In-Depth Exploration of Catalytic Sites on Amorphous Solid Water: I. The Astrosynthesis of Aminomethanol
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| Format: | Preprint |
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2024
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| _version_ | 1866914857882746880 |
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| author | Bovolenta, Giulia M. Silva-Vera, Gabriela Bovino, Stefano Molpeceres, German Kästner, Johannes Vogt-Geisse, Stefan |
| author_facet | Bovolenta, Giulia M. Silva-Vera, Gabriela Bovino, Stefano Molpeceres, German Kästner, Johannes Vogt-Geisse, Stefan |
| contents | Chemical processes taking place on ice-grain mantles are pivotal to the complex chemistry of interstellar environments. In this study, we conducted a comprehensive analysis of the catalytic effects of an amorphous solid water (ASW) surface on the reaction between ammonia (NH$_3$) and formaldehyde (H$_2$CO) to form aminomethanol (NH$_2$CH$_2$OH) using density functional theory. We identified potential catalytic sites based on the binding energy distribution of NH$_3$ and H$_2$CO reactants, on a set-of-clusters surface model composed of 22 water molecules and found a total of 14 reaction paths. Our results indicate that the catalytic sites can be categorized into four groups, depending on the interactions of the carbonyl oxygen and the amino group with the ice surface in the reactant complex. A detailed analysis of the reaction mechanism using Intrinsic Reaction Coordinate and reaction force analysis revealed three distinct chemical events for this reaction: formation of the C--N bond, breaking of the N--H bond, and formation of the O--H hydroxyl bond. Depending on the type of catalytic site, these events can occur within a single, concerted, albeit asynchronous, step, or can be isolated in a step-wise mechanism, with the lowest overall transition state energy observed at 1.3 kcal mol$^{-1}$. A key requirement for the low-energy mechanism is the presence of a pair of dangling OH bonds on the surface, found at 5\% of the potential catalytic sites on an ASW porous surface. |
| format | Preprint |
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arxiv_https___arxiv_org_abs_2407_03493 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | In-Depth Exploration of Catalytic Sites on Amorphous Solid Water: I. The Astrosynthesis of Aminomethanol Bovolenta, Giulia M. Silva-Vera, Gabriela Bovino, Stefano Molpeceres, German Kästner, Johannes Vogt-Geisse, Stefan Astrophysics of Galaxies Chemical processes taking place on ice-grain mantles are pivotal to the complex chemistry of interstellar environments. In this study, we conducted a comprehensive analysis of the catalytic effects of an amorphous solid water (ASW) surface on the reaction between ammonia (NH$_3$) and formaldehyde (H$_2$CO) to form aminomethanol (NH$_2$CH$_2$OH) using density functional theory. We identified potential catalytic sites based on the binding energy distribution of NH$_3$ and H$_2$CO reactants, on a set-of-clusters surface model composed of 22 water molecules and found a total of 14 reaction paths. Our results indicate that the catalytic sites can be categorized into four groups, depending on the interactions of the carbonyl oxygen and the amino group with the ice surface in the reactant complex. A detailed analysis of the reaction mechanism using Intrinsic Reaction Coordinate and reaction force analysis revealed three distinct chemical events for this reaction: formation of the C--N bond, breaking of the N--H bond, and formation of the O--H hydroxyl bond. Depending on the type of catalytic site, these events can occur within a single, concerted, albeit asynchronous, step, or can be isolated in a step-wise mechanism, with the lowest overall transition state energy observed at 1.3 kcal mol$^{-1}$. A key requirement for the low-energy mechanism is the presence of a pair of dangling OH bonds on the surface, found at 5\% of the potential catalytic sites on an ASW porous surface. |
| title | In-Depth Exploration of Catalytic Sites on Amorphous Solid Water: I. The Astrosynthesis of Aminomethanol |
| topic | Astrophysics of Galaxies |
| url | https://arxiv.org/abs/2407.03493 |