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.     

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.     

X-ray photoelectron spectroscopic studies of PbO surfaces bombarded with He+, Ne+, Ar+, Xe+ and Kr+

The surface composition of PbO has been studied with X-ray photoelectron spectroscopy after bombardment with several inert gas ions of 400 eV. The results show reduction of PbO to metallic Pb with the degree of damage following the order He⁺ > Ne⁺ >Ar⁺. Both Kr⁺ and Xe⁺ did not reduce the oxide. The depth of damage varied from ≈9 Å for He⁺ to ≈1 Å for Ar⁺ bombardment. The results were compared to a collisional and a thermal model of the sputtering process.     

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.     

Ion survival probabilities for 3 keV He+, Ne+, and Ar+ scattering from La and adsorbate covered La surfaces

TOF spectra of scattered neutrals and ions for 3 keV He⁺, Ne⁺, and Ar⁺ bombardment of La and adsorbate covered La surfaces show that the scattered ion fractions are 21.1% and 10.7% for Ar⁺ on clean and adsorbate covered La, respectively, and < 1% for all of the other systems. These results are consistent with a model in which Auger and resonant neutralization (AN and RN) transitions govern the ion survival probability.     

Influence of argon ion bombardment on the formation of intermetallic compounds in the nickel-aluminum system

The formation of Ni _x Al _y intermetallic compounds in two-layer (Ni/Al) structures (nickel films deposited on aluminum substrates in vacuum) under bombardment by Ar⁺ ions has been studied experimentally. The method based on Rutherford backscattering of He⁺ ions is used to demonstrate that argon ion bombardment causes the formation of intermetallic compounds in the near-surface layer. The thickness of the intermetallic layer formed in the near-surface region substantially exceeds the projective ion path. The composition and thickness of the intermetallic layer depend mainly on the implantation dose and the substrate temperature, rather than on the ion current density. In the intermetallic layer, the content of nickel increases with increasing temperature. It has been established that, in the absence of bombardment, intermetallic phases are not observed at temperatures lower than T = 400°C and that, in the presence of bombardment, the Ni₃Al intermetallic layer arises at a temperature of 320°C.     

Effect of the bombarding-ion mass in alloy sputtering

It is shown experimentally that a change in the mass of bombarding ions from ⁴⁰Ar⁺ to ⁴He⁺ has a strong effect on the spatial distributions of the components sputtered from the alloy NiMoRe. A mechanism of sputtering by backscattered ions is proposed to describe the observed preferential ejection of the light component in the direction normal to the surface of the sample under bombardment by ⁴He⁺ ions. Pis’ma Zh. éksp. Teor. Fiz. 63, No. 7, 507–510 (10 April 1996)     

Investigation on surface compositions of CuNi alloy under Ar+ ion bombardment by ISS and in situ AES measurements

Surface compositions of CuNi(50 wt%) alloy under 3 keV Ar⁺ ion bombardment were measured by Auger electron spectroscopy (AES) and ion scattering spectroscopy (ISS). In situ AES measurement of sputter-deposited layer and sputtered sample surface indicated that surface composition became Ni-rich due to Ar⁺ ion sputtering at steady state, in accord with previous reports of preferential sputtering. ISS measurements with 3 keV Ar⁺ ions, however, have suggested that the composition of the outermost atom layer is not Ni-rich but slightly copperrich. This leads to the conclusion that the degree of preferential sputtering is small and that the question of preferential sputtering, particularly, the ratio of the sputtering yields, $\text{S}{}_{\mathrm{<mtext>Cu</mtext>}}\text{S}{}_{\mathrm{<mtext>Ni</mtext>}}$, based on AES measurement requires further examination.     

Sputtering of metals at ion-electron irradiation

It has been found that, in contrast to the commonly accepted opinion, simultaneous irradiation by 15-keV Ar⁺ ions and 2.5-keV electrons at temperatures above 0.5T _m (T _m is the melting temperature) induces much larger sputtering of metallic copper, nickel, and steel than irradiation only by Ar⁺ ions. The effect increases with the temperature. At T = 0.7T _m, the sputtering coefficients in the case of ion-electron irradiation are more than twice as large as the sputtering coefficients in the case of irradiation by Ar⁺ ions. The experiments on the sublimation of copper show that the sublimation rate in the case of the heating of a sample by an electron beam is higher than that in the case of heating in an electric vacuum oven. The revealed effects are explained by the electron-induced excitation of adatoms (atoms stuck over the surface, which appear owing to ion bombardment). Excited adatoms have a smaller binding energy with the surface and are sputtered more easily.     

Metastable Decomposition of Ar3+ Cluster Ions Into Ar2+ and Ar+

In this note we present the first account of a study of metastable (unimolecular decay) and collision-induced dissociation of Ar₃+ cluster ions using an experimental setup consisting of a molecular beam-electron impact ion source and a double focussing (reversed Nier Johnson geometry) mass spectrometer. The existence of the following metastable decay processes (accessible by our sampling time window) could be demonstrated: Ar₃⁺* → Ar₂+ and Ar₃⁺* → Ar⁺. The processes were studied as a function of electron impact energy. The present results are of importance in order to provide some guidance for the development of appropriate theoretical models for the dissociation of cluster ions.     

On the nature of ion bombardment-induced phase transformations in films of transition metals

Abstract

Electron diffraction studies have been made of polycrystalline Ni films irradiated with well separated beams of ions of different nature, namely ions of inert (He⁺, Ne⁺, Ar⁺, Kr⁺, Xe⁺) and reactive (N⁺ and O⁺) gases. The Ni films were prepared under vacuum conditions (P? 3·10^?6Pa during evaporation) preventing an appreciable contamination of the films with impurities. The samples were irradiated at T? 300 K with ion beams of energies from 10 to 100 keV in the dose range between 5·10¹⁶ cm^?2 and the value leading to sample destruction.

Irradiation with noble gas ions revealed no phase transitions in the Ni films. A similar result was obtained in irradiation of Fe and Cr films with He⁺ ions. The bombardment of Ni films with reactive gas ions does cause changes in the lattice structure of the samples under study, depending on the nature of the bombarding ions. The N⁺ ion bombardment gives rise to the hcp phase with the lattice parameters typical of the Ni₃N compound, and the O⁺ ion bombardment results in the fcc phase with the NiO-type parameter.

The conclusion is drawn on the chemical origin of the phase transformations in the Ni films under ion bombardment. The necessity of revising the concept about the polymorphous nature of phase transformations induced in the films of transition metals by ion bombardment is substantiated.     

Radiation damage of material surfaces under prolonged irradiation with He+ and Ar+ ions with broad energy spectra

The results of studying the redistribution of Be, Al, Ti, Fe, Cu, Zr, Mo, and W atoms incorporated in polycrystalline metal samples under irradiation with He⁺, (He⁺ + Ar⁺), and Ar⁺ ion beams with a broad energy spectrum and an average energy of 10 keV at irradiation doses of 1 × 10²¹ ion/cm² are studied. It is discovered that irradiation at doses exceeding 1 × 10¹⁹ ion/cm² results in local small-crystal formations being produced in a near-surface substrate layer. Their typical dimensions are less than 1–5 μm, and their the density is up to 1–100. They contain incorporated atoms and impurity atoms with a concentration of 0.1–10 at %. Subsequent irradiation at a dose of 1 × 10²⁰ ions/cm² or more leads to disappearance of these formations, mainly because of sputtering processes.     

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.     

The influence of ion bombardment on emission properties of small dust grains

Dust grains that are present in many plasma and vacuum systems and in the space usually carry a non-negligible charge. Their charging significantly depends on surface properties of the grain material. In cold plasma, charging is mainly given by electron attachment, nevertheless, when plasma becomes hot, other processes (secondary electron emission, field emission, etc.) take place. Emission properties of the grain surface could be modified by grain baking or by ion bombardment. Our study is carried out at the dust charging experiment dealing with a single dust grain electro-dynamically levitated in a 3D quadrupole trap. The grain can be exposed to the ion beam in the energy range of 100 eV–5 keV and to the electron beam in the energy range of 100 eV–10 keV. We have chosen He⁺ and Ar⁺ ions for the surface treatment and the observed influence on the surface properties is discussed in terms of secondary emission. A non-negligible shift of the secondary electron emission yield, as well as a change of energy distribution of secondary electrons, were measured after Ar⁺ bombardment. A preliminary study suggests that the effects of He⁺ and Ar⁺ are comparable.     

Study on the orientation of silver films by ion-beam assisted deposition

Low energy ion beam assisted deposition (IBAD) was employed to prepare Ag films on Mo/Si (100) substrate. It was found that Ag films deposited by sputtering method without ion beam bombardment were preferred (111) orientation. When the depositing film was simultaneously bombardment by Ar⁺ beam perpendicular to the film surface at ion/atom arrival ratio of 0.18, the prepared films exhibited weak (111) and (200) mixed orientations. When the direction of Ar⁺ beam was off-normal direction of the film surface, Ag films showed highly preferred (111) orientation. Monte Carlo method was used to calculate the sputtering yields of Ar⁺ ions at various incident and azimuth angles. The effects of channeling and surface free energy on the crystallographic orientation of Ag films were discussed.     

Absolute measurement of sputtered ion fractions using matrix isolation spectroscopy

Sputtering yields for neutrals and ions have been measured by collecting the sputtered species in a noble gas matrix and determining their amounts from optical absorption spectroscopy. The atomic ion fractions for Ti and Zr bombarded by O₂⁺ at 2 keV are 0.8 and 0.4, respectively, whereas TiO and ZrO are sputtered largely as neutrals. Neutral sputtering yields from Ar⁺ bombardment arc consistent with previous measurements. The experimental results are compared with various theoretical models for the sputtering process.     

On the use of the saha-eggert equation for quantitative sims analysis using argon primary ions

Samples of known composition have been bombarded by Ar⁺ ions. The resulting secondary ion mass spectra, obtained with two different types of SIMS instruments, were used to check the validity of the Saha-Eggert equation for the case of Ar⁺ ion bombardment.     

Calculations of the level of primary radiation defects (displacements per atom) taking into account surface sputtering

The results of analytical estimates and computer simulations of the primary radiation damage level in the number of displacements per atom (dpa) in solids are presented and compared, taking into account the material sputtering under ion bombardment. Calculations were performed for the bombardment of carbon-based materials by Ar⁺, Ne⁺, and N⁺ ions with energies of 2?C30 keV, when considerable ion-induced changes in the material??s structure are observed. A comparison shows the close fit of the analytical and computer calculations.     

Damage formation in Ge during Ar and He implantation at 15 K

Ar⁺ and He⁺ ions were implanted into Ge samples with (1 0 0), (1 1 0), (1 1 1) and (1 1 2) orientations at 15 K with fluences ranging from 1×10¹¹ to 1×10¹⁴ cm⁻² for the Ar⁺ ions and fluences ranging from 1×10¹² to 6×10¹⁵ cm⁻² for the He⁺ ions. The Rutherford backscattering (RBS) technique in the channelling orientation was used to study the damage built-up in situ. Implantation and RBS measurements were performed without changing the target temperature. The samples were mounted on a four axis goniometer cooled by a close cycle He cryostat. The implantations were performed with the surface being tilt 7° off the ion beam direction to prevent channelling effects. After each 300 keV Ar⁺ and 40 keV He⁺ implantation, RBS analysis was performed with 1.4 MeV He⁺ ions.For both the implantation ions, there is about no difference between the values found for the damage efficiency per ion for the four different orientations. This together with the high value (around 5 times higher than that found in Si), gives rise to the assumption of amorphous pocket formation per incident ion, i.e. direct impact amorphization, already at low implantation fluences. At higher fluences, when collision cascades overlap, there is a growth of the already amorphized regions.     

Relation between surface structures and sputtering ratios of copper single crystals

Polished (100) Cu crystals have been bombarded at target temperatures of 204 K, 294 K and 456 K by 10 and 20 keV Ne⁺ ions up to a total dose of 1.7 × 10¹⁹ ions/cm². The plane of incidence was chosen to be a {100} plane perpendicular to the surface. Measurements have been performed for incident angles between 36° and 44° with respect to the surface normal. In this angular interval the sputtering ratio and the surface structure have been studied by weightloss and replica electron microscope techniques respectively. At target temperatures of 204 K and 294 K an anomaly was observed in the curve of the sputtering ratio versus angle of incidence. A small peak appears where the curve slopes towards the 〈110〉 minimum. The position and height of the peak is a function of target temperature and ion energy.

This sputtering submaximum is accompanied by the formation of {100} orientated furrows perpendicular to the ion beam. The nucleation of this relief is tentatively discussed in terms of local deviations from perfection of the surface, which might be due to a singularity in the production of focusing collisions influencing the damage structure. The growth of the furrows and the submaximum in the sputtering ratio are discussed in terms of the angle between the ion beam and the characteristic {110} side of the furrows.

These sputtering and faceting phenomena have not been observed at 20 keV Ar⁺ ion bombardment nor generally under bombardment at a target temperature of 456 K.