Ultrafast relaxation of photoexcited superfluid He nanodroplets

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 decouple...

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Authors: Mudrich, M., LaForge, A.C., Ciavardini, A., O'Keeffe, P., Callegari, C., Coreno, M., Demidovich, A., Devetta, M., Di Fraia, M., Drabbels, M., Finetti, P., Gessner, O., Grazioli, C., Hernando, A., Neumark, D.M., Ovcharenko, Y., Piseri, P., Plekan, Oksana, Prince, Kevin C., Richter, R., Ziemkiewicz, M.P., Möller, T., Eloranta, J., Pi Pericay, Martí, Barranco Gómez, Manuel, Stienkemeier, F.
Format: article
Status:Published version
Publication Date:2020
Country:España
Institution:Universidad de Barcelona
Repository:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/178863
Online Access:https://hdl.handle.net/2445/178863
Access Level:Open access
Keyword:Nanotecnologia
Nanotechnology
Description
Summary: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 pho- toelectron 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.