Abstract

No clear resonance is present in the resonant valence band photoemission spectrum of a Mn6 (S=4) single molecule magnet grafted on Au (111) for photon energy at the L2 resonance edge. This is due to the L2-hole’s dominant decay by the L2–L3V Coster–Kronig (CK) decay. The excess energy of the photon at which the Mn resonant Raman scattering regime transits to the normal Mn Auger-decay regime in MnO depends on the Mn Auger-decay channels. This is because of the localization and delocalization of two holes in the Auger final states. The Mn resonant Auger-electron spectroscopy spectra of MnO are analyzed.

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