Mobility-Driven Design of PDMS-Modified Glassy Polymer Networks for Thermally Activated Shape Memory in Vat...

Glass-transition-driven shape memory polymers are promising materials for 4D printing because their thermally activated transition enables programmed deformation and recovery without relying on melting or crystallization-driven switching. In this study, PDMS-MMA-modified photocurable networks were designed for vat photopolymerization-based 4D printing by varying PDMS-MMA content and switching monomer structure while maintaining a fixed TMPTMA crosslinker content. The resin formulations were prepared using tert-butyl acrylate (tBA) or isobornyl acrylate (IBOA) as switching monomers, PDMS-MMA as a flexible mobility-regulating segment, and TMPTMA as a multifunctional crosslinker. The effects of formulation composition on printability, network formation, thermal stability, thermomechanical transition, mechanical properties, and shape memory behavior were systematically investigated. FT-IR analysis confirmed effective photocuring of the acrylate/methacrylate networks, while rheological evaluation showed that resin viscosity depended on monomer structure and PDMS-MMA content. DMA results revealed thermomechanical transition, although some formulations exhibited broad tan δ responses due to network heterogeneity and distributed segmental relaxation. Based on resin printability, printed-part resolution, and relatively well-defined tan δ transitions, T-15 and I-15 were selected as representative formulations for quantitative shape memory evaluation. Shape memory testing was conducted under force-control mode because stable strain-controlled programming was not achievable for the printed specimens. Both T-15 and I-15 exhibited high shape fixity over two programming-recovery cycles. I-15 showed stable recovery behavior with recovery ratios of 91.51% and 95.87%, whereas T-15 showed apparent over-recovery with recovery ratios exceeding 100%, likely due to residual stress release during reheating. Overall, these results demonstrate that thermally activated shape-memory performance is governed not only by the nominal transition temperature but also by the coupled effects of PDMS-mediated segmental mobility, switching monomer structure, mechanical integrity, and elastic energy storage within a fixed crosslinked network framework.