Relative photoionization cross sections for O + and O 2+ produced by the Auger decay of a 1s hole in atomic oxygen were measured by using synchrotron radiation between 525 and 553 eV. Energies and quantum defects of the members of the two Rydberg series converging to [1s]2s 2 2p 4 ( 4 P) and [1s]2s 2 2p 4 ( 2 P) ionization thresholds were determined. In addition, the 2 P and 4 P ionization thresholds were calculated from the two Rydberg series. The 182 meV resolution of the monochromator allowed a detailed study over both thresholds revealing evidence for post-collision interaction and allowing a comparison of the ionization continuum above both 2 P and 4 P thresholds with that of the ionization continuum above the Ar L 2-3 edges. This comparison indicates that the lifetimes of the Ar(2p) and O(1s) hole states are approximately the same.

No abstract

The independent particle approximation is shown to break down for the photoionization of both inner and outer nᐉ ͑ᐉ . 0͒ electrons of all atoms, at high enough energy, owing to interchannel interactions with the nearby ns photoionization channels. The effect is illustrated for Ne 2p in the 1 keV photon energy range through a comparison of theory and experiment. The implications for x-ray photoelectron spectroscopy of molecules and condensed matter are discussed. [S0031-9007 (97)03382-6] PACS numbers: 32.80.Fb

By exploiting the core-excitation-induced dissociation of O2, we find that the Auger emission exhibits a Doppler-like energy shift. We show this to be a manifestation of localization of the core hole and propose that the problem of core-hole localization versus delocalization in core-hole spectroscopies may be resolved by considering the nature of the measurement.

International audienceA Doppler-type shift in the kinetic energy of atomic Auger electrons emitted after fast dissociation of O3 molecules is observed. The resonant Auger spectrum from the decay of repulsive core-excited states reflects both the early molecular ozone decay and that from excited dissociation fragments. The kinetic energy of the fragment is manifested as an energy shift of the atomic Auger lines when the measurement is made under certain conditions. We report measurements of the energy-split atomic fragment emission lines arising from dissociation on a time scale comparable to the core-hole lifetime. For the O 1s–* states the kinetic energy release amounts to several electron volts. We report measurements for excitation of both the terminal and central oxygen 1s electrons. A simple kinematic model for extracting a lower limit for the kinetic-energy release is presented and is compared with the result of a Born–Haber cycle, which may be seen as an estimate of the maximum energy releas