Role of Material Composition in Photothermal Actuation of DASA-Based Polymers

We investigate the influence of the host matrix on the photothermally driven actuation performance of negatively photochromic, donor-acceptor Stenhouse adduct (DASA)-based polymers. Using a modular Diels-Alder click platform, we designed polymeric materials with varying DASA incorporation and investigated the relationships between the material composition and the resulting physical, mechanical, and photoswitching properties. We demonstrate that increasing the DASA concentration in polymer conjugates has a dramatic effect on the materials physical and mechanical properties, such as the glass transition temperature (T-g) and elastic modulus, as well as the photoswitching properties, which are found to be highly dependent on T-g. We establish using a simple photoresponsive bilayer that actuation performance is controlled by the bilayer stiffness rather than the photochrome incorporation of DASA. Finally, we report and compare the light-induced property changes in T-g and the elastic modulus between the materials comprising the open or closed forms of DASAs. Our results demonstrate the importance of designing a material that is stiff enough to provide the mechanical strength required for actuation under load, but soft enough to reversibly switch at the operational temperature and provide key considerations for the development of application-geared photoswitchable materials.

Automated summary

This study investigates the influence of the host matrix on the photothermally driven actuation performance of DASA-based polymers. By designing polymeric materials with varying DASA incorporation, the relationships between material composition and physical, mechanical, and photoswitching properties are examined. Results demonstrate the importance of designing a material that is stiff enough for mechanical strength required for actuation, yet soft enough for reversible switching, providing key considerations for application-oriented photoswitchable materials.