Interatomic processes play a crucial role in weakly bound complexes exposed to ionizing radiation; therefore, gaining a thorough understanding of their efficiency is of fundamental importance. Here, we directly measure the timescale of interatomic Coulombic decay (ICD) in resonantly excited helium nanodroplets using a high-resolution, tunable, extreme ultraviolet free-electron laser. Over an extensive range of droplet sizes and laser intensities, we discover the decay to be surprisingly fast, with decay times as short as 400 fs, nearly independent of the density of the excited states. Using a combination of time-dependent density functional theory and ab initio quantum chemistry calculations, we elucidate the mechanisms of this ultrafast decay process, where pairs of excited helium atoms in one droplet strongly attract each other and form merging void bubbles, which drastically accelerates ICD.

Ultrafast Resonant Interatomic Coulombic Decay Induced by Quantum Fluid Dynamics / A.C. Laforge, R. Michiels, Y. Ovcharenko, A. Ngai, J.M. Escartin, N. Berrah, C. Callegari, A. Clark, M. Coreno, R. Cucini, M. Di Fraia, M. Drabbels, E. Fasshauer, P. Finetti, L. Giannessi, C. Grazioli, D. Iablonskyi, B. Langbehn, T. Nishiyama, V. Oliver, P. Piseri, O. Plekan, K.C. Prince, D. Rupp, S. Stranges, K. Ueda, N. Sisourat, J. Eloranta, M. Pi, M. Barranco, F. Stienkemeier, T. Moller, M. Mudrich. - In: PHYSICAL REVIEW. X. - ISSN 2160-3308. - 11:2(2021 Apr 12), pp. 021011.021011-1-021011.021011-11. [10.1103/PhysRevX.11.021011]

Ultrafast Resonant Interatomic Coulombic Decay Induced by Quantum Fluid Dynamics

P. Piseri;
2021

Abstract

Interatomic processes play a crucial role in weakly bound complexes exposed to ionizing radiation; therefore, gaining a thorough understanding of their efficiency is of fundamental importance. Here, we directly measure the timescale of interatomic Coulombic decay (ICD) in resonantly excited helium nanodroplets using a high-resolution, tunable, extreme ultraviolet free-electron laser. Over an extensive range of droplet sizes and laser intensities, we discover the decay to be surprisingly fast, with decay times as short as 400 fs, nearly independent of the density of the excited states. Using a combination of time-dependent density functional theory and ab initio quantum chemistry calculations, we elucidate the mechanisms of this ultrafast decay process, where pairs of excited helium atoms in one droplet strongly attract each other and form merging void bubbles, which drastically accelerates ICD.
Settore FIS/03 - Fisica della Materia
12-apr-2021
Article (author)
File in questo prodotto:
File Dimensione Formato  
PhysRevX.11.021011.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 1.2 MB
Formato Adobe PDF
1.2 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/911118
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 18
  • ???jsp.display-item.citation.isi??? 19
social impact