No abstract

Anion-yield spectroscopy using x rays is shown to be a selective probe of molecular core-level processes, providing unique experimental verification of shape resonances. For CO, partial anion and cation yields are presented for photon energies near the C K edge. The O- yield exhibits features above threshold related only to doubly excited states, in contrast to cation yields which also exhibit pronounced structure due to the well-known sigma* shape resonance. Because the shape resonance is completely suppressed for O-, anion spectroscopy thus constitutes a highly selective probe, yielding information unobtainable with absorption or electron spectroscopy.

Partial-anion and-cation yields from H 2 O are presented for photon energies near the oxygen K edge. The O Ϫ yield exhibits a feature above threshold attributed to doubly excited states, in contrast to the H Ϫ and cation yields, which are nearly featureless above threshold. Additionally, the lack of the OH Ϫ fragment indicates radiative decay and provides a negligible amount of anion formation.

Absolute cross-section measurements for valence-shell photoionization of Ar + ions are reported for photon energies ranging from 27.4 to 60.0 eV. The data, taken by merging beams of ions and synchrotron radiation at a photon energy resolution of 10 meV, indicate that the primary ion beam was a statistically weighted mixture of the 2 P o 3/2 ground state and the 2 P o 1/2 metastable state of Ar + . Photoionization of this Cl-like ion is characterized by multiple Rydberg series of autoionizing resonances superimposed on a direct photoionization continuum. Observed resonance line shapes indicate interference between indirect and direct photoionization channels. Resonance features are spectroscopically assigned and their energies and quantum defects are tabulated. The measurements are satisfactorily reproduced by theoretical calculations based on an intermediate coupling semirelativistic Breit-Pauli approximation.

Mass-resolved anion and cation partial-yield spectra following photoexcitation of CO2 have been recorded in the vicinity of the C 1s and O 1s thresholds. Anion production was found to be site specific: a weak production of O− was observed on the π* resonance near the C K edge, whereas both C− and O− fragments were observed near the O K edge. Due to suppression of the shape resonances that dominate the cross section above the core thresholds, the anion-partial-yield spectra at the O K edge reveal several previously unobserved electronic states. In addition, several cations such as CO2+ and O2+ were observed for the first time.