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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

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We report on an experimental and theoretical investigation of x-ray absorption and resonant Auger electron spectra of gas phase O(2) recorded in the vicinity of the O 1s-->sigma(*) excitation region. Our investigation shows that core excitation takes place in a region with multiple crossings of potential energy curves of the excited states. We find a complete breakdown of the diabatic picture for this part of the x-ray absorption spectrum, which allows us to assign an hitherto unexplained fine structure in this spectral region. The experimental Auger data reveal an extended vibrational progression, for the outermost singly ionized X (2)Pi(g) final state, which exhibits strong changes in spectral shape within a short range of photon energy detuning (0 eV>Omega>-0.7 eV). To explain the experimental resonant Auger electron spectra, we use a mixed adiabatic/diabatic picture selecting crossing points according to the strength of the electronic coupling. Reasonable agreement is found between experiment and theory even though the nonadiabatic couplings are neglected. The resonant Auger electron scattering, which is essentially due to decay from dissociative core-excited states, is accompanied by strong lifetime-vibrational and intermediate electronic state interferences as well as an interference with the direct photoionization channel. The overall agreement between the experimental Auger spectra and the calculated spectra supports the mixed diabatic/adiabatic picture.

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