Publications

Abstract Here, a self‐powered optical switch (OS) composed of a surface‐etched single‐electrode triboelectric nanogenerator (TENG) and a polymer‐dispersed liquid crystal (PDLC) film is reported. The working principle of the developed OS is that the liquid crystal alignment can be driven by triboelectrification‐generated voltage, inducing the PDLC film to rapidly switch its initial translucent state to an instantaneous transparent state. An output voltage of 360 V is generated upon the PDLC film when a nitrile rubber film contacts with the TENG at an area of 25 cm 2 and a velocity of 0.4 m s −1 . As such, a wide dimming range with the relative transmitted light intensity from 0.05 to 0.85 can be achieved for the OS. Enabled by the unique mechano‐electro‐optical reaction, the effects of a series of structural parameters on the performance of the OS are methodically studied. Particularly, through integrating the OS with a visible‐light‐operated signal‐processing circuit, a complete wireless sensing system with a fully power‐free sensing node is developed. The paradigms of hand touching and foot stepping triggered wireless alarms are demonstrated, explicitly showing great potential for the system in many possible interactive human–machine interface applications, such as surveillance, security systems, remote operation, and automatic control.

Domains play an essential role in determining the piezoelectric properties of polymers. The conventional method for achieving ultrafine piezoelectric domain structures for polymers is multiphase polymerization, which is not the primary choice for industrial-scale applications because of its complex synthesis and weak mechanical properties. In this study, it is demonstrated for the first time that a nanoscale domain design can be achieved in a commercially available polyvinylidene fluoride (PVDF) homopolymer through a simple fabrication method involving cyclic compression and rapid freezing. The domain-engineered PVDF exhibits largely enhanced piezoelectric output with a record-breaking piezoelectric coefficient (d

Textile-based triboelectric nanogenerators (T-TENGs), combining the functions of energy harvesting and self-powered sensing with advantages of breathability and flexibility, have received intensive attention, which is vital to the rapid advancements in smart textiles. However, there exists few reports of T-TENGs applied to fires under the intelligent era of high requirements for devices with versatility and multiscenario practicability. Here, in combination with flame-retardant conductive cotton fabric, polytetrafluoroethylene-coated cotton fabric, and a divider, a low-cost and environmentally friendly flame-retardant textile-based triboelectric nanogenerator (FT-TENG) is developed, which is endowed with excellent fire resistance and outstanding energy harvesting capabilities. The cotton fabrics treated with a layer-by-layer self-assembly method show great self-extinguishing performance. Besides, the maximum peak power density of the FT-TENG can reach 343.19 mW/m2 under the tapping frequency of 3 Hz. Furthermore, the FT-TENG still keeps 49.2% of the initial electrical output even after being burned at 17 different positions; 34.48% of the electrical output is also retained when the FT-TENG is exposed to 220 °C. Moreover, the FT-TENGs are successfully applied as energy harvesters for firefighters and self-powered sensors for forest self-rescue and fire alarm systems. This work may provide a promising potential for multifunctional smart textiles in energy harvesting, self-powered sensing, and life or property security.

The rapid development of wearable electronics requires its energy supply part to be flexible, wearable, integratable and sustainable. However, some of the energy supply units cannot meet these requirements at the same time, and there is also a capacity limitation of the energy storage units, and the development of sustainable wearable self-charging power supplies is crucial. Here, we report a wearable sustainable energy harvesting-storage hybrid self-charging power textile. The power textile consists of a coaxial fiber-shaped polylactic acid/reduced graphene oxide/polypyrrole (PLA-rGO-PPy) triboelectric nanogenerator (fiber-TENG) that can harvest low-frequency and irregular energy during human motion as a power generation unit, and a novel coaxial fiber-shaped supercapacitor (fiber-SC) prepared by functionalized loading of a wet-spinning graphene oxide fiber as an energy storage unit. The fiber-TENG is flexible, knittable, wearable and adaptable for integration with various portable electronics. The coaxial fiber-SC has high volumetric energy density and good cycling stability. The fiber-TENG and fiber-SC are flexible yarn structures for wearable continuous human movement energy harvesting and storage as on-body self-charging power systems, with light-weight, ease of preparation, great portability and wide applicability. The integrated power textile can provide an efficient route for sustainable working of wearable electronics.

Excellent triboelectric and mechanical properties are achieved on the same material for the first time by developing an effective, general, straightforward, and area‐scalable approach to surface modification of a polyethylene terephthalate (PET) film via inductive‐coupled plasma etching. The modification enables gigantic enhancement of triboelectric charge density on the PET surface. Based on the modified PET as a contact material, a triboelectric nanogenerator (TENG) exhibits significantly promoted electric output compared to the one without the modification. The obtained electric output is even superior to a TENG made of conventional polytetrafluoroethylene that is known for its strongest ability of being charged by triboelectrification among all engineering plastics. Detailed characterizations reveal that the enhancement of triboelectric charge density on the PET is attributed to both chemical modification of fluorination and physical modification of roughened morphology in nanoscale. Therefore, this work proposes a new route to obtaining high‐performance TENGs by manipulating and modifying surface properties of materials.

High dielectric characteristics polymer dielectrics are crucial for high-power, high-integration, and high-energy storage density electrical devices and film capacitors. However, polymer dielectrics accumulate much charge during operation, causing local electric field distortion and flashover or breakdown. The deep-level defect state (electron/hole accumulation center) is a fundamental factor affecting dielectric strength. Unfortunately, related research, especially on passivating deep-level defects in polymer dielectrics, is minimal. In this paper, based on experiments and first-principles calculations, it is found that KX (X=F, Cl, Br, I) effectively passivates deep-level defect states in polymer dielectrics. Further analysis of the physical passivation mechanism reveals that the deep-level defect cation passivation principle is the cation dipole effect on polymers. The principle of anion passivation of deep-level defects by suspending anions and cations is the key to producing more stable C covalent bonds. This stable covalent bond transfers the local charge from the C with the lone electron pair that originally contains the hanging bond. Therefore, some transfer occurs and the anion implements effective passivation. This paper addresses the design of high-performance polymer dielectrics, providing a reference for experimental and theoretical analyses.

Real-time monitoring of flow turbulence is very difficult but extremely important in fluid dynamics, which plays an important role in flight safety and control. Turbulence can cause airflow to detach at the end of the wings, potentially resulting in the aerodynamic stall of aircraft and causing flight accidents. Here, we developed a lightweight and conformable system on the wing surface of aircraft for stall sensing. Quantitative data about airflow turbulence and the degree of boundary layer separation are provided in situ using conjunct signals provided by both triboelectric and piezoelectric effects. Thus, the system can visualize and directly measure the airflow detaching process on the airfoil, and senses the degree of airflow separation during and after a stall for large aircraft and unmanned aerial vehicles.

As a green and eco-friendly technology, triboelectric nanogenerator (TENG) can harvest energy from human motion to generate electricity, so TENGs have been widely applied in wearable electronic devices to replace traditional batteries. However, the surface of these TENGs is easily contaminated and breeds bacteria, which is a threat to human health. Here, we report an antibacterial composite film-based triboelectric nanogenerator (ACF-TENG) that uses Ag-exchanged zeolite (Ag-zeolite) and polypropylene (PP) composite film as the triboelectric layer. Adding a small amount of Ag-zeolite with excellent antibacterial properties can increase the dielectric permittivity and improve the surface charge density of composite films, which enhances the output performance of the ACF-TENG. The open-circuit voltage (VOC), short-circuit current (ISC), and transferred charge (QTr) of the ACF-TENG are about 193.3, 225.4, and 233.3% of those of a pure PP film-based TENG, respectively. Because of the silver in the Ag-zeolite, the ACF-TENG can effectively kill Escherichia coli and fungi. When used in insoles, the ACF-TENG can resist the athlete’s foot fungus effectively and work as a power source to light up light-emitting diodes and charge capacitors. The ACF-TENG has wide application prospects in self-powered medical and healthcare electronics.

Abstract Despite recent progress in producing perovskite nanowires (NWs) for optoelectronics, it remains challenging to solution‐print an array of NWs with precisely controlled position and orientation. Herein, we report a robust capillary‐assisted solution printing (CASP) strategy to rapidly access aligned and highly crystalline perovskite NW arrays. The key to the CASP approach lies in the integration of capillary‐directed assembly through periodic nanochannels and solution printing through the programmably moving substrate to rapidly guide the deposition of perovskite NWs. The growth kinetics of perovskite NWs was closely examined by in situ optical microscopy. Intriguingly, the as‐printed perovskite NWs array exhibit excellent optical and optoelectronic properties and can be conveniently implemented for the scalable fabrication of photodetectors.

Abstract Triboelectric nanogenerator (TENG) operates on the principle of utilizing contact electrification and electrostatic induction. However, visualization and standardized quantification of surface charges for triboelectric materials remain challenging. Here, we report a surface charge visualization and standardized quantification method using electrostatic surface potential measured by Kevin probe and the iterative regularization strategy. Moreover, a tuning strategy on surface charge is demonstrated based on the corona discharge with a three-electrode design. The long-term stability and dissipation mechanisms of the injected negative or positive charges demonstrate high dependence on deep carrier traps in triboelectric materials. Typically, we achieved a 70-fold enhancement on the output voltage (~135.7 V) for the identical polytetrafluoroethylene (PTFE) based TENG (neg-PTFE/PTFE or posi-PTFE/PTFE triboelectric pair) with stable surface charge density (5% decay after 140 days). The charged PTFE was demonstrated as a robot e-skins for non-contact perception of object geometrics. This work provides valuable tools for surface charge visualization and quantification, giving a new strategy for a deeper understanding of contact electrification.