Probing the role of polycyclic aromatic hydrocarbons in the photoelectric heating within photodissociation regions

Abstract

We observationally investigate the relation between the photoelectric heating efficiency in PDRs and the charge of PAHs, which are considered to play a key role in photoelectric heating. Using PACS onboard Herschel, we observed six PDRs spanning a wide range of FUV radiation fields (G_0=100-10^5). To measure the photoelectric heating efficiency, we obtained the intensities of the main cooling lines, i.e., the [OI]63um, 145um, and [CII]158um, as well as the FIR continuum intensity. We used Spitzer/IRS spectroscopic mapping observations to investigate the MIR PAH features in the same regions. We decomposed the MIR PAH emission into that of neutral (PAH^0) and positively ionized (PAH^+) species to derive the fraction of the positively charged PAHs, and compare it to the photoelectric heating efficiency. The heating efficiency traced by ([OI]63um+[OI]145um+[CII]158um) / TIR, ranges between 0.1% and 0.9% in different sources, and the fraction of PAH^+ relative to (PAH^0 + PAH^+) spans from 0(+11)% to 87(+/-10)%. All positions with a high PAH^+ fraction show a low heating efficiency, and all positions with a high heating efficiency have a low PAH^+ fraction, supporting the scenario in which a positive grain charge results in a decreased heating efficiency. Theoretical estimates of the photoelectric heating efficiency show a stronger dependence on the charging parameter gamma=G_0 T^{1/2}/n_e than the observed efficiency reported in this study, and the discrepancy is significant at low gamma. The photoelectric heating efficiency on PAHs, traced by ([OI]63um+[OI]145um+[CII]158um) / (PAH+[OI]63um+[OI]145um+[CII]158um), shows a much better match between the observations and the theoretical estimates. The good agreement of the photoelectric heating efficiency on PAHs with a theoretical model indicates the dominant contribution of PAHs to the photoelectric heating. (abridged for arXiv)