Stereodynamics at the Gas−Liquid Interface: Orientation and Alignment of CO2 Scattered from Perfluorinated Liquid Surfaces
journal contributionposted on 28.01.2010, 00:00 by Bradford G. Perkins, David J. Nesbitt
Rotational orientation/alignment dynamics of CO2 scattered from a perfluorinated polyether (PFPE) liquid surface has been investigated via direct absorption experimental studies and theoretical molecular dynamics (MD) simulations. Experimentally, polarization modulation of a single mode diode laser is combined with lock-in detection to measure circular/linear IR polarizance due to CO2 scattering from the surface at θinc = 60° and Einc = 10.6(8) kcal/mol and probed over a series of final scattering angles. The differential absorption intensities are related through Fano−Macek theory to the three lowest multipole moments (A0, A2+, and O1−) which describe collisionally induced orientation and alignment at the liquid surface. The total scattering population reflects both trapping-desorption (TD) and impulsive scattering (IS) components, with a strong positive anisotropy in the MJ distribution that indicates preferential CO2 scattering from the surface with a forward (i.e., “topspin”) sense of end-over-end tumbling. Theoretical trajectory simulations provide 3D CO2 flux and J state distributions scattering from fluorinated self-assembled monolayers (F-SAMs) and are compared with experimental results as a function of final rotational state. Specifically, trends in the theoretical orientation/alignment moments are in remarkable agreement over the full range of J states but with values consistently overpredicted by nearly 2-fold, which may reflect a higher level of local ordering for F-SAMS vs a gas−PFPE liquid interface.