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Christine Joblin

Publications and source records attributed to Christine Joblin.

47 records · Page 3Linked to original sources

Laboratory Photo-chemistry of PAHs: Ionization versus Fragmentation

Interstellar polycyclic aromatic hydrocarbons (PAHs) are expected to be strongly processed by vacuum ultraviolet photons. Here, we report experimental studies on the ionization and fragmentation of coronene (C24H12), ovalene (C32H14) and hexa-peri-hexabenzocoronene (HBC; C42H18) cations by exposure to synchrotron radiation in the range of 8--40 eV. The results show that for small PAH cations such as coronene, fragmentation (H-loss) is more important than ionization. However, as the size increases, ionization becomes more and more important and for the HBC cation, ionization dominates. These results are discussed and it is concluded that, for large PAHs, fragmentation only becomes important when the photon energy has reached the highest ionization potential accessible. This implies that PAHs are even more photo-stable than previously thought. The implications of this experimental study for the photo-chemical evolution of PAHs in the interstellar medium are briefly discussed.

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Absolute evaporation rates of non-rotating neutral PAH clusters

Clusters of polycyclic aromatic hydrocarbons (PAHs) have been proposed as candidates for evaporating very small grains, which are thought to be precursors of free-flying PAHs. Evaporation rates have been calculated so far only for species containing up to a few 100 C atoms, whereas interstellar PAH clusters could contain up to ~1000 C atoms. We present a method that generalises the calculation of the statistical evaporation rate of large PAH clusters and provides rates for species containing up to ~1000 C-atoms. The evaporation of non-rotating neutral homo-molecular PAH clusters containing up to 12 molecules from a family of highly symmetric compact PAHs is studied. Statistical calculations were performed and completed with molecular dynamics simulations at high internal energies to provide absolute values for the evaporation rate and distributions of kinetic energy released. The calculations used explicit atom-atom Lennard-Jones potentials in the rigid molecule approximation. A new method is proposed to take both inter- and intra-molecular vibrations into account. Without any parameter adjustment, the calculated evaporation rates agree well with available experimental data. We find that the non-rotation assumption has a limited impact on the evaporation rates. The photostability of PAH clusters increases dramatically with the size of molecules in the clusters, and to a lesser extent with the number of molecules in the clusters. For values of the UV radiation field that are typical of the regions where evaporating very small grains are observed, the smallest clusters in this study (~50 C-atoms) are found to be quickly photo-evaporated, whereas the largest clusters (~1000 C-atoms) are photostable. Our results support the idea that large PAH clusters are good candidates for evaporating very small grains.

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Detection of the buckminsterfullerene cation (C60+) in space

In the early 90s, C60+ was proposed as the carrier of two diffuse interstellar bands (DIBs) at 957.7 and 963.2 nm, but a firm identification still awaits gas-phase spectroscopic data. Neutral C60, on the other hand, was recently detected through its infrared emission bands in the interstellar medium and evolved stars. In this contribution, we present the detection of C60+ through its infrared vibrational bands in the NGC 7023 nebula, based on spectroscopic observations with the Spitzer space telescope, quantum chemistry calculation, and laboratory data from the literature. This detection supports the idea that C60+ could be a DIB carrier, and provides robust evidence that fullerenes exist in the gas-phase in the interstellar medium. Modeling efforts to design specific observations, combined with new gas-phase data, will be essential to confirm this proposal. A definitive attribution of the 957.7 and 963.2 nm DIBs to C60+ would represent a significant step forward in the field.

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

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)

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Interstellar C60+

Buckminsterfullerene (C60) was recently detected through its infrared emission bands in the interstellar medium (ISM), including in the proximity of massive stars, where physical conditions could favor the formation of the cationic form, C60+. In addition, C60+ was proposed as the carrier of two diffuse interstellar bands in the near-IR, although a firm identification still awaits for gas-phase spectroscopic data. We examined in details the Spitzer IRS spectra of the NGC 7023 reflection nebula, at a position close (7.5") to the illuminating B star HD 200775, and found four previously unreported bands at 6.4, 7.1, 8.2 and 10.5 μm in addition to the classical bands attributed to Polycylic Aromatic Hydrocarbons (PAHs) and neutral C60. These 4 bands are observed only in this region of the nebula, while C60 emission is still present slightly further away from the star, and PAH emission even further away. Based on this observation, on theoretical calculations we perform, and on laboratory studies, we attribute these bands to C60+. The detection of C60+ confirms the idea that large carbon molecules exist in the gas-phase in these environments. In addition, the relative variation of the C60, and C60+, band intensities constitutes a potentially powerful probe of the physical conditions in highly UV-irradiated regions.

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Blind decomposition of Herschel-HIFI spectral maps of the NGC 7023 nebula

Large spatial-spectral surveys are more and more common in astronomy. This calls for the need of new methods to analyze such mega- to giga-pixel data-cubes. In this paper we present a method to decompose such observations into a limited and comprehensive set of components. The original data can then be interpreted in terms of linear combinations of these components. The method uses non-negative matrix factorization (NMF) to extract latent spectral end-members in the data. The number of needed end-members is estimated based on the level of noise in the data. A Monte-Carlo scheme is adopted to estimate the optimal end-members, and their standard deviations. Finally, the maps of linear coefficients are reconstructed using non-negative least squares. We apply this method to a set of hyperspectral data of the NGC 7023 nebula, obtained recently with the HIFI instrument onboard the Herschel space observatory, and provide a first interpretation of the results in terms of 3-dimensional dynamical structure of the region.

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Excitation of H$_2$ in photodissociation regions as seen by Spitzer

We present spectroscopic observations obtained with the infrared Spitzer Space Telescope, which provide insight into the H$_2$ physics and gas energetics in photodissociation Regions (PDRs) of low to moderate far-ultraviolet (FUV) fields and densities. We analyze data on six well known Galactic PDRs (L1721, California, N7023E, Horsehead, rho Oph, N2023N), sampling a poorly explored range of excitation conditions ($χ\sim 5-10^3$), relevant to the bulk of molecular clouds in galaxies. Spitzer observations of H$_2$ rotational lines are complemented with H$_2$ data, including ro-vibrational line measurements, obtained with ground-based telescopes and ISO, to constrain the relative contributions of ultraviolet pumping and collisions to the H$_2$ excitation. The data analysis is supported by model calculations with the Meudon PDR code. The observed column densities of rotationally excited H$_2$ are observed to be much higher than PDR model predictions. In the lowest excitation PDRs, the discrepancy between the model and the data is about one order of magnitude for rotational levels $J \ge $3. We discuss whether an enhancement in the H$_2$ formation rate or a local increase in photoelectric heating, as proposed for brighter PDRs in former ISO studies, may improve the data-model comparison. We find that an enhancement in the H$_2$ formation rates reduces the discrepancy, but the models still fall short of the data. This large disagreement suggests that our understanding of the formation and excitation of H$_2$ and/or of PDRs energetics is still incomplete. We discuss several explanations, which could be further tested using the Herschel Space Telescope

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C$_{60}$ in Reflection Nebulae

The fullerene C$_{60}$ has four infrared-active vibrational transitions at 7.0, 8.5, 17.4 and 18.9 $μ$m. We have previously observed emission features at 17.4 and 18.9 $μ$m in the reflection nebula NGC 7023 and demonstrated spatial correlations suggestive of a common origin. We now confirm our earlier identification of these features with C$_{60}$ by detecting a third emission feature at 7.04 $\pm$ 0.05 $μ$m in NGC 7023. We also report the detection of these three C$_{60}$ features in the reflection nebula NGC 2023. Our spectroscopic mapping of NGC 7023 shows that the 18.9 $μ$m C$_{60}$ feature peaks on the central star and that the 16.4 $μ$m emission feature due to polycyclic aromatic hydrocarbons peaks between the star and a nearby photodissociation front. The observed features in NGC 7023 are consistent with emission from UV-excited gas-phase C$_{60}$. We find that 0.1-0.6% of interstellar carbon is in C$_{60}$; this abundance is consistent with those from previous upper limits and possible fullerene detections in the interstellar medium. This is the first firm detection of neutral C$_{60}$ in the interstellar medium.

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Interstellar OH+, H2O+ and H3O+ along the sight-line to G10.6-0.4

We report the detection of absorption lines by the reactive ions OH+, H2O+ and H3O+ along the line of sight to the submillimeter continuum source G10.6$-$0.4 (W31C). We used the Herschel HIFI instrument in dual beam switch mode to observe the ground state rotational transitions of OH+ at 971 GHz, H2O+ at 1115 and 607 GHz, and H3O+ at 984 GHz. The resultant spectra show deep absorption over a broad velocity range that originates in the interstellar matter along the line of sight to G10.6$-$0.4 as well as in the molecular gas directly associated with that source. The OH+ spectrum reaches saturation over most velocities corresponding to the foreground gas, while the opacity of the H2O+ lines remains lower than 1 in the same velocity range, and the H3O+ line shows only weak absorption. For LSR velocities between 7 and 50 kms$^{-1}$ we estimate total column densities of $N$(OH+) $> 2.5 \times 10^{14}$ cm$^{-2}$, $N$(H2O+) $\sim 6 \times 10^{13}$ cm$^{-2}$ and $N$(H3O+) $\sim 4.0 \times 10^{13}$ cm$^{-2}$. These detections confirm the role of O$^+$ and OH$^+$ in initiating the oxygen chemistry in diffuse molecular gas and strengthen our understanding of the gas phase production of water. The high ratio of the OH+ by the H2O+ column density implies that these species predominantly trace low-density gas with a small fraction of hydrogen in molecular form.

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Star Formation Near Photodissociation Regions: Detection of a Peculiar Protostar Near Ced 201

We present the detection and characterization of a peculiar low-mass protostar (IRAS 22129+7000) located ~0.4 pc from Ced 201 Photodissociation Region (PDR) and ~0.2 pc from the HH450 jet. The cold circumstellar envelope surrounding the object has been mapped through its 1.2 mm dust continuum emission with IRAM-30m/MAMBO. The deeply embedded protostar is clearly detected with Spitzer/MIPS (70 um), IRS (20-35 um) and IRAC (4.5, 5.8, and 8 um) but also in the K_s band (2.15 um). Given the large "near- and mid-IR excess" in its spectral energy distribution, but large submillimeter-to-bolometric luminosity ratio (~2%), IRAS 22129+7000 must be a transition Class 0/I source and/or a multiple stellar system. Targeted observations of several molecular lines from CO, 13CO, C18O, HCO+ and DCO+ have been obtained. The presence of a collimated molecular outflow mapped with the CSO telescope in the CO J=3-2 line suggests that the protostar/disk system is still accreting material from its natal envelope. Indeed, optically thick line profiles from high density tracers such as HCO+ J=1-0 show a red-shifted-absorption asymmetry reminiscent of inward motions. We construct a preliminary physical model of the circumstellar envelope (including radial density and temperature gradients, velocity field and turbulence) that reproduces the observed line profiles and estimates the ionization fraction. The presence of both mechanical and (non-ionizing) FUV-radiative input makes the region an interesting case to study triggered star formation.

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Blind Signal Separation Methods for the Identification of Interstellar Carbonaceous Nanoparticles

The use of Blind Signal Separation methods (ICA and other approaches) for the analysis of astrophysical data remains quite unexplored. In this paper, we present a new approach for analyzing the infrared emission spectra of interstellar dust, obtained with NASA's Spitzer Space Telescope, using FastICA and Non-negative Matrix Factorization (NMF). Using these two methods, we were able to unveil the source spectra of three different types of carbonaceous nanoparticles present in interstellar space. These spectra can then constitute a basis for the interpretation of the mid-infrared emission spectra of interstellar dust in the Milky Way and nearby galaxies. We also show how to use these extracted spectra to derive the spatial distribution of these nanoparticles.

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