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Infrared free electron laser induced photodesorption of CO and N2 from solid amorphous water at cryogenic temperatures

  • Kerry H. Jones
  • , Jack E. Fulker*
  • , Domantas Laurinavicius
  • , Ali Ozel
  • , Johanna G. M. Schrauwen
  • , Britta Redlich
  • , Jennifer A. Noble
  • , Sergio Ioppolo
  • , Martin R. S. McCoustra
  • , Wendy A. Brown*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Photon induced processing of molecular ices is known to be important in a number of astrophysical environments. However, to date, astrophysical models tend to only incorporate ultra-violet induced photoprocesses. This is despite the fact that the flux of infrared (IR) photons is comparable to, and sometimes exceeds that of, ultra-violet photons in a number of environments. In order to determine whether IR photoprocesses are important under astrophysical conditions, we have undertaken experiments to investigate the IR-induced desorption of CO and N2 from CO:H2O and N2:H2O mixed ices grown at 9 K. These studies were performed at FELIX, the free electron laser facility at Radboud University, Nijmegen, The Netherlands. Irradiation of the ices was performed in the mid-IR range from 2.9 – 12 μm and shows that photon induced desorption (PID) of CO and N2 only occurs when the ices are irradiated at wavelengths that excite the vibrational modes of the H2O ice. No PID is observed when the internal stretching modes of the dopant molecules are excited. The observed PID traces, recorded during the irradiation with a mass spectrometer, can be fitted with a biexponential decay function that shows the presence of a fast and a slow photodesorption process. These can be assigned to direct and indirect substrate-mediated resonant photodesorption processes. Power dependence studies show saturation and suggest that a complex process is leading to the observed PID. The data reported here clearly show that IRdriven photodesorption should be considered in astrophysical models.
Original languageEnglish
Pages (from-to)8186-8198
Number of pages13
JournalPhysical Chemistry Chemical Physics
Volume28
Issue number13
Early online date9 Mar 2026
DOIs
Publication statusPublished - 1 Apr 2026

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