Abstract
Understanding and control of the surface properties such as molecular orientations are of great importance in numerous applications of ionic liquids. However, there remain discrepancies among the previous experimental and theoretical studies on the surface orientation and structures of room temperature ionic liquids (RTIL) systems. In this article, the orientation of 1-butyl-3-methylimidazolium ([bmin]) cation at the air/liquid interface of a characteristic RTIL, 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]), was investigated by the sum frequency generation vibrational spectroscopy (SFG-VS). Detailed polarization and experimental configuration analyses of the SFG-VS spectra showed the possibility of a small spectral splitting in the CH3 symmetric stretching region, which can be further attributed to the probable existence of multiple orientations for the interfacial [bmim] cations. In addition, the (N)-CH3 vibrations were absent, ruling out the prediction by several recent molecular dynamics simulations which state that portions of the [bmim] cations orient with a standing-up (N)-CH3 group at the ionic liquid surface. Hence, new realistic theoretical models have to be developed to reflect the complex nature of the ionic liquid surface.
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Deng, G., Guo, Y., Li, X. et al. Surface of room temperature ionic liquid [bmim][PF6] studied by polarization- and experimental configuration-dependent sum frequency generation vibrational spectroscopy. Sci. China Chem. 58, 439–447 (2015). https://doi.org/10.1007/s11426-014-5241-5
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DOI: https://doi.org/10.1007/s11426-014-5241-5