We identified interatomic Coulombic decay (ICD) channels in argon dimers after spectator-type resonant Auger decay 2p −1 3d → 3p −2 3d,4d in one of the atoms, using momentum-resolved electron-ion-ion coincidence. The results illustrate that the resonant core excitation is a very efficient way of producing slow electrons at a specific site, which may cause localized radiation damage. We find also that ICD rate for 3p −2 4d is significantly lower than that for 3p −2 3d.

Cascade Si LVV Auger decays following KL(23)L(23) Auger transitions have been measured in SiF(4) molecule using an electron spectrometer combined with monochromatized undulator radiation. Molecular cascade processes from the two 2p holes states largely generate wide band structures in the spectra due to sequential electron emission leading to multiple valence holes. However, a peak with high yield is observed for the first time at about 103 eV, an energy being considerably higher than the energies of the normal LVV Auger electron, in the instance of the resonant excitation of Si 1s electron into the vacant molecular orbital. This peak is presumed to originate from the participator decay from the state with two 2p holes and one excited electron into the state with one 2p hole and one valence hole. A similar peak with less intensity is detected in the photoexcitation of the 1s electron into a Rydberg orbital. After the normal KL(23)L(23) Auger transition, the resultant cascade spectrum shows several peaks, e.g., 61 eV, 76 eV, and 82 eV. The former two peaks are assigned to the Auger transitions of Si atoms produced through molecular ion dissociation after cascade decays, and the latter is probably ascribed to the second step Auger decay into states having a 2p hole together with two valence holes.

Spectator resonant Auger electron spectra with the Si 1s photoexcitation of SiCl 4 have been measured using an electron spectroscopic technique combined with undulator radiation. The transition with the highest intensity in the total ion yield (TIY) spectrum, coming from excitation of a 1s electron into the 9t 2 valence orbital, generates the resonant Auger decay in which the excited electron remains in the 9t 2 orbital. A TIY peak positioned slightly above the 1s ionization threshold induces Auger decay in which the slow photoelectron is re-captured into a higher lying Rydberg orbital or the normal Auger peak shape is distorted due to a post-collision interaction effect. Another structure above the threshold, originating from a doubly excited state, yields the normal Auger peak with the distortion of peak shape and a resonant Auger peak with a higher kinetic energy. These findings provide a clear understanding of the properties of the excited orbitals which were ambiguous previously.

Spectator resonant KL(23)L(23) Auger electron spectra have been measured in the Si 1s photoexcitation region of Si(CH(3))(4) using monochromatized undulator radiation combined with a hemispherical electron spectrometer. The broad peak with high intensity in a total ion yield spectrum, coming mainly from excitation of a 1s electron into the 6t(2) vacant orbital, induces a spectator Auger decay in which the excited electron remains in its excited orbital. The component on the higher energy side of this peak through 1s excitation into a Rydberg orbital produces resonant Auger decays in which the excited Rydberg electron moves into a slightly higher Rydberg orbital, or is partly shaken up to a significantly higher Rydberg orbital. These findings of Si(CH(3))(4) indicate a clear contrast to those for SiF(4), in which the 1s excitation into a Rydberg orbital induces a shake-down phenomenon as well as a shake-up one. The results of these molecules exhibit a clear splitting effect among excited orbitals which are smeared out by overlapping due to lifetime widths and due to densely populated levels in the 1s electron excitation spectrum. This is consistent with the calculation on photoexcitation within the framework of density functional theory.

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