Physical Chemistry Chemical Physics · 2020 · 43 citations · 49 references
Natural SciencesChemistryPhysicsAnalytical ChemistryInorganic ChemistrySpectroscopyElectronic Band StructureElectronic SpectroscopyInorganic SpectroscopyPhotoelectron SpectroscopyX-ray Photoelectron SpectroscopyX-ray SpectroscopyDouble IonizationHigh-resolution X-ray SpectroscopyInitial State EffectsIonizationNear-edge X-ray Absorption Fine Structure SpectroscopyX-ray Absorption Near Edge StructureX-ray Absorption SpectroscopyX-ray Chemistry
We present and analyze high resolution near edge X-ray absorption fine structure (NEXAFS) spectra of CO+ at the carbon and oxygen K-edges. The spectra show a wealth of features that appear very differently at the two K-edges. The analysis of these features can be divided into three parts; (i) repopulation transition to the open shell orbital - here the C(1s) or O(1s) to 5σ transition, where the normal core hole state is reached from a different initial state and different interaction than in X-ray photoelectron spectroscopy; (ii) spin coupled split valence bands corresponding to C(1s) or O(1s) to π* transitions; (iii) remainder weak and long progressions towards the double ionization potentials containing a manifold of peaks. These parts, none of which has correspondence in NEXAFS spectra of neutral molecules, are dictated by the localization of the singly occupied 5σ orbital, adding a dimension of chemistry to the ionic NEXAFS technique.
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