Publications by authors named "R Geneaux"

We measure the light-driven response of a magnetic multilayer structure made of thin alternating layers of cobalt and platinum at the few-femtosecond timescale. Using attosecond magnetic circular dichroism, we observe how light rearranges the magnetic moment during and after excitation. The results reveal a sub-5 fs spike of magnetization in the platinum layer, which follows the shape of the driving pulse.

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We report on the generation of optical vortices with few-cycle pulse durations, 500μJ per pulse, at a repetition rate of 1 kHz. To do so, a 25 fs laser beam at 800 nm is shaped with a helical phase and coupled into a hollow-core fiber filled with argon gas, in which it undergoes self-phase modulation. Then, 5.

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Article Synopsis
  • The study investigates excitons in 2H-WSe_{2} using advanced spectroscopic techniques, focusing on how these excitons can be manipulated through the use of circularly polarized light.
  • The XUV photoemission method allows researchers to specifically measure the spin polarization of both bright and dark excitons at the surface level, revealing a difference in their behaviors.
  • Findings indicate that while bright excitons' spin polarization diminishes due to scattering, dark excitons may serve as a resource for local spin polarization, potentially benefiting spin injection in layered materials.
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Attosecond transient absorption spectroscopy (ATAS) is used to observe photoexcited dynamics with outstanding time resolution. The main experimental challenge of this technique is that high-harmonic generation sources show significant instabilities, resulting in sub-par sensitivity when compared to other techniques. This paper proposes edge-pixel referencing as a means to suppress this noise.

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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.

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