open access publication

Article, 2024

Spectroscopically resolved resonant interatomic Coulombic decay in photoexcited large He nanodroplets

PHYSICAL REVIEW RESEARCH, Volume 6, 1, 10.1103/PhysRevResearch.6.013019

Contributors

Ben Ltaief, L. (Corresponding author) [1] Sishodia, K. [2] [3] Richter, R. [4] Bastian, B. 0000-0003-3519-5752 [1] Asmussen, J. D. 0000-0001-9881-8617 [1] Mandal, S. [5] Pal, N. [4] Medina, C. [6] Krishnan, S. R. [2] [3] von Haeften, K. 0000-0002-2758-8030 [7] [8] [9] Mudrich, M. [1]

Affiliations

  1. [1] Aarhus Univ, Dept Phys & Astron, DK-8000 Aarhus C, Denmark
  2. [NORA names: AU Aarhus University; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Indian Inst Technol Madras, Chennai 600 036, India
  4. [NORA names: India; Asia, South];
  5. [3] Indian Inst Technol Madras, Chennai 600 036, India
  6. [NORA names: India; Asia, South];
  7. [4] Elettra Sincrotrone Trieste, I-34149 Trieste, Italy
  8. [NORA names: Italy; Europe, EU; OECD];
  9. [5] Indian Inst Sci Educ & Res, Pune 411008, India
  10. [NORA names: India; Asia, South];

Abstract

Interatomic Coulombic decay (ICD) processes play a crucial role in weakly bound complexes exposed to intense or high-energy radiation. Using large helium nanodroplets, we demonstrate that ICD is efficient even when the droplets are irradiated by weak synchrotron radiation at relatively low photon energies. Below the ionization threshold, resonant excitation of multiple centers efficiently induces resonant ICD as previously observed for intense pulses [A. C. LaForge et al., Phys. Rev. X 11, 021011 (2021)]. More surprisingly, we observe ICD even above the ionization threshold due to recombination of photoelectrons and ions into excited states which subsequently decay by ICD. This demonstrates the importance of secondary processes, in particular electron scattering and recombination, in inducing ICD in extended condensed phase systems. High-resolution ICD electron spectra in combination with coincidence imaging of electrons and ions reveal the relaxation dynamics of highly excited and ionized weakly bound nanosystems.

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