Single‐Thread‐Based Wearable and Highly Stretchable Triboelectric Nanogenerators and Their Applications in Cloth‐Based Self‐Powered Human‐Interactive and Biomedical Sensing

The development of wearable and large‐area fabric energy harvester and sensor has received great attention due to their promising applications in next‐generation autonomous and wearable healthcare technologies. Here, a new type of “single” thread‐based triboelectric nanogenerator (TENG) and its uses in elastically textile‐based energy harvesting and sensing have been demonstrated. The energy‐harvesting thread composed by one silicone‐rubber‐coated stainless‐steel thread can extract energy during contact with skin. With sewing the energy‐harvesting thread into a serpentine shape on an elastic textile, a highly stretchable and scalable TENG textile is realized to scavenge various kinds of human‐motion energy. The collected energy is capable to sustainably power a commercial smart watch. Moreover, the simplified single triboelectric thread can be applied in a wide range of thread‐based self‐powered and active sensing uses, including gesture sensing, human‐interactive interfaces, and human physiological signal monitoring. After integration with microcontrollers, more complicated systems, such as wireless wearable keyboards and smart beds, are demonstrated. These results show that the newly designed single‐thread‐based TENG, with the advantage of interactive, responsive, sewable, and conformal features, can meet application needs of a vast variety of fields, ranging from wearable and stretchable energy harvesters to smart cloth‐based articles.     

A Nonmetallic Stretchable Nylon‐Modified High Performance Triboelectric Nanogenerator for Energy Harvesting

As a new energy harvesting strategy, triboelectric nanogenerators which have a broad application prospect in collecting environmental energy, human body mechanical energy, and supplying power for low‐power electronic devices, have attracted extensive attention. However, technology challenges still exist in the stretchability for the preparation of some high‐performance triboelectric materials. In this work, a new strategy for nonmetallic nylon‐modified triboelectric nanogenerators (NM‐TENGs) is reported. Nylon is introduced as a high performance friction material to enhance the output performance of the stretchable TENG. The uniform matrix reduces the difficulty of heterogeneous integration and enhances the structural strength. The open‐circuit voltage (V_OC) and short‐circuit current (I_SC) of NM‐TENG can reach up to 1.17 kV and 138 µA, respectively. The instantaneous power density reaches 11.2 W m^?2 and the rectified output can directly light ≈480 LEDs. The transferred charge density is ≈100 µC m^?2 in one cycle when charging the capacitor. In addition, a low‐power electronic clock can be driven directly by the rectified signal without additional circuits. NM‐TENG also has high enough strain rate and can be attached to the human body for energy harvesting effectively. This work provides a new idea for fabrication of stretchable TENGs and demonstrates their potential application.     

A Wrinkled PEDOT:PSS Film Based Stretchable and Transparent Triboelectric Nanogenerator for Wearable Energy Harvesters and Active Motion Sensors

The functionalized conductive polymer is a promising choice for flexible triboelectric nanogenerators (TENGs) for harvesting human motion energy still poses challenges. In this work, a transparent and stretchable wrinkled poly(3,4‐ethylenedioxythiophene):poly(4‐styrenesulfonate) (PEDOT:PSS) electrode based TENG (WP‐TENG) is fabricated. The optimum conductivity and transparency of PEDOT:PSS electrode can reach 0.14 kΩ □⁻¹ and 90%, respectively, with maximum strain of ≈100%. Operating in single‐electrode mode at 2.5 Hz, the WP‐TENG with an area of 6 × 3 cm² produces an open‐circuit voltage of 180 V, short‐circuit current of 22.6 µA, and average power density of 4.06 mW m⁻². It can be worn on the wrist to harvest hand tapping energy and charge the capacitor to 2 V in ≈3.5 min, and then drive an electronic watch. Furthermore, the WP‐TENG as the human motion monitoring sensor could inspect the bending angle of the elbow and joint by analyzing the peak value of voltage and monitor the motion frequency by counting the peak number. The triboelectric mechanism also enables the WP‐TENG to realize high‐performance active tactile sensing. The assembled 3 pixel × 3 pixel tactile sensor array is fabricated for mapping the touch location or recording the shape of object contacted with the sensor array.     

Highly Porous Polymer Aerogel Film‐Based Triboelectric Nanogenerators

A novel class of high performance polymer porous aerogel film‐based triboelectric nanogenerators (A‐NGs) is demonstrated. The A‐NGs, made of a pair of highly porous polymer films, exhibit much higher triboelectric outputs than the corresponding dense polymer film‐based triboelectric nanogenerators (D‐NGs) under the same mechanical stress. The triboelectric outputs of the A‐NGs increase significantly with increasing porosity, which can be attributed to the increase in contact area and the electrostatic induction in the porous structure, thereby leading to additional charges on the porous surface. Remarkably, the A‐NG fabricated using porous chitosan aerogel film paired with the most porous polyimide (with a porosity of 92%) aerogel film demonstrates a very high voltage of 60.6 V and current of 7.7 µA, corresponding to a power density of 2.33 W m^?2, which is sufficient to power 22 blue light‐emitting‐diodes (LEDs). This is the first report on triboelectric nanogenerators (TENGs) employing porous polymer aerogel films as both positive and negative materials to enhance triboelectric outputs. Furthermore, enhancing the tribopositive polarity of the cellulose aerogel film via silanization using aminosilane can dramatically improve the triboelectric performance. Therefore, this study provides new insights into investigating porous materials with tunable triboelectric polarities for high performance TENGs.     

Waterproof,Breathable, and Antibacterial Self‐Powered e‐Textiles Based on Omniphobic Triboelectric Nanogenerators

Multifunctional electronic textiles (e‐textiles) incorporating miniaturized electronic devices will pave the way toward a new generation of wearable devices and human–machine interfaces. Unfortunately, the development of e‐textiles is subject to critical challenges, such as battery dependence, breathability, satisfactory washability, and compatibility with mass production techniques. This work describes a simple and cost‐effective method to transform conventional garments and textiles into waterproof, breathable, and antibacterial e‐textiles for self‐powered human–machine interfacing. Combining embroidery with the spray‐based deposition of fluoroalkylated organosilanes and highly networked nanoflakes, omniphobic triboelectric nanogenerators (R^F‐TENGs) can be incorporated into any fiber‐based textile to power wearable devices using energy harvested from human motion. R^F‐TENGs are thin, flexible, breathable (air permeability 90.5 mm s^?1), inexpensive to fabricate (<0.04$ cm^?2), and capable of producing a high power density (600 µW cm^?2). E‐textiles based on R^F‐TENGs repel water, stains, and bacterial growth, and show excellent stability under mechanical deformations and remarkable washing durability under standard machine‐washing tests. Moreover, e‐textiles based on R^F‐TENGs are compatible with large‐scale production processes and exhibit high sensitivity to touch, enabling the cost‐effective manufacturing of wearable human–machine interfaces.     

Stretchable Energy‐Harvesting Tactile Interactive Interface with Liquid‐Metal‐Nanoparticle‐Based Electrodes

Energy‐harvesting electronic skin (E‐skin) is highly promising for sustainable and self‐powered interactive systems, wearable human health monitors, and intelligent robotics. Flexible/stretchable electrodes and robust energy‐harvesting components are critical in constructing soft, wearable, and energy‐autonomous E‐skin systems. A stretchable energy‐harvesting tactile interactive interface is demonstrated using liquid metal nanoparticles (LM‐NPs)‐based electrodes. This stretchable energy‐harvesting tactile interface relies on triboelectric nanogenerator composed of a galinstan LM‐NP‐based stretchable electrode and patterned elastic polymer friction and encapsulation layer. It provides stable and high open‐circuit voltage (268 V), short‐circuit current (12.06 µA), and transferred charges (103.59 nC), which are sufficient to drive commercial portable electronics. As a self‐powered tactile sensor, it presents satisfactory and repeatable sensitivity of 2.52 V·kPa^?1 and is capable of working as a touch interactive keyboard. The demonstrated stretchable and robust energy‐harvesting E‐skin using LM‐NP‐based electrodes is of great significance in sustainable human–machine interactive system, intelligent robotic skin, security tactile switches, etc.     

Fully Elastic and Metal‐Free Tactile Sensors for Detecting both Normal and Tangential Forces Based on Triboelectric Nanogenerators

A tactile sensor should be able to detect both normal and tangential forces, which is mandatory for simulating human hands, but this fundamental function has been overlooked by most of the previous studies. Here, based on a triboelectric nanogenerator (TENG) with single‐electrode mode, the fully elastic and metal‐free tactile sensor that can detect both normal and tangential forces is proposed. With tiny burr arrays on the contact interface to facilitate the elastic deformation, the detected normal pressure by the device can reach to 1.5 MPa with a sensitivity of about 51.43 kPa V⁻¹, and a large range of tangential forces can be detected ranging from 0.5 to 40 N with rough sensitivity of 0.83 N V⁻¹ (0.5–3 N) and 2.50 N V⁻¹ (3–40 N). Meanwhile, the applied tangential forces from different directions can also be clearly distinguished by the four‐partitioned electrode structure. Moreover, a shield film is coated on the top surface of the device, which can screen the electrostatic interference and enhance the repeatability of the device. The demonstrated concept of this self‐powered tactile sensor has excellent applicability for industrial robotics, human–machine interactions, artificial intelligence, etc.     

Tunable Optical Modulator by Coupling a Triboelectric Nanogenerator and a Dielectric Elastomer

A conjunction system based on triboelectric nanogenerator (TENG) and dielectric elastomer actuator (DEA) is a promising demonstration for the application of TENG in the field of electronic skin and soft robotics. In this paper, a triboelectric tunable smart optical modulator (SOM) has been proposed based on this TENG‐DEA system. The SOM has a very simple structure of an elastomer film and electrodes made of dispersed silver nanowires. Owing to the voltage induced rippling of the elastomer, the output of the TENG for a contact‐separation motion at a velocity ranging from 0.5 to 10 cm s^?1 can decrease the SOM's transmittance from 72% to 40%, which is enough for realizing the function of privacy protection. Meanwhile, an effective operation method is also proposed for this SOM. By serially connecting an accessory DEA to the SOM, an external bias voltage can be applied on the SOM to tune its “threshold” voltage and the output from TENG can smoothly regulate the transmittance on the basis of the bias. The proposed operation method has excellent applicability for all DEA‐based devices, which can promote the practical study of TENG‐DEA system in the field of micro‐electro‐mechanical system and human–robots interaction.     

Theoretical Investigation and Structural Optimization of Single‐Electrode Triboelectric Nanogenerators

Single‐electrode triboelectric nanogenerators (SETENGs) significantly expand the application of triboelectric nanogenerators in various circumstances, such as touch‐pad technologies. In this work, a theoretical model of SETENGs is presented with in‐depth interpretation and analysis of their working principle. Electrostatic shield effect from the primary electrode is the main consideration in the design of such SETENGs. On the basis of this analysis, the impacts of two important structural parameters, that is, the electrode gap distance and the area size, on the output performance are theoretically investigated. An optimized electrode gap distance and an optimized area size are observed to provide a maximum transit output power. Parallel connection of multiple SETENGs with micro‐scale size and relatively larger spacing should be utilized as the scaling‐up strategy. The discussion of the basic working principle and the influence of structural parameters on the whole performance of the device can serve as an important guidance for rational design of the device structure towards the optimum output in specific applications.     

Self-Powered Syringe Pump for Insulin Pump Therapy Based on High-Voltage Triboelectric Nanogenerator and Dielectric Elastomer Actuator

Insulin pump therapy (IPT) is commonly utilized for treating type 1 diabetes. However, the insulin pump is generally rigid, and its prolonged use can cause discomfort to patients. Additionally, the device suffers from other drawbacks such as limited battery life. Herein, an IPT system consisting of a dielectric elastomer-based soft syringe pump (DE-SSP) and a high-voltage triboelectric nanogenerator (H-TENG) is introduced, which can achieve stable and adjustable liquid output depending on real-time blood glucose. The maximum pump volume of this IPT can reach 262.4 or 303.7 µL when powered by a DC source or H-TENG, respectively, which is generally sufficient to meet the requirements of the therapy. H-TENG possesses a sensitive self-protection mechanism that minimizes the risk of electrical damage and it can be easily fabricated or repaired and flexibly designed according to the application environment. The proposed IPT system is compatible with different placement angles and utilizes compliant electrodes with good biocompatibility that ensure its safety. It also overcomes common issues including rigidness, relatively fixed bolus delivery options, and short battery life associated with traditional insulin pumps. This study not only demonstrates a combination of H-TENG and DE-based actuators but also opens new avenues for microelectromechanical systems micropumps.     

All‐Plastic‐Materials Based Self‐Charging Power System Composed of Triboelectric Nanogenerators and Supercapacitors

Triboelectric nanogenerators (TENG) are a possible power source for wearable electronics, but the conventional electrode materials for TENG are metals such as Cu and Al that are easy to be oxidized or corroded in some harsh environments. In this paper, metal electrode material is replaced by an electrical conducting polymer, polypyrrole (PPy), for the first time. Moreover, by utilizing PPy with micro/nanostructured surface as the triboelectric layer, the charge density generated is significantly improved, more superior to that of TENG with metals as the triboelectric layer. As this polymer‐based TENG is further integrated with PPy‐based supercapacitors, an all‐plastic‐materials based self‐charging power system is built to provide sustainable power with excellent long cycling life. Since the environmental friendly materials are adopted and the facile electrochemical deposition technique is applied, the new self‐charging power system can be a practical and low cost power solution for many applications.     

Stretchable,Washable, and Ultrathin Triboelectric Nanogenerators as Skin-Like Highly Sensitive Self-Powered Haptic Sensors

Accompanying the boom in multifunctional wearable electronics, flexible, sustainable, and wearable power sources are facing great challenges. Here, a stretchable, washable, and ultrathin skin-inspired triboelectric nanogenerator (SI-TENG) to harvest human motion energy and act as a highly sensitive self-powered haptic sensor is reported. With the optimized material selections and structure design, the SI-TENG is bestowed with some merits, such as stretchability ( ≈ 800%), ultrathin ( ≈ 89 µ m), and light-weight ( ≈ 0.23 g), which conformally attach on human skin without disturbing its contact. A stretchable composite electrode, which is formed by homogenously intertwining silver nanowires (AgNWs) with thermoplastic polyurethane (TPU) nanofiber networks, is fabricated through synchronous electrospinning of TPU and electrospraying of AgNWs. Based on the triboelectrification effect, the open-circuit voltage, short-circuit current, and power density of the SI-TENG with a contact area of 2 × 2 cm² and an applied force of 8 N can reach 95 V, 0.3 µ A, and 6 mW m⁻², respectively. By integrating the signal-processing circuits, the SI-TENG with excellent energy harvesting and self-powered sensing capability is demonstrated as a haptic sensor array to detect human actions. The SI-TENG exhibits extensive applications in the fields of human–machine interface and security systems.     

Triboelectric Nanogenerators as a Self‐Powered Motion Tracking System

Motion tracking is a key area of sensor systems for security, transportation, and high‐tech industry. In this work, a self‐powered motion tracking system is developed to monitor moving speed, direction, acceleration, starting and ending positions, and even the moving path of a moving object. Such a system is based on a set of triboelectric nanogenerators (TENGs) that are composed of two friction layers with opposite triboelectric polarities (Kapton and Aluminum) and operates in the sliding mode. Velocities of a moving object are monitored from ?0.1 m s^‐1 to +0.1 m s^‐1 at a step of 0.01 m s^‐1, and accelerations from ?0.1 m s^‐2 to +0.1 m s^‐2 at a step of 0.02 m s^‐2. Furthermore, an 8 × 8 two‐dimensional coordinates system with 16 groups of TENGs is created, and the moving path of an object is obtained. This study opens up a new area of TENGs as active sensors with great potential in self‐powered systems, positioning detecting, motion tracking, environmental and infrastructure monitoring, and security.     

Triboelectric Nanogenerators Based on Melamine and Self‐Powered High‐Sensitive Sensors for Melamine Detection

Melamine (Mel) is added illegally to foods and feeds due to its high nitrogen content and high intake, and it causes serious health problems, so it is urgent to build a simple and quick method for detecting Mel in our daily life. In this work, a self‐powered Mel detection method is developed that is based on the newly invented triboelectric nanogenerator (TENG) by using the strong electronegativity property of Mel. In addition, Mel can enhance the electrical output signals of the TENGs by pairing with other triboelectric materials. Thus a high‐sensitive Mel sensor is designed based on polytetrafluoethylene (PTFE) TENG; the output current of TENG increases with the addition of Mel, resulting in largely improved detection limit of Mel with 0.5 ppb and a linear increase range from 1 to 500 ppb. This study not only develops a new type of material for TENG, but also demonstrates an innovative and convenient method for the detection of Mel and other biomaterials.     

Stretchable,Transparent, and Self‐Patterned Hydrogel‐Based Pressure Sensor for Human Motions Detection

In this study, a binary networked conductive hydrogel is prepared using acrylamide and polyvinyl alcohol. Based on the obtained hydrogel, an ultrastretchable pressure sensor with biocompatibility and transparency is fabricated cost effectively. The hydrogel exhibits impressive stretchability (>500%) and superior transparency (>90%). Furthermore, the self‐patterned microarchitecture on the hydrogel surface is beneficial to achieve high sensitivity (0.05 kPa^?1 for 0–3.27 kPa). The hydrogel‐based pressure sensor can precisely monitor dynamic pressures (3.33, 5.02, and 6.67 kPa) with frequency‐dependent behavior. It also shows fast response (150 ms), durable stability (500 dynamic cycles), and negligible current variation (6%). Moreover, the sensor can instantly detect both tiny (phonation, airflowing, and saliva swallowing) and robust (finger and limb motions) physiological activities. This work presents insights into preparing multifunctional hydrogels for mechanosensory electronics.     

High‐Performance Piezoelectric,Pyroelectric, and Triboelectric Nanogenerators Based on P(VDF‐TrFE) with Controlled Crystallinity and Dipole Alignment

Poly(vinylidenefluoride‐co‐trifluoroethylene) (P(VDF‐TrFE)), as a ferroelectric polymer, offers great promise for energy harvesting for flexible and wearable applications. Here, this paper shows that the choice of solvent used to dissolve the polymer significantly influences its properties in terms of energy harvesting. Indeed, the P(VDF‐TrFE) prepared using a high dipole moment solvent has higher piezoelectric and pyroelectric coefficients and triboelectric property. Such improvements are the result of higher crystallinity and better dipole alignment of the polymer prepared using a higher dipole moment solvent. Finite element method simulations confirm that the higher dipole moment results in higher piezoelectric, pyroelectric, and triboelectric potential distributions. Furthermore, P(VDF‐TrFE)‐based piezoelectric, pyroelectric, and triboelectric nanogenerators (NGs) experimentally validate that the higher dipole moment solvent significantly enhances the power output performance of the NGs; the improvement is about 24% and 82% in output voltage and current, respectively, for piezoelectric NG; about 40% and 35% in output voltage and current, respectively, for pyroelectric NG; and about 65% and 75% in output voltage and current for triboelectric NG. In brief, the approach of using a high dipole moment solvent is very promising for high output P(VDF‐TrFE)‐based wearable NGs.     

High‐Performance Triboelectric Nanogenerators Based on Electrospun Polyvinylidene Fluoride–Silver Nanowire Composite Nanofibers

The preparation of ferroelectric polymer–metallic nanowire composite nanofiber triboelectric layers is described for use in high‐performance triboelectric nanogenerators (TENGs). The electrospun polyvinylidene fluoride (PVDF)–silver nanowire (AgNW) composite and nylon nanofibers are utilized in the TENGs as the top and bottom triboelectric layers, respectively. The electrospinning process facilitates uniaxial stretching of the polymer chains, which enhances the formation of the highly oriented crystalline β‐phase that forms the most polar crystalline phase of PVDF. The addition of AgNWs further promotes the β‐phase crystal formation by introducing electrostatic interactions between the surface charges of the nanowires and the dipoles of the PVDF chains. The extent of β‐phase formation and the resulting variations in the surface charge potential upon the addition of nanowires are systematically analyzed using X‐ray diffraction (XRD) and Kelvin probe force microscopy techniques. The ability of trapping the induced tribocharges increases upon the addition of nanowires to the PVDF matrix. The enhanced surface charge potential and the charge trapping capabilities of the PVDF–AgNW composite nanofibers significantly enhance the TENG output performances. Finally, the mechanical stability of the electrospun nanofibers is dramatically enhanced while maintaining the TENG performances by applying thermal welding near the melting temperature of PVDF.     

Rolling Friction Enhanced Free‐Standing Triboelectric Nanogenerators and their Applications in Self‐Powered Electrochemical Recovery Systems

Heavy metals contained in wastewater are one of the most serious pollutions in natural resources. A self‐powered electrochemical recovery system for collecting Cu ions in wastewater by incorporating a rolling friction enhanced freestanding triboelectric nanogenerator (RF‐TENG) is developed here. The RF‐TENG utilizes integrated cylindrical surfaces using the conjunction of rolling electrification and freestanding electrostatic induction, which shows outstanding output performance and ultrarobust stability. By using the kinetic energy of flowing water, a collection efficiency of up to 80% for Cu²⁺ ions in wastewater has been achieved. Self‐powered electrochemical systems are one of the most promising applications of TENGs for independent and sustainable driving of electrochemical reactions without the need for any additional power supply. This research is a substantial advancement towards the practical applications of triboelectric nanogenerators and self‐powered electrochemical systems.     

Self‐Healing,Flexible, and Tailorable Triboelectric Nanogenerators for Self‐Powered Sensors based on Thermal Effect of Infrared Radiation

Self‐healing triboelectric nanogenerators (TENGs) with flexibility, robustness, and conformability are highly desirable for promising flexible and wearable devices, which can serve as a durable, stable, and renewable power supply, as well as a self‐powered sensor. Herein, an entirely self‐healing, flexible, and tailorable TENG is designed as a wearable sensor to monitor human motion, with infrared radiation from skin to promote self‐healing after being broken based on thermal effect of infrared radiation. Human skin is a natural infrared radiation emitter, providing favorable conditions for the device to function efficiently. The reversible imine bonds and quadruple hydrogen bonding (UPy) moieties are introduced into polymer networks to construct self‐healable electrification layer. UPy‐functionalized multiwalled carbon nanotubes are further incorporated into healable polymer to obtain conductive nanocomposite. Driven by the dynamic bonds, the designed and synthesized materials show excellent intrinsic self‐healing and shape‐tailorable features. Moreover, there is a robust interface bonding in the TENG devices due to the similar healable networks between electrification layer and electrode. The output electric performances of the self‐healable TENG devices can almost restore their original state when the damage of the devices occurs. This work presents a novel strategy for flexible devices, contributing to future sustainable energy and wearable electronics.     

Metal‐Free Growth of Nanographene on Silicon Oxides for Transparent Conducting Applications

Conventional methods to prepare large‐area graphene for transparent conducting electrodes involve the wet etching of the metal catalyst and the transfer of the graphene film, which can degrade the film through the creation of wrinkles, cracks, or tears. The resulting films may also be obscured by residual metal impurities and polymer contaminants. Here, it is shown that direct growth of large‐area flat nanographene films on silica can be achieved at low temperature (400 °C) by chemical vapor deposition without the use of metal catalysts. Raman spectroscopy and TEM confirm the formation of a hexagonal atomic network of sp²‐bonded carbon with a domain size of about 3–5 nm. Further spectroscopic analysis reveals the formation of SiC between the nanographene and SiO₂, indicating that SiC acts as a catalyst. The optical transmittance of the graphene films is comparable with transferred CVD graphene grown on Cu foils. Despite the fact that the electrical conductivity is an order of magnitude lower than CVD graphene grown on metals, the sheet resistance remains 1–2 orders of magnitude better than well‐reduced graphene oxides.