Charge exchange between low energy alkali ions and cerium oxide surfaces

The fraction of low energy Na⁺ ions neutralized during single scattering from CeO₂(1 0 0) surfaces was measured with time-of-flight spectroscopy. The projectile ionization level is resonant with the surface electronic states, so that the neutralization results from a non-adiabatic charge exchange process that depends on the exit velocity and the local electrostatic potential (LEP) along the exit trajectory at a point close to the surface. Variations of the measured neutral fraction with ion energy and exit angle differ from the results obtained from clean metals due to the inhomogeneity of the LEP on an oxide surface. The results suggest that neutral fraction data collected as a function of emission angle and ion energy could be used to quantitatively map the shape of an inhomogeneous LEP.     

Experimental and theoretical study of charge transfer in hydrogen ion scattering from a graphite surface

Ion scattering spectrometry (ISS) with time of flight (TOF) analysis is employed to measure the ion fraction of positively charged hydrogen (H⁺) projectiles scattered from a well characterized highly oriented pyrolitc graphite (HOPG) surface at a 45° scattering angle, various ingoing/outgoing angles and two different incoming energies (4 and 5 keV). In the theoretical approach, the negative ionization probability is calculated by employing a Green's function formalism to solve the dynamic collisional process. Both theoretical and experimental results are analyzed and contrasted. The theoretical negative ion fraction evolution during the collisional process is described in detail.     

Features of the electron exchange under grazing scattering of H− ions from a thin aluminum disk

The electron exchange under grazing scattering of a negative hydrogen ion from a thin Al disk is analyzed via the wave packet propagation method that does not use the perturbation theory. The probability of H^? ion fraction formation is calculated as a function of the ion velocity component (v_‖) parallel to the surface. It is shown that the yield of negative hydrogen ions has a bell-like dependence on the value of v_‖ under grazing scattering from a thin disk. The negative ion yield under grazing scattering from a disk is very close to the H^? ion yield under scattering from a film. The maximum of the probability of H^? fraction formation calculated for a thin disk is shifted to smaller values of v_‖ with respect to the maximum of the probability of H^? formation for a thin film.     

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.     

Energy and charge distributions of fast hydrogen ions and atoms reflected from Cu in the case of grazing incidence

The energy and charge distributions of protons and hydrogen atoms reflected from the Cu surface in the case of grazing incidence angles are measured at energies of incident particles (H⁺ and H⁰) of 200 and 250 keV. The charged fractions of reflected particles are analyzed. A weak dependence of the neutral fraction of reflected particles on the scattering angle is discovered for incidence angles of 1°–2° and an energy of scattered particles of 60 keV or less. It is shown that the neutral fraction of reflected particles with an energy of 60–80 keV or more is independent of the scattering angle and is determined by the ratio of the cross sections for the electron capture and loss by ions in the material.     

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.     

Mechanism of negative ion formation in low velocity collisions at surfaces

Theoretical calculations using the coupled angular modes (CAM) method have been used to interpret experimental findings related to the scattered oxygen negative ion fraction (O⁻) in collisions of low energy O⁺ with an Al(1 1 0) surface. The increasing O⁻ ion fraction observed experimentally at low O⁺ velocities can be explained in terms of the distance of closest approach Z_c to the Al surface and the specific charge state of the projectile at this distance. Both Z_c and the charge state influence the charge transfer process between the projectile and the surface at low collision energies.     

A global potential energy surface for H2S+(X 4A′′) and quasi-classical trajectory study of the S+(4S) + H2(X1Σ+g) reaction

A novel global potential energy surface for H₂S⁺(X?⁴A″) based on accurate ab initio calculations is presented. Energies are calculated at the multi-reference configuration interaction level with Davidson correction using aug-cc-pVQZ basis set plus core-polarisation high-exponent d functions. A grid of 4552 points is used for the least-square fitting procedure in the frame of a many-body expansion. The topographical features of the new potential energy surface are here discussed in detail. Such a surface is then employed for dynamic studies of the S(⁴S) + H₂(X?¹Σ⁺_g) →SH⁺(X?³Σ^?) + H(²S) reaction using the quasi-classical trajectory method. State specific trajectories are calculated, for both ground and ro-vibrationally excited initial states of H₂(X?¹Σ⁺_g). Corrections to the zero point energy leakage of the classical calculations are also presented. Calculated reaction cross sections and rate constants are here reported and compared with available literature.     

Electron dynamics in H/Na/Cu(1 1 1) collisions

Surface adsorbates induce strong local perturbations in the electronic structure and potentials in their surroundings. Consequently, charge transfer processes between projectiles and adsorbate-covered surfaces are strongly affected. The theoretical calculations and experiment measurements reported herein are focused on the H⁻/Na/Cu(1 1 1) system. The electron dynamics at the Na/Cu(1 1 1) surface and the influence of Na adsorbates on the H⁻-Cu(1 1 1) charge transfer are treated and discussed in detail. The ion fractions are mainly influenced by the ion exit trajectories. At low Na coverage, they exhibit a maximum near the 60° exit angle from surface. The calculations and experimental data are in good agreement.     

Anomalous enhancement of negative sputtered ion emission by oxygen

Enhancement of negative sputtered ion yields by oxygen (either O⁺₂ bombardment or O₂ gas with Ar⁺ bombardment) is demonstrated for Si^?, As^?, P^?, Ga^?, Cu^? and Au^?, sputtered from a variety of matrices. Because oxygen also enhances positive ion yields of the same species, this effect cannot be simply explained on the basis of existing sputtered ion emission models. To rationalize these phenomena, a surface polarization model is developed which invokes localized electron emissive or electron retentive sites associated with differently oriented surface dipoles in the oxygenated surface. Such sites are considered to dominate the emission of negative and positive ions respectively. The model is shown to correctly predict that Au⁺ and Au^? ion yields are much more strongly enhanced by oxygen in dilute Au-Al alloys than in pure gold.     

Generation of high-energy negative hydrogen ions upon the interaction of superintense femtosecond laser radiation with a solid target

The formation of a high-energy (～35 keV) beam of negative hydrogen ions was observed in the expanding femtosecond laser plasma produced at the surface of a solid target by radiation with an intensity of up to 2× 10¹⁶ W/cm². The energy spectra of the H⁺ and H^?-ions show a high degree of correlation.     

Electron stimulated desorption of H3O from 316L stainless steel

Surface ions generated by electron stimulated desorption from mass spectrometer ion source grids are frequently observed, but often misidentified. For example, in the case of mass 19, the source is often assumed to be surface fluorine, but since the metal oxide on grid surfaces has been shown to form water and hydroxides, a more compelling case can be made for the formation of hydronium. Further, fluorine is strongly electronegative, so it is rarely generated as a positive ion. A commonly used metal for ion source grids is 316L stainless steel. Thermal vacuum processing by bakeout or radiation heating from the filament typically alters the surface composition to predominantly Cr₂O₃. X-ray photoelectron spectral shoulders on the O 1s and Cr 2p_3/2 peaks can be attributed to adsorbed water and hydroxides, the intensity of which can be substantially increased by hydrogen dosing. On the other hand, the sub-peak intensities are substantially reduced by heating and/or by electron bombardment. Electron bombardment diode measurements show an initial work function increase corresponding to predominant hydrogen desorption (H₂) and a subsequent work function decrease corresponding to predominant oxygen desorption (CO). The fraction of hydroxide concentration on the surface was determined from X-ray photoelectron spectroscopy and from the deconvolution of temperature desorption spectra. Electron stimulated desorption yields from the surface show unambiguous H₃O⁺ peaks that can be significantly increased by hydrogen dosing. Time of flight secondary ion mass spectrometry sputter yields show small signals of H₃O⁺, as well as its constituents (H⁺, O⁺ and OH⁺) and a small amount of fluorine as F⁻, but no F⁺ or F⁺ complexes (HF⁺, etc.). An electron stimulated desorption cross-section of σ⁺ ∼ 1.4 × 10⁻²⁰ cm² was determined for H₃O⁺ from 316L stainless steel for hydrogen residing in surface chromium hydroxide.     

H− Formation in proton-metal collisions

Negative hydrogen ion formation is studied by scattering protons from a cesiated tungsten (110) surface. The primary energy ranges from 50 to 400 eV. The angle of incidence is 70° with respect to the surface normal. A maximum conversion efficiency $\text{H}{}^{\mathrm{?}}\text{(H}{}^{\mathrm{?}}\text{+ H}{}^0\text{)}$ of 67% is measured. The measurements can be described in terms of the probability model. The perturbation of the H^? ion by the metal is described within first order perturbation theory. A reasonable agreement between theory and experiment is obtained.     

Electrostatic cnoidal waves and soliton structures in multi‐ions plasmas

Using a reductive perturbation technique (RPT), the Korteweg‐de Vries (KdV) equation for nonlinear electrostatic waves in multi‐ion plasmas is derived with appropriate boundary conditions. Furthermore, compressive and rarefactive cnoidal wave and soliton solutions are discussed. In our model, the multi‐ion plasma consists of light dynamic warm ions, heavy cold ions, and inertialess electrons, which follows the Maxwell‐Boltzmann distribution. It is observed that in such an unmagnetized multi‐ion plasma, two characteristic electrostatic waves i.e., slow ion‐acoustic (SIA) waves and fast ion‐acoustic (FIA) waves, can propagate. The results are discussed by considering two types of multi‐ion plasmas i.e., H⁺–O⁺–e plasma and H^?–O⁺–e plasma that exist in space plasmas. It is found that for H⁺–O⁺–e plasma, the SIA cnoidal wave and soliton form both positive (compressive) and negative (rarefactive) potential pulses, which depend on the temperature and density of the light and warm ions. However, only electrostatic positive potential structures are obtained for FIA cnoidal wave and soliton in H⁺–O⁺–e plasma. In the case of H^?–O⁺–e plasma, the SIA cnoidal wave and soliton form only compressive structures, while the FIA cnoidal wave and soliton compose rarefactive structures. The effects of light ions' density and temperature on nonlinear potential structures are investigated in detail. The parametric results are also demonstrated, which are applicable to space and laboratory multi‐ion plasma situations.     

Negative-ion formation from surface scattering and the Anderson correlation energy U

A theoretical investigation of negative-ion formation from positive-ion-surface scattering is presented from a unified point of view. Based on the time-dependent Anderson-Newns model, the correlation energy U is seen to play an important role in the two-electron transfer process. Calculations of the probability of negative-ion formation are in good agreement with experiments on the conversion of H⁺(D⁺) to H^?(D^?) by scattering from a cesiated W(100) surface.     

Isotope effect in electron capture by protons into the 2S-state of hydrogen

We have investigated the isotope effect for electron capture into the 2S-state of hydrogen in close collisions for the processes H⁺ in H₂ and H⁺ in D₂. The differential cross sections and transition probabilities P_2S obtained for capture into H(2S) as a function of energy at a fixed angle of θ = 1° exhibit distinctive features, but no apparent isotope effects are detected.     

Integral Hellmann-Feynman theorem as a criterion of the quality of wave functions of atomic-molecular systems

It is proposed to use the integral Hellmann-Feynman theorem for the quality control and refinement of atomic and molecular wave functions. Its validity is verified for variational wave functions of the positronium ion e ⁺ e ^? e ^?, the negative ion of the hydrogen atom p _∞ ⁺ e ^? e ^? (H^?), and mesomolecules μ^?π⁺π⁺ and μ^? p ⁺ p ⁺. The relative violation of this theorem (10^?2) is six orders of magnitude larger than the error of the energy calculation (10^?8), which demonstrates its high sensitivity to the quality of wave functions. A way of refining wave functions on the basis of combination of the integral Hellmann-Feynman theorem for exactly solvable model and real atomic-molecular systems is proposed. A rule for verification of the mutual consistency of the wave functions of any three quantum-mechanical systems is formulated.     

Argon (10 keV) scattered from structures,induced by bombarding a Cu(100) surface; ionization and neutralization

The ion fractions, η⁺, of 10 keV argon particles, scattered from a damaged copper surface, are measured with a time of flight spectrometer. The damage was introduced by bombardment with argon ions. The scattering angle was 30°. The results for different angles of incidence, ψ, are reported. For Ψ < 10° the ion fraction is relatively high (～27% for Ψ = 4°) and decreases as Ψ increases. For Ψ = 15° the value of η⁺ is 7%, whereas for 21° < Ψ < 27° the value of η⁺ appears to be constant (～14%). An explanation is given by assuming interatomic ionization as well as neutralization processes along the trajectory of the scattered particles. The number of step-atoms, induced by ion bombardment, is estimated to be about 2 × 10¹⁴/cm².     

Comparative study on low energy ion beam modification of thermoplastic polymers

ABSTRACT

Polycarbonate (PC) and polyethylene terephthalate (PET) thermoplastic polymer films were irradiated by low energy ion beams such as 100 keV Hydrogen (H⁺) ions and 350 keV Nitrogen (N⁺) ions at varied fluence from 1?×?10¹³ ions/cm² to 5?×?10¹⁴ ions/cm². The depth profile concentration of ions was calculated using Stopping and Range of Ions in Matter (SRIM) software code. Fourier Transform Infrared (FTIR) technique shows decrement in the intensity of peaks and disappearance of peaks mainly related to carbonyl stretching at 1770?cm^?1 and C–C stretching at 1500?cm^?1. Scanning electron microscopy (SEM) of irradiated polymers showed the formation of pores. X-ray diffraction (XRD) analysis has showed decrease in the intensity indicating the decrease in crystallinity after irradiation. Mechanical studies revealed that the molecular weight and microhardness decrease with increase in ion fluence due to increase in chain scission. The contact angle increased with increase in ion fluence indicating the hydrophobic nature of polymer after irradiation. Antibiofilm activity test of irradiated films shows resistance to Salmonella typhi (S. typhi) pathogen responsible for typhoid. The study shows that Nitrogen ion induces more damage compared to Hydrogen ions and PC films get more modified than PET films.