Dissociative Electron Attachment to Polyatomic Molecules - I : Water

Details Dissociative Electron Attachment to Polyatomic Molecules - I : Water Dissociative Electron Attachment to Polyatomic Molecules - I : Water

2010-07-29

arxiv.org/abs/1007.5144v1

Physics

Chemical Physics

40 pages, 14 figures, More detailed version of the journal paper - J. Phys. B : At. Mol. Opt. Phys. 42, 225203 (2009)

Scientific paper

Using the velocity map imaging technique, we studied and characterized the process of Dissociative Electron Attachment (DEA) in polyatomic molecules like Water, Hydrogen Sulphide, Ammonia, Methane, Formic Acid and Propyl Amine. We present the details of these studies in a series of 5 articles. In the first article here, we discuss the DEA process in gas phase water ($H_{2}O$ and $D_{2}O$) molecules. Electrons of 6.5 eV, 8.5 eV and 12 eV are captured by water molecules in neutral ground state to form $H_{2}O^{-*}$ ($D_{2}O^{-*}$) resonant states which dissociate into an anion fragment and one or more neutrals. Kinetic energy and angular distributions of the fragment anions $H^{-}$($D^{-}$) and $O^{-}$ produced from the three negative ion resonant states in the entire $2\pi$ scattering range are obtained. Unique angular distribution patterns are observed at the 8.5 eV and 11.8 eV resonances showing dissociation dynamics beyond the axial recoil approximation.

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