Author
Listed:
- M. Mudrich
(Aarhus University)
- A. C. LaForge
(University of Freiburg
University of Connecticut)
- A. Ciavardini
(CNR-ISM
CERIC-ERIC Basovizza)
- P. O’Keeffe
(CNR-ISM)
- C. Callegari
(Elettra – Sincrotrone Trieste S.C.p.A.)
- M. Coreno
(CNR-ISM)
- A. Demidovich
(Elettra – Sincrotrone Trieste S.C.p.A.)
- M. Devetta
(Università degli Studi di Milano
CNR-IFN)
- M. Di Fraia
(Elettra – Sincrotrone Trieste S.C.p.A.)
- M. Drabbels
(Ecole Polytechnique Fédérale de Lausanne (EPFL))
- P. Finetti
(Elettra – Sincrotrone Trieste S.C.p.A.)
- O. Gessner
(Lawrence Berkeley National Laboratory)
- C. Grazioli
(CNR-IOM, Istituto Officina dei Materiali)
- A. Hernando
(Kido Dynamics
IFISC (CSIC-UIB), Instituto de Fisica Interdisciplinar y Sistemas Complejos)
- D. M. Neumark
(Lawrence Berkeley National Laboratory
University of California)
- Y. Ovcharenko
(Institut für Optik und Atomare Physik
European XFEL)
- P. Piseri
(Università degli Studi di Milano)
- O. Plekan
(Elettra – Sincrotrone Trieste S.C.p.A.)
- K. C. Prince
(Elettra – Sincrotrone Trieste S.C.p.A.)
- R. Richter
(Elettra – Sincrotrone Trieste S.C.p.A.)
- M. P. Ziemkiewicz
(Lawrence Berkeley National Laboratory
University of California)
- T. Möller
(Institut für Optik und Atomare Physik)
- J. Eloranta
(California State University at Northridge)
- M. Pi
(Universitat de Barcelona
Universitat de Barcelona)
- M. Barranco
(Universitat de Barcelona
Universitat de Barcelona
IRSAMC, UMR 5589, CNRS et Université Paul Sabatier-Toulouse 3)
- F. Stienkemeier
(University of Freiburg)
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.
Suggested Citation
M. Mudrich & A. C. LaForge & A. Ciavardini & P. O’Keeffe & C. Callegari & M. Coreno & A. Demidovich & M. Devetta & M. Di Fraia & M. Drabbels & P. Finetti & O. Gessner & C. Grazioli & A. Hernando & D. , 2020.
"Ultrafast relaxation of photoexcited superfluid He nanodroplets,"
Nature Communications, Nature, vol. 11(1), pages 1-7, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-13681-6
DOI: 10.1038/s41467-019-13681-6
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