Context.Recent JWST observations have measured the ice chemical composition towards two highly extinguished background stars, NIR38 and J110621, in the Chamaeleon I molecular cloud. The observed excess of extinction on the long-wavelength side of the H2O ice band at 3 μm has been attributed to a mixture of CH3OH with ammonia hydrates NH3·H2O), which suggests that CH3OH ice in this cloud could have formed in a water-rich environment with little CO depletion. Laboratory experiments and quantum chemical calculations suggest that CH3OH could form via the grain surface reactions CH3+ OH and/or C + H2O in water-rich ices. However, no dedicated chemical modelling has been carried out thus far to test their efficiency. In addition, it remains unexplored how the efficiencies of the proposed mechanisms depend on the astrochemical code employed. Aims.We modelled the ice chemistry in the Chamaeleon I cloud to establish the dominant formation processes of CH3OH, CO, CO2, and of the hydrides CH4and NH3(in addition to H2O). By using a set of state-of-the-art astrochemical codes (MAGICKAL, MONACO, Nautilus, UCLCHEM, and KMC simulations), we can test the effects of the different code architectures (rate equation vs. stochastic codes) and of the assumed ice chemistry (diffusive vs. non-diffusive). Methods.We consider a grid of models with different gas densities, dust temperatures, visual extinctions, and cloud-collapse length scales. In addition to the successive hydrogenation of CO, the codes’ chemical networks have been augmented to include the alternative processes for CH3OH ice formation in water-rich environments (i.e. the reactions CH3+ OH → CH3OH and C + H2O → H2CO). Results.Our models show that the JWST ice observations are better reproduced for gas densities ≥105cm−3and collapse timescales ≥105yr. CH3OH ice formation occurs predominantly (>99%) via CO hydrogenation. The contribution of reactions CH3+ OH and C + H2O is negligible. The CO2ice may form either via CO + OH or CO + O depending on the code. However, KMC simulations reveal that both mechanisms are efficient despite the low rate of the CO + O surface reaction. CH4is largely underproduced for all codes except for UCLCHEM, for which a higher amount of atomic C is available during the translucent cloud phase of the models. Large differences in the predicted abundances are found at very low dust temperatures (Tdust<12 K) between diffusive and non-diffusive chemistry codes. This is due to the fact that non-diffusive chemistry takes over diffusive chemistry at such low Tdust. This could explain the rather constant ice chemical composition found in Chamaeleon I and other dense cores despite the different visual extinctions probed. 
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                            Atomistic mechanisms of water vapor–induced surface passivation
                        
                    
    
            The microscopic mechanisms underpinning the spontaneous surface passivation of metals from ubiquitous water have remained largely elusive. Here, using in situ environmental electron microscopy to atomically monitor the reaction dynamics between aluminum surfaces and water vapor, we provide direct experimental evidence that the surface passivation results in a bilayer oxide film consisting of a crystalline-like Al(OH)3top layer and an inner layer of amorphous Al2O3. The Al(OH)3layer maintains a constant thickness of ~5.0 Å, while the inner Al2O3layer grows at the Al2O3/Al interface to a limiting thickness. On the basis of experimental data and atomistic modeling, we show the tunability of the dissociation pathways of H2O molecules with the Al, Al2O3, and Al(OH)3surface terminations. The fundamental insights may have practical significance for the design of materials and reactions for two seemingly disparate but fundamentally related disciplines of surface passivation and catalytic H2production from water. 
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                            - PAR ID:
- 10535246
- Publisher / Repository:
- Science
- Date Published:
- Journal Name:
- Science Advances
- Volume:
- 9
- Issue:
- 44
- ISSN:
- 2375-2548
- Page Range / eLocation ID:
- edah5565
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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