Electron impact cross sections for atmospheric species. II.
Electron impact excitation and ionization cross sections data of molecular nitrogen synthesized using modified Born approximation
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Electron impact excitation and ionization cross sections data of molecular nitrogen synthesized using modified Born approximation
Spectral line shapes broadened by electron impacts, taking into account contribution of radiation produced by perturbing electrons
The optical excitation function of prompt Lyman-Alpha radiation, produced by electron impact on atomic hydrogen, has been measured over the extended energy range from threshold to 1.8 keV. Measurements were obtained in a crossed-beams experiment using both magnetically confined and electrostatically focused electrons in collision with atomic hydrogen produced by an intense discharge source. A vacuum-ultraviolet mono- chromator system was used to measure the emitted Lyman-Alpha radiation. The absolute H(1s-2p) electron impact excitation cross section was obtained from the experimental optical excitation function by normalizing to the accepted optical oscillator strength, with corrections for polarization and cascade. Statistical and known systematic uncertainties in our data range from +/- 4% near threshold to +/- 2% at 1.8 keV. Multistate coupling affecting the shape of the excitation function up to 1 keV impact energy is apparent in both the present experimental data and present theoretical results obtained with convergent close- coupling (CCC) theory. This shape function effect leads to an uncertainty in absolute cross sections at the 10% level in the analysis of the experimental data. The derived optimized absolute cross sections are within 7% of the CCC calculations over the 14 eV-1.8 keV range. The present CCC calculations converge on the Bethe- Fano profile for H(1s-2p) excitation at high energy. For this reason agreement with the CCC values to within 3% is achieved in a nonoptimal normalization of the experimental data to the Bethe-Fano profile. The fundamental H(1s-2p) electron impact cross section is thereby determined to an unprecedented accuracy over the 14 eV - 1.8 keV energy range.
Metastable fragments produced by electron impact excitation of CH4 have been investigated for incident electron energies from threshold to 300 eV. Only metastable hydrogen and carbon atoms were observed. Onset energies for the production of metastable hydrogen atoms were observed at electron impact energies of 22.0 + or - .5 eV, 25.5 + or - .6 eV, 36.7 + or - .6 eV and 66 + or - 3 eV, and at 26.6 + or - .6 eV for the production of metastable carbon atoms. Most of the fragments appear to have been formed in high-lying Rydberg states. The total metastable hydrogen cross section reaches a maximum value of approximately 1 X 10 to the minus 18th power sq cm at 100 eV. At the same energy, the metastable carbon cross section is 2 x 10 to the minus 19th power sq cm.
The kinetic energy spectra of protons resulting from the dissociative ionization of H2 by electron impact have been measured for electron impact energies from threshold (approximately 17 eV) to 160 eV at 90 deg and 30 deg detection angles, using a crossed-beam experimental arrangement. To check reliability, two separate proton energy analysis methods have been employed, i.e., a time-of-flight proton energy analysis and an electrostatic hemispherical energy analyzer. The present results are compared with previous measurements.
The emission spectra resulting from electron impact excitation on molecular nitrogen and oxygen in the 500-1200 A spectral region are investigated. Electron energies are from 0 to 300 eV. Numerous bands of N2 are found between 800 and 1000 A. Excitation functions are measured for the NII 916 A, the OI 879 A, and the OII 834 multiplets, and nitrogen band emission. Cross sections were measured at 200 eV for several of the band emissions plus the NI 1135 A, NI 1164 A, NI 1177 A, NII 776 A, NII 1084 A, OI 1152 A, OI 1041 A, OI 999 A, OI 989 A, OI 879 A, OII 834 A, OII 616 A, OII 555 A, OII 539 A, and OII 718 A multiplets.
A framework is established for deriving true projection operators in electron resonance calculations involving many electron targets (ions and atoms). The analytical approach is based on Feshbach's formalism the true and quasi-projection operators (QPO) one-electron systems. In the case of QPOs, the formalism is explicitly generalized to treat autoionization states lying in the region of inelastic scattering. In order to illustrate the analytical method, a recent calculation of the lowest 2P0 resonance in He is described. The application of the modified Feshbach formalism to calculation of nonresonant phase shifts in many electron systems is also discussed.
The cross sections for the excitation of Ly-beta and H-alpha when methane is dissociated by electron impact have values of 17.1 by 10 to the -19th power sq cm and 26.0 by 10 to the -19th power sq cm, respectively, at an electron impact energy of 100 eV. These results are in disagreement with the implications of recent polarization measurements of H-alpha radiation that suggest negligible H(3p) excitation in the dissociation of CH4 by electron impact.
Published electron impact cross section data on halogens Cl2, F2, and halogen containing compounds such as Cx Fy, HCl, Cx Cly Fz are reviewed and critically evaluated based on the information provided by various researchers. The present work reports data on electron impact excitation, ionization, dissociation, electron attachment, electron detachment, and photo detachment. Elastic scattering cross sections and data on bulk properties such as diffusion coefficients in various background gases are also evaluated. Since some of the cross sectional data is derived from indirect measurements such as drift velocity, care has been taken to reconcile the differences among the reported data with due attention to the measurement technique. In conclusion, the processes with no or very limited amount of data and questionable set of data are identified and recommendation for further research direction is made.
Inelastic electron impact cross sections for ionization and vibrational excitation of atmospheric molecular oxygen
Electron impact ionization of hydrogen/2s/ and hydrogen/2p/
Electron impact ionization cross sections for second quantum level of atomic H, using Born exchange approximation and Vainshtein approximation
Electron impact cross sections for diatomic molecule ionization and excitation from modified Gryzinski theory, discussing results from molecular models
Glauber and Born approximations of electron impact excitations of hydrogen atomic energy levels
Electron impact excited carbon monoxide and dioxide 1260-5000 A spectral emission, discussing cross sections of Cameron and fourth positive bands
Absolute differential cross sections of electrons vibrationally elastically scattered from water vapor have been measured at room temperature by electron impact. A modulated crossed-beam method was used. The energy and angular range covered were from 2.2 to 20 eV and from 15 to 150 deg, respectively. Strong backward scattering has been observed as predicted by theory. The measured integrated and momentum-transfer cross sections are generally larger than others in the literature by 50 percent.
First measurements of electron impact excitation on the O2 a delta-one sub g metastable state to a higher bound state, pi-one sub u, is reported. The data were taken at an incident electron energy of 500 eV and scattering angles of 0 deg to 15 deg. A superelastic electron scattering experiment was performed on the pure oxygen target gas in order to establish the composition of the discharged oxygen and to confirm the existence of delta-one sub g molecules in the interaction region. The electron-impact energy loss spectrum obtained is shown. The electronic assignment of the upper state which produces the vibrational structure was determined to be pi-one sub u by examining the potential energy curves of O2 and applying the electric dipole selection rules. The relative line intensities were obtained and used to determine the Morse potential for the pi-one sub u state.
The dissociation of N2 by electron impact and by absorption of EUV photons was studied experimentally. It was shown that most of the N2 molecules excited to singlet states in the 12.5-14.86 eV range are depopulated by predissociation and not by the emission of EUV photons and that this is the principal mechanism by which N2 is dissociated by solar EUV absorption and by electron impact. The experiments provide a physical explanation for the near absence of N2 band radiation in airglow and auroral EUV spectra, and rule out the excitation of EUV radiation as a major factor in the overall energy economy of an auroral substorm.