Characterising the molecular line emission in the asymmetric Oph-IRS 48 dust trap: Temperatures, timescales, and sub-thermal excitation

TL;DR

This study investigates the excitation, temperature, and chemical timescales of molecules in the asymmetric Oph-IRS 48 disk, revealing sub-thermal excitation and molecular layer origins, with no clear vortex influence on temperature structure.

Contribution

It provides detailed temperature and excitation analysis of multiple molecules in the disk, highlighting sub-thermal excitation and molecular layer origins, and assesses the impact of vortex structures.

Findings

SO$_2$ originates from deep disk layers (~55 K)

CH$_3$OH$ and H$_2$CO$ are sub-thermally excited

Photodissociation explains molecular extents

Abstract

The ongoing physical and chemical processes in planet-forming disks set the stage for planet formation. The asymmetric disk around the young star Oph-IRS 48 has one of the most well-characterised chemical inventories, showing molecular emission from a wide variety of species at the dust trap. One of the explanations for the asymmetric structure is dust trapping by a perturbation-induced vortex. We aim to constrain the excitation properties of the molecular species SO$_2$, CH$_3$OH, and H$_2$CO. We further characterise the extent of the molecular emission, through the determination of important physical and chemical timescales at the location of the dust trap. We also investigate whether the potential vortex can influence the observable temperature structure of the gas. Through a pixel-by-pixel rotational diagram analysis, we create rotational temperature and column density maps for SO$_2$ and CH$_3$OH, while temperature maps for H$_2$CO are created using line ratios. We find temperatures of $T\sim$55 K and $T\sim$125 K for SO$_2$ and CH$_3$OH, respectively, while the line ratios point towards temperatures of T$\sim$150-300 K for H$_2$CO. The rotational diagram of CH$_3$OH is dominated by scatter and subsequent non-LTE RADEX calculations suggest that both CH$_3$OH and H$_2$CO must be sub-thermally excited. The temperatures suggest that SO$_2$ comes from a layer deep in the disk, while CH$_3$OH and H$_2$CO originate from a higher layer. While a potential radial gradient is seen in the temperature map of SO$_2$, we do not find any hints of a vortex influencing the temperature structure. The determined turbulent mixing timescale is not able to explain the emitting heights of the molecules, but the photodissociation timescales are able to explain the wider azimuthal extents of SO$_2$ and H$_2$CO compared to CH$_3$OH, where a secondary, gas-phase formation reservoir is required for H$_2$CO.