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Smart, stimuli‐responsive materials that are also environmentally friendly are highly desired in the fashion and textile industry. For example, thermoresponsive properties show potential in creating dynamic comfort by improving moisture wicking and breathability at high temperatures. Additionally, color change properties provide aesthetic appeal and can be used as flexible sensors for physiological or environmental monitoring. Herein, the integration of bioproduced, thermoresponsive polymers into textiles as coatings that can also deliver pH‐responsive color change is explored. Elastin‐like polypeptides (ELPs) are recombinant protein biopolymers that exhibit an inverse phase transition when temperature is raised above a tunable transition temperature. To incorporate these into cotton textiles, amino acid residues with functional groups are genetically introduced. These are covalently coupled to oxidized cotton fabric, as well as a pH indicator dye, and copper‐free “click” conjugation handles. Thus, a facile layer‐by‐layer assembly process is used to assemble coatings with tunable thickness. The chemical derivatization of ELPs is shown and how these modifications influence thermoresponsive properties in solution is demonstrated. Cotton fabric is oxidized to introduce carboxylic acid chemical handles and up to ten coats of ELP is layered onto the modified cotton. The coating demonstrates spatiotemporal pH responsive color change. [ABSTRACT FROM AUTHOR]

The seamless integration of emerging directional liquid transport (DLT) technology with traditional textile materials has ushered in the next‐generation multifunctional textiles, i.e., DLT textiles, which will play a vital role in areas such as wearable smart materials and ecological environmental protection. To further promote the combination of DLT technology and textile technology, a concise overview of the research progress in DLT textiles, including the basic transport mechanisms, various preparation strategies and diversified applications of DLT textiles is provided. In this review, the theoretical mechanisms of directional transport from the perspective of wetting and wicking is discussed. Besides, the preparation strategies of DLT textiles, and categorized them into three categories is summarized: fiber‐based DLT textiles, fabric‐based DLT textiles, and fiber/fabric hybrid‐based textiles. Subsequently, the current and potential applications of DLT textiles are classified and discussed, mainly focusing on functional clothing, oil‐water separation, fog collection, distillation, sensors, biomedicine, and so on. Finally, the challenges and prospects of DLT textile research to enhance the functionality and application performance is outlined. [ABSTRACT FROM AUTHOR]

Flexible sensors hold significant promise for wearable monitoring and rehabilitation training applications. However, current flexible strain sensors struggle to compatible their sensing performance and fabrication with textile substrate and weaving technologies, which limits the practical applications of flexible sensors in commercial markets for electronic wearables. Differing from traditional strategies that rely on sophisticated construction of functional materials, leveraging industrial braiding, and weaving technologies, an all‐textile‐based pseudo‐triaxial mechanosensory textile (PTMT) is designed by engineering the wrapping pattern, yarn twist, and fabric architecture. The switchable hierarchically‐structured morphing of the PTMT enables an ultra‐wide strain detection range (up to 140%) along with desirable sensitivity. Moreover, the PTMT shows outstanding air permeability (1915 mm s−1), moisture permeability (1922 g m−2 h−1), high washability, and electromagnetic interference shielding (20.25 dB). The potential applications of PTMT are also demonstrated, such as in simulating fetal‐movement in pregnant women, proving its effectiveness in fetal‐movement health monitoring. Furthermore, by integrating the PTMT into shoe vamps and combining it with machine learning algorithms (CNN, RF, and PSO‐SVM), it is proved that PSO‐SVM outperformed CNN and RF in accuracy and stability, achieving a combined recognition accuracy of 95.42%. [ABSTRACT FROM AUTHOR]

Textile‐based electromechanical sensors are increasingly used as wearable sensors for various applications, such as health monitoring and human‐machine interfaces. These sensors are becoming increasingly popular as they offer a comfortable and conformable sensing platform and possess properties that can be tuned by selecting different fiber materials, yarn‐spinning techniques, or fabric fabrication methods. Although it is still in its early stages, recent attempts have been made to introduce auxeticity to textile sensors to enhance their sensitivity. Having a negative Poisson's ratio, i.e., undergoing expansion laterally when subjected to tensile forces and contraction laterally under compressive forces, makes them distinct from conventional sensors with positive Poisson's ratio. This unique feature has demonstrated great potential in enhancing the performance of electromechanical sensors. This review presents an overview of electromechanical sensors based on auxetic textiles (textiles made from auxetic materials and/or non‐auxetic materials but with auxetic structures), specifically focusing on how the unique auxetic deformation impacts sensing performance. Sensors based on different working mechanisms, including piezoelectric, triboelectric, piezoresistive, and piezocapacitive, are covered. It is envisioned that incorporating auxeticity and electromechanical sensing capabilities into textiles will significantly advance wearable technology, leading to new sensors for health monitoring, fitness tracking, and smart clothing. [ABSTRACT FROM AUTHOR]

Textiles can be promising next‐generation wearable thermal management systems by exhibiting tunable infrared emissivity for dual‐mode control of cooling/warming, yet textiles often exhibit constant infrared emission. Herein, a dynamic thermoregulatory textile is woven from scalable‐manufactured radiative electrochromic fibers and is easily driven by a low voltage in a manner that results in a modulated emissivity of Δɛ≈0.35. Through a synergistic combination of the spiral outer electrode and electrochemically tunable carbon nanotube layer, excellent electrochemical controllability of the fibers is achieved over 100‐m length within 5s because of the decreased internal resistance with increasing length. As a result, the thermoregulatory textile suppresses substantial temperature variation and ensures excellent temperature regulation within ≈1.6 °C for simulated skin (much better than that of traditional textiles: ≈2.9 °C) under an ambient temperature fluctuation of 11.2 °C. Finally, wearable infrared camouflage and invisible infrared displays are also demonstrated by weaving or embroidering the radiative electrochromic fibers onto clothing. [ABSTRACT FROM AUTHOR]

Materials with contrary wettability have various functions and applications. Common methods such as chemical modification and secondary treatment with solid mask to achieve relevant wettability either have harmful additives or construct fixed shape. Herein, liquid is introduced as a plasma mask for constructing arbitrary area with contrary wettability on hydrophobic textiles. In atmospheric plasma working region, exposed area of textiles achieves hydrophilic while liquid shielding area maintains the original wettability. Water–ethanol mixtures with a broad range of surface tension are chosen as template liquid to meet most hydrophobic textiles with the property of erasable evaporation without residue. Liquid mask with fluidity can be drawn in any shape at any time, meanwhile, plasma treatment highlights the merit of no chemical additive. Higher resolution will be achieved when the operation process is further refined. This study may provide insights for constructing advanced infiltrating materials and replacing solid with liquid in more application scenarios. [ABSTRACT FROM AUTHOR]

Gallium‐based liquid metals with outstanding electrical conductivity and fluidity are widely used in wearable electronics for wireless communication, human–machine interaction, and smart textiles. However, their fluidity makes them easily leak from the embedded conductive circuits under repeatable stretching, mechanical damage, or exposure to acidic and alkaline environments, limiting their reliability in practical use. Here, highly stable LM–polymer composites are shown with the ability to endure significant mechanical or chemical stresses, maintaining low resistance changes (R/R0 = 3.3 and 2.4) after 10 times of standard washing and 24 h of storage in corrosive solutions. The use of fluoropolymer, providing robust interfacial binding with the gallium oxide layer, effectively serves as a barrier layer to withstand mechanical and chemical damage through the synergistic effect of adaptive dipole–dipole interactions among composites and enhanced hydrophobicity. The as‐prepared composites can be readily hot pressed onto commercial fabrics to develop electronic textiles with outstanding conductivity (10214 S m−1), high air permeability (148.6 mm s−1), and moisture permeability (30.3 g m−2). Taking advantage of their excellent stability and permeability, e‐textiles are demonstrated as washable thermal therapy patches and skin‐interfaced electrodes for epidermal biopotential recording. [ABSTRACT FROM AUTHOR]

Advanced innovation of flexible electrode with adequate redox activity and stably mechanical endurance that promotes charges kinetic migration and faradaic storage is pivotal for textile‐based supercapacitors (T‐SCs). Herein, this study reports a high‐performance T‐SCs electrode based on nickel–cobalt layered double hydroxides@black phosphorus (NiCo‐LDHs@BP) on a conductive silk (c‐silk) textile (NiCo‐LDHs@BP/c‐silk). Under negative voltage‐induced electrochemical exfoliation, the Ni2+ and Co2+ are embedded into bulk BP framework to form exfoliated BP nanosheets, and the NiCo‐LDHs are in situ grown within the BP networks, generating 3D NiCo‐LDHs@BP hetero‐nanostructure. Significantly, the NiCo‐LDHs@BP exhibits a large space‐charge area, enhanced adsorption energy for OH− and accelerated charges transfer/storage as confirmed using density functional theory calculations. Additionally, the T‐SCs electrode is fabricated by loading the blended NiCo‐LDHs@BP, sericin, and carbon nanotubes on fibroin textile via a silk reconstruction strategy, producing large area production, superior mechanical flexibility, and impressive electrochemical performance. The resultant NiCo‐LDHs@BP/c‐silk electrode exhibits large specific capacitance of 1291.3 F g−1 and considerable rate capacity in 1 M KOH electrolyte. Furthermore, the flexible solid‐state asymmetric T‐SCs deliver high specific areal energy density of 279.6 µWh cm−2 and robust folding capability (85.6% capacitance retention after 5000 folding cycles), which successfully power wearable watch and heart rate meter devices. [ABSTRACT FROM AUTHOR]

Hydration‐induced shape‐morphing behavior has been discovered in many natural fiber‐based materials, yet this smart behavior in regenerated fibers from biopolymers lacks investigation. Here, hierarchically structured silk fibers are developed with anisotropic long‐range molecular organization and water‐responsive effects resembling natural spider silk. The regenerated silk fibers exhibit the water‐triggered shape‐memory effect and a water‐driven cyclic response. The reversible hydrogen bonds and transformation in the metastable secondary structure from α‐helices/random coils to β‐sheets are explored as the mechanisms responsible for the water‐responsiveness. The silk fibers obtained possess a tensile strength higher than 104 MPa at a fracture strain of ≈100%, showing noticeable toughness. The water‐responsive silk fibers exhibit a shape recovery rate of ∼83% and generate a maximum actuation stress of up to 18 MPa during the water‐driven cyclic contraction that outperforms most traditional natural textile fibers. The regenerated silk fibers show potential for use in water‐driven actuators, artificial muscle, and smart fabrics based on the integration of suitable mechanical properties and water responsiveness. [ABSTRACT FROM AUTHOR]

The field of electronic textiles currently lacks n‐type polymer fibers that can complement the more established p‐type polymer fibers. Here, a highly conductive n‐type polymer fiber is obtained via wet‐spinning of n‐doped poly(3,7‐dihydrobenzo[1,2‐b:4,5‐b']difuran‐2,6‐dione) (n‐PBDF). The electrical conductivity of the fibers increases from 1000 to 1600 S cm−1 with increased draw during processing and correlates well with Young's modulus. Wide‐angle X‐ray scattering reveals the existence of a bimodal orientation of the polymer chains, favoring parallel alignment to the fiber axis with increased draw. After 14 d in 80% humid air, fiber conductivity stabilizes maintaining 81% of the initial conductivity. Although the electrical conductivity drops slightly over time, the Seebeck coefficient increases, resulting in the highest thermoelectric power factor being measured at 91 µW m−1 K−2 for the most drawn fiber 14 d after its fabrication. A proof‐of‐concept two‐couple thermoelectric textile is crafted by embroidering bundles of n‐type PBDF fibers and p‐type PEDOT:PSS fibers. The device generates 2.40 nW at a 22 °C temperature gradient. This work represents the initial steps and a crucial advancement toward fabricating high‐performance n‐type polymer fibers that can complement their p‐type counterparts to close the existing performance gap. [ABSTRACT FROM AUTHOR]

Man‐made superhydrophobic membranes are of interest for various applications in energy, environment, and medical fields. However, simultaneously achieving durable superhydrophobicity, robust waterproofness, and high breathability of the membranes is still challenging. Herein, an efficient and powerful strategy is reported to create superhydrophobic membranes with perdurable liquid repellency and robust breathability via combining humidity‐induced electrospinning with coat‐crosslinking technology. The micro/nano rough structure is in situ constructed based on manipulating the phase separation of electrospun jets; meanwhile, the waterborne acrylic resins are bridged to the surface of nanofiber to endow the membranes with stable low surface energy via coating and crosslinking treatment. Eventually, the resultant membranes present superhydrophobicity with a water contact angle of ≈154°, good self‐cleaning and anti‐icing properties, robust waterproofness of 83.4 kPa, and high breathability of 3.71 kg m−2 d−1. More interestingly, the nanomaterials can maintain durable superhydrophobicity even after exposure to various severe conditions. The successful creation of high‐performance superhydrophobic membranes opens a new avenue for synthesizing advanced functional materials for application in a variety of fields. [ABSTRACT FROM AUTHOR]

Textile‐based flexible alternating current electroluminescent devices have attracted extensive research interest due to their great potential in the fields of illumination and display, information interaction, smart wear, visual sensing, and trendy decoration. However, the challenge remains to easily and efficiently fabricate electroluminescent devices with high brightness and excellent durability. In this study, a fully sprayed method for fabricating electroluminescent devices on fabric is proposed. Based on the top‐emitting structure, light‐emitting e‐textiles with bright light emission are successfully prepared using highly conductive eutectic gallium–indium alloy and silver nanowires as the bottom and top electrodes, respectively, and high dielectric constant composites as the dielectric layer. Here, the brightness enhancement mechanism of high dielectric constant dielectric layers is explained for alternating current electroluminescence devices with top‐emitting structure. The devices have a brightness of up to 338.6 cd m−2 and are resistant to all forms of physical damage. This work may be a feasible path to simplify the process and reduce the cost, and may effectively promote the industrialization of wearable electroluminescent devices. [ABSTRACT FROM AUTHOR]

Liquid crystal elastomers (LCEs) are promising candidates for creating adaptive textile‐based devices that can actively and reversibly respond to the environment for sensing and communication. Despite recent advances in scalable manufacturing of LCE filaments for textile engineering, the actuation modes of various LCE filaments focus on contractual deformations. In this study, manufacture of polydomain LCE filaments with potential scalability by wet‐spinning is studied, followed by mechanical exploitation to program liquid crystal mesogen alignments, demonstrating both contractual and twisting actuation profiles. By plying these LCE filaments into yarns with different twist concentrations, yarn actuation, and mechanical performance is tuned. Yarns plied at 4 twists per cm can generate up to a seven‐fold increase in elastic modulus while maintaining 90% of actuation strain performance from their native filament. The contractual and twisting LCE filaments are then embroidered with varying stitch types to spatially program complex 2D‐to‐3D transformations in "inactive" fabrics. It is shown that a running stitch can actuate up to 15% in strain and create angular displacements in fabric with twisted mesogen alignments. It is envisioned that the wet‐spun polydomain LCE filaments for diverse plied yarn production together with textile engineering will open new opportunities to design smart textiles and soft robotics. [ABSTRACT FROM AUTHOR]

Intrinsically flexible photodetectors are compelling building blocks for next‐generation wearable optoelectronic systems owing to their distinctive advantages of reliable structural durability and versatile scalability for large‐scale production. However, their practical applications are still impeded by the inferior photodetection performance, irreversible device failure after breakage, and serious e‐waste accumulation after service life. Herein, a high‐performance intrinsically flexible, mechanically durable, self‐healable, closed‐loop recyclable, and screen‐printable Te NWs/MoS2 nanosheets/polyimine nanocomposite‐based photodetector are designed by engineering‐ordered‐bridged 1D/2D carrier percolation "fast lanes" in dynamic covalent polyimine matrix via a flow‐designed solution‐shearing method. Such a design provides a sixfold, 20.1‐fold, and 6.9‐fold enhancement in carrier mobility, responsivity (11.68 mA W−1), and detectivity (1.145 × 1010 Jones), respectively, as well as stable photoresponse over eight months or after 50 000 bending‐flattening times. Meanwhile, this photodetector presents excellent self‐healing efficiency and repeatable recyclability for device reconfiguration. Furthermore, these merits can be fully integrated onto textile by assembling nacre‐like Te NWs/MoS2/polyimine nanocomposite coatings on textiles via screen‐printing processes, enabling programmable patterning of photodetection arrays for large‐area image sensing. This work provides a viable approach for the design of shape‐tunable optoelectronics with reliable mechanical durability and customizable functionalities, demonstrating the tremendous potential for large‐scale applications in wearable optoelectronic systems. [ABSTRACT FROM AUTHOR]

Passive radiative cooling without energy consumption is increasingly being explored as an eco‐friendly alternative to electric cooling for mitigating heat stress caused by global warming. Incorporating radiative cooling into personal thermal management has garnered widespread interest. However, existing sub‐ambient radiative cooling textiles face challenges related to inferior solar reflectance, poor outdoor durability, or health concerns. Here, a durable multilayer silk textile (MST) is developed that achieves excellent comprehensive performance for the first time, including both ultrahigh solar reflectance (96.5%) and ultrahigh infrared emittance (97.1%), safety, air and moisture permeability, high mechanical strength, washability, abrasion resistance, surface hydrophobicity, and UV resistance. The MST achieves a remarkable sub‐ambient temperature drop of 5.1 °C under 892.4 W m−2 of ultra‐strong solar radiation and surpasses both commercial silk and cotton textiles at noon with temperature reductions of 6.0 and 8.3 °C, respectively. For proof of concept, a hat using the MST is fabricated, which shows improved cooling performance compared to commercial hats. Considering its outstanding cooling performance, durability, zero energy consumption, abundant raw materials, and scalable production ability, it is believed that the radiative cooling MST holds great promise for practical applications in daytime personal thermal management. [ABSTRACT FROM AUTHOR]

To achieve accurate monitoring of bioelectrical signals, it is essential to use customizable bioelectrodes that can self‐adapt to the skin's surface topography. Ion‐conducting hydrogel has received significant attention in this field due to its softness, adhesion, and skin‐like mechanical properties. However, these bioelectrodes currently suffer from degradation of adhesion, electrical conductivity, and skin‐compliance when exposed to aqueous environments. This significantly limits the application of bioelectrodes. Herein, a customizable biohydrogel that can be applied on skin or fabric by solvent volatilization for liquid ink‐gel film conversion is reported. The biohydrogel's distinct characteristic of transitioning between a liquid and hydrogel phase establishes superb conformal contact and dynamic compliance with the epidermis. This effectively eliminates motion artifacts and results in lower contact impedance and noise in both static and dynamic states when compared to existing bioelectrodes. The biohydrogel is applied to the cotton fabric to create electrocardiogram (ECG) monitoring garments. These garments enable the acquisition of ECG signals with high accuracy in aqueous environment for over 72 h. Besides, the biohydrogel‐based garments outperform the commercial gel electrodes by 83.5% in signal‐to‐noise ratio. Additionally, the cotton/biohydrogel electrode facilitates multi‐channel, high‐fidelity recording of ECG signals, enabling high‐performance capture and classification of ECG waveforms across multiple channels. [ABSTRACT FROM AUTHOR]

Seamlessly integrating biosensors into clothing for personalized stress level monitoring, specifically targeting cortisol, a stress‐related compound found in sweat, shows great potential for efficiently monitoring and managing individual mental and physical well‐being. Nevertheless, realizing the fabric biosensor faces a notable challenge, as it involves the persistent obstacle of ensuring reusability and washability. Here, a fabric sensing system constructed by a fiber electrode for rapid and reliable cortisol detection with high repeatability, breathability, and stability is reported. The fibers are assembled from aligned carbon nanotubes and functionalized with a molecularly imprinted polymer containing redox‐active nanoreporters. Through washing with ethanol, the fabricated fabric sensor exhibits high reusability for over 100 cycles detecting cortisol. The key is the large active surface area and elaborately designed channel distance in the fiber electrode, ensuring a stable interface between the polymer and the fiber electrode. The resulting fabric sensing system presents convenient monitoring of cortisol levels, allowing assessment of stress levels to understand emotions and health condition better. [ABSTRACT FROM AUTHOR]

Electromagnetic interference (EMI) shielding fabrics are crucial in addressing the increasingly serious electromagnetic pollution. To meet wearable requirements, stretchability and thermal comfortability are often desired, but which still are challenging. Herein, a stretchable EMI shielding fabric is fabricated via electrospinning coupled with biaxial pre‐stretching spraying, in which a block stacking wrinkled silver nanowire (AgNW)/Ti3C2Tx MXene network is coated on one side of electrospun thermoplastic polyurethane (TPU)/polydimethylsiloxane (PDMS) fabric. As expected, the wrinkled structure protects conductive network from fracture during stretching process, so as to realize the strain‐invariant electrical conductivity. Thus, the fabric exhibits a stretchable EMI shielding performance of over 40 dB when subjected to 10–50% uniaxial strains or 21–125% biaxial strains. More importantly, the white TPU/PDMS side and the black AgNW/MXene side enable the fabric passive radiative cooling and heating, respectively. The cooling side exhibits high mid‐infrared emissivity (97.5%) and solar reflectance (90%), thus reducing the skin temperature by ≈4.9 °C. The heating side with high solar absorptivity (86.6%) and photothermal effect increased the skin temperature by ≈5 °C. Therefore, the fabirc with stretchable EMI shielding and Janus‐type dual‐mode personal passive thermal management is promising in future wearable products. [ABSTRACT FROM AUTHOR]

For safe coexistence between robots and humans, it is important for robots to detect the presence of nearby humans as well as any physical contacts made to its body. The design of a modular textile sensor array and an algorithm for multi‐modal sensing of human touches and other contacts with their contact forces proposed. Each sensor module in the array is capable of multi‐modal sensing, and the entire array with multiple modules requires only two wires to read the outputs from all the modules using band‐stop filter circuits. The proposed sensor system shows the structural modularity, achieved by simple fabrication of sequential lamination of conductive and non‐conductive textile materials, realizing electrical connections through conductive snap buttons that connect the modules to the circuit. The functional modularity is also achieved through the compensation algorithm, derived from the analysis of the transfer function in the frequency domain. The algorithm significantly reduces signal interferences between modules. The multi‐modality, the textile‐based design, and the structural and functional modularity of the proposed system enable practical applications to various robotic systems, including robotic skin for a collaborative robot, a wearable sensor, a robot hand sensor, and a human–computer interface, as demonstrated in this study. [ABSTRACT FROM AUTHOR]

As a distributed environmental energy harvesting device, triboelectric nanogenerators (TENGs) inevitably encounter different and extreme application scenarios, such as environment with high temperature, high humidity, corrosion condition, frequent mechanical stimulus, and physical damages, which resulting in triboelectric performance degradation either by damaging device structure or reducing surface potential, and accelerating dissipation of surface bound charge. Therefore, tremendous efforts are dedicated to improving the TENG performance, enabling devices are competent in sustaining various challenging conditions. This review summarizes and highlights the latest research progress of strategy to achieve TENGs with high environmental adaptivity in three representative application fields of interfacial devices, wearable devices and implantable devices, aiming to gain insights in terms of material selection, structural design, preparation technology, working mode and integration strategy. The future development of the TENG would transform from static to dynamic device that possesses multifunction, high stability, autonomous response and actuation ability to adapt complex application environment. It is hoped that this review article could steer the development of environment‐adaptive TENGs to a higher level. [ABSTRACT FROM AUTHOR]

Amorphous tungsten oxide (WO3) is widely exploited in the fields of photochromism and electrochromism. Despite its widespread use, the tractable synthesis of amorphous WO3 nanodots is still on the drawing board, even though the WO3 nanodots possess superior chromatic performance owing to their large surface‐to‐volume ratio. Therefore, a new efficient strategy to synthesize amorphous WO3 nanodots, which exhibit both excellent electrochromic and photochromic properties, is reported. For the first time, the ligand effects of the amorphous WO3 nanodots on chromatic applications are elucidated. The presence of the ligand on amorphous WO3 nanodots inhibits the electrochromic color switching, while promoting photochromic performance. As a proof of concept, zinc‐WO3 electrochromic devices, WO3‐polyvinyl alcohol (PVA) transparent hydrogels, and PVA/WO3 textiles are prepared for diverse rapid‐switching chromatic applications. These results present a new strategy for the synthesis of widely used amorphous WO3 nanodots and open new opportunities for the development of WO3‐based chromatic applications. [ABSTRACT FROM AUTHOR]

The article titled "Protein-Engineered Elastin Fibers as Building Blocks for The Textile-Based Assembly of Tissue Equivalents" discusses the development of protein-engineered elastin fibers with customized molecular composition and microstructure. These fibers are autoclavable and do not have any negative effects on their mechanical or biological properties. They can be used to create hierarchically organized structures through textile-based assembly, opening up new possibilities for medical textiles and long-lasting stretch fabrics. The authors of the article are Alicia Fernández-Colino, Ikram El Maachi, Alexander Loewen, Sergio Acosta, Stephan Rütten, J. Carlos Rodríguez-Cabello, Stefan Jockenhoevel. [Extracted from the article]

Textiles with a freedom of form factor, unlimited scalability, and high programmability provide an ideal platform for constructing wearable optoelectronic systems. The emerging wearable technologies, like artificial intelligence and Internet of Things, have driven the development of textile optoelectronics from simple functional blocks to sophisticated logic systems, offering a seamless, breathable, and programmable on‐body platform to synergistically sense, analyze, store, and feedback information in response to complex commands. In the past few years, the creation of such smart textile optoelectronics‐based logic systems is boosted by nanomaterial science and manufacturing integration technologies and has revolutionized human–machine interaction paradigms in numerous emerging fields. Herein, in this review, the recent progress of smart textile optoelectronics for human‐interfaced logic systems is timely summarized. This review begins with a concise discussion about the wearability evaluation and integration consideration of textile optoelectronic devices. Then, important breakthroughs in human‐interfaced logic systems based on smart textile optoelectronics are demonstrated by highlighting their representative device, working principle, and application scenarios. Finally, the existing challenges and potential directions in the field of textile optoelectronics‐integrated logic systems are analyzed. [ABSTRACT FROM AUTHOR]

2D transition metal carbide/nitride (MXene) show significant potential for fabricating flexible wearables due to its outstanding electroactive characteristic. However, the complex processes in rheology regulation and easy agglomeration of MXene nanosheets hinder their applications as inks for homogeneous printing and coating. Herein, an electroactive gel‐ink with a low concentration of MXene (20 mg mL−1) using poly(3,4‐ethylenedioxythiophene):poly(sodium 4‐styrenesulfonate) (PEDOT:PSS) as a dopant and conductive binder is developed. The dopamine‐involved modification and PEDOT:PSS doping together promote the formation of ordered lamellar structure of MXene nanosheets, and in turn the nanosheets can regulate the interconnected electronic structure of PEDOT:PSS, which enables the transition from micellar to linear structures. Through adjusting the combination ratio of dopamine‐modified MXene (MD) to PEDOT:PSS, the viscosity of MXene inks (MDP) is tunable within 1–104 Pa·s to realize scalable printing and other processing. Screen‐printing with MDP gel‐ink endows textiles with excellent conductive stability while retaining the inherent wearability of the original fabric. With high conductivity (109.6 S m−1) and low mid‐infrared emissivity (0.34), the decorated textiles exhibit remarkable multi‐protective abilities. This work provides a novel strategy for formulating versatile MXene inks that will facilitate the large‐scale fabrication of high‐performance personal wearable multi‐protective textiles. [ABSTRACT FROM AUTHOR]

Bio‐inspired unidirectional flow of tiny aqueous droplets across the fibrous substrate paved the way for the emergence of various advanced materials. In the past, textiles decorated with noncontact‐based wettability‐patterns enabled unidirectional water flow—without flooding the top surface by the transferred water. However, such approaches mostly suffer from a low (≈0.176 µL mm−2 s−1) flow rate and are likely to delay the overall liquid ejection process. Here, a chemically reactive coating capable of tailoring water wettability (121.3° ± 2.4° to 153.3° ± 1.8°) is introduced on commercially available textiles to develop chemically modulated wettability‐pattern for achieving a rapid (2.57 ± 0.28 µL mm−2 s−1) flow rate of water against the gravity with an ability to roll the accumulated liquids on the top surface. The spatially selected and controlled chemical modification with hydrophilic and hydrophobic small molecules through a 1, 4‐conjugate addition reaction yielded a 3D channel with a customized wettability gradient. The pinning and depinning of invaded water through such chemically decorated channels enabled unidirectional and fast penetration of liquid, where the water penetration resistance largely depends on the water penetration direction and dimension of the chemically modulated channels. [ABSTRACT FROM AUTHOR]

Currently, multifunctional MXene‐integrated wearable textiles (MWTs) are particularly appealing due to their various applications such as health monitoring, smart protection, and medical treatment. However, scalable manufacture of durable, stable, and high‐performance multifunctional MWTs still face challenges due to the poor oxidation stability of MXene and low utilization of precursor titanium aluminum carbide (MAX). Herein, an improved preparation strategy for zinc ion (Zn2+) intercalation is proposed to create high antioxidative MXene (ZM) and exceptionally conductive and printable gel ink based on MXene sediments (ZMS‐ink), while multifunctional wearable textiles are fabricated using spray‐coating and screen‐printing techniques on cellulosic nonwoven textiles (CNWs), achieving the complete utilization of MXene precursor. Benefiting from the inherent disordered stacking and porous structure of CNWs, along with the highly conductive ZM and ZMS‐ink, as‐prepared smart, wearable and green‐based pressure sensor offered proper breathability, high sensitivity (2602.26 kPa−1), wide sensing range (0–141 kPa), and excellent cycling stability (>5000 cycles). Additionally, the sensor exhibited efficient photothermal/photodynamic therapy antibacterial activity and exceptional electromagnetic interference shielding performance (57.5 dB). Therefore, this work paves the way for the future development of integrated and scalable multifunctional wearable devices building on the environmental‐friendly CNWs incorporated with fully utilized MAX, offering a green and cost‐effective approach. [ABSTRACT FROM AUTHOR]

The rise of the Internet of Things has spurred extensive research on integrating conductive materials into textiles to turn them into sensors, antennas, energy storage devices, and heaters. MXenes, owing to their high electrical conductivity and solution processability, offer an efficient way to add conductivity and electronic functions to textiles through simple dip coating. However, manual development of MXene‐coated textiles restricts their quality, quantity, and variety. Here, a versatile automated yarn dip coater tailored for producing continuously high‐quality MXene‐coated yarns and conducted the most comprehensive MXene‐yarn dip coating study to date is developed. Compared to manual methods, the automated coater provides lower resistance, superior uniformity, faster speed, and reduced MXene consumption. It also enables rapid coating parameter optimization, resulting in a thin Ti3C2 coating uniform over a 1 km length on a braided Kevlar yarn while preserving its excellent mechanical properties (over 800 MPa) and adding Joule heating and damage sensing to composites reinforced by the yarns. By dip‐coating five different yarns of varying materials, diameters, structures, and chemistries, new insights into MXene‐yarn interactions are gained. Thus, the automated dip coating presents ample opportunities for scalable integration of MXenes into a wide range of yarns for diverse functions and applications. [ABSTRACT FROM AUTHOR]

Phase‐change textiles can achieve temperature regulation in variable ambient environments, however, augmenting the amounts of phase‐change materials (PCMs) in textiles remains a significant challenge due to the occurrence of leakage with higher amounts. Herein, a novel approach is proposed for the fabrication of a hierarchical nanofiber textile embedded with a substantial quantity of phase‐change microcapsules (PCMC) using electrospinning. Such nanofiber textile is composed of a polyvinylidene fluoride‐hexafluoropropylene fibers (PVDF‐HFP) layer and a polyvinyl butyral fibers doped with 60 wt% of PCMC (PVB/PCMC‐60) layer. Gratifyingly, doped PCMC shows no signs of rupture and exhibits excellent cycling stability. Furthermore, the incorporation of the PCMC does not affect the spectral characteristics of the PVDF‐HFP layer while providing a substantial enthalpy of fusion (92.6 J g−1) to the PVB/PCMC‐60 layer. This serves to compensate for the deficiency in radiative cooling capacity and effectively mitigates temperature fluctuations and overheating of the textile. Outdoor test results indicate that the nanofiber textile can achieve temperature drops of 3.7 and 14.8 °C compared to textile without the PCMC (namely PVDF‐HFP/PVB) and cotton, and attains a subambient temperature drop of 6.5 °C. Additionally, the nanofiber textile exhibits desirable mechanical strength, flexibility, washability, breathability, moisture permeability, and sun protection. [ABSTRACT FROM AUTHOR]

The development of wearable heat supply textiles in cold conditions utilizing the photothermal conversion effect is crucial for the advancement of wearable thermal management textiles that do not require any power supply connection or other external energy input. Here, a dual gelation strategy under gravity‐enhanced orientation is proposed to construct super‐strong bacterial cellulose (BC) aerogel fiber using BC as the matrix material and hydroxylated carbon nanotubes (HCNT) as the photothermal conversion material. Under the assistance of orientation property and dual network structure with soft–hard synergy, the silanized BC/HCNT (SBT) aerogel fiber has rich network, tensile strength up to 26.0 MPa, flexibilityand knittability. Thanks to the enhanced network backbone, after the introduction of the phase change material eicosane in SBT aerogel fiber (SBTE), the SBTE fiber achieves high enthalpy of 105 J g−1, low leakage, storage stabilityand super‐strong and tough mechanical properties of 23.9 MPa and 8.7 MJ m−3, while maintaining flexibility, knittabilityand hydrophobicity. The textile woven by SBTE fiber also exhibits a long‐lasting heat supply capacity at low temperatures and under real‐world conditions. Therefore, the finely designed SBTE fiber has the potential to be used in solar‐driven wearable heat supply textiles in cold weather. [ABSTRACT FROM AUTHOR]

Wearable electronic textiles (e‐textiles) have emerged as promising healthcare solutions, offering point‐of‐care diagnostics while maintaining breathability, comfort, durability, and environmental stability with strong mechanical performance. However, the lack of thin and flexible power supplies hinders their practical adoption. In this regard, textile‐based micro‐energy storage devices present an appealing solution. Inkjet printing offers the capability to produce high‐quality prints with sharp details and versatile substrate compatibility, making it an ideal choice for a wide array of printing applications. Here, the preparation of a range of inkjet‐printable 2D material inks is reported for the fabrication of ultra‐flexible and machine‐washable textile micro‐supercapacitors. Then 2D material heterostructures are proposed to enhance the performance of textile supercapacitors. This study reveals that a unique combination of highly conductive graphene with an insulator hexagonal boron nitride (h‐BN) can enhance the areal capacitance of graphene‐based textile supercapacitors by ≈82.48%. The heterostructure‐based supercapacitors also demonstrate higher energy (≈18.06 µWh cm−2) and power densities (≈4333.33 µW cm−2) with excellent capacitance retention (≈95% after 1000 cycles). These findings on inkjet‐printed heterostructure‐based supercapacitors may herald a new era for the future application of high‐performance micro‐supercapacitors within textile‐based wearable technology. [ABSTRACT FROM AUTHOR]

Personal thermal management textiles have garnered a lot of attention because they can efficiently preserve the body's thermal and moisture comfort while saving energy consumption. Nonetheless, conduction cooling‐based textile research is scarce and frequently encounters obstacles like overlooking through‐plane heat conduction, moisture management, and durability assurance. Here, a dual‐cooling textile (DCT) that combines high‐efficiency heat dissipation and sweat evaporation with a 3D thermal conductive network and Janus wetting structure is demonstrated. The DCT achieves notable in‐plane and through‐plane thermal conductivity (8.57 and 0.70 W m−1 K−1), along with practical mechanical qualities (tensile fracture strength of 65 MPa), under the influence of the 3D multistage thermal conduction network. Additionally, the DCT benefits from its Janus wetting structure, exhibiting unidirectional moisture‐wicking capability (transport index of 1081%) and fast water evaporation performance (0.34 g h−1). Rapid heat dissipation and sweat evaporation are advantageous features for the cooling of the human body in both static and dynamic situations. Compared to cotton fabric, DCT can lower the temperature by up to 3.7 °C. This strategy provides a fresh perspective on the development of advanced functional textiles for personalized cooling and energy savings in buildings. [ABSTRACT FROM AUTHOR]

With the advancement of functional textile technology, there is a growing demand for functional enhancements in textiles from both industrial and societal perspectives. Recently, nanopattern transfer technology has emerged as a potential approach for fabricating functional textiles. However, conventional transfer methods have some limitations such as transfer difficulties on curved fiber surfaces, polymer residues, and delamination of transferred nanopatterns. In this study, an advanced nanopattern transfer method based on surface modification and thermoforming principles is applied to microscale electrospun fibers. This transfer method utilizes covalent bonding and mechanical interlocking between nanopatterns and the fibers without requiring extra adhesives. Various nanopatterns transferred electrospun fibers possess significant potential for diverse wearable healthcare applications. This work introduces two specific application scenarios in the field of wearable healthcare, both of which leverage the light: diagnostics and antimicrobials. Versatile textile with silver nanogap‐pattern detects glucose in sweat, diagnosing hypoglycemia and diabetes by shifting Raman peaks from 1071.0 to 1075.4 cm−1 for 0 to 150 µm glucose. Additionally, a bactericidal mask using visible light to induce the photocatalytic degradation effect of titanium dioxide and silver nanopatterns is developed. Bactericidal efficacy against Escherichia coli and Staphylococcus aureus is 99.9% due to photolysis from visible light irradiation. [ABSTRACT FROM AUTHOR]

The moisture‐enabled electricity generators (MEGs) represent an appealing clean power strategy within the realm of hydrovoltaic technology. However, their stable operation under all‐weather conditions is still challengeable due to the effect of ambient humidity. Herein, a self‐water‐storage MEGs with multifunctionality was developed. Gel textiles are employed as the proton‐release layer, while graphite fibers loaded with tin‐bismuth alloy liquid metal serve as water‐storing electrode. The gel textiles absorb water permeating down from the electrodes, releasing protons, which then react with the active electrode to enhance output performance. The experiment demonstrates that a device can generate a voltage of 0.55 V and a current of 7.08 μA after water storage, with a maximum power density of 1.14 μW·cm‐². The device's performance output can remain stable within a wide temperature range. The experiment confirms that the electrical output of the device originates from ionic diffusion, while density functional theory (DFT) and molecular dynamics (MD) calculations reveal the importance of the strong hydrolysis ability of the polymer and the high adsorption energy of the liquid metal for H3O+ on the output performance of the device. Furthermore, the integrated device has demonstrated effective applications in driving microelectronic devices, charging capacitors and, self‐powered health monitoring. [ABSTRACT FROM AUTHOR]

Achieving highly efficient self‐powered fibrous sensing systems is desirable for smart electronic textiles but remains a great challenge. Here, a bifunctional hydrogel is proposed by introducing of polyacrylic acid grafted MXene (MXene‐g‐PAA) into polyacrylamide/chitosan, achieving high‐sensitivity sensor and a stable hydrogel electrolyte of battery. The MXene‐g‐PAA flakes act as ion transport "highway", significantly enhance ionic conductivity, thereby increasing the sensitivity of sensors and facilitating Zn2+ diffusion in Zn‐ion battery (ZIB). The rich hydrogen bonding network in the hydrogel improves its mechanical properties and limits water molecule movement, thus reducing side reactions and prolonging the stability of ZIB. As a result, the fibrous sensor exhibits high strain sensitivity (gauge factor of 2.4) with a wide detection range (0–800%), and the fibrous Zn‐ion battery exhibits high capacity (353 mAh cm−3) with long cycling stability (400 cycles). The hydrogel‐based sensor and ZIB can be easily integrated into a flexible self‐powered sensing system, which effectively detects human movement and 3D ball motion. The bifunctional hydrogel with the integrated fibrous system will shed light on the development of next‐generation smart electronic textiles. [ABSTRACT FROM AUTHOR]

Over the past two decades, significant advancements have been made in the scalable production and commercialization of microbially‐produced recombinant protein polymers. This perspective presents the evolution from early research efforts to the development of market‐ready products, with a focus on recombinant silk‐like proteins. Initial attempts to synthesize spider silk proteins in microbial hosts faced challenges with solubility, stability, and yield. Recent advancements in synthetic biology, protein engineering, and bioprocess development have enabled the substantial progress on these challenges. Early commercial efforts highlight the complexities and high costs involved in silk production and more recent strategies have shifted toward processes with better scalability, techno‐economics, and product properties. Significant commercial progress has been made, with products launched in textiles and personal care. Although market penetration is limited so far, substantial groundwork is laid for future success. Key challenges remain, such as continued high production costs and the need for cost‐effective purification and fiber spinning techniques. However, the convergence of scientific, technological, and market developments –including a growing number of product launches – suggests that recombinant silk and protein polymers can soon become widespread sustainable materials across various industries. [ABSTRACT FROM AUTHOR]

Natural melanin polymers, biosynthesized from free tyrosine, assemble into microstructures that interact with light, producing a wide range of photonic properties. These structures are formed by mechanisms that are difficult to control to create new optical materials. Here, simple pentapeptides YXXXY is presented, where the XXX controls self‐assembly into microstructures, after which the Y's are polymerized by tyrosinase into melanin. It sought to computationally predict peptides that will assemble into two‐layer films that exhibit structural color and infrared (IR) scattering. Three peptides (YPIIY, YLPIY, YVPAY) are synthesized and found to form a two‐layer film exhibiting structural color. YLPIY‐melanin also forms a stable coating with scattering peaks in the near‐ and mid‐IR. This coating reduces the signature of a hotplate (37 °C) as seen by a thermal camera. This synthetic peptidic material is the first to exhibit IR‐scattering, opening the possibility of incorporating this function into bio‐compatible fibers, textiles, and plastics. [ABSTRACT FROM AUTHOR]

Healthcare textiles serve as key reservoirs for pathogen proliferation, demanding an urgent call for innovative interventions. Here, a new class of Smart Fabrics (SF) is introduced with integrated “Repel, Kill, and Detect” functionalities, achieved through a blend of hierarchically structured microparticles, modified nanoparticles, and an acidity‐responsive sensor. SF exhibit remarkable resilience against aerosol and droplet‐based pathogen transmission, showcasing a reduction exceeding 99.90% compared to uncoated fabrics across various drug‐resistant bacteria, Candida albicans, and Phi6 virus. Experiments involving bodily fluids from healthy and infected individuals reveal a significant reduction of 99.88% and 99.79% in clinical urine and feces samples, respectively, compared to uncoated fabrics. The SF's colorimetric detection capability coupled with machine learning (96.67% accuracy) ensures reliable pathogen identification, facilitating accurate differentiation between healthy and infected urine and fecal contaminated samples. SF holds promise for revolutionizing infection prevention and control in healthcare facilities, providing protection through early contamination detection. [ABSTRACT FROM AUTHOR]

Counterfeit goods are pervasive, being found in products as diverse as textiles and optical media to pharmaceuticals and sensitive electronics. Here, an anti‐counterfeit platform is reported in which plasmonic nanoparticles (NPs) are used to create unique image tags that can be authenticated quickly and reliably. Specifically, plasmonic NPs are assembled into periodic arrays of NP clusters by template‐assisted self‐assembly (TASA), where the light scattering responses from the arrays are analyzed by dark‐field optical microscopy. Tag design proved modular as plasmonic NPs with different optical responses can be selected and paired with Templates with different features (e.g., well size, well shape, and number and arrangement of wells in an array), giving access to a variety of color responses and unique images. These images can be differentiated from one another and authenticated by image analysis. Authentication methods based on shallow and deep neural networks are compared, where deep neural networks authenticated TASA tags with higher accuracy. Given the ease of tag fabrication and rapid image analysis, these platforms are ideal for on‐the‐fly tagging and supply‐chain authentication of critical goods. [ABSTRACT FROM AUTHOR]

In this study, a novel and sustainable triboelectric material is successfully designed and developed by extracting keratin from recycled fur and combining it with chitosan to create a keratin/chitosan triboelectric nanogenerator (CK‐TENG) device. The device is designed for the simultaneous treatment of waste and the generation of green and clean energy, crucial for addressing global challenges. CK is prepared through a freeze‐drying method to overcome the weak mechanical properties of keratin and achieve a high surface contact area, which is important for triboelectric properties. The results showed that the output voltage is improved by 375% compared to the TENG without keratin, with values reaching 322 V under a 6 N. It produced a high power density of 14.4 W m−2 and excellent cyclic stability for more than 8000 cycles, which are crucial for practical applications. Further, the potential applications are also studied, and the results showed that it can turn on over 250 light‐emitting diodes (LEDs), display liquid crystal display (LCD), and charge capacitors under 6 N. Moreover, it is successful in harvesting energy from waste vibrations, acoustic energy, and as a shoe, and the electrical output is utilized to power electronic devices. Furthermore, the power density harvested by the device is higher than that of TENG devices made with keratin‐rich materials. Therefore, this study paves the way for the use of keratin‐based bio‐waste materials for clean and green energy production, which can play significant roles in applications such as the charging of electronic devices, biomedicine, sensors, and smart textiles. [ABSTRACT FROM AUTHOR]

Solar steam generation has emerged as a promising approach to address water scarcity issues globally. However, a few challenges remain, including high cost, limited scalability, and salt accumulation, before this technique can be adopted by the general population. Here, an all‐in‐one photothermal fabric is reported such as a solar steam generator (SSG), consisting of commercial hydrophilic superfine denier polypropylene fiber and water‐repellent expandable polyethylene foam, manufactured via a conventional weaving machine. By tailoring the yarn twist and density, optimized micro‐macro hierarchical channels can be created in the SSG to provide sufficient water supplementation and continuous steam generation. Due to the Marangoni effect introduced by the temperature gradient along the yarns water with high salinity transports to the bulk water, realizing a salt‐rejecting property. As a result, the SSG demonstrates a rapid evaporation rate of 1.408 kg m−2 h−1 and energy efficiency of 92.43% under 1 sun, as well as outstanding stability for desalination of high salinity brine (10 wt% NaCl). Furthermore, this strategy provides a new solution to achieve excellent cost‐effectiveness in clean water production at ≈1700 g h−1 $−1. This work provides a sustainable fabric‐based SSG for practical large‐scale clean water production, and can potentially inspire other textiles‐based water treatment. [ABSTRACT FROM AUTHOR]

This study presents a novel method to fabricate scalable photovoltaic fibers (PVFs) by leveraging crystalline silicon (c‐Si) solar cell technology, known for its high‐power conversion efficiency (PCE), stable performance, and low cost. The c‐Si PVF is built on a flexible circuit strip as narrow as 400 µm, and c‐Si cells as small as 0.35 mm2 are surface‐mounted on the strip. The cells are diced from an interdigitated back‐contact c‐Si solar cell (≈153 cm2). A c‐Si PVF including a 1 mm2 cell reaches PCE up to 9.6% and 11.0% under simulated AM 1.5G illumination without and with encapsulation, respectively, the highest reported for c‐Si PVFs, while a 1.5 ft‐long fiber produces ≈37 mW m−1. Additionally, the PVF can tolerate bending fatigue with no sign of performance loss after 8000 bending cycles. To demonstrate practical applicability, the c‐Si PVFs are also woven into textile swatches. They deliver ≈10 mW cm−2 under a halogen lamp and successfully power a light‐emitting‐diode. This PVF technology is scalable with regards to both achieving thin fibers and its compatibility with roll‐to‐roll fabrication processes. The fiber concept presented here can also be extended to any chip‐scale surface mountable devices, enabling cell‐agnostic fiber technologies for multifunctional electronic textiles. [ABSTRACT FROM AUTHOR]

Fiber crossbars are an emerging architecture in electronic devices, and they have become the favored fundamental units for state‐of‐the‐art smart textiles. Fiber crossbar sensors with high linearity can provide more realistic pressure feedback, faster circuit response time, and simpler data processing systems. However, due to the unique crossbar structure, replicating existing linear response strategies presents challenges. To address this issue, a fiber crossbar sensor is prepared that incorporates a low modulus coupling circuit (LCFS). The hollow conductive network significantly reduces the sensor's electrode modulus, thereby enhancing its initial sensitivity. The coupling of the parallel and series circuits within the fiber crossbar maintains a linear increase in capacitance. As a result, propelled by the low modulus coupling circuit, the LCFS achieves a highly sensitive linear response. This strategy, independent of intricate microstructures in dielectric layers, has significant implications for fiber crossbar sensor design. Experimental tests and theoretical analyses confirm the effectiveness of this linear response strategy. Because of its high sensitivity and linearity, the LCFS consistently generates reliable and discernible pulse signals, unaffected by pre‐pressures. This empowers the LCFS to recognize various pulse patterns in Chinese medicine, heralding promising applications in daily health monitoring. [ABSTRACT FROM AUTHOR]

Shape memory polymers (SMPs) are one of the primary directions in the development of modern high‐tech new materials, which are integrated with sensing, actuation, information processing, and autonomous deformation. Here, multifunctional shape memory polymers are focused and a detailed introduction to the characteristics of self‐deformation, self‐sensing, self‐healing, and self‐learning is provided. Integrating with other functional materials to form shape memory polymer composites (SMPC), designing and controlling the material structure and organization at the microscale, thereby achieving more precise and controllable shape memory effects and expanding the potential of material applications. Ultimately, it is shown that SMPs and their composites have a wide range of fascinating applications in the fields of robotics, smart clothing, smart textiles, biomedical devices, and wearable technology. SMPs will thus continue to play a significant role in future deeper exploration. [ABSTRACT FROM AUTHOR]

Intrinsically stretchable light‐emitting polymer semiconductors are essential building blocks for bioelectronics and display textiles. Stretchability is challenging for rigid conjugated polymers unless sacrificing charge mobility by introducing amorphous domains. High‐performance light‐emitting properties designed with twisted angle are undesirable for conductive materials. Hence, the concurrent strategies hardly satisfy the balance of stretchability, light‐emitting and mobility. Herein, a morphology engineering is proposed by controlling micro‐crystalline and limiting aggregation, that four intrinsically stretchable emissive polymers with good charge mobility based on indacenodithiophene (IDT) are obtained. Polymers reveal good emission properties with high photoluminescence quantum yields (PLQY) of about 20%, while stretchable modulus and charge mobility are tunable by backbone and weight. Specifically emphasizing, IDT‐2T‐H retains high performance of charge mobility and PLQY even at 100% strain. Therefore, organic light emitting diodes are fabricated based on it and showing the luminance of 176.2 cd cm−2, which verifies the potential of technique to reconcile integration of stretchability, light‐emitting, and mobility. This is the first attempt to integrate balanced mechanical, optical, and electrical properties through micro‐crystalline aggregation‐limited morphology in one polymer, offering a feasible approach to advanced integrated circuit and multi‐functional electronics in the future. [ABSTRACT FROM AUTHOR]

Stretchable supercapacitors (SCs) have attracted attention as energy storage devices for wearable electronics due to their excellent power performance, low heat generation, and ease of integration into clothing. This paper presents a stretchable SC composed of liquid metal current collectors on textile substrates. For the liquid metal and textile‐based supercapacitors (LM/Tex SCs), the wetting characteristics and electrical resistance of the liquid metal on different types of textile substrates are investigated. The wettability of the carbon nanotube suspension for an electrochemically active material is also affected by the chemical and structural properties of the textile substrates. The intrinsically stretchable LM/Tex SCs are fabricated by sandwiching a soft gel electrolyte layer between the two liquid metal and textile‐based electrodes. The optimized SCs based on the polyester/neoprene textile exhibit a high areal capacitance of 527.8 mF cm−2 and maintain more than 90% of their initial capacitance after 1000 repetitive stretching cycles. Finally, it is demonstrated that the LM/Tex SC is readily integrated into a shirt and reliably supplies electrical energy to light up a light‐emitting diode even under human motion. [ABSTRACT FROM AUTHOR]

Aqueous zinc‐ion batteries (AZIBs) have attracted more and more attention owing to their high safety, low cost, and environmental friendliness. Mn‐based materials are considered as one of the most promising cathode materials for AZIBs because of their high output voltage, eco‐friendliness, and abundance. However, the low electrochemical activity and the manganese dissolution of Mn3O4 lead to the low specific capacity and inferior cycling stability, hindering its practical applications. Herein, a facile and low‐cost strategy is designed that combines cationic vacancy modulation with Mn ion‐confinement effect in a synergistic action to boost zinc ion energy storage capability of inert Mn3O4 (designated as VMn‐Mn3O4@C). The cationic vacancy endows Mn3O4 with more active sites, resulting in an increased specific capacity. Meanwhile, the manganese dissolution is inhibited via the Mn ion‐confinement effect of the carbon framework, thereby improving the cycling stability of the cathode. Consequently, the developed Zn/VMn‐Mn3O4@C batteries deliver a high specific capacity of 280.9 mAh g−1 and 98.4% capacity retention after 100 cycles at 0.1 A g−1. More importantly, VMn‐Mn3O4@C cathodes maintain superior cycling stability of 5000 cycles with nearly 100% capacity retention at 1 A g−1. [ABSTRACT FROM AUTHOR]

Toward addressing the aesthetic demand, IR emissivity, and fire hazards of radiative cooling materials in the practical application, chameleon‐inspired is tactfully employed, dipole moment‐increasing, and fire‐retardant strategies to manufacture an advanced polyurea‐based composite coating through incorporating thermochromic microcapsules, boron nitride nanosheets, and montmorillonite nanosheets. The chameleon‐inspired thermochromic microcapsules and admirable IR emissivity (supported by the original IR emittance spectra) realized by the increasing dipole moment allow the composite coatings to spontaneously adjust the solar absorption and reflection during hot daytime, while enabling high‐efficiency radiative cooling throughout the day. The IR emissivity higher than most literature is attributed to the strong interfacial interactions within polyurea composite coatings which improve the dipole moment of C─O─C, Si─O, and B─N bonds by increasing the distance between the centers of positive and negative charges, thus producing more IR emissions. Furthermore, the thermally melted montmorillonite nanosheets can form a ceramic protective layer enhanced by boron nitride nanosheets, further suppressing combustion behavior to improve the fire safety performance of polyurea coatings. The integration of thermochromic functionality, high fire safety, and admirable IR emissivity not only contribute to promoting the practical application of radiative cooling materials, but also provide a precious reference route to design high IR emissivity. [ABSTRACT FROM AUTHOR]

Liquid metal (LM) micro‐nano droplets show the superiority in reducing the high surface tension applicable in conductive inks for flexible electronics. However, the dynamic surface makes LM droplets susceptible to be oxidized, facing challenges in storage and applications. Herein, a bifunctional groups cross‐linking strategy is adopted to encapsulate LM droplets into a robust shell. During sonicating LM in carboxymethyl chitosan (CMCS) solution with bifunctional groups (i.e., carboxyl and amino groups), a robust interface shell is constructed by anchoring effect, thereby providing high chemical stability (>7d). When directionally freezing‐drying LM dispersions, aerogel with Janus architecture is produced driven by the gravity of LM droplets. Due to the unique heterogeneous structure, the resultant aerogel exhibits a selective multifunctional response toward directional bending. In addition, owing to the gradient distribution of CMCS within aerogel, moisture electricity generator can be built with a high output voltage of 460 mV. Thus, this bifunctional groups cross‐linking strategy not only improves the chemical stability of LM micro‐nano droplets, but also renders a new method for producing multifunctional aerogel with energy harvesting and selective directional recognition, and applicable in smart sensors and power supplying devices. [ABSTRACT FROM AUTHOR]

Constructing heterostructures containing multiple active components is proven to be an efficient strategy for enhancing the sodium storage capability of anode materials in sodium‐ion batteries (SIBs). However, performance enhancement is often attributed to the unclear synergistic effects among the active components. A comprehensive understanding of the reaction mechanisms on the interfaces at the atomic level remains elusive. Herein, the carbon‐coated Fe3Se4/CoSe (Fe3Se4/CoSe‐C) anode material as a model featuring atomic‐scale contact interfaces is synthesized. This unique heterogeneous architecture offers an adjustable electronic structure, which facilitates rapid reaction kinetics and enhances structural integrity. In situ microscopic and ex situ spectral characterization techniques, along with theoretical simulations, confirm that the heterointerface with strong electric fields promotes Na+ ion migration. Based on solid‐state nuclear magnetic resonance (NMR) analysis, an interface charge storage mechanism is revealed, resulting in the enhanced specific capacity of the anode materials. When employed as an anode in SIBs, the Fe3Se4/CoSe‐C electrode demonstrates excellent rate capabilities (218 mAh g−1 at 7 A g−1) and prolonged cycling stability (258 mAh g−1 at 5 A g−1 after 1000 cycles). This work highlights the significance of heterointerface engineering in electrode material design for rechargeable batteries. [ABSTRACT FROM AUTHOR]

High electrochemical and durability anion exchange membranes (AEMs) are a vital material for Flexible zinc‐air batteries (F‐ZAB) and AEM water electrolysis (AEMWE) to achieve green economy and environmental protection. However, the existing AEMs possess the disadvantages of a complicated preparation process, poor homogeneity, and unsatisfactory electrochemical performance. Here, a novel alkaline exchange membrane is synthesized using bacterial cellulose (BC) as the matrix, incorporating constrained in situ Poly (diallyldimethylammonium chloride) (PDDA) polymerization and double chemical cross‐linking techniques. By adjusting the microstructure, a unique long‐range order and dense internal structure to address the issue of loose bonding between PDDA and BC is established and achieve the purpose of rapid OH− conduction. The membranes exhibit excellent application properties, with excellent ionic conductivity (145.12 mS cm−1) and superb mechanical strength (73.26 MPa). Consequently, the membrane is assembled into the F‐ZAB, and the unprecedented power density of 258.7 mW cm−2 can be achieved at room temperature. Moreover, the membrane also can reach 3.0 A cm−2 at 2.3 V, indicating good prospects in the field of water electrolysis in 6 m KOH. The approach paves a new path for manufacturing AEMs for green energy and environmental applications. [ABSTRACT FROM AUTHOR]