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Interaction of H2S with H atoms on grain surfaces under molecular cloud conditions

2023/08/15 by Julia C. Santos, Santos, Julia C., H. Linnartz +3 · 1 citation
Earth and Planetary Sciences · Physics and Astronomy · #Astrophysics and Star Formation Studies #Astrophysics of Galaxies (astro-ph.GA) #Atmospheric Ozone and Climate #Atmospheric chemistry and aerosols #FOS: Physical sciences

paper · pdf · doi:10.48550/arxiv.2308.07960

openalex publication_date 2023/08/15 · openalex created_date 2023/08/18 · openalex updated_date 2026/07/28

Abstract

Hydrogen sulfide (H2S) is thought to be efficiently formed on grain surfaces through the successive hydrogenation of S atoms. Its non-detection so far in astronomical observations of icy dust mantles thus indicates that effective destruction pathways must play a significant role in its interstellar abundance. While chemical desorption has been shown to remove H2S very efficiently from the ice, in line with H2S gas-phase detections, possible solid-state chemistry triggered by the related HS radical have been largely disregarded so far -- despite it being an essential intermediate in the H2S + H reaction scheme. We aim to thoroughly investigate the fate of H2S upon H-atom impact under molecular cloud conditions, providing a comprehensive analysis combined with detailed quantification of both the chemical desorption and ice chemistry that ensues. Experiments are performed in an ultrahigh vacuum chamber at temperatures between 10--16 K. The changes in the solid phase during H-atom bombardment are monitored in situ by means of reflection absorption infrared spectroscopy (RAIRS), and desorbed species are measured with a quadrupole mass spectrometer (QMS). We confirm the formation of H2S2 via reactions involving H2S + H, and quantify its formation cross section under the employed experimental conditions. Additionally, we directly assess the chemical desorption of H2S by measuring the gas-phase desorption signals with the QMS, providing unambiguous desorption cross sections. Chemical desorption of H2S2 was not observed. The relative decrease of H2S ices by chemical desorption changes from ~85% to ~74% between temperatures of 10 and 16 K, while the decrease as the result of H2S2 formation is enhanced from ~5% to ~26%, suggesting an increasingly relevant sulfur chemistry induced by HS radicals at warmer environments. The astronomical implications are further discussed.

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