Highly Oxidation-Resistant and Self-Healable MXene-Based Hydrogels for Wearable Strain Sensor

Very recently, MXene-based wearable hydrogels have emerged as promising candidates for epidermal sensors due to their tissue-like softness and unique electrical and mechanical properties. However, it remains a challenge to achieve MXene-based hydrogels with reliable sensing performance and prolonged service life, because MXene inevitably oxidizes in water-containing system of the hydrogels. Herein, catechol-functionalized poly(vinyl alcohol) (PVA-CA)-based hydrogels is proposed to inhibit the oxidation of MXene, leading to rapid self-healing and superior strain sensing behaviors. Sufficient interaction of hydrophobic catechol groups with the MXene surface reduces the oxidation-accessible sites in the MXene for reaction with water and eventually suppresses the oxidation of MXene in the hydrogel. Furthermore, the PVA-CA-MXene hydrogel is demonstrated for use as a strain sensor for real-time motion monitoring, such as detecting subtle human motions and handwriting. The signals of PVA-CA-MXene hydrogel sensor can be accurately classified using deep learning models.     

Conductive MXene Nanocomposite Organohydrogel for Flexible,Healable, Low‐Temperature Tolerant Strain Sensors

Conductive hydrogels are attracting tremendous interest in the field of flexible and wearable soft strain sensors because of their great potential in electronic skins, and personalized healthcare monitoring. However, conventional conductive hydrogels using pure water as the dispersion medium will inevitably freeze at subzero temperatures, resulting in the diminishment of their conductivity and mechanical properties; meanwhile, even at room temperature, such hydrogels suffer from the inevitable loss of water due to evaporation, which leads to a poor shelf‐life. Herein, an antifreezing, self‐healing, and conductive MXene nanocomposite organohydrogel (MNOH) is developed by immersing MXene nanocomposite hydrogel (MNH) in ethylene glycol (EG) solution to replace a portion of the water molecules. The MNH is prepared from the incorporation of the conductive MXene nanosheet networks into hydrogel polymer networks. The as‐prepared MNOH exhibits an outstanding antifreezing property (?40 °C), long‐lasting moisture retention (8 d), excellent self‐healing capability, and superior mechanical properties. Furthermore, this MNOH can be assembled as a wearable strain sensor to detect human biologic activities with a relatively broad strain range (up to 350% strain) and a high gauge factor of 44.85 under extremely low temperatures. This work paves the way for potential applications in electronic skins, human?machine interactions, and personalized healthcare monitoring.     

Flexible MXene-Based Hydrogel Enables Wearable Human–Computer Interaction for Intelligent Underwater Communication and Sensing Rescue

Conductive hydrogels have recently attracted extensive attention in the field of smart wearable electronics. Despite the current versatility of conductive hydrogels, the balance between mechanical properties (tensile properties, strength, and toughness) and electrical properties (electrical conductivity, sensitivity, and stability) still faces great challenges. Herein, a simplified method for constructing hydrophobic association hydrogels with excellent mechanical and electrical properties is proposed. The prepared conductive hydrogels exhibit high tensile properties (≈1224%), high linearity in the whole-strain–range (R² = 0.999), and a wide strain sensing range (2700%). The conductive hydrogel can realize more than 1000 cycles of sensing under 500% tensile strain. As an application demonstration, an underwater communication device is assembled in combination with polydimethylsiloxane/Triton X-100 film coating, which successfully transmits underwater signals and provides warning of potential hazards. This study provides a new research method for developing underwater equipment with excellent mechanical properties and sensing properties.     

Zwitterionic Osmolyte‐Based Hydrogels with Antifreezing Property,High Conductivity,and Stable Flexibility at Subzero Temperature

Conductive hydrogels have emerged as fascinating materials applied in flexible electronics because of their integrated conductivity and mechanical flexibility. However, the large amounts of water in conductive hydrogels inevitably freeze at subzero temperature, causing a reduction of their ionic transport ability and elasticity. Herein, the bioinspired antifreezing agents—zwitterionic osmolytes (e.g., betaine, proline) are first proposed to prevent ammonium chloride‐containing Ca‐alginate/polyacrylamide hydrogels from freezing. With a facile one‐pot solvent displacement method, the zwitterionic osmolytes can displace the water molecules inside the hydrogels. Due to the excellent freeze tolerance of zwitterionic osmolytes, the resulting zwitterionic osmolyte‐based hydrogels exhibit outstanding ionic conductivity (up to ≈2.7 S m^?1) at ?40 °C, which exceeds the conductivities of most reported conductive hydrogels. Meanwhile, they present stable mechanical flexibility over a wide temperature range (?40 to 25 °C). More importantly, two types of the resulting hydrogel‐based flexible electronics, including a capacitive sensor and a resistive sensor, can maintain their response function at ?40 °C. This work offers a new solution to fabricate conductive hydrogels with antifreezing ability, which can broaden the working temperature range of flexible electronics.     

MXene Functionalized,Highly Breathable and Sensitive Pressure Sensors with Multi-Layered Porous Structure

Breathable, flexible, and highly sensitive pressure sensors have drawn increasing attention due to their potential in wearable electronics for body-motion monitoring, human-machine interfaces, etc. However, current pressure sensors are usually assembled with polymer substrates or encapsulation layers, thus causing discomfort during wearing (i.e., low air/vapor permeability, mechanical mismatch) and restricting their applications. A breathable and flexible pressure sensor is reported with nonwoven fabrics as both the electrode (printed with MXene interdigitated electrode) and sensing (coated with MXene/silver nanowires) layers via a scalable screen-printing approach. Benefiting from the multi-layered porous structure, the sensor demonstrates good air permeability with high sensitivity (770.86–1434.89 kPa⁻¹), a wide sensing range (0–100 kPa), fast response/recovery time (70/81 ms), and low detection limit (≈1 Pa). Particularly, this sensor can detect full-scale human motion (i.e., small-scale pulse beating and large-scale walking/running) with high sensitivity, excellent cycling stability, and puncture resistance. Additionally, the sensing layer of the pressure sensor also displays superior sensitivity to humidity changes, which is verified by successfully monitoring human breathing and spoken words while wearing a sensor-embedded mask. Given the outstanding features, this breathable sensor shows promise in the wearable electronic field for body health monitoring, sports activity detection, and disease diagnosis.     

Super-Stretchable,Anti-Freezing,Anti-Drying Organogel Ionic Conductor for Multi-Mode Flexible Electronics

Due to their intrinsic flexibility, tunable conductivity, multiple stimulus-response, and self-healing ability, ionic conductive hydrogels have drawn significant attention in flexible/wearable electronics. However, challenges remain because traditional hydrogels inevitably faced the problems of losing flexibility and conductivity because of the inner water loss when exposed to the ambient environment. Besides, the water inside the hydrogel will freeze at the water icing temperatures, making the device hard and fragile. As a promising alternative, organogels have attracted wide attention because they can, to some extent, overcome the above drawbacks. Herein, a kind of organogel ionic conductor (MOIC) by a self-polymerization reaction is involved, which is super stretchable, anti-drying, and anti-freezing. Meanwhile, it can still maintain high mechanical stability after alternately loading/unloading at the strain of 600% for 600 s (1800 cycles). Using this MOIC, high-performance triboelectric nanogenerator (TENG) is constructed (MOIC-TENG) to harvest small mechanical energy even the MOIC electrode underwent an extremely low temperature. In addition, multifunctional flexible/wearable sensors (strain sensor, piezoresistive sensor, and tactile sensor) are realized to monitor human motions in real time, and recognize different materials by triboelectric effect. This study demonstrates a promising candidate material for flexible/wearable electronics such as electronic skin, flexible sensors, and human-machine interfaces.     

Highly Conductive MXene/PEDOT:PSS-Integrated Poly(N-Isopropylacrylamide) Hydrogels for Bioinspired Somatosensory Soft Actuators

Sophisticated sensing and actuation capabilities of many living organisms in nature have inspired scientists to develop biomimetic somatosensory soft robots. Herein, the design and fabrication of homogeneous and highly conductive hydrogels for bioinspired somatosensory soft actuators are reported. The conductive hydrogels are synthesized by in situ copolymerization of conductive surface-functionalized MXene/Poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) ink with thermoresponsive poly(N-isopropylacrylamide) hydrogels. The resulting hydrogels are found to exhibit high conductivity (11.76 S m⁻¹), strain sensitivity (GF of 9.93), broad working strain range (≈560% strain), and high stability after over 300 loading–unloading cycles at 100% strain. Importantly, shape-programmable somatosensory hydrogel actuators with rapid response, light-driven remote control, and self-sensing capability are developed by chemically integrating the conductive hydrogels with a structurally colored polymer. As the proof-of-concept illustration, structurally colored hydrogel actuators are applied for devising light-driven programmable shape-morphing of an artificial octopus, an artificial fish, and a soft gripper that can simultaneously monitor their own motions via real-time resistance variation. This work is expected to offer new insights into the design of advanced somatosensory materials with self-sensing and actuation capabilities, and pave an avenue for the development of soft-matter-based self-regulatory intelligence via built-in feedback control that is of paramount significance for intelligent soft robotics and automated machines.     

Multifunctional Ionic Skin with Sensing,UV-Filtering,Water-Retaining,and Anti-Freezing Capabilities

Conductive polymer hydrogels are receiving considerable attention in applications such as soft robots and human-machine interfaces. Herein, a transparent and highly ionically conductive hydrogel that integrates sensing, UV-filtering, water-retaining, and anti-freezing performances is achieved by the organic combination of tannic acid-coated hydroxyapatite nanowires (TA@HAP NWs), polyvinyl alcohol (PVA) chains, ethylene glycol (EG), and metal ions. The highly ionic conductivity of the hydrogel enables tensile strain, pressure, and temperature sensing capabilities. In particular, in terms of the hydrogel strain sensors based on ionic conduction, it has high sensitivity (GF = 2.84) within a wide strain range (350%), high linearity (R² = 0.99003), fast response (≈50 ms) and excellent cycle stability. In addition, the incorporated TA@HAP NWs act as a nano-reinforced filler to improve the mechanical properties and confer a UV-shielding ability upon the hydrogel due to its size effect and the characteristics of absorbing ultraviolet light waves, which can reflect and absorb short ultraviolet rays and transmit visible light. Meanwhile, owing to the water-locking effect between EG and water molecules, the hydrogel exhibits freezing resistance at low temperatures and moisture retention at high temperatures. This biocompatible and multifunctional conductive hydrogel provides new ideas for the design of novel ionic skin devices.     

Lightweight,Superelastic, and Hydrophobic Polyimide Nanofiber /MXene Composite Aerogel for Wearable Piezoresistive Sensor and Oil/Water Separation Applications

Inspired by the ultralight and structurally robust spider webs, flexible nanofibril-assembled aerogels with intriguing attributes have been designed for achieving promising performances in various applications. Here, conductive polyimide nanofiber (PINF)/MXene composite aerogel with typical “layer-strut” bracing hierarchical nanofibrous cellular structure has been developed via the freeze-drying and thermal imidization process. Benefiting from the porous architecture and robust bonding between PINF and MXene, the PINF/MXene composite aerogel exhibits an ultralow density (9.98 mg cm⁻³), intriguing temperature tolerance from -50 to 250 °C, superior compressibility and recoverability (up to 90% strain), and excellent fatigue resistance over 1000 cycles. The composite aerogel can be used as a piezoresistive sensor, with an outstanding sensing capacity up to 90% strain (corresponding 85.21 kPa), ultralow detection limit of 0.5% strain (corresponding 0.01 kPa), robust fatigue resistance over 1000 cycles, excellent piezoresistive stability and reproductivity in extremely harsh environments. Furthermore, the composite aerogel also exhibits superior oil/water separation properties such as high adsorption capacity (55.85 to 135.29 g g⁻¹) and stable recyclability due to its hydrophobicity and robust hierarchical porous structure. It is expected that the designed PINF/MXene composite aerogel can supply a new multifunctional platform for human bodily motion/physical signals detection and high-efficient oil/water separation.     

Skin‐Inspired Antibacterial Conductive Hydrogels for Epidermal Sensors and Diabetic Foot Wound Dressings

Recently, artificial intelligence research has driven the development of stretchable and flexible electronic systems. Conductive hydrogels are a class of soft electronic materials that have emerging applications in wearable and implantable biomedical devices. However, current conductive hydrogels possess fundamental limitations in terms of their antibacterial performance and a mechanical mismatch with human tissues, which severely limits their applications in biological interfaces. Here, inspired by animal skin, a conductive hydrogel is fabricated from a supramolecular assembly of polydopamine decorated silver nanoparticles (PDA@Ag NPs), polyaniline, and polyvinyl alcohol, namely PDA@Ag NPs/CPHs. The resultant hydrogel has many desirable features, such as tunable mechanical and electrochemical properties, eye‐catching processability, good self‐healing ability as well as repeatable adhesiveness. Remarkably, PDA@Ag NPs/CPHs exhibit broad antibacterial activity against Gram‐negative and Gram‐positive bacteria. The potential application of this versatile hydrogel is demonstrated by monitoring large‐scale movements of the human body in real time. In addition, PDA@Ag NPs/CPHs have a significant therapeutic effect on diabetic foot wounds by promoting angiogenesis, accelerating collagen deposition, inhibiting bacterial growth, and controlling wound infection. To the best of the authors' knowledge, this is the first time that conductive hydrogels with antibacterial ability are developed for use as epidermal sensors and diabetic foot wound dressing.     

Knittable and Washable Multifunctional MXene‐Coated Cellulose Yarns

Textile‐based electronics enable the next generation of wearable devices, which have the potential to transform the architecture of consumer electronics. Highly conductive yarns that can be manufactured using industrial‐scale processing and be washed like everyday yarns are needed to fulfill the promise and rapid growth of the smart textile industry. By coating cellulose yarns with Ti₃C₂T_x MXene, highly conductive and electroactive yarns are produced, which can be knitted into textiles using an industrial knitting machine. It is shown that yarns with MXene loading of ≈77 wt% (≈2.2 mg cm^?1) have conductivity of up to 440 S cm^?1. After washing for 45 cycles at temperatures ranging from 30 to 80 °C, MXene‐coated cotton yarns exhibit a minimal increase in resistance while maintaining constant MXene loading. The MXene‐coated cotton yarn electrode offers a specific capacitance of 759.5 mF cm^?1 at 2 mV s^?1. A fully knitted textile‐based capacitive pressure sensor is also prepared, which offers high sensitivity (gauge factor of ≈6.02), wide sensing range of up to ≈20% compression, and excellent cycling stability (2000 cycles at ≈14% compression strain). This work provides new and practical insights toward the development of platform technology that can integrate MXene in cellulose‐based yarns for textile‐based devices.     

Flexible and Multifunctional Silk Textiles with Biomimetic Leaf‐Like MXene/Silver Nanowire Nanostructures for Electromagnetic Interference Shielding,Humidity Monitoring,and Self‐Derived Hydrophobicity

Although flexible and multifunctional textiles are promising for wearable electronics and portable device applications, the main issue is to endow textiles with multifunctionalities while maintaining their innate flexible and porous features. Herein, a vacuum‐assisted layer‐by‐layer assembly technique is demonstrated to conformally deposit electrically conductive substances on textiles for developing multifunctional and flexible textiles with superb electromagnetic interference (EMI) shielding performances, superhydrophobicity, and highly sensitive humidity response. The formed leaf‐like nanostructure is composed of silver nanowires (AgNWs) as the highly conductive skeleton (vein) and transition metal carbide/carbonitride (MXene) nanosheets as the lamina. The presence of MXene protects AgNWs from oxidation and enhances the combination of AgNWs with the fabric substrate, and the transformation of its functional groups leads to self‐derived hydrophobicity. The flexible and multifunctional textile exhibits a low sheet resistance of 0.8 Ω sq^?1, outstanding EMI shielding efficiency of 54 dB in the X‐band at a small thickness of 120 µm, and highly sensitive humidity responses, while retaining its satisfactory porosity and permeability. The self‐derived hydrophobicity with a large contact angle of >140° is achieved by aging the hydrophilic MXene coated silk. The wearable multifunctional textiles are highly promising for applications in intelligent garments, humidity sensors, actuators, and EMI shielding.     

Large-Area Smooth Conductive Films Enabled by Scalable Slot-Die Coating of Ti3C2Tx MXene Aqueous Inks

Large-area flexible transparent conductive electrodes (TCEs) featuring excellent optoelectronic properties (low sheet resistance, R_s, at high transparency, T) are vital for integration in transparent wearable electronics (i.e., antennas, sensors, supercapacitors, etc.). Solution processing (i.e., printing and coating) of conductive inks yields highly uniform TCEs at low cost, holding great promise for commercially manufacturing of transparent electronics. However, to formulate such conductive inks as well as to realize continuous conductive films in the absence of percolation issue are quite challenging. Herein, the scalable slot-die coating of Ti₃C₂T_x MXene aqueous inks is reported for the first time to yield large-area uniform TCEs with outstanding optoelectronic performance, that is, average DC conductivity of 13 000 ± 500 S cm⁻¹. The conductive MXene nanosheets are forced to orientate horizontally as the inks are passing through the moving slot, leading to the rapid manufacturing of highly aligned MXene TCEs without notorious percolation problems. Moreover, through tuning the ink formulations, such conductive MXene films can be easily adjusted from transparent to opaque as required, demonstrating very low surface roughness and even mirror effects. These high-quality, slot-die-coated MXene TCEs also demonstrate excellent electrochemical charge storage properties when assembled into supercapacitors.     

Fishing Net-Inspired Mutiscale Ionic Organohydrogels with Outstanding Mechanical Robustness for Flexible Electronic Devices

Mechanically robust and electrically conductive organohydrogels/hydrogels are increasingly required in flexible electronic devices, but it remains a challenge to achieve organohydrogels/hydrogels with integrated high performances. Herein, inspired by the geometric deformability and robustness of fishing nets, multiscale ionic organohydrogels with outstanding isotropic mechanical robustness are developed. The organohydrogels are prepared by introducing polyacrylamide (PAM) hydrogel, Zn²⁺ and a binary solvent of glycerol-water into a crosslinked fibrous mat which is electrospun from poly(acrylic acid) (PAA) and poly(vinyl alcohol) (PVA). Because of the unique structure, the resultant organohydrogels, being mentioned as PAA-PVA/PAM/Zn²⁺ organohydrogels, exhibit outstanding tensile strength (9.45 MPa), high stretchability, excellent anti-fatigue property, skin-like mechanical behaviors and ionic conductivity. Importantly, the organohydrogels are promising in flexible electronic devices capable of operating properly over a wide temperature range and under harsh mechanical conditions, such as mechanical-electrical signal transducing materials in flexible mechanosensors and robust electrolytes in zinc ion hybrid supercapacitors. Not only the multiscale design strategy will provide a clue to improve the mechanical properties of soft materials, but also the organohydrogels offer promising materials for future flexible electronic devices.     

Tough and Stretchable Phenolic-Reinforced Double Network Deep Eutectic Solvent gels for Multifunctional Sensors with Environmental Adaptability

Conductive gels are perfect for various sensor applications due to their inherent stretchability, flexibility, and electrical conductivity. However, their poor environmental adaptability and low fracture toughness restrict their potential applications. In this study, resorcinol-formaldehyde resin (RF) is used for the first time as a rigid network compounded with a flexible polyacrylic acid (PAA) network to successfully prepare a double network (DN) deep eutectic solvent gel (RF/PAA DN gel). The gel has high stress strength (1.04 MPa), compressive strength (10.63 MPa), and toughness (1.07 MJ m⁻³). The addition of RF significantly improves the mechanical properties and gives the RF/PAA DN gel certain photothermal effects, swelling resistance, and flame retardancy, broadening the scope of use and application of the gel. Importantly, as a multifunctional sensor, it can combine deformation sensing, temperature sensing, optical sensing, humidity sensing, and underwater sensing into one, with a wide range of stimuli responses and excellent sensing properties. Excellent environmental suitability also allows its use in a wide range of temperatures (−20−90 °C), humidity (55%−90% RH), underwater, and in fire conditions. The work provides new ideas for choosing rigid networks and a novel strategy for developing multifunctional sensors with excellent performance in complex environments.     

Flexible Breathable Nanomesh Electronic Devices for On‐Demand Therapy

Flexible electronics are drawing tremendous interest for various applications in wearable healthcare biomonitoring, on‐demand therapy, and human–machine interactions. However, conventional plastic substrates with uncomfortableness, mechanical mismatches, and impermeability have limited the application of flexible on‐skin electronic devices for healthcare biomonitoring and on‐demand therapy. Herein, flexible breathable electronic devices with the capabilities of real‐time temperature sensing and timely on‐demand anti‐infection therapy at wound sites are presented. These devices are assembled from a crosslinked electrospun moxifloxacin hydrochloride (MOX)‐loaded thermoresponsive polymer nanomesh film with a conductive pattern. The conductive polymer nanomesh film demonstrates excellent flexibility, reliable breathability, and robust environmental stability. Furthermore, the assembled temperature sensor displays a linear relationship between the electrical resistance and temperature, potentially enabling real‐time biomonitoring of tissue temperature at the wound site. Smart artificial electronic skins (E‐skins) are assembled from the thermoresponsive polymer nanomesh film for spatial touching sensing mapping of temperature changes. Furthermore, the flexible temperature sensor is coupled with a wireless transmitter for real‐time wireless temperature monitoring. Notably, the thermoresponsive polymer nanomesh film can also be assembled as a highly efficient flexible heater to trigger the on‐demand release of antibiotics loaded in the fibers to eliminate bacterial colonization in the wound site once infection has occurred.     

Low-Molecular-Weight Supramolecular-Polymer Double-Network Eutectogels for Self-Adhesive and Bidirectional Sensors

Ionic conducting eutectogels have attracted enormous attention as an alternative to the conventional temperature-intolerant hydrogels and costly ionic liquid gels in constructing flexible electronic devices. However, current eutectogels prepared via cross-linked polymer or low-molecular-weight gelators suffer from limited stretchability and insufficient surface-adaptive adhesion. Herein, a low-molecular-weight supramolecular network is introduced into a covalent polymer network in a eutectogel architecture, and a novel supramolecular-polymer double-network (SP-DN) strategy is demonstrated to fabricate conductive SP-DN eutectogels with high stretchability (>4000% elongation) and toughness (≈800 J m⁻²), as well as self-healing, self-adhesive and anti-freezing/anti-drying characteristics. These unique features lead to the successful realization of SP-DN eutectogels in wearable self-adhesive strain sensors, which can conformally deform with the skin and dynamically monitor body movements with high sensitivity and long-term stability over a wide temperature range (−40 to 60 °C). Furthermore, the strain sensors can accurately detect body movements along two opposite directions (bend up or bend down), which are rarely reported in the literature. Distinct from the widely explored polymer double-network (P-DN) hydrogels, the developed SP-DN eutectogel platform is capable of well-regulating molecular-scale noncovalent and covalent interactions, providing a paradigm for the creation of smart soft materials with versatile performance and high environmental adaptability.     

Bio-Inspired Stimuli-Responsive Ti3C2Tx/PNIPAM Anisotropic Hydrogels for High-Performance Actuators

Near-infrared (NIR) light-responsive hydrogels have the advantages of high precision, remote control and excellent biocompatibility, which are widely used in soft biomimetic actuators. The process by which water molecules diffuse can directly affect the deformation of hydrogel. Therefore, it remains a serious challenge to improve the response speed of hydrogel actuator. Herein, an anisotropic photo-responsive conductive hydrogel is designed by a directional freezing method. Due to the anisotropy of the MXene-based PNIPAM/MXene directional (PMD) hydrogel, its mechanical properties and conductivity are enhanced in a specific direction. At the same time, with the presence of the internal directional channels and the assistance of capillary force, the PMD hydrogel can achieve a volume deswelling of 70% in 2 s under light irradiation, further building a hydrogel actuator with a fast response performance. Additionally, the hydrogel actuator can lift an object 40 times its weight by a distance of 6 mm, realizing the advantages of both rapid responsiveness and high driving strength, which makes the hydrogel actuator have important application significance in remote control, microflow valve, and soft robot.     

Recent Advances in MXene-Based Aerogels: Fabrication,Performance and Application

As one of the “miracle materials” in the 21st century, aerogels with ultra-low weight and remarkable mechanical performance have emerged and shown incredible immunity to harsh working environments, attracting substantial research interests across a wide range of areas. Recently, exploitation of MXene nanosheets into aerogels represents a new research focus in the field of materials science, on account of their unique structures and outstanding properties. In this review, the aim is to provide a timely and insightful overview for the recent advances in the fabrication, performance, and application of MXene-based aerogels. The main strategies for constructing MXene-based aerogels, directly from MXene-dispersion or in the presence of other functional components, are summarized. Furthermore, the desirable performance of MXene-based aerogels and their related applications in the areas including electromagnetic management, sensors, solar steam generators, and energy storage are highlighted. A thorough investigation and comparison of their mechanical, electrical, sensing, and other properties are performed to understand the structure-property relationships. At last, this study is concluded with summary and outlook section on the future development as well as challenges that remained, thus bringing new research opportunities for the material engineering and functional application of MXene-based aerogels.     

Multifunctional,Ultra-Tough Organohydrogel E-Skin Reinforced by Hierarchical Goatskin Fibers Skeleton for Energy Harvesting and Self-Powered Monitoring

E-skins based on conductive hydrogels are regarded as ideal candidates for sensing application. However, limited by the constructed materials and strategies, the current conductive hydrogels have poor mechanical properties, single function, and unsatisfactory conductivity, which seriously hinder their development and application. Herein, the natural goatskin with hierarchical 3D network structure weaved by collagen fibers is used as the substrate material for the construction of ultra-tough hydrogel through a “top-down” strategy, in which acrylic acid monomer is first vacuum-impregnated into the interstices of goatskin fibers skeleton and is then polymerized in situ to produce the skin-based hydrogel with unique 3D wrapping structure. Based on the skin-based hydrogel, a substrate with load-carrying capacity, after loaded with a new multifunctional nanoscale-conductive medium nanosilver particles (AgNPs) and 1,3-propanediol, a goatskin-derived multifunctional organohydrogel S@HCP is constructed with excellent mechanical properties, self-adhesion, transparency, ultraviolet shielding, antibacterial, biocompatibility, environmental stability, and conductivity. Notably, the stretchable S-TENG assembled using S@HCP can be perfectly suited for real-life applications including biomechanical energy harvesting, self-powered tactile-sensing, and motion monitoring. It is believed that, by combining natural animal skin with different functional materials, it is possible to reuse animal skin, “dead skin,” which provides a new platform for developing multifunctional flexible e-skin.