MPG.PuRe (Max Planck Society) · 2019 · 71 citations · 79 references
Natural SciencesMaterials SciencePhysicsCondensed Matter PhysicsPhotonicsSpectroscopyPhotoelectron SpectroscopyTime-resolved SpectroscopyUltrafast OpticsUltraviolet SpectroscopyAngle-resolved Photoelectron SpectroscopyAngle-resolved Photoemission SpectroscopyExtreme Ultraviolet SpectroscopyHarmonic GenerationHigh-harmonic GenerationHigh-order Harmonic GenerationTime-resolved Photoelectron SpectroscopyUltrafast Spectroscopy
With its direct correspondence to electronic structure, angle-resolved photoemission spectroscopy (ARPES) is a ubiquitous tool for the study of solids. When extended to the temporal domain, time-resolved (TR)-ARPES offers the potential to move beyond equilibrium properties, exploring both the unoccupied electronic structure as well as its dynamical response under ultrafast perturbation. Historically, ultrafast extreme ultraviolet sources employing high-order harmonic generation (HHG) have required compromises that make it challenging to achieve a high energy resolution-which is highly desirable for many TR-ARPES studies-while producing high photon energies and a high photon flux. We address this challenge by performing HHG inside a femtosecond enhancement cavity, realizing a practical source for TR-ARPES that achieves a flux of over 10(11) photons/s delivered to the sample, operates over a range of 8-40 eV with a repetition rate of 60 MHz. This source enables TR-ARPES studies with a temporal and energy resolution of 190 fs and 22 meV, respectively. To characterize the system, we perform ARPES measurements of polycrystalline Au and MoTe2, as well as TR-ARPES studies on graphite. Published under license by AIP Publishing
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Plasma perspective on strong field multiphoton ionization
P. B. Corkum · Physical Review Letters · 1993 · 7.1K citations · Full text
Natural Sciences, Physics, Optics +14
Ultrashort-pulse fiber ring lasers
L.E. Nelson, David J. Jones, K. Tamura et al. · Applied Physics B · 1997 · 834 citations