0000000000997269

AUTHOR

Jessica Walkenhorst

showing 2 related works from this author

Tailored pump-probe transient spectroscopy with time-dependent density-functional theory: controlling absorption spectra

2016

Recent advances in laser technology allow us to follow electronic motion at its natural time-scale with ultra-fast time resolution, leading the way towards attosecond physics experiments of extreme precision. In this work, we assess the use of tailored pumps in order to enhance (or reduce) some given features of the probe absorption (for example, absorption in the visible range of otherwise transparent samples). This type of manipulation of the system response could be helpful for its full characterization, since it would allow us to visualize transitions that are dark when using unshaped pulses. In order to investigate these possibilities, we perform first a theoretical analysis of the non…

Physics010304 chemical physicsSolid-state physicsAtomic Physics (physics.atom-ph)AttosecondQuantum dynamicsComplex systemFOS: Physical sciencesContext (language use)Time-dependent density functional theoryCondensed Matter Physics01 natural sciences7. Clean energySettore FIS/03 - Fisica Della MateriaPhysics - Atomic Physics3. Good healthElectronic Optical and Magnetic MaterialsCharacterization (materials science)Computational physicsCondensed Matter - Other Condensed Matter0103 physical sciences010306 general physicsAbsorption (electromagnetic radiation)Other Condensed Matter (cond-mat.other)Computational MethodsThe European Physical Journal B
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Simulating pump-probe photo-electron and absorption spectroscopy on the attosecond time-scale with time-dependent density-functional theory

2013

Molecular absorption and photoelectron spectra can be efficiently predicted with real-time time-dependent density functional theory. We show herein how these techniques can be easily extended to study time-resolved pump-probe experiments, in which a system response (absorption or electron emission) to a probe pulse is measured in an excited state. This simulation tool helps with the interpretation of fast-evolving attosecond time-resolved spectroscopic experiments, in which electronic motion must be followed at its natural timescale. We show how the extra degrees of freedom (pump-pulse duration, intensity, frequency, and time delay), which are absent in a conventional steady-state experimen…

Time-resolved spectroscopyTime FactorsAbsorption spectroscopyAtomic Physics (physics.atom-ph)AttosecondAttosecond dynamicsFOS: Physical sciencesPump probesingle-molecule studies01 natural sciencestime-resolved spectroscopySettore FIS/03 - Fisica Della MateriaPhysics - Atomic PhysicsAb initio quantum chemistry methodsPhysics - Chemical Physics0103 physical sciencesPhysics - Atomic and Molecular ClustersLaser spectroscopyPhysical and Theoretical Chemistry010306 general physicsSpectroscopyPhysicsChemical Physics (physics.chem-ph)010304 chemical physicsEuropean researchab initio calculationsPhotoelectron SpectroscopySingle-molecule studiesattosecond dynamicsTime-dependent density functional theoryAtomic and Molecular Physics and OpticsPhysics - Plasma PhysicsPlasma Physics (physics.plasm-ph)X-Ray Absorption Spectroscopylaser spectroscopyQuantum TheoryAtomic physicsTime-resolved spectroscopyAtomic and Molecular Clusters (physics.atm-clus)
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