| Autor: |
Mudrich, M., LaForge, A. C., Ciavardini, A., O'Keeffe, P., Callegari, C., Coreno, M., Demidovich, A., Devetta, M., Fraia, M. Di, Drabbels, M., Finetti, P., Gessner, O., Grazioli, C., Hernando, A., Neumark, D. M., Ovcharenko, Y., Piseri, P., Plekan, O., Prince, K. C., Richter, R. |
| Předmět: |
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| Zdroj: |
Nature Communications; 1/8/2020, Vol. 11 Issue 1, p1-7, 7p |
| Abstrakt: |
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. There is interest in understanding the relaxation mechanisms of photoexcitation in atoms, molecules and other complex systems. Here the authors unravel the photoexcitation and ultrafast relaxation of superfluid helium nanodroplets using a pump-probe experiment with FEL pulses. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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