Bio-inspired hydrogel actuator with rapid self-strengthening behavior

Inspired by intelligent biomaterials which often have flexible responsiveness to multiple environmental cues and strengthen their mechanical properties by trainings, emerging soft actuators require programmable manipula-tion. Currently, the integration of such characteristics as rapid self-strengthening, strain-adaptive stiffening and smart actuation, into a single hydrogel actuator is urgently needed. Here, we report a self-strengthened hydrogel actuator based on the semi-interpenetrating polymer network consisting of polyvinyl alcohol (PVA) and poly(N-isopropylacrylamide) (PNIPAm), which can display diverse programmable actuations by responding to tem-perature/salt stimuli. In the design, the layer of freeze-thawed PNIPAm/PVA (PPGel-F) is assembled with another original PNIPAm/PVA hydrogel layer (PPGel) into one device. By taking advantage of the PVA crys-talline nanofibrils in the PPGel-F matrix, the differentiated swelling degree across the bilayer structure gives rise to asymmetric deformations and the resultant shape transformation. Moreover, upon the mechanical training with less than 100 cycles, the anisotropic arrangement of PVA nanofibrils through strong hydrogen bonding interactions can swiftly immobilize the amorphous polymer chains orientation along the tensile direction. This enhances the strain-induced crystallization, thereby generating the rapid self-strengthening behavior. The proposed work provides potential solution for constructing dynamically adaptive hydrogel systems that can mimic biological tissues for more intelligent soft robotics and bionic research.

Automated summary

Inspired by intelligent biomaterials, this study presents a self-strengthened hydrogel actuator based on a semi-interpenetrating polymer network, which can display diverse programmable actuations by responding to temperature/salt stimuli. The actuator consists of freeze-thawed PNIPAm/PVA (PPGel-F) layer and an original PNIPAm/PVA hydrogel layer (PPGel), and the differential swelling degree across the bilayer structure leads to asymmetric deformations and shape transformations. Mechanical training induces anisotropic arrangement of PVA nanofibrils, enhancing strain-induced crystallization and resulting in rapid self-strengthening behavior. This work provides a potential solution for constructing dynamically adaptive hydrogel systems for intelligent soft robotics and bionic research.