Thermoresponsive Reflective Scattering of Meso-Scale Phase Separation Structures of Uniaxially Orientation-Ordered Liquid Crystals and Reactive Mesogens.

Abstract

Polymer network liquid crystals (PNLCs) capable of thermoresponsive change in reflective scattering were fabricated using a self-organization technique called photopolymerization-induced phase separation. These PNLCs exhibit nonscattering states at temperatures τ below the nematic-to-isotropic (NI) phase transition temperature τNI but reflective scattering states at τ values above τNI. The magnitude of change of optical clarity is 80% and of solar transmittance is 20% in PNLCs with a thickness of 50 μm. The microscopic structures consist of wavelength- or meso-scale phase separation domains of liquid crystals (LCs) and polymerized reactive mesogens (RMs) in which cyanobiphenyl (CB) groups are thermoresponsively transformed between uniaxially orientation-co-ordered and disordered states. Such thermoresponsive structures were fabricated by employing the CB groups as mesogenic bodies, which were expected to mutually associate due to their physicochemical structures. Cross-linkers stabilized the meso-scale domains and made the PNLCs durable through repeated temperature changes. Polarizing optical microscopy (POM) and scanning electron microscopy showed meso-scale composites that reflectively scatter visible and near-infrared light. POM and Fourier-transform infrared spectroscopy at different temperatures suggest that the orientation order of the CB groups changes in the LC phase in response to temperature but remains ordered in the RM phase. Such a thermoresponsive change in the orientation order produces the switchability in meso-scale nonuniformity and consequently in reflective light scattering. The thermoresponsive PNLCs are not only effective as energy-saving smart windows but also advantageous at stages of manufacture, installation, and operation.