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Stretchable strain sensor detects a wide range of strain variation and is therefore a key component in various applications. Unlike traditional ones made of elastomers doped with conductive components or fabricated with liquid conductors, ionically conductive hydrogel-based strain sensors remain conductive under large deformations and are biocompatible. However, dehydration is a challenging issue for the latter. Researchers have developed hydrogel-elastomer-based strain sensors where an elastomer matrix encapsulates a hydrogel circuit to prevent its dehydration. However, the reported multi-step approaches are generally time-consuming. Our group recently reported a multimaterial 3D printing approach that enables fast fabrication of such sensors, yet requires a self-built digital-light-processing-based multimaterial 3D printer. Here, we report a simple projection lithography method to fabricate hydrogel-elastomer-based stretchable strain sensors within 5 minutes. This method only requires a UV projector/lamp with photomasks; the chemicals are commercially available; the protocols for preparing the polymer precursors are friendly to users without chemistry background. Moreover, the manufacturing flexibility allows users to readily pattern the sensor circuit and attach the sensor to a 3D printed soft pneumatic actuator to enable strain sensing on the latter. The proposed approach paves a simple and versatile way to fabricate hydrogel-elastomer-based stretchable strain sensors and flexible electronic devices.

Soft composite actuators can be fabricated by embedding shape memory alloy (SMA) wires into soft polymer matrices. Shape retention and recovery of these actuators are typically achieved by incorporating shape memory polymer segments into the actuator structure. However, this requires complex manufacturing processes. This work uses multimaterial 3D printing to fabricate composite actuators with variable stiffness capable of shape retention and recovery. The hinges of the bending actuators presented here are printed from a soft elastomeric layer as well as a rigid shape memory polymer (SMP) layer. The SMA wires are embedded eccentrically over the entire length of the printed structure to provide the actuation bending force, while the resistive wires are embedded into the SMP layer of the hinges to change the temperature and the bending stiffness of the actuator hinges via Joule heating. The temperature of the embedded SMA wire and the printed SMP segments is changed sequentially to accomplish a large bending deformation, retention of the deformed shape, and recovery of the original shape, without applying any external mechanical force. The SMP layer thickness was varied to investigate its effect on shape retention and recovery. A nonlinear finite element model was used to predict the deformation of the actuators.

Shape-shifting structures have gained growing interest recently and found wide applications in areas such as soft robotics, biomedical devices and self-folding origami, attributed to their ability to construct complicated shapes directly from simple structures. However, an efficient method to design and fabricate programmable 3D shape-shifting structures from 2D polymer films still lacks. In this work, we design programmable shape-shifting 3D structures via the release of internal gradient stress using the frontal photopolymerization (FPP) method. First, the relation between the non-uniformly distributed material and loading parameters, and the geometric and fabrication parameters are established theoretically. The finite element (FE) model is then developed based on the theoretically obtained material and loading parameters. Next, the elastic instability in the shape-shifting behaviors of a cured film is captured through an elastic energy minimization. Furthermore, by using grayscale light patterns, it is shown that we can selectively manipulate the geometric and fabrication parameters to improve the design freedom of various complex 3D structures.

Spatial control of material properties is highly desirable in additive manufacturing of functional structures with complex geometries. Whereas most previous efforts focused on developing new printing or material systems, we propose a new voxel design strategy of constructing digital materials to provide the additively manufactured polymeric structures with spatially customized thermomechanical properties. In our approach, a matrix-inclusion composite layout is adopted in the linearly patterned voxels that perform as building blocks to construct bulk material. Through rational design of voxel size and inclusion content, the printed polymeric digital material displays a tunable storage modulus up to three orders of magnitude and glass transition temperature ranging from 0 °C to 60 °C. By taking advantage of the design freedom, we demonstrate a sequential folding structure with spatially tunable actuation speed, and multi-stable configurations that trap elastic energy in deterministic collapse sequences. Overall, our approach provides an effective and convenient way of spatially customizing material properties for additive manufacturing and offers instructive inspirations to the realm of digital fabrication.

Extraordinary optical, electrical and chemical properties of 2D materials have potential to be useful for quick and sensitive detection of pathological diseases. One important example is malaria disease that can progress rapidly and cause death within days. Therefore, fast, accurate and cost-effective malaria diagnosis available at the point of care is urgently needed to facilitate precise treatment. Here we report rapid and highly sensitive malaria detection with an inexpensive graphene-protected copper surface plasmon resonance biosensor. Using phase sensitive surface plasmon resonance technique and a graphene functionalization protocol for attaching end-tethered DNA probes that were complementary to a malaria specific DNA target, we were able to significantly improve the detection limit of the malarial plasmodium parasite. The phase sensitivity of our graphene-enhanced sensors exceeds by two orders of magnitude the sensitivity of analogous optical biosensors. This enhanced sensitivity could provide means to detect low copy number bacterial infectious agents and to associate dormant bacterial populations with chronic inflammatory diseases using simple label-free optical detection.

Four-dimensional (4D) printing of shape memory polymer (SMP) imparts time responsive properties to 3D structures. Here, we explore 4D printing of a SMP in the submicron length scale, extending its applications to nanophononics. We report a new SMP photoresist based on Vero Clear achieving print features at a resolution of ~300 nm half pitch using two-photon polymerization lithography (TPL). Prints consisting of grids with size-tunable multi-colours enabled the study of shape memory effects to achieve large visual shifts through nanoscale structure deformation. As the nanostructures are flattened, the colours and printed information become invisible. Remarkably, the shape memory effect recovers the original surface morphology of the nanostructures along with its structural colour within seconds of heating above its glass transition temperature. The high-resolution printing and excellent reversibility in both microtopography and optical properties promises a platform for temperature-sensitive labels, information hiding for anti-counterfeiting, and tunable photonic devices., Four-dimensional (4D) printing of shape memory polymer (SMP) imparts time responsive properties to 3D structures. Here, the authors explore 4D printing of a SMP in the submicron length scale, extending its applications to nanophononics.

In this paper, Au nanoshell arrays, serving as a photo-activated material, are fabricated via the combination of self-assembled nanosphere lithography and the thermal decomposing polymer method. The intensity and position of surface plasmonic resonance can be tuned from the visible region to the near-infrared region by changing the size of Au nanoshell arrays. When resonance absorption peaks of metal nanoparticles are matched with emission wavelengths of core-shell CdSe/CdS quantum dots, fluorescent intensity of CdSe/CdS quantum dots can be strongly enhanced. The physical mechanism of fluorescent enhancement is explained.

Microlattices make marvelous materials Framework or lattice structures can be remarkably strong despite their very low density. Using a very precise technique known as projection microstereolithography, Zheng et al. fabricated octet microlattices from polymers, metals, and ceramics. The design of the lattices meant that the individual struts making up the materials did not bend under pressure. The materials were therefore exceptionally stiff, strong, and lightweight. Science , this issue p. 1373