The light scattering and electro-optic response of new material with display potential are investigated. The materials consist of microdroplets of nematic liquid crystals which are spontaneously formed in a solid polymer at the time of its polymerization. Droplet size, spacing, and distribution are readily controlled in these materials to allow optimization of displays based upon electrically controlled light scattering from the liquid crystal droplets. Preliminary experimental and theoretical studies of the light scattering properties show these materials to offer new features suitable for many display applications.

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Polymer-dispersed liquid crystal (PDLC) films are potentially useful in applications requiring electrically controllable light transmission. In these applications, both a high on-state transmittance and a strong off-state attenuation are often needed over a wide operating temperature range. These transmittance characteristics depend strongly on the refractive indices of the materials in the PDLC films. We have measured the temperature dependent refractive indices of typical PDLC film materials and the temperature dependent electro-optic transmittance of a PDLC film composed of liquid crystal microdroplets dispersed in an epoxy matrix. We show that our refractive index measurements can account for all the features in the measured transmittance characteristics and discuss several methods for controlling refractive indices to optimize electro-optic transmittance over an extended temperature range. We have also measured the room temperature refractive indices of mixtures of epoxy resins and hardeners as a function of composition. We discuss the problems associated with predicting the refractive indices of such mixtures in terms of either the volume fractions or mole fractions of the mixture components. These considerations are important in matching refractive indices of droplets and matrix materials to maximize on-state transmittance. The refractive indices of epoxy matrix materials increase monotonically with time during their chemical cure. The measured time dependence can be described by a simple model in which the concentrations of the reacting resin and hardener each decay exponentially in time with their own characteristic time constants while the concentration of the cured polymer increases. Finally, we relate the measured rates of index change with temperature to the coefficients of volume expansion of PDLC film materials; the results are used to discuss the mechanical stability of PDLC films.