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Resonant 3<i>d</i>, 3<i>p</i>and 3<i>s</i>Photoemission in Transition Metal Oxides Predicted at 2<i>p</i>Threshold
355
Citations
19
References
1994
Year
EngineeringInorganic PhotochemistryAbsorption SpectroscopyChemistryElectronic Excited StateQuantum MaterialsTransition MetalTransition Metal OxidesPhotophysical PropertyResonant 3PhysicsPhotochemistryOxide ElectronicsPhysical ChemistryD RpeQuantum ChemistryTransition Metal ChalcogenidesExcited State PropertyTransition Metal IonsNatural SciencesSpectroscopyApplied PhysicsCondensed Matter Physics
We present calculated 3 d , 3 p and 3 s resonant photoemission (RPE) spectra in the transition metal (TM) compounds CuO, NiO, CoO, FeO, MnO and TiO 2 at TM 2 p core threshold on the basis of a cluster model. Our model includes the intraatomic multipole electron-electron interactions and the hybridization between transition metal ions and ligand. The imaginary part of the self-energy matrix of the intermediate state is calculated by taking into account the 2 p 3 d 3 d , 2 p 3 d 3 p , 2 p 3 d 3 s and 2 p 3 p 3 p Coster-Kronig decay, which guarantees a sum rule between the integrated RPE spectra and absorption spectra. The dependence of RPE on the incident photon energy tuned to various multiplet structures of TM 2 p absorption spectra is shown to be useful to identify the second order optical process, which is argued to include much Auger decay component. It is also shown, by a comparison with experiment, that the present 3 d RPE contributes to a removal of discrepancies of estimated parameter values among analyses of other spectra.
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