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Carbon Isotope Fractionation of Complex Organic Molecules in Star-Forming Cores

Published 5 Jun 2024 in astro-ph.SR, astro-ph.EP, and astro-ph.GA | (2406.02961v2)

Abstract: Recent high-resolution and sensitivity ALMA observations have unveiled the carbon isotope ratios (${12}$C/${13}$C) of Complex Organic Molecules (COMs) in a low-mass protostellar source. To understand the ${12}$C/${13}$C ratios of COMs, we investigated the carbon isotope fractionation of COMs from prestellar cores to protostellar cores with a gas-grain chemical network model. We confirmed that the ${12}$C/${13}$C ratios of small molecules are bimodal in the prestellar phase: CO and species formed from CO (e.g., CH${3}$OH) are slightly enriched in ${13}$C compared to the local ISM (by $\sim$ 10 $\%$), while those from C and C${+}$ are depleted in ${13}$C owing to isotope exchange reactions. COMs are mainly formed on the grain surface and in the hot gas ($>$ 100 K) in the protostellar phase. The ${12}$C/${13}$C ratios of COMs depend on which molecules the COMs are formed from. In our base model, some COMs in the hot gas are depleted in ${13}$C compared to the observations. Thus, We additionally incorporate reactions between gaseous atomic C and H${2}$O ice or CO ice on the grain surface to form H$_2$CO ice or \ce{C2O} ice, as suggested by recent laboratory studies. The direct C-atom addition reactions open pathways to form \ce{13C}-enriched COMs from atomic C and CO ice. We find that these direct C-atom addition reactions mitigate ${13}$C-depletion of COMs, and the model with the direct C-atom addition reactions better reproduces the observations than our base model. We also discuss the impact of the cosmic ray ionization rate on the ${12}$C/${13}$C ratio of COMs.

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