The interaction of free cationic silicon oxide clusters, Si O ( = 2-5, ≥ ), with dilute water vapor, was investigated in a flow tube reactor. Product mass distributions indicate cluster size-dependent dissociative water adsorption. To probe the structure and vibrational spectra of the resulting Si O H ( = 2-4) clusters, we employed infrared multiple photon dissociation spectroscopy and density functional theory calculations. The planar rhombic cluster core of the disilicon oxides ( = 2) appears to be retained upon dissociative adsorption of one HO unit, whereas a significant structural transformation of the tri- and tetra-silicon oxides ( = 3 and 4) is induced, resulting in an increased coordination of the Si atoms and more 3D cluster structures. In an astronomical context, we discuss the potential relevance of Si O H clusters as seeds for dust nucleation and catalysts for carbon-based chemistry in diffuse or translucent interstellar clouds, where all the necessary conditions for producing these species are found. In the produced clusters, the frequency of the isolated silanol Si-OH stretching vibrational mode is considerably blue-shifted compared to that in hydroxylated bulk silica and small inorganic compounds. This mode has a characteristic frequency range between 1200 cm (8.3 μm) and 1090 cm (9.2 μm) and is associated with the anomalously small Si-OH bond lengths in these ionised species. In infrared observations such high frequency Si-O stretching modes are usually associated with a pure bulk silica component of silicate cosmic dust. The presence of Si O H clusters in low silica astrophysical environments could thus potentially be detected via their signature Si-O band using the James Webb space telescope.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11194846 | PMC |
http://dx.doi.org/10.1021/acsearthspacechem.3c00346 | DOI Listing |
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