Angle-resolution techniques in combination with a tunable synchrotron radiation source are used in resonant photoemission from bulk, multilayer, and monolayer Cr. The striking double-peak structure of the resonant 3p{→}3d transition in bulk Cr is found to turn gradually into a single peak when going to a multilayer and eventually to a monolayer of Cr. The evolution of the double peak into a single peak is also confirmed in electron-energy-loss spectra. The constant-initial-state (CIS) spectra of bulk Cr are strongly angle dependent. This is an indication of a multichannel autoionization process in the neighborhood of the M₂,3 absorption threshold. We attempt to describe this angle dependence by the empirical Kabachnik-Sazhina two-channel autoionization formula. For describing the two-peak-structure angular dependence in Cr we find the following values for the Fano-profile parameters q and the level widths {Γ}: q₁=+0.8, q₂=-1.5, Γ₁=5 eV, and Γ₂=7 eV. The double-peak structure in the Cr M₂,3 resonant transition is found to disappear in high-energy transmission electron-energy-loss spectroscopy of a Cr₂₀{Au}₈₀$ alloy. For comparison reasons angle-integrated resonant photoemission studies were also carried out on vanadium for photon energies around the ${M}₂$,3 binding energy and only a single peak was detected, in agreement with previously published results.
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Bader et al. (1986) studied this question.
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