Anchoring and electro-optical dynamics of thin liquid crystalline films in a polyimide cell: Experiment and theory

Abstract

The surface-dependent anchoring and electro-optical (EO) dynamics of thin liquid crystalline films have been examined using Fourier transform infrared spectroscopy. A simple nematic liquid crystal, 4-n-pentyl-4'-cyanobiphenyl (5CB), is confined as 40, 50, and 390 nm thick films in nanocavities defined by gold interdigitated electrode arrays (IDEAs) patterned on polyimide-coated zinc selenide (ZnSe) substrates [Noble et al., J. Am. Chem. Soc. 124, 15020 (2002)]. New strategies for controlling the anchoring interactions and EO dynamics are explored based on coating a ZnSe surface with an organic polyimide layer in order to both planarize the substrate and induce a planar alignment of the liquid crystalline film. The polyimide layer can be further treated so as to induce a strong alignment of the nematic director along a direction parallel to the electrode digits of the IDEA. Step-scan time-resolved spectroscopy measurements were made to determine the rate constants for the electric-field-induced orientation and thermal relaxation of the 5CB films. In an alternate set of experiments, uncoated ZnSe substrates were polished unidirectionally to produce a grooved surface presenting nanometer-scale corrugations. The dynamical rate constants measured for several nanoscale film thicknesses and equilibrium organizations of the director in these planar alignments show marked sensitivities. The orientation rates are found to vary strongly with both the magnitude of the applied potential and the initial anisotropy of the alignment of the director within the IDEA. The relaxation rates do not vary in this same way. The marked variations seen in EO dynamics can be accounted for by a simple coarse-grained dynamical model.