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Ion beam neutralization

To overcome this problem, we have modified a commercial ion gun to generate a diffuse fast-atom beam [116, 117]. The ion beam neutralizer shown in Figure 7 consists of a multi-hole metal plate through which the primary ions pass. The ions are neutralized by the ion/surface interactions that occur as the beam passes through the metal aperatures and by charge-exchange reactions that occur within the gun assembly. A repeller grid is used to remove the residual ions from the neutralized beam. [Pg.180]

Figure 7. Schematic diagram of commercial ion gun modified with an ion beam neutralizer. Reproduced with permission from Ref. 116. Copyright 1983, Elsevier Science Publishing Co. Figure 7. Schematic diagram of commercial ion gun modified with an ion beam neutralizer. Reproduced with permission from Ref. 116. Copyright 1983, Elsevier Science Publishing Co.
D. Gardner, W. Sainty, Ion current measurement and ion beam neutralization using a novel Faraday Cup operable during deposition, in Proceedings of the 50th Annual Technical Conference, Society of Vacuum Coaters, 2007, p. 534. [Pg.192]

These equations indicate that the energy of the scattered ions is sensitive to the mass of the scattering atom s in the surface. By scanning the energy of the scattered ions, one obtains a kind of mass spectrometric analysis of the surface composition. Figure VIII-12 shows an example of such a spectrum. Neutral, that is, molecular, as well as ion beams may be used, although for the former a velocity selector is now needed to define ,. ... [Pg.309]

As with most methods for studying ion-molecule kinetics and dynamics, numerous variations exist. For low-energy processes, the collision cell can be replaced with a molecular beam perpendicular to the ion beam [106]. This greatly reduces the thennal energy spread of the reactant neutral. Another approach for low energies is to use a merged beam [103]. In this system the supersonic expansion is aimed at the tluoat of the octopole, and the ions are passed tluough... [Pg.812]

Figure Bl.7.7. Summary of the other collision based experiments possible with magnetic sector instruments (a) collision-mduced dissociation ionization (CIDI) records the CID mass spectrum of the neutral fragments accompanying imimolecular dissociation (b) charge stripping (CS) of the incident ion beam can be observed (c) charge reversal (CR) requires the ESA polarity to be opposite that of the magnet (d) neutiiralization-reionization (NR) probes the stability of transient neutrals fonned when ions are neutralized by collisions in the first collision cell. Neutrals surviving to be collisionally reionized in the second cell are recorded as recovery ions in the NR mass spectrum. Figure Bl.7.7. Summary of the other collision based experiments possible with magnetic sector instruments (a) collision-mduced dissociation ionization (CIDI) records the CID mass spectrum of the neutral fragments accompanying imimolecular dissociation (b) charge stripping (CS) of the incident ion beam can be observed (c) charge reversal (CR) requires the ESA polarity to be opposite that of the magnet (d) neutiiralization-reionization (NR) probes the stability of transient neutrals fonned when ions are neutralized by collisions in the first collision cell. Neutrals surviving to be collisionally reionized in the second cell are recorded as recovery ions in the NR mass spectrum.
In TOF-SARS [9], a low-keV, monoenergetic, mass-selected, pulsed noble gas ion beam is focused onto a sample surface. The velocity distributions of scattered and recoiled particles are measured by standard TOF methods. A chaimel electron multiplier is used to detect fast (>800 eV) neutrals and ions. This type of detector has a small acceptance solid angle. A fixed angle is used between the pulsed ion beam and detector directions with respect to the sample as shown in figure Bl.23.4. The sample has to be rotated to measure ion scattering... [Pg.1805]

The critical requirements for the ion source are that the ions have a small energy spread, there are no fast neutrals in the beam and the available energy is 1-10 keV. Both noble gas and alkali ion sources are conunon. Por TOP experunents, it is necessary to pulse the ion beam by deflecting it past an aperture. A beam line for such experiments is shown in figure B1.23.5 it is capable of producing ion pulse widths of 15 ns. [Pg.1807]

Static Secondary Ion Mass Spectrometry (SIMS) involves the bombardment of a sample with an energetic (typically 1-10 keV) beam of particles, which may be either ions or neutrals. As a result of the interaction of these primary particles with the sample, species are ejected that have become ionized. These ejected species, known as secondary ions, are the analytical signal in SIMS. [Pg.41]

In Dynamic Secondary Ion Ma s Spectrometry (SIMS), a focused ion beam is used to sputter material from a specific location on a solid surface in the form of neutral and ionized atoms and molecules. The ions are then accelerated into a mass spectrometer and separated according to their mass-to-charge ratios. Several kinds of mass spectrometers and instrument configurations are used, depending upon the type of materials analyzed and the desired results. [Pg.528]

In Surface Analysis by Laser Ionization (SAU) ionized and neutral atoms are sputtered from the sample surface, typically using an ion beam (like SIMS) or a... [Pg.528]

In other articles in this section, a method of analysis is described called Secondary Ion Mass Spectrometry (SIMS), in which material is sputtered from a surface using an ion beam and the minor components that are ejected as positive or negative ions are analyzed by a mass spectrometer. Over the past few years, methods that post-ion-ize the major neutral components ejected from surfaces under ion-beam or laser bombardment have been introduced because of the improved quantitative aspects obtainable by analyzing the major ejected channel. These techniques include SALI, Sputter-Initiated Resonance Ionization Spectroscopy (SIRIS), and Sputtered Neutral Mass Spectrometry (SNMS) or electron-gas post-ionization. Post-ionization techniques for surface analysis have received widespread interest because of their increased sensitivity, compared to more traditional surface analysis techniques, such as X-Ray Photoelectron Spectroscopy (XPS) and Auger Electron Spectroscopy (AES), and their more reliable quantitation, compared to SIMS. [Pg.559]

Figure 2 Relationship of SIMS, separate bombardment SNMSs and direct bombardment SNMSd. (a) Materials for SIMS analysis are those ions formed In the sputtering with a focused primary ion beam. The largest fraction of the particles sputtered from the surface are neutral atoms, (b) Ions for SNMS analysis are formed by ionization of the sputtered neutrals, (c) When the plasma is used as an ionizer, plasma ions can also be used to sputter the sample surface at low energies. Figure 2 Relationship of SIMS, separate bombardment SNMSs and direct bombardment SNMSd. (a) Materials for SIMS analysis are those ions formed In the sputtering with a focused primary ion beam. The largest fraction of the particles sputtered from the surface are neutral atoms, (b) Ions for SNMS analysis are formed by ionization of the sputtered neutrals, (c) When the plasma is used as an ionizer, plasma ions can also be used to sputter the sample surface at low energies.
Nearly all these techniques involve interrogation of the surface with a particle probe. The function of the probe is to excite surface atoms into states giving rise to emission of one or more of a variety of secondary particles such as electrons, photons, positive and secondary ions, and neutrals. Because the primary particles used in the probing beam can also be electrons or photons, or ions or neutrals, many separate techniques are possible, each based on a different primary-secondary particle combination. Most of these possibilities have now been established, but in fact not all the resulting techniques are of general application, some because of the restricted or specialized nature of the information obtained and others because of difficult experimental requirements. In this publication, therefore, most space is devoted to those surface analytical techniques that are widely applied and readily available commercially, whereas much briefer descriptions are given of the many others the use of which is less common but which - in appropriate circumstances, particularly in basic research - can provide vital information. [Pg.2]

The limitations of SIMS - some inherent in secondary ion formation, some because of the physics of ion beams, and some because of the nature of sputtering - have been mentioned in Sect. 3.1. Sputtering produces predominantly neutral atoms for most of the elements in the periodic table the typical secondary ion yield is between 10 and 10 . This leads to a serious sensitivity limitation when extremely small volumes must be probed, or when high lateral and depth resolution analyses are needed. Another problem arises because the secondary ion yield can vary by many orders of magnitude as a function of surface contamination and matrix composition this hampers quantification. Quantification can also be hampered by interferences from molecules, molecular fragments, and isotopes of other elements with the same mass as the analyte. Very high mass-resolution can reject such interferences but only at the expense of detection sensitivity. [Pg.122]

Ion beam spectrochemical analysis (IBSCA) is a sputtering-based surface analytical technique similar to SIMS/SNMS. In IBSCA the radiation emitted by excited sputtered secondary neutrals or ions is detected. IBSCA was developed parallel to SIMS in the nineteen-sixties and early nineteen-seventies [4.246, 4.247]. It is also known... [Pg.240]


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See also in sourсe #XX -- [ Pg.328 , Pg.330 , Pg.331 ]




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Ion neutralization

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