Resonant infrared irradiation of CO and CH3OH interstellar ices

Abstract

Context. Solid-phase photo-processes involving icy dust grains greatly affect the chemical evolution of the interstellar medium by leading to the formation of complex organic molecules and by inducing photodesorption. So far, the focus of laboratory studies has mainly been on the impact of energetic ultraviolet (UV) photons on ices, but direct vibrational excitation by infrared (IR) photons is expected to influence the morphology and content of interstellar ices as well. However, little is still known about the mechanisms through which this excess vibrational energy is dissipated, as well as its implications for the structure and ice photochemistry. Aims. In this work, we present a systematic investigation of the behavior of interstellar relevant CO and CH3OH ice analogs following the resonant excitation of vibrational modes using tunable IR radiation. We seek to quantify the IR-induced photodesorption and gain insights into the impact of vibrational energy dissipation on ice morphology. Methods. We utilized an ultrahigh vacuum setup at cryogenic temperatures to grow pure CO and CH3OH ices, as well as mixtures of the two. We exposed the ices to intense, near-monochromatic mid-IR (MIR) free-electron-laser radiation using the LISA end-station at the FELIX free electron laser facility to selectively excite the species. Changes to the ice are monitored by means of reflection-absorption IR spectroscopy combined with quadrupole mass-spectrometry. These methods also allowed us to characterize the photodesorption efficiency. Results. The dissipation of vibrational energy is observed to be highly dependent on the excited mode and the chemical environment of the ice. All amorphous ices undergo some degree of restructuring towards a more organized configuration upon on-resonance irradiation. Moreover, IR-induced photodesorption is observed to occur for both pure CO and CH3OH ices, with interstellar photodesorption efficiencies on the order of 10 molecules cm−2 s−1. This result is comparable to or higher than what is found for UV-induced counterparts. An indirect photodesorption of CO upon vibrational excitation of CH3OH in ice mixtures is also observed to occur, particularly in environments that are rich in methanol. Here, we discuss the astrochemical implications of these IR-induced phenomena.