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Bérenger Gans

Publications and source records attributed to Bérenger Gans.

4 recordsLinked to original sources

Angle-resolved photoelectron spectroscopy of the DABCO molecule probed with VUV radiation

We report a study of the diazabicyclo[2.2.2]octane (DABCO) molecule photoionized using VUV synchrotron radiation in combination with an ion--electron coincidence spectrometer. We determine accurately the adiabatic ionization energy to $7.199\pm0.006$~eV. Two vibrational progressions of DABCO cation ground state are resolved at $847~\text{cm}^{-1}\pm27~\text{cm}^{-1}$ and $1257~\text{cm}^{-1}\pm67~\text{cm}^{-1}$, which we assign to modes of $e'$ symmetry. Analysis of the photoelectron angular distribution shows that the anisotropy parameter depends on the vibrational excitation. This dependence of the $β$ parameter with the vibrational excitation is attributed to the scattering of the outgoing wavefunction mediated by high-lying Rydberg states.

physics.atom-ph↗

PDRs4All XI. Detection of infrared CH$^+$ and CH$_3^+$ rovibrational emission in the Orion Bar and disk d203-506: evidence of chemical pumping

The methylidyne cation (CH$^+$) and the methyl cation (CH$_3^+$) are building blocks of organic molecules, yet their coupled formation and excitation mechanisms remain mainly unprobed. The James Webb Space Telescope (JWST), with its high spatial resolution and good spectral resolution, provides unique access to the detection of these molecules. Our goal is to use the first detection of CH$^+$ and CH$_3^+$ rovibrational emission in the Orion Bar and in the protoplanetary disk d203-506, irradiated by the Trapezium cluster, to probe their formation and excitation mechanisms and constrain the physico-chemical conditions. We use spectro-imaging acquired using both the NIRSpec and MIRI-MRS instruments to study the CH$^+$ and CH$_3^+$ spatial distribution at very small scales, and compare it to excited H$_2$ emission. CH$^+$ and CH$_3^+$ emissions originate from the same region as highly excited H$_2$. Our comparison between the Bar and d203-506 reveals that both CH$^+$ and CH$_3^+$ excitation and/or formation are highly dependent on gas density. The excitation temperature of the observed CH$^+$ and CH$_3^+$ rovibrational lines is around $T$ ~ 1500 K in the Bar and $T$ ~ 800 K in d203-506. Moreover, the column densities derived from the rovibrational emission are less than 0.1 % of the total known (CH$^+$) and expected (CH$_3^+$) column densities. These results show that CH$^+$ and CH$_3^+$ level populations strongly deviate from ETL. CH$^+$ rovibrational emission can be explained by chemical formation pumping with excited H$_2$ via C$^+$ + H$_2^*$ = CH$^+$ + H. These results support a gas phase formation pathway of CH$^+$ and CH$_3^+$ via successive hydrogen abstraction reactions. However, we do not find any evidence of CH$_2^+$ emission in the JWST spectrum. Finally, observed CH$^+$ intensities coupled with chemical formation pumping model provide a diagnostic tool to trace the local density.

astro-ph.GA↗

Formation of the Methyl Cation by Photochemistry in a Protoplanetary Disk

Forty years ago it was proposed that gas phase organic chemistry in the interstellar medium was initiated by the methyl cation CH3+, but hitherto it has not been observed outside the Solar System. Alternative routes involving processes on grain surfaces have been invoked. Here we report JWST observations of CH3+ in a protoplanetary disk in the Orion star forming region. We find that gas-phase organic chemistry is activated by UV irradiation.

astro-ph.GA↗

High-resolution photoelectron-spectroscopic investigation of the H$_2$O$^+$ cation in its ${\mathrm {\tilde A^+}}$ electronic state

The photoelectron spectrum of water has been recorded in the vicinity of the ${\mathrm {\tilde A^+}}$ $\leftarrow$ $\tilde{\mathrm{X}}$ transition between 112 000 and 116 000 cm$^{-1}$ (13.89-14.38 eV). The high-resolution allowed the observation of the rotational structure of several bands. Rotational assignments of the transitions involving the $Π(080)$, $Σ(070)$ and $Π(060)$ vibronic states of the $\tilde{\mathrm{A}}^+$ electronic state are deduced from previous studies of the $\tilde{\mathrm{A}}^+ - \tilde{\mathrm{X}}^+$ band system of H$_2$O$^+$ (Lew, Can. J. Phys. 54, 2028 (1976) and Huet et al., J. Chem. Phys. 107, 5645 (1997)) and photoionization selection rules. The transition to the $Σ(030)$ vibronic state is tentatively assigned.

physics.chem-ph↗