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

Ryota Ichimura, Hideko Nomura, Kenji Furuya

Published 2024-06-05Version 1

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.