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Abstract Materials that exhibit varied optical responses to different modes of mechanical stimuli are attractive for complex sensing and adaptive functionalities. However, most mechanochromic materials are fabricated from films or fibers with limited actuation modes. Here, hollow tubes of a symmetric sheath are created using cholesteric liquid crystal elastomers (CLCEs) at the sub‐millimeter scale. The oligomeric precursor is sheared in an elastomeric microchannel to form uniform thickness, overcoming gravity effect and Plateau‐Rayleigh instability. In addition, the coloration is achieved to be faster and have higher reflectivity compared to that of solid fibers. The tube can undergo axial, circumferential, and radial strains upon extension and inflation. The combination of molecular anisotropy and geometry of the tube enables highly sensitive mechanochromic responses in both azimuthal and axial directions: inflation causes red‐to‐violet shift (≈220 nm) at a circumferential strain of 0.57. The inflation of a bent tube generates another mechanochromic mode with a higher sensitivity to strain. Finally, display of 26 alphabets is achieved using 5 tubes, of which the positions can be reconfigured, and curvature‐dependent 3D photonic skins are demonstrated from tubes wrapped around 3D objects. The multi‐mode mechanochromic tubes will find applications for soft robotics, adaptive displays, wearable sensors, and spectrometers. 

Abstract Direct ink writing (DIW) of core‐shell structures allows for patterning hollow or composite structures for shape morphing and color displays. Cholesteric liquid crystal elastomers (CLCEs) with liquid crystal mesogens assembled in a helix superstructure are attractive for generating tunable iridescent structural colors. Here, by fine‐tuning the rheology of the core and shell materials, respectively, this study creates droplets or a continuous filament in the core from the precursors of polydimethylsiloxane (PDMS) or poly(vinyl alcohol), whereas CLCE forms the outer shell. By introducing a dye in the droplets, the skin structures of cephalopods, consisting of chromatophores and iridocytes, are mimicked for enhanced color saturation, lightness, and camouflage. After removal of the core material, a CLCE hollow fiber is obtained, which can switch colors upon mechanical stretching and pneumatic actuation, much like papilla along with iridocytes. Further, liquid crystal mesogens assembled in the bulk of the fiber are in polydomain. Thus, the skin appears opalescent at room temperature, much like how leucophores enhance reflectins. Upon heating above the nematic to isotropic transition temperature, the skin becomes transparent. Lastly, a cephalopod model is constructed, where different parts of the model can change colors independently based on different mechanisms. 

Atmospheric water vapor is an abundant and renewable resource that can alleviate growing water scarcity. Hybrid hydrogel desiccants composed of hygroscopic salts hold significant promise for atmospheric water harvesting (AWH) due to their increased capacity for water uptake. Thus far, many efforts in fabricating these desiccants require multistep processes, where the salt impregnation is achieved post-hydrogel fabrication. Here, we develop a scalable wet spinning methodology using aramid nanofibers (ANFs) to template and coagulate hydroxypropyl cellulose (HPC) into filaments in a coagulation bath consisting of water and lithium chloride (LiCl). HPC serves as the matrix to retain the captured water vapor, and later releases it upon heating. ANFs serve as the physical cross-linker between HPC, allowing for wet spinning at a speed up to 61 m h–1. The composite filaments achieve up to 0.55 g g–1 water uptake at 30% relative humidity (RH) and 21 °C, reaching 80% saturation in 40 min. With a lower critical solution temperature of 39 °C, the desiccant filaments can release up to 72% of the captured water at 60 °C after 30 min. In an AWH chamber, the filaments can achieve daily water production of 5.21 L kg–1 day–1 at 30% RH and 21 °C. 

This paper directly links the abstract geometry of structural form-finding to the fabrication-aware design of discrete shells and spatial structures for 3D concrete printing through a bidirectional approach, where it creates surface-toolpath twins for the components, optimizing the buildability of the parts and their surface quality. The design-to-production process of efficient structural systems for 3D printing is often a top-down unidirectional process involving form-finding, segmentation, and slicing, where results face printability challenges due to incompatibility between the initial geometry and the printing system, as well as material constraints. We introduce surface-toolpath twins that can be interconverted and synchronized through efficient slicing and surface reconstruction algorithms to allow the combination of optimizations and modifications on either part of the twin in flexible orders. We provide two core methods for fabrication rationalization: (1) global buildability optimization on the surface mesh by normal-driven shape stylization and (2) local surface quality optimization on toolpath curves through intra-layer iterative adjustments. The result is a bidirectional design-to-production process where one can plug and play different form-finding results, assess and optimize their fabrication schemes, or leverage knowledge in fabrication design, model toolpath curves as sections, reconstruct surfaces, and merge them into form-finding and segmentation in an inverse way. The proposed framework enables the integration of form-finding expertise with fabrication-oriented design, allowing the realization of spatial shell structures with complex topologies or extreme geometrical features through 3D concrete printing. 

Cellular solids composed of a network of interconnected pores offer low‐density and high strength‐to‐weight ratio as exemplified by wood, bones, corks, and shells. However, the slender edges and low connectivity of the structs in cellular lattices make them vulnerable to buckle, fracture, or collapse. Here, by taking advantage of the continuity of a thin film that can follow curvatures and dissipate energy, shellular materials are created by dip coating a wireframe of the primitive triply periodic minimal surface (TPMS) with an aqueous solution of lyotropic liquid crystalline graphene oxide (GO)/polymer composites. Regulated by surface tension, GO nanosheets align on the polymer soap film as the stress builds up during drying. When the wireframe mesh density is low, the shellular material is film‐dominated, demonstrating superior mechanical strength (384.30 Nm kg⁻¹) and high specific energy absorption (1.59 kJ kg⁻¹) yet lightweight (equivalent density, 0.063 g cm⁻³), with an energy absorption rate comparable to that of carbon nanotube‐based lattices but a lower equivalent density. The study offers insights into designing lightweight yet high‐strength structural materials that also function as impact energy absorbers. 

Biocompatible polymers have emerged as essential materials in medical 3D printing, enabling the fabrication of scaffolds, tissue constructs, drug delivery systems, and biosensors for applications in and on the human body. This review aims to provide a comprehensive overview of the current state of 3D-printable biocompatible polymers and their composites, with an emphasis on their processing methods, properties, and biomedical uses. The scope of this work includes both natural and synthetic biocompatible polymers, polymer–nanocomposite systems, and bioinks that do not require photo initiators. The relevant literature was critically examined to classify materials by type, evaluate their compatibility with major 3D printing techniques such as stereolithography, selective laser sintering, and fused deposition modeling, and assess their performance in various medical applications. Key findings highlight that reinforced polymer composites, tailored surface chemistries, and hybrid printing strategies significantly expand the range of functional, customizable, and affordable biomedical devices. This review concludes by discussing present-day applications and emerging trends, underscoring that 3D-printable biocompatible polymers are rapidly transitioning from research to clinical practice, offering transformative potential for patient-specific healthcare solutions.