scholarly journals Auger neutralization and ionization processes for charge exchange between slow noble gas atoms and solid surfaces

2014 ◽  
Vol 89 (1) ◽  
pp. 80-125 ◽  
Author(s):  
R. Carmina Monreal
1997 ◽  
Vol 11 (06) ◽  
pp. 685-706 ◽  
Author(s):  
Ryutaro Souda

Various aspects of charge exchange between low-energy ions (10 eV–2 keV) and solid surfaces are discussed with particular emphasis placed on the effects of valence orbital hybridization on the electronic transition probabilities, and uniqueness of surface scattering relative to diatomic gas-phase collision is highlighted. Two classes of projectiles are explored, i.e. inert noble-gas ions and a reactive hydrogen ion. One or two core vacancies are created in noble-gas projectiles during collisions with specific target atoms, leading to (re)ionization and autoionization. In contrast to gas-phase collision, it is found that one-electron excitation predominates over simultaneous two-electron excitation. This result is basically ascribed to the band effect of energy-level crossing. Neutralization of the slow hydrogen ion at a surface is rather unique compared to the noble-gas ions and its probability is sensitively dependent upon ionicity of target atoms or the nature of the valence band. This is because a valence electron is captured via a new class of resonance neutralization which is mediated by a short-lived chemisorption state of hydrogen on a surface.


Atoms ◽  
2019 ◽  
Vol 7 (4) ◽  
pp. 96
Author(s):  
Steven Bromley ◽  
Corey Ahl ◽  
Chad Sosolik ◽  
Joan Marler

Charge transfer of an electron from a neutral atom to an ion is a fundamental interaction that plays a dominant role in the energy balance of atmospheric and astrophysical plasmas. The present investigation measured the charge exchange cross sections of noble gas ions (He + , Ne + , Ar + , Kr + ) with N 2 in the intermediate energy range 0.2–5.0 keV. The systems were chosen because there remains a lack of consensus amongst previous measurements and regions where there were no previous measurements. A description of the mechanical design for an electrically floated gas cell is described herein.


1987 ◽  
Vol 186 (3) ◽  
pp. 278
Author(s):  
Shinji Tsuneyuki ◽  
Nobuyuki Shima ◽  
Masaru Tsukada

2021 ◽  
pp. 101397
Author(s):  
Anton V. Nazarov ◽  
Vladimir S. Chernysh ◽  
Andrey D. Zavilgelsky ◽  
Andrey A. Shemukhin ◽  
Alvaro Lopez-Cazalilla ◽  
...  

2000 ◽  
Vol 14 (11) ◽  
pp. 1139-1177 ◽  
Author(s):  
RYUTARO SOUDA

In this article, the mechanism of electronic transitions during scattering and stimulated desorption of ions from solid surfaces is discussed. Reactive ions such as H + and O + experience transient chemisorption during scattering from solid surfaces. These ions are neutralized almost completely on metal and semiconductor surfaces due to the band effect on resonance neutralization. The neutralization probability of H + is suppressed considerably on highly ionic compound surfaces and is dependent on the target species due to the formation of the bound state (on cations) or the surface molecule (on anions). Because of this, the H - ion is formed preferentially on the cationic site rather than on the anionic site. The noble-gas ions are neutralized via the Auger process so that the neutralization probability is basically independent of the band effect. The stimulated desorption of secondary O + and F + ions does not exhibit the band effect. This is because the desorption is initiated by the core hole state, which is followed by ionization via the intra-atomic Auger decay after breakage of the chemisorptive bond. The stimulated desorption of H + might occur from the valence holes but is more likely to be caused by the core-excited OH species via the interatomic Auger decay. The core hole is created not only by the electron and photon irradiation but also by the energetic ion bombardment due to the nonadiabatic transition of the primary ion/s core hole. Also presented are some applications of ion scattering and ion stimulated desorption for the analysis of the diffusion/segregation dynamics of oxygen and hydrogen on solid surfaces.


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