Dynamics of electron impact ionization of the outer and inner valence (1t2 and 2a1) molecular orbitals of CH4 at intermediate and large ion recoil momentum

• Published in: Journal of physics. B, Atomic, molecular, and optical physics Vol. 42; no. 16; pp. 165201 - 165201 (8)
• Main Authors: Lahmam-Bennani, A, Naja, A, Staicu Casagrande, E M, Okumus, N, Dal Cappello, C, Charpentier, I, Houamer, S
• Format: Journal Article
• Language: English
• Published: Bristol IOP Publishing 28.08.2009; Institute of Physics
• Subjects: Atomic and molecular collision processes and interactions; Atomic and molecular physics; Electron scattering; Exact sciences and technology; Molecular excitation and ionization by electron impact; Physics; Methane; Molecular orbital; Electron impact ionization; Triply differential cross section; Hydrocarbons; Momentum; Electron-molecule collisions; Cross sections; Organic compounds
• ISSN: 0953-4075; 1361-6455
• DOI: 10.1088/0953-4075/42/16/165201

The triply differential cross section has been measured for electron-impact ionization of the outer valence 1t2 and the inner valence 2a1 orbitals of methane using the (e,2e) technique with coplanar asymmetric kinematics. The measurements are performed at scattered electron energy of 500 eV, ejected electron energy of 12, 37 and 74 eV and for scattering angle of the fast outgoing electron of 6 deg. This kinematics is characterized by a target ion recoil momentum ranging from moderate (0.25 au) to very large (3.2 au) values. The results are compared with theoretical cross sections calculated using the 1CW and the BBK models recently extended to molecules. The experimental cross sections exhibit a very large recoil scattering, especially for the inner 2a1 molecular orbital, which is not predicted by the theory. The differences between experiment and theory are attributed to the very strong scattering from the ion, not properly accounted for by theory. This indicates the need for further theoretical developments as well as experimental investigations in order to correctly model the process of molecular ionization.