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Register a new userMolecular ion abundances in the diffuse ISM : CF+, HCO+, HOC+, and C3H+
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The transition between atomic and molecular hydrogen is associated with important changes in the structure of interstellar clouds, and marks the beginning of interstellar chemistry. Because of the relatively simple networks controlling their abundances, molecular ions are usually good probes of the underlying physical conditions including for instance the fraction of gas in molecular form or the fractional ionization. In this paper we focus on three possible probes of the molecular hydrogen column density, HCO+, HOC+, and CF+. We presented high sensitivity ALMA absorption data toward a sample of compact HII regions and bright QSOs with prominent foreground absorption, in the ground state transitions of the molecular ions HCO+, HOC+, and CF+ and the neutral species HCN and HNC, and from the excited state transitions of C3H+(4-3) and 13CS(2-1). These data are compared with Herschel absorption spectra of the ground state transition of HF and p-H2O. We show that the HCO+, HOC+, and CF+ column densities are well correlated with each other. HCO+ and HOC+ are tightly correlated with p-H2O, while they exhibit a different correlation pattern with HF depending on whether the absorbing matter is located in the Galactic disk or in the central molecular zone. We report new detections of C3H+ confirming that this ion is ubiquitous in the diffuse matter, with an abundance relative to H2 of ~7E-11. We confirm that the CF+ abundance is lower than predicted by simple chemical models and propose that the rate of the main formation reaction is lower by a factor of about 3 than usually assumed. In the absence of CH or HF data, we recommend to use the ground state transitions of HCO+, CCH, and HOC+ to trace diffuse molecular hydrogen, with mean abundances relative to H2 of 3E-9, 4E-8 and 4E-11.
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This paper assesses the roles of the presence of warm H2, and the increased formation rate due to the ion-neutral drift. We performed ideal MHD simulations that include the heating and cooling of the multiphase ISM, and where we treat dynamically the formation of H2. In a post-processing step we compute the abundances of species at chemical equilibrium. We show that CH+ is efficiently formed at the edge of clumps, in regions where the H2 fraction is low, but nevertheless higher than its equilibrium value, and where the gas temperature is high. We show that warm and out of equilibrium H2 increases the integrated column densities of CH+ by one order of magnitude, up to values still 3-10 times lower than those observed in the diffuse ISM. We balance the Lorentz force with the ion-neutral drag to estimate the ion-drift velocities (vd). We find that the vd distribution peaks around 0.04 km s-1, and that high vd are too rare to have a significant statistical impact on the abundances of CH+. Compared to previous works, our multiphase simulations reduce the spread in vd, and our self-consistent treatment of the ionisation leads to much reduced vd. Nevertheless, our resolution study shows that this velocity distribution is not converged: the ion-neutral drift has a higher impact on CH+ at higher resolution. On the other hand, our ideal MHD simulations do not include ambipolar diffusion, which would yield lower drift velocities. Within these limitations, we conclude that warm H2 is a key ingredient in the efficient formation of CH+ and that the ambipolar diffusion has very little influence on the abundance of CH+, mainly due to the small drift velocities obtained. However, we point out that small-scale processes and other non-thermal processes not included in our MHD simulation may be of crucial importance, and higher resolution studies with better controlled dissipation processes are needed.
Molecular abundances are sensitive to UV-photon flux and cosmic-ray ionization rate. In starburst environments, the effects of high-energy photons and particles are expected to be stronger. We examine these astrochemical signatures through multiple transitions of HCO$^+$ and its metastable isomer HOC$^+$ in the center of the starburst galaxy NGC 253 using data from the ALMA large program ALCHEMI. The distribution of the HOC$^+$(1-0) integrated intensity shows its association with superbubbles, cavities created either by supernovae or expanding HII regions. The observed HCO$^+$/HOC$^+$ abundance ratios are $sim 10-150$, and the fractional abundance of HOC$^+$ relative to H$_2$ is $sim 1.5times 10^{-11} - 6times 10^{-10}$, which implies that the HOC$^+$ abundance in the center of NGC 253 is significantly higher than in quiescent spiral-arm dark clouds in the Galaxy and the Galactic center clouds. Comparison with chemical models implies either an interstellar radiation field of $G_0gtrsim 10^3$ if the maximum visual extinction is $gtrsim 5$, or a cosmic-ray ionization rate of $zeta gtrsim 10^{-14}$ s$^{-1}$ (3-4 orders of magnitude higher than that within clouds in the Galactic spiral-arms) to reproduce the observed results. From the difference in formation routes of HOC$^+$, we propose that a low-excitation line of HOC$^+$ traces cosmic-ray dominated regions, while high-excitation lines trace photodissociation regions. Our results suggest that the interstellar medium in the center of NGC 253 is significantly affected by energy input from UV-photons and cosmic rays, sources of energy feedback.
We study the behavior of eight diffuse interstellar bands (DIBs) in different interstellar environments, as characterized by the fraction of hydrogen in molecular form [$f$(H$_2$)], with comparisons to the corresponding behavior of various known atomic and molecular species. The equivalent widths of the five normal DIBs ($lambdalambda$5780.5, 5797.1, 6196.0, 6283.8, and 6613.6), normalized to $E(B-V)$, show a Lambda-shaped behavior: they increase at low $f$(H$_2$), peak at $f$(H$_2$) ~ 0.3, and then decrease. The similarly normalized column densities of Ca, Ca$^+$, Ti$^+$, and CH$^+$ also decline for $f$(H$_2$) > 0.3. In contrast, the normalized column densities of Na, K, CH, CN, and CO increase monotonically with $f$(H$_2$), and the trends exhibited by the three C$_2$ DIBs ($lambdalambda$4726.8, 4963.9, and 4984.8) lie between those two general behaviors. These trends with $f$(H$_2$) are accompanied by cosmic scatter, the dispersion at any given $f$(H$_2$) being significantly larger than the individual errors of measurement. The Lambda-shaped trends suggest the balance between creation and destruction of the DIB carriers differs dramatically between diffuse atomic and diffuse molecular clouds; additional processes besides ionization and shielding are needed to explain those observed trends. Except for several special cases, the highest $W$(5780)/$W$(5797) ratios, characterizing the so-called sigma-zeta effect, occur only at $f$(H$_2$) < 0.2. We propose a sequence of DIBs based on trends in their pair-wise strength ratios with increasing $f$(H$_2$). In order of increasing environmental density, we find the $lambda$6283.8 and $lambda$5780.5 DIBs, the $lambda$6196.0 DIB, the $lambda$6613.6 DIB, the $lambda$5797.1 DIB, and the C$_2$ DIBs.
We present recent UV laboratory spectra of various polycyclic aromatic hydrocarbons (PAHs) and explore the potential of these molecules as carriers of the DIBs. From a detailed comparison of gas-phase and Ne-matrix absorption spectra of anthracene, phenanthrene, pyrene, 2,3-benzofluorene, benzo[ghi]perylene, and hexabenzocoronene with new interstellar spectra, we infer upper limits in the abundance of these PAHs in the interstellar medium. Upper limits in the column densities of anthracene of $0.8 - 2.8 times 10^{12}$ cm$^{-2}$ and of pyrene and 2,3-benzofluorene ranging from $2 - 8 times 10^{12}$ cm$^{-2}$ are inferred. Upper limits in the column densities of benzo[ghi]perylene are $0.9 - 2.4 times 10^{13}$ and $10^{14}$ cm$^{-2}$ for phenanthrene. The measurements indicate fractional abundances of anthracene, pyrene, and 2,3-benzofluorene of a few times $10^{-10}$. Upper limits in the fractional abundance of benzo[ghi]perylene of a few times $10^{-9}$ and of phenanthrene of few times $10^{-8}$ are inferred. {Toward CPD $-32^circ 1734$, we found near 3584 {AA} an absorption line of OH$^+$, which was discovered in the interstellar medium only very recently. The fractional abundances of PAHs inferred here are up to two orders of magnitude lower than estimated total PAH abundances in the interstellar medium. This indicates that either neutral PAHs are not abundant in translucent molecular clouds, or that a PAH population with a large variety of molecules is present.
Near ultraviolet observations of OH+ and OH in diffuse molecular clouds reveal a preference for different environments. The dominant absorption feature in OH+ arises from a main component seen in CH+ (that with the highest CH+/CH column density ratio), while OH follows CN absorption. This distinction provides new constraints on OH chemistry in these clouds. Since CH+ detections favor low-density gas with small fractions of molecular hydrogen, this must be true for OH+ as well, confirming OH+ and H2O+ observations with the Herschel Space Telescope. Our observed correspondence indicates that the cosmic ray ionization rate derived from these measurements pertains to mainly atomic gas. The association of OH absorption with gas rich in CN is attributed to the need for high enough density and molecular fraction before detectable amounts are seen. Thus, while OH+ leads to OH production, chemical arguments suggest that their abundances are controlled by different sets of conditions and that they coexist with different sets of observed species. Of particular note is that non-thermal chemistry appears to play a limited role in the synthesis of OH in diffuse molecular clouds.
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