Excitation of hydrogen molecules by electron impact. II - Excitation to D/3ppi 1piu/ state
Excitation of hydrogen molecules by electron impact
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Excitation of hydrogen molecules by electron impact
Vainshteins approximation method applied to electron impact excitation and ionization of atoms
First-order many-body theory has been used to calculate collision-frame magnetic-sublevel differential cross sections for electron-impact excitation of the n 1P (n = 2,3,4,5,6) levels of helium for electrons with incident energy in the 25-500-eV range. By combining results from electron-impact differential-cross-section measurements and electron-photon coincidence measurements, experimental magnetic-sublevel cross sections have also been derived for the excitation of the 2 1P and 3 1P levels. The theory predicts a pronounced minimum for the M = 0 magnetic-sublevel differential cross section for incident electron energies around 30 eV. The theoretical results are compared to the experimental data and some other theoretical results.
The polarization of Lyman-a radiation, produced by electron-impact excitation of atomic hydrogen, has been measured over the extended energy range from near threshold to 1800 eV. Measurements were obtained in a crossed-beam experiment using a silica-reflection linear polarization analyzer in tandem with a vacuum-ultraviolet monochromator to isolate the emitted line radiation. Comparison with various theoretical calculations shows that the present experimental results are in good agreement with theory over the entire range of electron-impact energies and, in particular, are in excellent agreement with theoretical convergent-close-coupling (CCC) calculations performed in the present work. Our polarization data are significantly different from the previous experimental measurements of Ott, Kauppila, and Fite.
The electron impact induced fluorescence spectrum of N2 is measured in the 102-134 nm range at a 0.05 nm spectral resolution. The spectral measurements provide the emission cross sections of the transitions of the b 1Pi(u)-X 1Sigma(+)g Birge-Hopfield I-band system. The structure and vibrational population distribution of this system are strongly affected by a configuration interaction of the valence b 1Pi(u) and Rydberg c 1Pi(u) and o 1Pi(u) states. The excitation function (0-400 eV) for the b-X (1,2) transition is measured and a modified Born approximation analytic model is applied to calculate the oscillator strength for the b 1Pi(u)-X band system. With the exception of the v-prime = 1 level, vibrational levels of the b 1Pi(u) state predissociate with a branching ratio of between 0.95 and 1.00. Predissociation of the b 1Pi(u) state contributes approximately six percent of the total dissociation cross section of N2 by electron impact at 100 eV.
Dissociation cross section of hydrogen molecule exchange excited by electron impact from ground to triplet state, using one-center wave functions
Dissociative ionization cross sections for the production of singly charged energetic ions by electron impact on N2 and CO2 have been measured. The ions were divided into two groups: one with energies less than 1 eV and the other with energies greater than 1 eV. The ions detected were N+ from N2 and C+, O+, and CO+ from CO2. The electron impact energy range, and cross section data on ions is given.
Cross section calculations for electron impact ionization and excitation of hydrogen molecules
The threshold behavior of the ultraviolet photon excitation function for electron impact on carbon monoxide was studied for the pseudo-resonance signal reported elsewhere. Time of flight spectrometer techniques were not able to confirm the resonant feature in excited CO states under electron impact.
Electron impact excitation rates of bound electronic states of hydrogen, helium and alkali atoms
Electron impact excitation of the electronic states of SO2 was investigated. Differential, integral, and inelastic momentum transfer cross sections were obtained by normalizing the relative measurements to the elastic cross sections. The cross sections are given for seven spectral ranges of the energy-loss spectra extending from the lowest electronic state to near the first ionization limit. Most of the regions represent the overlap of several electronic transitions. No measurements for these cross sections have been reported previously.
Utilizing a crossed electron-beam-molecular-beam scattering technique, differential electron impact cross sections (DCS) for the excitation of the nu prime = 2 vibrational band of the B (1-Sigma-u +) state of H2 have been measured and are presented for the first time. These measurements were made at electron impact energies of 15, 20, 30, 40, 50 and 60 eV. At each energy, DCS between scattering angles of 10 and 135 deg were determined. They were then extrapolated to 0 and 180 deg scattering angles to obtain the integral cross sections. These integral cross sections and the Frank-Condon factor for the nu prime = 2 band were used to calculate the total cross sections for the excitation of the B (1-Sigma-u +).
Spectrograms from 2200 to 20 A of optical emissions produced by a simple lamp using fast (3-10-keV) electron impact on tungsten and tantalum targets are presented. The lamp dissipated up to 5 kW/sq cm on the target surface, simultaneously cleaning the surface and generating bremsstrahlung in the soft X-ray region with 3-keV electron impact and longer wavelength transition radiation at the higher energy. In both the bremsstrahlung and transition radiation modes, the lamp emissions were of sufficient strength and reproducibility to qualify the two mechanisms as potential processes for use in a secondary standard light source. Calculated spectral distributions of transition radiation for normally incident electrons on tungsten, tantalum, and aluminum targets, with a viewing direction 45 deg from the normal, are also shown.
Excitation of hydrogen molecule from ground state to B and C electronic states by electron impact, using one-center wave functions of Huzinaga together with Born approximation
The electron impact induced fluorescence spectrum of NO at 200 eV was measured for the vacuum UV range (40-170 nm) and the mid-UV range (170-270 nm). The absolute electron impact excitation cross sections are studied by calibrating to the Ly-alpha cross section of H2. The cross section of the N I 120-nm transition by dissociative excitation is found to be 1.73 + or - 0.38 X 10 to the -18th sq cm. Measurements of the cross sections of other features in the vacuum UV and mid-UV are presented. A band model of the far-UV (120-170 nm) is developed. Also, it is found that great care must be taken if NO is the target for relative calibration in the Mid-UV using the molecular branching ratio techniques.
Ionization of hydrogen and hydrogenic positive ions by electron impact
Electron impact broadening in isolated lines from ions explained by quantum mechanics
Cyanohydrins and O-acylcyanohydrins fragmentation upon electron impact correlated with mass spectra molecular structure