously subjected to fluxes of XeF₂ or Cl₂ molecules. Etch yields as high as 25 Si atoms/ion are observed for XeF₂ and Ar⁺ on Si. A discussion is presented of the extent to which these results clarify the mechanisms responsible for ion-enhanced gas-surface chemistry.     

ISS measurement of surface composition of AuCu alloys by simultaneous ion bombardments with Ar+ and He + ions

Surface composition of Au-Cu(43 at%) alloy under 1.5–5 keV argon ion bombardment has been investigated by ion scattering spectroscopy (ISS). In this experiment, we adopted a specific technique to use mixed He⁺ and Ar⁺ ions as primary beam in order to perform sputtering (Ar⁺) and ISS measurement (He⁺) simultaneously. The outermost atom layer of Au-Cu alloys under Ar⁺ ion bombardment is Au-rich leading to the conclusion that Ar⁺ ion bombardment of AuCu alloys causes the preferential sputtering of Cu atoms, resulting in a Au-rich outermost atom layer and a depletion layer of Au atoms beneath the outermost atom layer due to ion-beam-enhanced surface segregation. This result explains the experimental results obtained by AES as well.