Ice as a Photochemical Shield: Adsorption Energetics and Spectroscopic Modulation of Interstellar Thiocyanates HCSCN and HCSCCH in TMC-1
Saptarshi G. Dastider, Amit Singh Negi, Krishnakanta Mondal, Jobin Cyriac

TL;DR
This study combines computational chemistry and astrochemical modeling to understand how interstellar thiocyanates adsorb on ice, affecting their spectral features and survival, with implications for their detection and stability in space.
Contribution
It provides detailed site-specific adsorption energetics and spectroscopic effects of HCSCN and HCSCCH on amorphous water ice, revealing their complex desorption and photodissociation behavior.
Findings
Adsorption energies range from 1500 to 4900 K.
Cavity sites cause Stark shifts in vibrational modes.
Deeply bound species have enhanced UV absorption cross-sections.
Abstract
The recent detections of thioformyl cyanide (HCSCN) and propynethial (HCSCCH) in TMC-1 provide critical insights into the interstellar sulfur inventory, yet their sequestration and survivability on dust grain mantles remain poorly constrained. Here, we present a computational study of the site-specific adsorption of HCSCN and HCSCCH on amorphous solid water (ASW), modelled via water clusters (H2O)n, n = 6-16, at the wB97X-D/def2-TZVP level of theory, corroborated by QTAIM topological analyses and TD-DFT vertical excitations. Our results reveal a highly heterogeneous binding environment, with desorption energies spanning 1500 to 4900 K. Strongly bound cavity sites induce significant Stark shifts in the C=S stretching modes. Crucially, while the ice matrix exerts a negligible solvatochromic shift on UV transition wavelengths, deeply bound CN-cavity configurations exhibit a pronounced…
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