skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Channel-interaction effects on the chlorine 3P-subshell photoionization cross sections and photoelectron angular distributions

Thesis/Dissertation ·
OSTI ID:5421413

In this investigation the photoionization cross sections and photoelectron angular distributions (asymmetry parameters) were obtained for 3p-subshell ionization of the chlorine ground state using the multiconfiguration Hartree-Fock (MCHF) technique. By employing a multiconfiguration description of the ground state and residual ionic core, a substantial amount of electron correlation could be taken into account. Both the independent-channel and channel-interaction final states were used in evaluating the length and velocity forms of the dipole transition amplitudes. This accommodation of channel interaction was performed via the reaction matrix (K-matrix) method which diagonalized the total N-electron atomic Hamiltonian in the manifold of single-channel basis states of the model Hamiltonian (Hartree-Fock). For 3p-subshell ionization the residual ion can produce three LS-coupled multiplets: Cl/sup +/(3p/sup 4/,/sup 3/P), CL/sup +/(3p/sup 4/,/sup 1/D), and Cl/sup +/(3p/sup 4/,/sup 1/S) in order of ascending ionization thresholds. From the conditions imposed by the electric dipole transition operator, the 3p/sup 5/,/sup 2/P ground state can undergo a photoionization transition to either a /sup 2/D, /sup 2/P, or /sup 2/S final state. These ionic and final state multiplets, taken together with the dipole operator constraint on the possible photoelectron orbital angular momentum quantum numbers, yield a large number of channels resulting from the n = 3 shell ionization which interact through the Coulomb operator. In all cases the photoabsorption transition probabilities exhibit a significant amount of channel interaction. For the partial cross sections of the /sup 2/D and /sup 2/P channels the K-matrix values are all depressed at threshold with respect to the Hartree-Fock values.

Research Organization:
Johns Hopkins Univ., Baltimore, MD (USA)
OSTI ID:
5421413
Resource Relation:
Other Information: Thesis (Ph. D.)
Country of Publication:
United States
Language:
English