The Effects of Doubly Ionized Chemistry on SH+ and S^+2 Abundances in X-ray Dominated Regions
N. P. Abel, S. R. Federman, P. C. Stancil

TL;DR
This study investigates how doubly ionized sulfur chemistry influences the formation and destruction of SH+ and S^+2 in X-ray dominated regions, revealing significant increases in SH+ abundance and implications for astrophysical diagnostics.
Contribution
It introduces the impact of increased S^+2 + H2 reaction rates on sulfur chemistry in XDRs, highlighting the dominant pathway to SH+ formation and its observational consequences.
Findings
SH+ column density can increase by up to 2 dex near AGNs.
Doubly ionized sulfur chemistry can dominate SH+ formation if the branching ratio exceeds a few percent.
High S^+2 + H2 reaction rates lead to efficient destruction of S^+2 in molecular regions.
Abstract
Recent laboratory measurements for the S^+2 + H2 reaction find a total rate coefficient significantly larger than previously used in theoretical models of X-ray dominated regions (XDRs). While the branching ratio of the products is unknown, one energetically possible route leads to the SH+ molecule, a known XDR diagnostic. In this work, we study the effects of S^+2 on the formation of SH+ and the destruction of S^+2 in XDRs. We find the predicted SH+ column density for molecular gas surrounding an Active Galactic Nucleus (AGN) increases by as much as 2 dex. As long as the branching ratio for S^+2 + H2 -> SH+ + H+ exceeds a few percent, doubly ionized chemistry will be the dominant pathway to SH+, which then initiates the formation of other sulfur-bearing molecules. We also find that the high rate of S^+2 + H2 efficiently destroys S^+2 once H2 forms, while the S^+2 abundance remains high…
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