Abstract
Ionic liquids have been shown to form extended ordered structures near surfaces and in bulk. Identifying fundamental driving force(s) for this organization has been elusive. In this paper, we test a hypothesis that the ionic liquid asymmetry, inherent in many of the IL formulations to frustrate crystallization, is a significant contributor to the observed ordering. We have carried out measurements to track the ordering of ionic liquids composed of "spherical" cations, namely, tetraoctylphosphonium ([P8888]) and tetra(propoxymethyl)phosphonium [P(3O1)4] paired with tetracyanoborate anion [B(CN)4]. Analysis of the infrared signatures for films of these ionic liquids shows very little evidence of ordered structures. These liquids instead remain in a more isotropic environment even when confined to volumes of few micrometer dimensions.