Abstract
Electro-optic properties of polymer stabilized ferroelectric liquid crystal (PSFLC) systems are examined as a function of varying concentrations of either a linear or crosslinked thiol-ene polymer. The thiol-ene method of polymer stabilization is a drastic change from previous studies designed to avert the problem of polymer phase separation. FLC rise time and tilt angle measurements were used to determine the effects of the polymer network on the optical properties of the system. The addition of monomer impurities to both systems demonstrated a reduction in tilt angle, which translated into decreased switching speeds in both systems prior to polymerization. The crosslinked thiol-ene system showed increased switching times due to the creation of polymer in the interlayer spacing of the FLC, but exhibited minimal increase in the rotational viscosity of the system. In addition, the crosslinked polymer systems resulted in an increase in the liquid crystalline order, which produced an increase in the contrast ratio of the system. The linear polymer system showed drastically different results as compared with the crosslinked system. The rise time and tilt angle measurements decreased upon polymerization of the linear thiol-ene and the rotational viscosity and contrast ratio values also decreased. We suggest that the linear thiol-ene polymer phase separation from the interlayer spacing leads to a microscopic misalignment of the FLC molecules, causing a decrease in the optical properties of the LC.