Low-energy neon-ion scattering and neutralization on first and second layers of a Ni(001) surface

The scattering and neutralization of 2.4 and 5 keV Ne⁺ ions on the Ni(001) surface have been studied by time-of-flight (TOF) and electrostatic analyzer (ESA) techniques. The scattering yield of neutrals plus ions (by TOF) is strongly dependent on crystal orientation, in one direction being reduced by the shadowing of 2nd layer atoms by 1st layer atoms, or in another being increased by focussing of ions onto the 2nd layer by 1st layer atoms. Ion yields (by ESA) show little of this variation since the ions are largely neutralized on scattering from the second layer. The results thus demonstrate and explain the first layer selectivity of low-energy ion scattering by ESA for a case in which there is no shadowing of second layer atoms by the first layer. On the other hand, the ability to measure and distinguish first and second layer scattering of neutrals and ions by TOF suggests the possibility of composition analysis of individual layers of single crystal alloys and compound semiconductors.     

Multiple scattering of low-energy rare-gas ions at solid surfaces

We have studied the multiple scattering of He⁺, Ne⁺, and Ar⁺ from a TaC(001) surface in the energy region of the order of 1 keV. The experimental data revealed large differences between the energy spectra of these ions. The spectral peak corresponding to quasi-double scattering is clearly observed for Ar⁺ but not observed for Ne⁺. The multiple scattering effect appearing in the energy spectra of rare-gas ions is discussed on the basis of electron exchange between these ions and solid surfaces.     

Low energy ion scattering from a Ni(100) surface

We have tudied the scattering of He and Ne ione from a clean Ni(001) surface in the energy range of 0.5 to 5 keV. The spectra are dominated by scattering from atoms in the first layer for energies belowe 2 keV, whereas for higher energies contributions from the second layer can be identified. In the impact collision mode of ion scattering spectroscopy with a scattering angle =164°, the shape of the shadow cone can be determined. These experimental shadow cone radii agree over a wide range of parameters well with calculations using a Thomas-Fermi-Molière potential with a reduced screening length.     

Theory of ion scattering from single crystals

The scattering of He⁺, Ne⁺ and Ar⁺ ions at 600 eV from Ni(110) in the [11̄0] direction is modeled using classical dynamics. The distributions of final scattering angles of the primary ions are displayed as contour plots over the surface impact zone. From the contour plots the regions of the surface that give rise to scattering at specific angles can be isolated. The majority of the inplane scattering arises from collisions of the primary ion with second layer or “valley” atoms. However, to correctly reproduce the experimental energy distribution curves of Heiland and Taglauer (J. Vacuum Sci. Technol. 9 (1971) 620), we must include a simple collision time correction to account for neutralization of the ion beam. This analysis predicts that the ions which collide with second layer atoms of the solid are preferentially neutralized. The energy distributions due to first layer collisions agree well with experiment. We find that a full molecular three dimensional model is needed to describe all of the ion scattering events since for most of the collisions, the ion is simultaneously interacting with at least two atoms of the solid. However, in agreement with other workers we find only a single collision is responsible for the “binary” peak in the energy distribution. In addition the relative scattering intensity at different angles is dependent on having a three-dimensional solid.     

Oxygen adsorption on Cu(110): Determination of atom positions with low energy ion scattering

The position of adsorbed oxygen on Cu($\text{1}$10) surfaces was determined with Low Energy Ion Scattering (LEIS). The experiments were performed by bombarding the copper surface at small angles of incidence with low energy Ne⁺ ions (3–5 keV). Measurements of the Ne⁺ ions scattered by adsorbed oxygen showed regular peaks in the azimuthal distribution of the scattered ions due to a shadowing effect. From the symmetry of the azimuthal distributions it follows that the centre of an adsorbed oxygen atom on the Cu(1̄10) surface lies about 0.6 Å below the midpoint between two neighbouring Cu atoms in a 〈001〉 row. A comparison of the azimuthal distributions of Ne⁺ ions scattered from clean Cu surfaces and oxygen-covered Cu surfaces showed that hardly any surface reconstruction had occurred in the oxygen-covered surfaces. The applied method seems to be an appropriate one for locating adsorbed atoms because it uses only simple qualitative considerations about azimuthal distributions of scattered ions.     

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.     

Electron transfer in low energetic Ne2+/Ar,Kr collisions

Single electron capture processes in Ne²⁺/Ar, Kr collisions were studied by aid of the high-resolution translational spectroscopy. At low collision energies (<1 keV) the dominant contribution to the Ne⁺-spectrum arises from Ne²⁺ ions in the metastable¹ S ₀-state, although it is the weakest component of the primary Ne²⁺ beam. Ne²⁺(³ P) and Ne^2+*(¹ D) projectiles play no important role due to unfavourable energy defects. Target excitation processes as well as transfer ionisation are considered as a possible explanation for different structures in the measured Ne⁺ spectra.     

Multiple scattering and neutralization aspects of low energy noble gas ions incident on a Cu (110) crystal

Experiments have been done with 1 keV Ne⁺ ions bombarding a Cu (110) single crystal in a (111) plane. From the measured energy spectra of the scattered ions the minimum and maximum scattering angles for multiple scattering on the surface are determined. These minimum and maximum scattering angles were also calculated using a computer model. The parameters for an interatomic potential function between ion and metal atom are determined by comparison of the experimental and calculated scattering angles. A neutralization model for an energetic ion at an atomic surface is given. The reliability of this model is tested by comparison of the results of computer calculations and the measured peak intensity distributions as a function of the scattering angle.     

A comparison of radiation from sputtered atoms with radiation from projectiles scattered on oxidized magnesium at varying angle of incidence

The intensity of light emitted from sputtered atoms and neutralized, scattered primary ions, excited during 4 keV Ne⁺ and Ar⁺ bombardment of oxidized magnesium has been measured as a function of the incidence angle. It was found that the photon yield of sputtered atoms increases with the angle of incidence much more rapidly than the theoretical sputtering yield and the photon yield of scattered projectiles. In order to explain the experimental results a numerical approach was made based on the following assumptions: (1) the sputtered atom can be excited when it crosses the surface after getting the momentum from the collision cascade; (2) at oblique incidence the sputtered excited atom can be directly emitted after a gentle collision between the incident ion and the surface atom; (3) the neutralized primary ion can only be excited in a violent collision with the surface atom.     

Randomisation of crystal structure within energetic collision cascades revealed by the sputtering of Au single crystals during ion bombardment

The ratio of random to preferential atomic ejection which occurs from the surface of a gold single crystal during ion bombardment has been found to be very sensitive to the ion mass. For instance, in the case of 50 keV Ne⁺ ion bombardment preferential ejection dominates, whereas in the case of 50 keV Au⁺ ion bombardment preferential ejection is only a small fraction of the total. These results are interpreted in terms of a dynamic randomisation of the crystal lattice which occurs during the creation of energetic atomic collision cascades. The disorder occurs so rapidly that a substantial fraction of atoms sputtered from the surface are ejected from an essentially random structure. It is thought that such gross disorder is only a transient phenomenon, and leaves no significant permanent effects, except perhaps for a few clustered defects.     

Auger study of preferred sputtering on binary alloy surfaces

Auger Electron Spectroscopy has been used to investigate the preferred sputtering behavior on homogeneous Cu/Ni alloy surfaces. Measurements were made on a range of alloy compositions with Ar⁺ sputter ions of 0.5 to 2 keV energy. A kinetic model has been formulated to describe the time variation of the surface composition during sputtering. Based on this model, we were able to determine the individual sputter yields for Cu and Ni atoms in the alloy and the depth of the surface layer where the composition is altered by sputtering. The sputter yields were found to be relatively independent of the alloy composition but increased almost linearly with energy. The depth of the altered layer was comparable to the Auger sampling depth with its value increasing from 10 Å to more than 20 Å when ion energy increased from 0.5 to 2 keV.     

Theoretical energy distributions of atoms sputtered from elastic collision spikes by monomer and dimer ion bombardment

The energy spectra of atoms sputtered from metal targets by bombardment with heavy monomer and dimer ions have been investigated on the basis of a standard model for elastic collision spikes. In particular we calculated the energy distributions for a Au sample bombarded by 4 keV I⁺ and 8 keV I ₂ ⁺ ions. The results were compared with the recent time of flight measurements performed by de Vries and coworkers. It was shown that the model described accurately most of the experimental observations: the count rates and the relative cascade to spike ratios for both I⁺ and I ₂ ⁺ projectiles, and the energy spectrum for dimer sputtering. The spectrum for monomer bombardment, however, was shifted towards lower energies in comparison to the experimental one. The possible source of this discrepancy is discussed.This work was supported by the Central Research Program CPBP 01.09     

The energy distributions of atoms sputtered from HfC

The energy spectra of Hf and C atoms sputtered from an HfC target with a 6 keV Xe⁺ beam have been measured. It was found that the target constituents of widely different masses were sputtered with energy distributions of the same form. The results are compared with the collision cascade theory for compound targets.     

低能原子簇轰击金属簿膜引起的级联碰撞(Ⅱ)——注入簇原子的加速

研究了能量为１ｋｅＶ／ａｔｏｍ的金原子簇和０．２ｋｅＶ／ａｔｏｍ的铝原子簇轰击金薄膜产生的级联碰撞。用分子动力学模拟计算了注入靶后的簇原子能量分布及其随时间的演化。结果表明，在原子簇注入引起的级联碰憧中，簇原子除了将能量传递给靶原子外，尚有可能破加速。簇原子的最高能量可大于它的初始能量；分析了原子簇注入引起的多次碰撞效应，并用经典力学守恒定律计算了一个簇原子发生二次散射后的能量增益，用以解释注入原子的加速机制。 关键词：     

Émission d'électrons auger caractéristiques du néon et du sodium,observée lors de collisions de ces ions avec différentes cibles solides

The Ne and Na Auger emission observed from collisions of these ionized gases with different solid targets, in an energy range from 5 to 50 keV, has been investigated. The Auger electron distributions were analyzed. Moreover, for the Ne⁺-Mg and Na⁺-Mg collisions, the Auger yield variation as a function of various parameters which influence the implantation, was studied. The experimental Auger yields ρ_A were compared to the calculated ones in a model which takes into account the stationnary concentration profiles of implanted atoms inside the target. For the Ne, the experimental results are in good agreement with the proposed model but this model is inadequate to explain the Na ρ_A variations as a function of ionic energy and incidence angle, at the room temperature.     

Influence of “travelling velocities” on molecular autoionization electron spectra

We present electron energy spectra that arise in Li⁺ —He collisions in the laboratory collision energy range from 1.4 to 3 keV, and that are observed at 0° and 180° with respect to the Li⁺ beam. The spectra are composed of a component due to atomic autoionization of doubly excited He in the field of Li⁺, and a component due to molecular autoionization of the collision system. The variation of the latter component with collision energy and observation angle is analyzed in terms of a newly developed spectral shape function for molecular autoionization that implies a “distribution of travelling velocities” of the collision system during electron emission. From the comparison of calculated and measured spectra it is concluded that the physical interpretation on which the analysis is based is correct. Two parameters of the distribution of travelling velocities are determined.     

Charge transfer in the collision system He<Superscript>2+</Superscript> + C<Stack><Subscript>60</Subscript><Superscript>+</Superscript></Stack>: Theory and experiment

Fullerenes are a direct link between atoms with discrete electronic energy levels and solids with a band structure and a well-defined surface. In this paper, we report on a quantum mechanical treatment of charge transfer and ionization in the ion-ion collision system ³He²⁺ + C ₆₀ ⁺ . This approach considers under- and over-barrier transitions through the one-dimensional barrier between the collision partners. The calculated cross sections for charge transfer compare favorably with experimental data measured in the center-of-mass energy range from 27 to 196 keV employing the crossed beams technique.     

Scattering of keV H+ from Au(110)—comparison between experiment and simulation

Abstract

Angle resolved energy spectra for H⁺ ₂ scattering from Au(110) have been compared to simulations using MARLOWE and SABRE binary collision codes. The results of both simulations agree with each other but only qualitatively with the experiment. The simulations indicate that (i) contributions to the surface peak in the energy spectra come from both single and double scattering at the surface (ii) the amount of inelastic loss suffered by the scattered ion is sensitive to the loss model and (iii) azimuthal scans around the double alignment direction can be simulated quite well if an increased experimental background is included.     

Point-defect properties of and sputtering events in the {001} surfaces of Ni3Al I. Surface and point-defect properties

Constant-area and fully relaxed molecular dynamics methods are employed to study the properties of the surface and point defects at and near {001} surfaces of bulk and thin-film Ni, Al and Ni₃Al respectively. The surface tension is larger than the surface energy for all {001} surfaces considered in the sequence: Al (1005?mJ?m^?2)<?Ni₃Al (mixed Ni–Al plane outermost, 1725?mJ?m^?2)<?Ni₃Al (all-Ni-atoms plane outermost, 1969?mJ?m^?2)<?Ni (1993?mJ?m^?2). For a surface of bulk Ni₃Al crystal with a Ni–Al mixed plane outermost, Al atoms stand out by 0.0679?Å compared with the surface Ni atoms and, for the all-Ni-atoms surface, Al atoms in the second layer stand out by 0.0205?Å compared with Ni atoms in the same layer. Vacancy formation energies are about half the bulk values in the first layer and reach a maximum in the second layer where the atomic energy is close to the bulk value but the change in embedding energy of neighbouring atoms before and after vacancy formation is greater than that in the bulk. Both the vacancy formation energy and the surface tension suggest that the fourth layer is in a bulk state for all the surfaces. The formation energy of adatoms, antisite defects and point-defect pairs at and near {001} surfaces of Ni₃Al are also given.     

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.