Attosecond Time-Domain Measurement of Core-Level-Exciton Decay in Magnesium Oxide.

Excitation of ionic solids with extreme ultraviolet pulses creates localized core-level excitons, which in some cases couple strongly to the lattice. Here, core-level-exciton states of magnesium oxide are studied in the time domain at the Mg L_{2,3} edge with attosecond transient reflectivity spectroscopy. Attosecond pulses trigger the excitation of these short-lived quasiparticles, whose decay is perturbed by time-delayed near-infrared pulses. Combined with a few-state theoretical model, this reveals that the infrared pulse shifts the energy of bright (dipole-allowed) core-level-exciton states as well as induces features arising from dark core-level excitons. We report coherence lifetimes for the two lowest core-level excitons of 2.3±0.2 and 1.6±0.5  fs and show that these are primarily a consequence of strong exciton-phonon coupling, disclosing the drastic influence of structural effects in this ultrafast relaxation process

Ultrafast Hidden Spin Polarization Dynamics of Bright and Dark Excitons in 2H-WSe2_2

We performed spin-, time- and angle-resolved extreme ultraviolet photoemission spectroscopy (STARPES) of excitons prepared by photoexcitation of inversion-symmetric 2H-WSe$_2$ with circularly polarized light. The very short probing depth of XUV photoemission permits selective measurement of photoelectrons originating from the top-most WSe$_2$ layer, allowing for direct measurement of hidden spin polarization of bright and momentum-forbidden dark excitons. Our results reveal efficient chiroptical control of bright excitons' hidden spin polarization. Following optical photoexcitation, intervalley scattering between nonequivalent K-K' valleys leads to a decay of bright excitons' hidden spin polarization. Conversely, the ultrafast formation of momentum-forbidden dark excitons acts as a local spin polarization reservoir, which could be used for spin injection in van der Waals heterostructures involving multilayer transition metal dichalcogenides

Separation of kinetic rate orders in extreme ultraviolet transient grating spectroscopy

We present an Extreme Ultraviolet (EUV) transient grating (TG) experiment of the spinel Co3O4 compound using tuneable incident energies across the Co M2,3-edge and a 395 nm probe pulse, detecting both the first and the second diffraction orders. While the first diffraction order shows a monotonous behaviour as a function of time, with a sharp response at t=0, followed by a weak sub-picosecond component and a nearly constant signal thereafter, the time dependence of second diffraction order varies dramatically with the incident energy as it is tuned across the Co M-edge, with the appearance of a component at t>1 ps that grows with increasing energy. The results are rationalised in terms of the deviations of the initial grating from sinusoidal to non-sinusoidal, namely a flattening of the grating pattern, that introduces new Fourier components. These deviations are due to higher order, three-body terms in the population relaxation kinetics. These results highlight the use of the response of the second diffraction order in EUV TG as a tool to identify higher order terms in the population kinetics