Spectroscopic measurement of H(1S) and H sub 2 (v double prime ,J double prime ) in an H sup minus ion source plasma
Abstract
Low pressure H{sub 2} discharges have been used for some time as sources of H{sup {minus}} ions. These discharges contain many different species of particles which interact with each other and with the walls of the discharge chamber. Models exist that predict the populations of the various species for given macroscopic discharge parameters. However, many of the cross sections and wall catalyzation coefficients are unknown or somewhat uncertain. Therefore, it is of interest to measure the populations of as many of these species as possible, in order to determine the validity of the models. These models predict that H{sup {minus}} is created predominantly by the two-step process of vibrational excitation of hydrogen molecules followed by dissociative attachment of slow electrons to these vibrationally-excited hydrogen molecules. Many different collisional processes must be included in the models to explain the dependence of the various populations upon macroscopic parameters. This work presents results of spectroscopic measurements of the density and translational temperature of hydrogen atoms and of specific rotationally- and vibrationally-excited states of electronic ground-state H{sub 2}, in a discharge optimized for H{sup {minus}} production, as well as conventional measurements of the various charged species within the plasma. The spectroscopic measurements are performedmore »
- Authors:
- Publication Date:
- Research Org.:
- Lawrence Berkeley Lab., CA (USA)
- Sponsoring Org.:
- USDOE; USDOE, Washington, DC (USA)
- OSTI Identifier:
- 5836451
- Report Number(s):
- LBL-30541
ON: DE91011879
- DOE Contract Number:
- AC03-76SF00098
- Resource Type:
- Technical Report
- Resource Relation:
- Other Information: Thesis (Ph.D.)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 74 ATOMIC AND MOLECULAR PHYSICS; HYDROGEN; ABSORPTION SPECTROSCOPY; DISSOCIATION; EXPERIMENTAL DATA; HYDROGEN IONS 1 MINUS; HYSTERESIS; ION SOURCES; MOLECULES; ULTRAVIOLET SPECTRA; VIBRATIONAL STATES; ANIONS; CHARGED PARTICLES; DATA; ELEMENTS; ENERGY LEVELS; EXCITED STATES; HYDROGEN IONS; INFORMATION; IONS; NONMETALS; NUMERICAL DATA; SPECTRA; SPECTROSCOPY; 640302* - Atomic, Molecular & Chemical Physics- Atomic & Molecular Properties & Theory
Citation Formats
Stutzin, G.C. Spectroscopic measurement of H(1S) and H sub 2 (v double prime ,J double prime ) in an H sup minus ion source plasma. United States: N. p., 1990.
Web. doi:10.2172/5836451.
Stutzin, G.C. Spectroscopic measurement of H(1S) and H sub 2 (v double prime ,J double prime ) in an H sup minus ion source plasma. United States. doi:10.2172/5836451.
Stutzin, G.C. Wed .
"Spectroscopic measurement of H(1S) and H sub 2 (v double prime ,J double prime ) in an H sup minus ion source plasma". United States.
doi:10.2172/5836451. https://www.osti.gov/servlets/purl/5836451.
@article{osti_5836451,
title = {Spectroscopic measurement of H(1S) and H sub 2 (v double prime ,J double prime ) in an H sup minus ion source plasma},
author = {Stutzin, G.C.},
abstractNote = {Low pressure H{sub 2} discharges have been used for some time as sources of H{sup {minus}} ions. These discharges contain many different species of particles which interact with each other and with the walls of the discharge chamber. Models exist that predict the populations of the various species for given macroscopic discharge parameters. However, many of the cross sections and wall catalyzation coefficients are unknown or somewhat uncertain. Therefore, it is of interest to measure the populations of as many of these species as possible, in order to determine the validity of the models. These models predict that H{sup {minus}} is created predominantly by the two-step process of vibrational excitation of hydrogen molecules followed by dissociative attachment of slow electrons to these vibrationally-excited hydrogen molecules. Many different collisional processes must be included in the models to explain the dependence of the various populations upon macroscopic parameters. This work presents results of spectroscopic measurements of the density and translational temperature of hydrogen atoms and of specific rotationally- and vibrationally-excited states of electronic ground-state H{sub 2}, in a discharge optimized for H{sup {minus}} production, as well as conventional measurements of the various charged species within the plasma. The spectroscopic measurements are performed directly by narrowband, single-photon absorption in the vacuum ultraviolet.},
doi = {10.2172/5836451},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Wed Aug 01 00:00:00 EDT 1990},
month = {Wed Aug 01 00:00:00 EDT 1990}
}
-
To check the adequacy and develop the theoretical models used in a semiempirical determination of the probabilities of rovibronic transitions, it is proposed to carry out a comparative optimization analysis of experimental data on the relative probabilities and radiative lifetimes of two or more isotopes. A program package has been developed for a semiempirical determination of an entire matrix set of probabilities of vibronic radiative transitions that makes it possible to conduct a study of the adequacy of a theoretical model (adiabatic approximation and type of approximation of the electron moment as a function of internuclear distance {ital M}{sup ({italmore »
-
Generation of H sup minus , H sub 2 (v double prime ), and H atoms by H sub 2 sup + and H sub 3 sup + ions incident upon barium surfaces
The generation of vibrationally excited molecules by electron excitation collisions and the subsequent generation of negative ions by dissociative attachment to these molecules has become a standard model for volume source operation. These processes have been supplemented recently by the demonstration of atom-surface recombination to form vibrationally excited molecules, and enhanced negative ion formation by protons incident upon barium electrodes. In this paper we consider the additional processes of molecular vibrational excitation generated by recombination of molecular ions on the electrode surfaces, and negative ion formation by vibrationally excited molecules rebounding from low work-function electrodes. 10 refs., 4 figs. -
Generation of H sup minus , H sub 2 ( v double prime ), and H atoms by H sub 2 sup + and H sub 3 sup + ions incident upon barium surfaces
Molecular vibrational excitation generated by recombination of molecular ions on barium electrode surfaces is presented. Negative hydrogen ion formation by vibrationally excited molecules rebounding from the surface is also calculated (AIP). -
Recombination and dissociation of H sub 2 sup + and H sub 3 sup + ions on surfaces to form H sub 2 ( v double prime ): Negative-ion formation on low-work-function surfaces
The recombination and dissociation of H{sup +}{sub 2} and H{sup +}{sub 3} ions incident upon metal surfaces leads to H, H{sub 2}({ital v}{double prime}), and H{sup {minus}} products rebounding from the surface. A four-step model for H{sup +}{sub 2} -ion recombination generates H{sub 2}({ital v}{double prime}) via resonant electron capture through the {ital b} {sup 3}{Sigma}{sup +}{sub {ital u}} and {ital X} {sup 1}{Sigma}{sup +}{sub {ital g}} states. A molecular trajectory analysis provides final-state H{sub 2}({ital v}{double prime}) distributions for incident energies of 1, 4, 10, and 20 eV. The calculated H{sub 2}:H{sup +}{sub 2} yields compare favorably with themore » -
Resonance-enhanced Raman scattering in the near-infrared region. Preliminary studies of charge transfer in the symmetric dimers (2,2 prime -bpy) sub 2 ClRu-4,4 prime -bpy-RuCl(2,2 prime -bpy) sub 2 sup 4+/3+/2+ , (H sub 3 N) sub 5 Ru-4,4 prime -bpy-Ru(NH sub 3 ) sub 5 sup 6+/5+/4+ , and (NC) sub 5 Fe-4,4 prime -bpy-Fe(CN) sub 5 sup 4 minus /5 minus /6 minus
Three symmetrical mixed-valence dimers (and their oxidized and reduced congeners) have been examined in solution by Raman spectroscopy with use of near-infrared excitation (1,064 nm, Nd:YAG source). The specific systems were (2,2{prime}-bpy){sub 2}ClRu-4,4{prime}-bpy-RuCl(2,2{prime}bpy){sub 2}{sup 4+/3+/2+}, (H{sub 3}N){sub 5}Ru-4,4{prime}-bpy-Ru(NH{sub 3}){sub 5}{sup 6+/5+/4+}, and (NC){sub 5}Fe-4,4{prime}-bpy-Fe(CN){sub 5}{sup 4{minus}/5{minus}/6{minus}}. For two of the mixed-valence ions, resonance-enhanced Raman scattering is found. (For the third, the decacyano ion, extensive thermal degradation occurs.) Studies of the corresponding fully reduced ions show, however, that the enhancement effects are due not to intervalence excitation but to weakly preresonant metal-to-ligand excitation.