Fast prototype and rapid construction of three-dimensional and multi-scaled pitcher for controlled drainage by systematic biomimicry

Biomimetic materials that use natural wisdom to solve practical problems are developing rapidly.The trend for systematic biomimicry is towards in-situ characterization of naturalcreatures with high spatial resolutions.Furthermore,rapid reconstruction of digital twin models with the same complex features as the prototype is indispensable.However,it faces bottlenecks and limits in fast characterization and fabrication,precise parameter optimization,geometricdeviations control,and quality prediction.To solve these challenges,here,we demonstrate astate-of-the-art method taking advantage of micro-computed tomography and three-dimensional printing for the fast characterization of the pitcher plant Nepenthes x ventrata and fabrication of its biomimetic model to obtain a superior drainage controller with multiscale structures withprecise surface morphology optimization and geometric deviation control.Thefilm-rupture-based drainage dynamic and mechanisms are characterized by x-ray and high-speed videography,which determines the crucial structures for unique directionaldrainage.Then the optimized artificial pitchers are further developed into sustained drainage devices with novel applications,such as detection,reaction,and smoke control.

Self-recoverable semi-crystalline hydrogels with thermomechanics and shape memory performance

Stimuli-responsive hydrogels have become one of the most popular artificial soft materials due to their excellent adaption to complex environments. Thermoresponsive hydrogels triggered by temperature change can be efficiently utilized in many applications. However, these thermoresponsive hydrogels mostly cannot recover their mechanical states under large strain during the process. Herein, we utilize the heterogeneous comb-type polymer network with semicrystalline hydrophobic side chains to design self-recovery semi-crystalline hydrogels. Based on hydrophilic/hydrophobic cooperative complementary interaction and heterogeneous polymer network, hydrogels can be endowed with excellent thermosensitive properties and mechanical performance. The hydrogels exhibit high compressive strength(7.57 MPa) and compressive modulus(1.76 MPa) due to the semi-crystalline domains formed by association of the hydrophobic poly(ε-caprolactone) PCL. The melting-crystalline transition of PCL and elastic polymer network provide the hydrogels excellent thermomechanical performance and self-recovery property. Furthermore, the hydrogels exhibit shape memory behavior, which can be realized by simple process and smart surface patterning. With these excellent properties, our hydrogels can be applied in sensors, flexible devices and scaffolds for tissue engineering.

Super-tough and strong nanocomposite fibers by flow-induced alignment of carbon nanotubes on grooved hydrogel surfaces

Nanocomposite fibers have attracted intensive attentions owing to their promising applications in various fields. However, the fabrication of nanocomposite fibers with super toughness and strong strength under mild conditions remains a great challenge. Here we present a facile flow-induced assembly strategy for the development of super-tough and strong nanocomposite fibers with highly ordered carbon nanotubes (CNTs), which can be induced by directional and fast flow on a grooved hydrogel surface. The prepared nanocomposite fibers show excellent mechanical properties, with a tensile strength up to 643±27 MPa and toughness as high as 77.3±3.4 MJ m^-3 at ultimate strain of 14.8±1.5%. This versatile and efficient flow-induced alignment strategy represents a promising direction for the development of high-performance nanocomposites for practical applications.

Magnetic-programmable organohydrogels with reconfigurable network for mechanical homeostasis

Synthetic materials with tunable mechanical properties have great potential in soft robotics and biomedical engineering.However,current materials are limited to the mechanical duality altering their mechanical properties only between soft and hard states and lack of consecutively programmable mechanics.Herein,the magnetic-programmable organohydrogels with heterogeneous dynamic architecture are designed by encasing oleophilic ferrofluid droplets into hydrogel matrix.As magnetic field increases,the mechanical properties of organohydrogels can be consecutively modulated owing to the gradual formation of chain-like assembly structures of nanoparticles.The storage modulus G'increases by 2.5 times when magnetic field goes up to 0.35 T.Small-Angle X-ray Scattering(SAXS)confirms the reconfigurable orientation of nanoparticles and the organohydrogels show reversible modulus switching.Besides,the materials also exhibit high stretchability,magnetic actuation behavior and effective self-healing capability.Furthermore,the organohydrogels are applied into the design of effectors with mechanical adaptivity.When subjected to serious external perturbations,the effector can maintain mechanical homeostasis by regulating modulus of organohydrogel under applied magnetic field.Such materials are applicable to homeostatic systems with mechanically adaptive behaviors and programmed responses to external force stimuli.