Vibrational excitation cross section and V → T rate constants in molecular hydrogen

1979 ◽  
Vol 38 (1) ◽  
pp. 97-108 ◽  
Author(s):  
F.A. Gianturco ◽  
U.T. Lamanna
1988 ◽  
Vol 41 (4) ◽  
pp. 573 ◽  
Author(s):  
JP England ◽  
MT Elford ◽  
RW Crompton

Measurements of electron drift velocities have been made in 1�160% and 2�892% hydrogen-neon mixtures at 294 K and values of EI N from 0�12 to 1�7 Td. The measurements are highly sensitive to the region of the threshold of the v = 0 → 1 vibrational excitation cross section for hydrogen and have enabled more definitive tests of proposed cross sections to be made than was possible using drift velocity data for H2−He and H2−Ar mixtures. The theoretical v = 0 → 1 vibrational excitation cross section of Morrison et al. (1987) is shown to be incompatible with the present measurements. A new set of hydrogen cross sections has been derived from the available electron swarm measurements in pure hydrogen and hydrogen mixtures.


Atoms ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 64
Author(s):  
Luis A. Poveda ◽  
Marcio T. do N. Varella ◽  
José R. Mohallem

The vibrational excitation cross-section of a diatomic molecule by positron impact is obtained using wave-packet propagation techniques. The dynamics study was carried on a two-dimensional potential energy surface, which couples a hydrogenlike harmonic oscillator to a positron via a spherically symmetric correlation polarization potential. The cross-section for the excitation of the first vibrational mode is in good agreement with previous reports. Our model suggests that a positron couples to the target vibration by responding instantly to an interaction potential, which depends on the target vibrational coordinate.


The scattering formalism of Arthurs & Dalgarno (1960) is generalized to take account of exchange (but not polarization) in the scattering of slow electrons by molecular hydrogen. The use of a single-centre molecular wavefunction is discussed, and representative calcula­tions of the j = 0→ j = 2 rotational excitation cross-section are carried out in the distorted wave approximation. The inclusion of exchange results in a significant increase (rising from 12% at 0.1 eV to over 70% at 0.5 eV) in the dominant ( p -wave) contribution to the cross-section. It is concluded that exchange effects cannot be ignored in the theoretical discussion of electron energy loss by rotational excitation in swarm experiments.


Author(s):  
M. Isaacson

In an earlier paper1 it was found that to a good approximation, the efficiency of collection of electrons that had lost energy due to an inner shell excitation could be written as where σE was the total excitation cross-section and σE(θ, Δ) was the integral cross-section for scattering within an angle θ and with an energy loss up to an energy Δ from the excitation edge, EE. We then obtained: where , with P being the momentum of the incident electron of velocity v. The parameter r was due to the assumption that d2σ/dEdΩ∞E−r for energy loss E. In reference 1 it was assumed that r was a constant.


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