Calculation of Electron-Hydrogen, Deuterium and Oxygen Molecules.

Abstract

Calculations are made on the vibrational transition cross sections of e-H2, D2 scatterings in the energy range of 0 appox. 10eV. Both hybrid theory and the simultaneous vibrational and rotational adiabatic-nuclei approximation are employed in the calculation. It turns out that the latter approximation scheme yields better results than the hybrid theory approach when compared with experimental measurements on 0 yields v vibrational excitation. The resonance peaks of the elastic scattering and vibrational excitation cross section obtained from the vibrational and rotational adiabatic-nuclei approximation are quite broad between 2 approx. 3 eV, which are in good agreements with experimental data. This seems to indicate that the periods of the vibrational and rotational motions are comparable to each other and longer than the lifetime of the compound molecule. In general, the rate of the vibrational transition decreases as the quantum number change increases. The e-02 vibrational transition cross sections have also been explored with a semi-quantitative analysis.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 1981
Accession Number
ADA110689

Entities

People

  • B. H. Choi
  • R. T. Poe

Organizations

  • University of California, Riverside

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Agreements
  • Differential Cross Sections
  • Differential Equations
  • Elastic Scattering
  • Energy Levels
  • Equations
  • Excitation
  • Experimental Data
  • Inelastic Scattering
  • Ionization Potentials
  • Measurement
  • Molecules
  • Quantum Numbers
  • Resonance
  • Scattering
  • Transitions
  • United States

Fields of Study

  • Physics

Readers

  • Materials Science and Engineering.
  • Quantum Dot Semiconductor Device Photonics and Graphene Optoelectronic Materials and THz Physics.
  • Structural Dynamics.

Technology Areas

  • Microelectronics
  • Quantum Computing