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Updated: Aug 6, 2026

Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals
Published on: May 29, 2018
Dynamics of ternary mixtures with photosensitive chemical reactions: creating three-dimensionally ordered blends
Olga Kuksenok1, Rui D M Travasso, Anna C Balazs
1Chemical Engineering Department, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA.
Abstract:
Using computer simulations, we establish an approach for creating defect-free, periodically ordered polymeric materials. The system involves ABC ternary mixtures where the A and B components undergo a reversible photochemical reaction. In addition, all three components are mutually immiscible and undergo phase separation. Through the simulations, we model the effects of illuminating a three-dimensional (3D) sample with spatially and temporally dependent light irradiation. Experimentally, this situation can be achieved by utilizing both a uniform background light and a spatially localized, higher intensity light, and then rastering a higher-intensity light over the 3D sample. We first focus on the case where the higher-intensity light is held stationary and focused in a distinct region within the system. The C component is seen to displace the A and B within this region and replicate the pattern formed by the higher-intensity light. In effect, one can write a pattern of C onto the AB binary system by focusing the higher-intensity light in the desired arrangement. We isolate the conditions that are necessary for producing clearly written patterns of C (i.e., for obtaining sharp interfaces between the C and A/B domains). We next consider the effect of rastering a higher-intensity light over this sample and find that this light "combs out" defects in the AB blend as it moves through the system. The resulting material displays a defect-free structure that encompasses both a periodic ordering of the A and B domains and a well-defined motif of C. In this manner, one can create hierarchically patterned materials that exhibit periodicity over two distinct length scales. The approach is fully reversible, noninvasive, and points to a novel means of patterning with homopolymers, which normally do not self-assemble into periodic structures.
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