4.8 Article

Ultrafast relaxation of photoexcited superfluid He nanodroplets

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NATURE COMMUNICATIONS
卷 11, 期 1, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-13681-6

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资金

  1. Deutsche Forschungsgemeinschaft [MU 2347/8-1, STI 125/19-1, 1840 QUTIF]
  2. Carlsberg Foundation
  3. National Science Foundation [DMR-1828019]
  4. Carl-Zeiss-Stiftung [FIS2017-87801-P]
  5. Swiss National Science Foundation [200020_162434]
  6. U.S. Department of Energy, Office of Basic Energy Sciences, Chemical Sciences, Geosciences and Biosciences Division [DE-AC02-05CH11231]
  7. Swiss National Science Foundation (SNF) [200020_162434] Funding Source: Swiss National Science Foundation (SNF)

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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.

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