Publications by authors named "Guillaume Thiam"

Reaction induced by slow electrons is implicated in a large field of research and applications. Below 3-4 eV, dissociative electron attachment efficiently fragments molecules via (1) shape resonance or (2) mediated by the formation of a dipole bound anion. While the temperature dependence of process 1 is well-known, that of 2 is not clearly established.

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Benzonitrile (BZN) and carbon tetrachloride (CCl) are versatile solvents used as a precursor for the synthesis of many products. As multi-usage molecules, these compounds may be involved in sustainable chemistry processes such as the cold plasma techniques for which the generated electrons are known to be responsible for reactions. Therefore, it is desirable to explore the interaction of low energy electrons with the co-compounds in the gas phase.

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Weakly bound non-valence anions are molecular systems where the excess electron stabilizes in a very diffuse orbital whose size, shape, and binding energy (∼1-100 meV) are governed by the long-range electrostatic potential of the molecule. Its binding energy comes mainly from charge-dipole or charge-multipole interactions or dispersion forces. While highly correlated methods, like coupled cluster methods, are considered to be the state of the art for describing anionic systems, especially when the electron lies in a very diffuse orbital, we consider here the possibility to use DFT-based calculations.

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The interaction of low-energy electron collisions with molecules may lead to temporary anions via resonant processes. While experimental measurements, e.g.

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In this contribution the dissociative electron attachment to metabolites found in aerobic organisms, namely oxaloacetic and citric acids, was studied both experimentally by means of a crossed-beam setup and theoretically through density functional theory calculations. Prominent negative ion resonances from both compounds are observed peaking below 0.5 eV resulting in intense formation of fragment anions associated with a decomposition of the carboxyl groups.

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