Generalization of the nonlocal resonance model for low-energy electron collisions with hydrogen halides: the variable threshold exponent

Article

Generalization of the nonlocal resonance model for low-energy electron collisions with hydrogen halides: the variable threshold exponent

Horáček, J.; Čížek, M.; Domcke, W.

Theor. Chem. Acc. 100(0), 31-35 (1998)

Abstract

The nonlocal resonance model developed previously for the description of low-energy electron collisions with hydrogen halides is generalized to include the dependence of the dipole-modified threshold exponent on the internuclear distance. An efficient computational scheme has been developed to deal with the resulting nonseparability of the nonlocal complex potential for the nuclear motion within the Schwinger-Lanczos approach. The results reveal that the R-dependence of the threshold exponent has a significant effect on the threshold peaks in the vibrational excitation cross sections of HCl. The shape and intensity of the calculated threshold peak in the 01 vibrational excitation channel, in particular, are in much better agreement with experimental data than previous results. For the electron-HBr and electron-HI collision systems the effects of the R-dependence of the threshold exponent are not significant.

Institute authors

BibTeX

@article{UTF218,
  author        = {Horáček, J. and Čížek, M. and Domcke, W.},
  title         = {{Generalization of the nonlocal resonance model for low-energy electron collisions with hydrogen halides: the variable threshold exponent}},
  journal       = {Theor. Chem. Acc.},
  volume        = {100},
  number        = {0},
  pages         = {31-35},
  year          = {1998},
  doi           = {10.1007/s002140050363},
  url           = {http://www.springerlink.com/content/b2980fyue4x0pnbe/},
}