Revamping Triboelectric Output by Deep Trap Construction.

High output performance is critical for building triboelectric nanogenerators (TENGs) for future multifunctional applications. Unfortunately, the high triboelectric charge dissipation rate has a significant negative impact on its electrical output performance. Herein, a new tribolayer is designed through introducing self-assembled molecules with large energy gaps on commercial PET fibric to form carrier deep traps, which improve charge retention while decreasing dissipation rates. The deep trap density of the PET increases by two orders of magnitude, resulting in an 86% reduction in the rate of charge dissipation and a significant increase in the charge density that can be accumulated on tribolayer during physical contact. The key explanation is that increasing the density of deep traps improves the dielectric's ability to store charges, making it more difficult for the triboelectric charges trapped by the tribolayer to escape from the deep traps, lowering the rate of charge dissipation. This TENG has a 1300% increase in output power density as a result of altering the deep trap density, demonstrating a significant improvement. This work describes a simple yet efficient method for building TENGs with ultra-high electrical output and promotes their practical implementation in the sphere of the Internet of Things.

Visualization of Charge Dynamics when Water Droplets Bounce on a Hydrophobic Surface.

Visualizing the motion of water droplets and understanding their electrification behavior holds significance for applications related to droplet transport, self-cleaning, and anti-icing/deicing and for providing a comprehensive explanation of the solid-liquid triboelectrification mechanism. Here, by constructing microcolumnar structures on the polytetrafluoroethylene surface, a water droplet-based single electrode triboelectric nanogenerator was fabricated for visualizing charge dynamics when a water droplet bounces on a hydrophobic surface. The motion state of the water droplet is closely linked to its electrification behavior through the integration of a high-speed camera and an ammeter. The electrification behavior stemming from the bounce of the water droplet is dynamically captured in real-time. The results show that the magnitude and polarity of the electrical signal have strong dependence on the motion state of the water droplet. For instance, when a water droplet approaches or moves away from the substrate in a single direction, a unipolar electrical signal is generated. However, when the water droplet reaches its limit in the initial motion direction, it signifies a static equilibrium state, resulting in the electrical signal being at zero. Furthermore, we examine the impact of factors such as impact speed, drop contact area, contact line spreading/retraction speed, and impact angle on electrification. Finally, based on the close relationship between poly(ethylene oxide) (PEO) droplet bounce dynamics and electrical signals, the bouncing details of PEO droplets with different concentrations are tracked by electrical signals. This study digitally presents the whole process of droplet bounce in situ and provides a means for monitoring and tracking droplet movement.

High-Output Single-Electrode Droplet Triboelectric Nanogenerator Based on Asymmetrical Distribution Electrostatic Induction Enhancement.

Droplet-based triboelectric nanogenerators (D-TENGs) have recently gained much attention due to their great potential in harvesting energy. However, the output performance of conventional single-electrode droplet-based TENGs is limited owing to low induced electrification efficiency. The asymmetric distribution of electric fields on both sides of the electrode edge enhances the electrostatic induction process and improves the output performance of D-TENG. Herein, an induced electrification-enhanced droplet-based triboelectric nanogenerator (IED-TENG) is developed to effectively enhance the output performance by simultaneously optimizing the electrode structure and the dynamics of the water droplet. One droplet falling from a height of 30 cm results in a -70 V output voltage and -6 µA short-circuit current, which is 70 times and 20 times the full-inductive-electrode mode, respectively. The working principle and the relationship between electric signal and droplet dynamics are analyzed in detail. Moreover, the peak output voltage can reach -110 V, and the peak current can get -140 µA by using the power generation of multiple water droplets. The present protocol provides an easy and reproducibility strategy in energy harvesting and sensing areas.

Monolayer NbSe2 Favors Ultralow Friction and Super Wear Resistance.

The urgent demand for atomically thin, superlubricating, and super wear-resistant materials in micro/nanoelectromechanical systems has stimulated the research of friction-reducing and antiwear materials. However, the fabrication of subnanometer-thick films with superlubricating and super wear-resistant properties under ambient conditions remains a huge challenge. Herein, high-quality monolayer (ML) NbSe2 (∼0.8 nm) with ultralow friction and super wear resistance in an atmospheric environment was successfully grown by chemical vapor deposition (CVD) for the first time. Moreover, compared with few-layered (FL) NbSe2, ML NbSe2 has a lower friction coefficient and better wear resistance. On the basis of density function theory (DFT) calculations, the adhesion and the degree of charge transfer between ML NbSe2 and the substrate is larger than that of the topmost layer to the underlying layers of NbSe2 with two or more layers, which can be used to explain that the ML NbSe2 favors ultralow friction and super wear resistance.

Macroscale Superlubricity with Ultralow Wear and Ultrashort Running-In Period (∼1 s) through Phytic Acid-Based Complex Green Liquid Lubricants.

Liquid superlubricity has attracted much attention, due to its ability to significantly reduce friction on the macroscale. However, the severe wear caused by the long running-in period is still one of the bottlenecks restricting the practical application of liquid superlubricating materials. In this work, the obtained polyethylene glycol-phytic acid (PEG-PA) composite liquid lubricants showed outstanding superlubricating properties (µ ≈ 0.006) for Si3N4/glass friction pairs with an ultrashort running-in period (∼1 s) under high Hertzian contact pressure of ∼758 MPa. More importantly, even after up to 12 h (∼700 m of travel), only about 100 nm deep wear scars were found on the surface of the glass sheet (wear rate = 2.51× 10-9 mm3 N-1 m-1). From the molecular point of view, the water molecules anchored between the two friction pairs have extremely low shear force during the friction process, and the strong hydrogen bond interaction between PEG and PA greatly improves the bearing capacity of the lubricant. This work addresses the challenge of liquid superlubricant simultaneously exhibiting low shear force and high load-carrying capacity and makes it possible to obtain liquid superlubrication performance with an extremely short running-in time.

Deep Trap Boosted Ultrahigh Triboelectric Charge Density in Nanofibrous Cellulose-Based Triboelectric Nanogenerators.

For their use in self-powered implantable or wearable electronics, cellulose nanofiber (CNF)-based triboelectric nanogenerators (TENGs) have drawn a lot of attention. However, the low triboelectric charge density (TECD) hinders its further application as a tribolayer for TENGs. In this work, a sulfonated cellulose nanofiber was prepared as an electropositive tribolayer for TENGs to obtain ultrahigh electrical output performance. Since the introduction of sulfonic acid effectively increased the dielectric properties and hole deep trap density of the CNF film, the triboelectric charge storage capacity of the CNF-SO3Na film was improved. The results showed that the TECD of the CNF-SO3Na film increased by 460% compared with the pristine CNF film. Furthermore, the dielectric constant and deep trap density of the CNF-SO3Na film increased by 2.4 times and 8.1 times. This work encourages the use of TENGs in real-world wireless transmission applications by outlining an easy and effective method for building high-performance TENGs.

Gas-liquid two-phase flow-based triboelectric nanogenerator with ultrahigh output power.

Solid-liquid triboelectric nanogenerators (SL-TENGs) have shown promising prospects in energy harvesting and application from water resources. However, the low contact separation speed, small contact area, and long contacting time during solid-liquid electrification severely limit their output properties and further applications. Here, by leveraging the rheological properties of gas-liquid two-phase flow and the Venturi-like design, we circumvent these limitations and develop a previously unknown gas-liquid two-phase flow-based TENG (GL-TENG) that can achieve ultrahigh voltage and volumetric charge density of 3789 volts and 859 millicoulombs per cubic meter, respectively. With a high-power output of 143.6 kilowatts per cubic meter, a 24-watt commercial lamp can be directly lighted by a continuous-flow GL-TENG device. The high performance displayed SL-TENGs in this work provides a promising strategy for the practical application of solid-liquid TENGs in energy harvesting and sensing applications.

Control of triboelectrification on Al-metal surfaces through microstructural design.

The instantaneous discharge of accumulated static charge due to contact electrification can cause irreversible damage to electrostatic-sensitive systems. Despite major advances in reducing tribo-charges, the problem remains intractable. Here, four alumina microstructures are fabricated on aluminum (Al) by combining chemical etching and anodic oxidation, and the effects of surface composition and structure on the triboelectric performance are studied by assembling them with a polytetrafluoroethylene membrane into a solid-solid triboelectric nanogenerator. The results show that the short-circuit current of the hierarchical nanoporous anodic aluminum oxide (micro/nano-AAO) modified Al is 8.77 times smaller than that of pristine Al, which is attributed to the reduced contact area and presence of an oxide film on the surface of the modified metal. By regulating the diameter of alumina nanotubes, a positive correlation between the contact area and the measured charge density is theoretically demonstrated, which establishes the size of the contact area as the main factor affecting triboelectric outputs. In addition, the micro/nano-AAO based phone shell could provide more effective electrostatic protection than that based on an acrylic coating. This novel regulation of the triboelectric output by microstructural design provides a new direction for the development of antistatic materials in a vacuum and non-grounded environment.

Quantifying Wetting Dynamics with Triboelectrification.

Wetting is often perceived as an intrinsic surface property of materials, but determining its evolution is complicated by its complex dependence on roughness across the scales. The Wenzel (W) state, where liquids have intimate contact with the rough surfaces, and the Cassie-Baxter (CB) state, where liquids sit onto air pockets formed between asperities, are only two states among the plethora of wetting behaviors. Furthermore, transitions from the CB to the Wenzel state dictate completely different surface performance, such as anti-contamination, anti-icing, drag reduction etc.; however, little is known about how transition occurs during time between the several wetting modes. In this paper, wetting dynamics can be accurately quantified and tracked using solid-liquid triboelectrification. Theoretical underpinning reveals how surface micro-/nano-geometries regulate stability/infiltration, also demonstrating the generality of the authors' theoretical approach in understanding wetting transitions. It can clarify the functioning behavior of materials in real environment.

A New Reversible Thermosensitive Liquid-Solid TENG Based on a P(NIPAM-MMA) Copolymer for Triboelectricity Regulation and Temperature Monitoring.

Intelligent and highly precise control of liquid-solid triboelectricity is of great significance for energy collection and electrostatic prevention. However, most of the traditional methods are irreversible and complex, greatly limiting their applicability. Here, a reversible thermosensitive liquid-solid triboelectric nanogenerator (L-S TENG) is assembled based on P(NIPAM-MMA) (PNM) copolymer for tunable triboelectrification. Through temperature regulation, the conformation between acylamino and isopropyl groups changes with the interfacial wettability and triboelectricity of PNM. When the temperature rises from 20 to 60 °C, the contact angle of PNM rises from 22.49° to 82.08°, and the output of the PNM-based L-S TENG shows a 27-fold increase. In addition, this transformation is reversible and repeatable with excellent durability for up to 60 days. Other organic liquids, such as glycol, exhibit positive response to temperature for this PNM-based L-S TENG. Polymers including polymethylmethacrylic, polytetrafluoroethylene, and polyimide are verified to not have such thermo-sensitivity properties. In addition, a droplet-based wireless warning system based on PNM is designed and actuated for monitoring specific temperature. The introduction of thermal PNM not only provides new material for reversible manipulation of L-S TENG, but also provides a new method for designing highly sensitive temperature warning sensors.

A New Self-Healing Triboelectric Nanogenerator Based on Polyurethane Coating and Its Application for Self-Powered Cathodic Protection.

With the increasing demand for carbon neutrality, the development of renewable and recycle green energy has attracted wide attention from researchers. A novel self-healing triboelectric nanogenerator (TENG) was constructed by applying a linear silicone-modified polyurethane (PU) coating as a triboelectric layer, which was obtained by reacting hydroxypropyl silicone oil and hexamethylene diisocyanate under the catalysis of Sn. The linear self-healing coating as the friction electrode could effectively alleviate the damages of TENG devices during long-term energy harvesting. When the triboelectric layer of the TENG device shows abrasion, the broken silicone-modified polyurethane polymer chains would gradually be cross-linked again through hydrogen bonding to achieve a self-healing effect. The entire self-healing process of the friction coating could be completed in 30 min at room temperature. The PU-based self-healing TENG exhibits an evident and stable output performance with a short-circuit current of 31.9 µA and output voltage of 517.5 V after multiple cutting-healing cycles, which could light 480 commercial LEDs. Besides, a self-powered cathodic protection system supplied by the self-healing TENG was constructed, which could transfer negative triboelectric charges to the protected metal surface to achieve an anti-corrosion effect by harvesting mechanical energy. Due to the self-healing characteristics of the TENG device as the power supply part, this intelligent system possesses great application potential in the long-term corrosion protection of multiple metal application industries, such as the marine industry.

Concealed Wireless Warning Sensor Based on Triboelectrification and Human-Plant Interactive Induction.

With the continuous development of artificial intelligence, the demand for sensors with simple preparation and strong concealment continues to increase. However, most of the high-sensitivity sensors have complex manufacturing methods, high costs, and single functions. In this paper, a sensitive motion sensor based on the triboelectric interaction between a living plant and the human body was designed to detect the real-time movements of human beings and provide danger warning. A certain relationship exists between the triboelectric signal and the distance between the plant and the human body, with effective signals being detected in the range of 1.8 m. In addition, the triboelectric signal generated by each person is unique like a fingerprint, which can be used for biometrics. On the basis of the triboelectric signal, a wireless character entry warning system is designed. This sensor can not only send out a wireless warning signal at a specific distance but also allow one to receive the warning information synchronously on a mobile phone in real time. The wireless movement sensor receives signals through a living plant, and it has the characteristics of convenient use, strong concealment, and shielding difficulty. This sensor has the potential to be widely used in person recognition, danger warning, and motion monitoring.

Manipulating Electrical Properties of Silica-Based Materials via Atomic Oxygen Irradiation.

Regulated triboelectrification has attracted considerable research attention due to its potential applications in harvesting energy and importance in antistatic protection. Irradiation is an effective and stable modification method due to its adjustable and uniform irradiation parameters. Moreover, atomic oxygen (AO) irradiation is an important component in the low earth orbit, which is a considerable factor for promoting triboelectric nanogenerators (TENGs) in the outer space. AO irradiation was utilized to manipulate the surface structure and chemical composition to regulate electrical properties. AO irradiation can increase electron-donating groups and enhance electrical positivity of polydimethylsiloxane (PDMS) films due to the transition from Si-C bonds to Si-O bonds. Therefore, different trends of polytetrafluoroethylene (PTFE) and polystyrene (PS) were caused by their TENG composition with irradiated PDMS. Tribocharge cross-over polarity and charge generation were prevented completely in PS- and PDMS-based TENGs by adjusting the irradiation time to 4.1 h. Short-circuit current enhanced from 5 to 22 µA and the output voltage increased from 160 to 760 V when PDMS films in PTFE- and PDMS-based TENGs were subjected to AO irradiation for 6 h. This study demonstrated that AO irradiation can manipulate triboelectric properties of silica-based materials, which are potential components for harvesting energy and preventing electrostatic hazard in the outer space.

A ß-cyclodextrin enhanced polyethylene terephthalate film with improved contact charging ability in a high humidity environment.

Moisture in the environment can severely decrease the contact charging properties of polymers, which usually reduce the output of solid-solid triboelectric nanogenerators (TENGs), hindering their further practical applications. To solve this problem, in this paper we fabricated a new type of polyethylene terephthalate (PET) based TENG, which can work stably in a high humidity environment with high output performance. The surface of the PET film is modified with ß-cyclodextrin to introduce hydroxyl groups, which increase the ability to form hydrogen bonds with water molecules in a high humidity environment, immobilizing water molecules to participate in contact charging. Since water molecules are a more positive material, the PET film combined with water molecules will acquire more positive charges during the contact charging process, which will greatly increase the electrical output of PET-based TENGs. Different from the PET film-based TENG without hydroxyl on the surface, the electrical output of the ß-cyclodextrin-modified PET-based TENG increases with the increase of environmental humidity. The circuit current (I sc) of the TENG increases from 3.7 µA to 16 µA when the humidity increases from 15% to 95%. Moreover, the dielectric properties of the PET film increase due to the introduction of amino groups in ß-cyclodextrin, which causes the I sc of the TENG to increase by 3.7 times at 15% RH. This strategy highly expands the application scope of TENGs for energy harvesting and self-powered sensors in high humidity environments, especially in cloudy and foggy days or under water and sweat conditions.

New Self-Healing Triboelectric Nanogenerator Based on Simultaneous Repair Friction Layer and Conductive Layer.

A new self-healing triboelectric nanogenerator (TENG) was fabricated by combining a temperature responsive polymer material of polycaprolactone (PCL) with flexible silver nanowires (Ag NWs), which could cope with the damages of TENGs in the long-term use of energy harvesting. Two different structured TENGs were designed to investigate their properties of self-recovery of the friction surfaces and conducting layers. When the top surface of the friction electrode is damaged, the healable PCL polymer will intenerate by heating and flow to the wound to realize the self-healing purpose. If the conductive layer at the bottom of the TENG electrode is also damaged, PCL will also drive the Ag NW network at the bottom of the electrode to move for healing during the heating process. This type of self-healing TENGs with a sandwich structure can exhibit a stable and high output performance with an output voltage of 800 V and a short-circuit current of 30 µA after several cutting-healing cycles, which can easily light up 372 commercial light-emitting diodes. This work proposes a simple and effective method to design a self-healing TENG, which has a widespread application prospect to prolong the life of TENGs for restoring the loss of output caused by rapid and repeated cutting.

New Hydrophobic Organic Coating Based Triboelectric Nanogenerator for Efficient and Stable Hydropower Harvesting.

Liquid-solid triboelectrification technology provides a new way to collect hydropower, while the high cost, complexity, and easily damaged microstructures of the triboelectric nanogenerator electrode materials highly limit their practical applications. In this study, a new type of organic coating triboelectric nanogenerator is fabricated using acrylate resin as the friction layer material. To further improve the solid-liquid triboelectrification performance and the hydrophobicity of the coating, fluorine-containing materials were added to the acrylic resin. As a non-microstructure-dependent film, its preparation process is simple and large area prepared, which can be achieved by modifying some commonly used anticorrosion and antifouling coatings in engineering. This packaged organic coating triboelectric nanogenerator provides good stability and high-output performance, which can easily light several commercial light-emitting diodes (LEDs) on a model ship by collecting the wave energy during the voyage. This new type of triboelectric nanogenerator based on the coating material has the advantages of simple process, low cost, and large-area preparation, which combines the performance of the coating itself with the power generation function, and have potential promising practical applications in ocean energy collection and utilization, self-powered sensing, and other fields.

Enhanced Photoelectrochemical Water-Splitting Property on TiO2 Nanotubes by Surface Chemical Modification and Wettability Control.

We report a simple method to control the photoelectrochemical (PEC) water-splitting performance of TiO2 nanotube arrays (NTs) by surface chemical modification. Four types of modifier molecules with different surface energy and functional groups, including amine (-NH2), n-alkane (-CnH2n+1), perfluoroalkyl (-F), and polymer molecule (-polymer), were self-assembled to the surface of TiO2 NTs, which could change the surface chemical composition and wettability from superhydrophilicity to hydrophobicity. Interestingly, different from expected results, photoelectrochemical measurement results show that the n-octadecyltrichlorosilane-modified TiO2 nanotube arrays with a contact angle of about 134° present the highest PEC property with doubled photocurrent density and more negative onset potential. And the total PEC performance order of the monolayers-modified TiO2 NTs is (-CnH2n+1) > (-F) > (-NH2) > (-OH, pristine TiO2) > (-polymer), which is due to the molecular monolayers modification being able to suppress the recombination of photogenerated electrons and holes and facilitate water oxidation by regulating the interface electric double layer, whereas a thick polymer layer on the photoelectrode surface would affect the light absorbance and decrease the PEC performance. Further investigation indicates that the surface energy and wettability of the TiO2 photoelectrode adjusted by surface modification also have an important influence on the interface reaction of water oxidation and the adsorption/desorption of newly formed oxygen, which also provides a new method for controlling the surface photocatalytic reactions.

New Coating TENG with Antiwear and Healing Functions for Energy Harvesting.

In view of the limitations of practical applications of current triboelectric nanogenerators (TENGs), a new type of coating TENGs with antiwear and healing properties have been fabricated to collect the large-scale dissipative energy in the environment. To enhance the triboelectrification performance of the coating TENG, mesoporous silica filled with perfluorooctylethanol is added to the acrylate resin material, in addition to improving the antiwear properties of the frictional coating. The result shows that when the mesoporous silica is used as a carrier and perfluorooctylethanol is loaded, the short-circuit current (Isc) and output voltage (Vo) of the coating TENG reach as high as 10 µA and 220 V, respectively, which are 4-5 times higher than those of pure acrylate. More importantly, the coefficient of friction of the new coating decreases from 0.11 to 0.04 with the wear volume reducing by approximately 89%, indicating a better friction-reducing property of the coating for long-term working. As a new coating material based on the traditional acrylic resin, it can be widely sprayed onto various walls, metals, and hulls as protection coating as well as power-generation coating. Interestingly, when the coating is damaged due to long-term aging or external mechanical forces, it can restore its triboelectric performance by encapsulating the repair agent within the pore structure of silica. Owing to the large-area fabrication, low cost, high output performance, and antiwear properties, the new coating TENGs have promising potential for practical applications in energy-harvesting, self-energy supplies, and self-powered sensors.

Anti-corrosion of amphoteric metal enhanced by MAO/corrosion inhibitor composite in acid, alkaline and salt solutions.

An anticorrosive composite coating with enhanced corrosion resistance in acid, alkaline and salt solutions was fabricated by compounding micro- and nanoporous inorganic structure and organic corrosion inhibitor, which was used to improve the corrosion resistance of amphoteric metal and its oxides in various corrosive medium. Micro- and nanoporous structure was prepared by microarc oxidation (MAO) coatings on 2024 aluminium alloy, which was used both as the inorganic anticorrosion coating and the container for organic corrosion inhibitor (M16). Electrochemical impedance spectroscopy, Tafel plots and salt spray resistance were measured to research the anticorrosion performance of the MAO/M16 composite coating. Enhanced corrosion resistance was observed for the MAO/M16 coating compared to the MAO by itself. When the concentration of corrosion inhibitor M16 is at 2 w%, the best anticorrosive properties of the composite coating were obtained. Moreover, the MAO/M16 composite coating showed better corrosion-resistant performance than pure MAO coating and Al alloy substrate in the corrosion environment of 1 M HCl, 0.1 M NaOH and 3.5 w% NaCl solutions, respectively. The enhancement of corrosion resistance for MAO/M16 composite coating was achieved by a unique synergy between the microarc oxidation layer and the corrosion inhibitor. The composite coating indicates its promising applications in acid, alkaline and salt solutions environments and other harsh environments.

New Method for the Corrosion Resistance of AZ31 Mg Alloy with a Porous Micro-Arc Oxidation Membrane as an Ionic Corrosion Inhibitor Container.

This work introduces a new composite anticorrosion coating for the AZ31 magnesium alloy, based on the synergistic effect of an organic/inorganic composite coating with a micro- and nanoporous micro-arc oxidation (MAO) membrane as the container of ionic corrosion inhibitor (M-16). The surface morphologies and size of the micro/nanocontainers in the porous MAO membrane before and after filling with M-16 corrosion inhibitor are examined by scanning electron microscopy (SEM). The effectiveness of M-16 for corrosion suppression on AZ31 Mg alloy with and without epoxy coating as the top sealing layer is demonstrated by electrochemical impedance spectroscopy (EIS) and salt spray tests. The potentiodynamic polarization and electrochemical impedance spectroscopy measurements show that, compared with the bare AZ31 Mg alloys, the composite coating has superior corrosion resistance with the a lower corrosion current (9.7 × 10-9 A/cm2) and a higher protection efficiency (99.3%) after immersion in 3.5 wt % NaCl solution and, meanwhile, has stronger salt spray resistance within 30 days. The results demonstrate the synergistic effect of the isolation protection of the micro-arc oxidation layer and the inhibition of M-16 and that the epoxy coating contributed to the protection for AZ31 Mg substrate to some extent. Therefore, it is anticipated that the composite coating has a potential application in the protection of metals and their alloys.