Electron and positron scattering from 1,1-C₂H₂F₂

Abstract

1,1-difluoroethylene (1,1-C₂H₂F₂) molecules have been studied for the first time experimentally and theoretically by electron and positron impact. 0.4-1000 eV electron and 0.2-1000 eV positron impact total cross sections (TCSs) were measured using a retarding potential time-of-flight apparatus. In order to probe the resonances observed in the electron TCSs, a crossed-beam method was used to investigate vibrational excitation cross sections over the energy range of 1.3-49 eV and scattering angles 90 degrees and 120 degrees for the two loss energies 0.115 and 0.381 eV corresponding to the dominant C-H (ν₂ and ν₉) stretching and the combined C-F (ν₃) stretching and CH₂ (ν₁₁) rocking vibrations, respectively. Electron impact elastic integral cross sections are also reported for calculations carried out using the Schwinger multichannel method with pseudopotentials for the energy range from 0.5 to 50 eV in the static-exchange approximation and from 0.5 to 20 eV in the static-exchange plus polarization approximation. Resonance peaks observed centered at about 2.3, 6.5, and 16 eV in the TCSs have been shown to be mainly due to the vibrational and elastic channels, and assigned to the B₂, B₁, and A₁ symmetries, respectively. The pi* resonance peak at 1.8 eV in C₂H₄ is observed shifted to 2.3 eV in 1,1-C₂H₂F₂ and to 2.5 eV in C₂F₄; a phenomenon attributed to the decreasing C=C bond length from C₂H₄ to C₂F₄. For positron impact a conspicuous peak is observed below the positronium formation threshold at about 1 eV, and other less pronounced ones centered at about 5 and 20 eV. Show more