Nature Communications · 2018 · 167 citations · 51 references
Natural SciencesChemistryPhysicsAtomic PhysicsQuantum MechanicsSpectroscopyAtomic SpectraAtomic TransitionsPhotoelectron SpectroscopyAngular DependenceExcitationPhotoionization Cross SectionsPhotoionization KineticsResonant ExcitationTime-resolved Photoelectron SpectroscopyUltrafast Electron Dynamics
Abstract Electron correlation and multielectron effects are fundamental interactions that govern many physical and chemical processes in atomic, molecular and solid state systems. The process of autoionization, induced by resonant excitation of electrons into discrete states present in the spectral continuum of atomic and molecular targets, is mediated by electron correlation. Here we investigate the attosecond photoemission dynamics in argon in the 20–40 eV spectral range, in the vicinity of the 3 s −1 np autoionizing resonances. We present measurements of the differential photoionization cross section and extract energy and angle-dependent atomic time delays with an attosecond interferometric method. With the support of a theoretical model, we are able to attribute a large part of the measured time delay anisotropy to the presence of autoionizing resonances, which not only distort the phase of the emitted photoelectron wave packet but also introduce an angular dependence.
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Effects of Configuration Interaction on Intensities and Phase Shifts
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Natural Sciences, Physics, Optics +13