Data di Pubblicazione:
2020
Abstract:
The relaxation of photoexcited nanosystems is a fundamental process of light-matter interaction. Depending on the couplings of the internal degrees of freedom, relaxation can be ultrafast, converting electronic energy in a few fs, or slow, if the energy is trapped in a metastable state that decouples from its environment. Here, we study helium nanodroplets excited resonantly by femtosecond extreme-ultraviolet (XUV) pulses from a seeded free-electron laser. Despite their superfluid nature, we find that helium nanodroplets in the lowest electronically excited states undergo ultrafast relaxation. By comparing experimental photoelectron spectra with time-dependent density functional theory simulations, we unravel the full relaxation pathway: Following an ultrafast interband transition, a void nanometer-sized bubble forms around the localized excitation (He*) within 1 ps. Subsequently, the bubble collapses and releases metastable He* at the droplet surface. This study highlights the high level of detail achievable in probing the photodynamics of nanosystems using tunable XUV pulses.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Atomic and molecular interactions with photons; Macromolecules and clusters; free electron laser; clusters; superfluid helium
Elenco autori:
Grazioli, Cesare; Prince, KEVIN CHARLES; Ciavardini, Alessandra; DI FRAIA, Michele; Callegari, Carlo; Finetti, Paola; Piseri, Paolo; Coreno, Marcello; O'Keeffe, PATRICK KEVIN; Devetta, Michele
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