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Rotational excitation elastic case

At low projectile ion energies, in the region close to the elastic scattered peak one sees pure rotational excitation. At present it is only in the case of the Li+ — H2 where clean cut resolution has been realized. [Pg.231]

The energy analysis of these inelastically scattered electrons is carried out by a cylindrical sector identical to the monochromator. The electrons are finally detected by a channeltron electron multiplier and the signal is amplified, counted and recorded outside of the vacuum chamber. A typical specularly reflected beam has an intensity of 10 to 10 electrons per second in the elastic channel and a full width at half maximum between 7 and 10 meV (60-80 cm l 1 meV = 8.065 cm-- -). Scattering into inelastic channels is between 10 and 1000 electrons per second. In our case the spectrometer is rotatable so that possible angular effects can also be studied. This becomes important for the study of vibrational excitation by short range "impact" scattering (8, 9, 10). [Pg.164]

As in Chapter 9 we discuss first the elastic limit (no exit channel excitation) in Section 10.1 and subsequently the more interesting inelastic case in Section 10.2. In Section 10.3 we consider the decay of long-lived resonance states and the impact of exit channel dynamics on the product distributions. A simple approximation, the so-called impulsive model, which is frequently employed to analyze experimental distributions in the absence of a PES, is discussed critically in Section 10.4. The chapter ends with a more qualitative assessment of thermal broadening of rotational state distributions in Section 10.5... [Pg.225]

The interaction of an electron with a molecule is described as a collision or impact, although the electron is so small that there is no collision in the usual sense of the word. The collision process may be termed elastic (the electron is merely deflected), inelastic (energy is transferred from the electron to the molecule), and superelastic (energy is transferred from the molecule to the electron). Electron-impact ionization is an example of an inelastic collision. The energy imparted to a molecule during an inelastic collision can lead to rotational, electronic, and vibrational excitation with or separate from ionization. Further, multiple-electron excitation can occur followed by autoionization, and the latter process has been shown to lead to a substantial fraction of total ionized species in many cases (S. Meyerson et al., 1963). Thus, an electron of energy 20 eV may lead to any of the above excitations of a molecule. The gas pressures used in a mass spectrometer and the density of electrons in the electron-beam are such that multiple electron-molecule interactions leading to ionization are improbable. [Pg.157]

Similar problems are encountered in a description of elastic or rotationally inelastic collisions of the electrons with molecules that have permanent dipole moment. However in this case K is never zero because k0 and ki have different norms due to an energy transfer to the vibrational excitation. [Pg.133]

It must be pointed out that considering only elastic collisions in deriving an electron temperature of several e.v. is unrealistic for molecular gases of interest to the chemist. Inelastic collisions leading to excitation of rotational, vibrational, and low-lying electronic states in molecules can enter the picture in major ways. Understanding in detail the way in which an electron energy distribution is established in most real cases of... [Pg.14]


See other pages where Rotational excitation elastic case is mentioned: [Pg.11]    [Pg.76]    [Pg.78]    [Pg.236]    [Pg.229]    [Pg.93]    [Pg.430]    [Pg.226]    [Pg.58]    [Pg.671]    [Pg.84]    [Pg.86]    [Pg.2404]    [Pg.494]    [Pg.163]    [Pg.154]    [Pg.1450]    [Pg.194]    [Pg.173]    [Pg.272]    [Pg.284]    [Pg.4]    [Pg.40]    [Pg.496]    [Pg.222]    [Pg.233]    [Pg.75]    [Pg.35]    [Pg.616]    [Pg.116]    [Pg.117]    [Pg.13]    [Pg.49]    [Pg.438]    [Pg.110]    [Pg.65]    [Pg.193]    [Pg.110]    [Pg.124]   
See also in sourсe #XX -- [ Pg.225 , Pg.226 , Pg.227 , Pg.228 , Pg.229 , Pg.230 , Pg.231 , Pg.232 ]




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