High-performance Triboelectric Nanogenerators Research Articles

Charge Generation and Enhancement of Key Components of Triboelectric Nanogenerators: A Review.

The past decade has witnessed remarkable progress in high-performance Triboelectric nanogenerators (TENG) with the design and synthesis of functional dielectric materials, the exploration of novel dynamic charge transport mechanisms, and the innovative design of architecture, making it one of the most crucial technologies for energy harvesting. High output charge density is fundamental for TENG to expand its application scope and accelerate industrialization; it depends on the dynamic equilibrium of charge generation, trapping, de-trapping, and migration within its core components. Here, this review classifies and summarizes innovative approaches to enhance the charge density of the charge generation, charge trapping, and charge collection layers. The milestone of high charge density TENG is reviewed based on material selection and innovative mechanisms. The state-of-the-art principles and techniques for generating high charge density and suppressing charge decay are discussed and highlighted in detail, and the distinct charge transport mechanisms, the technologies of advanced materials preparation, and the effective charge excitation strategy are emphatically introduced. Lastly, the bottleneck and future research priorities for boosting the output charge density are summarized. A summary of these cutting-edge developments intends to provide readers with a deep understanding of the future design of high-output TENG.

High-Performance Triboelectric Nanogenerator with Double-Side Patterned Surfaces Prepared by CO2 Laser for Human Motion Energy Harvesting

The triboelectric nanogenerator (TENG) has demonstrated exceptional efficiency in harvesting diverse forms of mechanical energy and converting it into electrical energy. This technology is particularly valuable for powering low-energy electronic devices and self-powered sensors. Most traditional TENGs use single-sided patterned friction pairs, which restrict their effective contact area and overall performance. Here, we propose a novel TENG that incorporates microwave patterned aluminum (MC-Al) foil and microcone structured polydimethylsiloxane (MC-PDMS). This innovative design utilizes two PMMA molds featuring identical micro-hole arrays ablated by a CO2 laser, making it both cost-effective and easy to fabricate. A novel room imprinting technique has been employed to create the micromorphology of aluminum (Al) foil using the PMMA mold with shallower micro-hole arrays. Compared to TENGs with flat friction layers and single-side-patterned friction layers, the double-side-patterned MW-MC-TENG demonstrates superior output performance due to increased cone deformation and contact area. The open-circuit voltage of the MW-MC-TENG can reach 141 V, while the short-circuit current can attain 71.5 μA, corresponding to a current density of 2.86 µA/cm2. The power density reaches 1.4 mW/cm2 when the resistance is 15 MΩ, and it can charge a 0.1 μF capacitor to 2.01 V in 2.28 s. In addition, the MW-MC-TENG can function as an insole device to harvest walking energy, power 11 LED bulbs, monitor step speed, and power a timer device. Therefore, the MW-MC-TENG has significant application potential in micro-wearable devices.

High‐performance triboelectric nanogenerators boosted by synergistically aligned piezoelectric/conductive composite nanofibers

AbstractTo address the need for efficient, flexible, and wearable power sources for portable electronics, a high performance triboelectric nanogenerator (TENG) was proposed by incorporating vertically‐aligned barium titanate (BaTiO3)/antimony tin oxide (ATO) nanofibers in polydimethylsiloxane (PDMS) negative triboelectric layer, where BaTiO3 served as piezoelectric material, and ATO served as conductive filler. Silver‐coated conductive fabric was used as electrode to ensure integrability and wearability. By strategically coupling the triboelectric effect of PDMS, the piezoelectric effect of BaTiO3 nanofibers, and the charge transfer effect of ATO nanofibers, the TENG exhibited the optimum output voltage and current of approximately 119 V and 28 μA, and power density of 11.74 μW/cm2, respectively. This device demonstrates its potential applications in energy supply by effectively illuminating 174 commercial green LEDs and charging capacitors for powering electronics. Additionally, the successful integration of the TENG into a smart fencing jacket highlights its utility in practical applications.Highlights TENGs with vertically‐aligned BaTiO3/ATO composite nanofibers was constructed. The output performance of TENGs were enhanced by coupling triboelectric and piezoelectric effects. Conductive ATO nanofibers were incorporated to enhance charge transfer for performance enhancement. A smart fencing jacket with scoring system was developed using the wearable TENG.

High-performance triboelectric nanogenerator with aminated barium titanate composite nanoparticles for early Parkinson’s disease diagnosis

High dielectric constant nanoparticles into polymer matrices have attracted much attention because this process can improve the nanofriction generator performance. However, the dispersion of the developed materials remains a challenge. In this paper, we present a novel high-performance nanofriction generator (FBT-TENG) based on composite nanoparticles of Amino-functionalized barium titanate and functionalized graphite oxide (FGO/ABTO) with Polyimide (PI) as substrate, which can be used as a sensor for intelligent monitoring systems. Specifically, we introduced amino groups on the surface of barium titanate to improve its dispersion in the PI solution, and the dual effect composite with functionalized graphite oxide improved the TENG performance of the PI film. Due to the FGO/ABTO synergy, the FBT-TENG can generate high output voltages, currents and power densities of 75 V, 13 µA and 4.6 W/m2, respectively, which is a 9 times increase in power density compared to the original PI film. FBT-TENG is capable of powering capacitors. In addition, the FBT-TENG can be used as a sensor to build an early Parkinson’s disease detection system, which provides a more convenient option for the early diagnosis of Parkinson’s patients and has the potential for a wide range of medical applications.

Biodegradable, stretchable, and high-performance triboelectric nanogenerators through interfacial polarization in bilayer structure

The increasing demand for wearable electronics has led to the development of triboelectric nanogenerators (TENGs) as a promising energy harvesting and sensing technology. However, conventional TENGs often utilize non-biodegradable materials, contributing to environmental pollution. In this work, we present a stretchable and biodegradable TENG based on hydroxyethyl cellulose (HEC) and gelatin (HG-TENG). The HG-TENG features a bilayered structure, where the large difference in their relative permittivity between HEC and gelatin induces interfacial polarization, effectively mitigating charge recombination and enhancing triboelectric performance. The optimized HG-TENG achieves an open-circuit voltage (Voc) of 93 V, a maximum power density of 57.8 µW/cm2, and can power 38 blue light-emitting diodes. The device exhibits a stretchability of 150 % and biodegrades within 3 hours in phosphate-buffered saline. Furthermore, we demonstrate the application of the HG-TENG as a wearable sensor by modifying it with trichloro(1H, 1H, 2H, 2H-perfluorooctyl)silane (FOTS) (FHG-TENG). The FHG-TENG-based smart glove, integrated with machine learning algorithms, enables real-time monitoring of blood pressure waveforms and finger motions, showcasing its potential for human-machine interfaces. The smart glove, equipped with five FHG-TENGs on the proximal interphalangeal joints of each finger, detects diverse finger gestures and generates voltage signals that control a robotic hand in real-time, demonstrating effective human-machine interaction through synchronized motion. Moreover, the smart glove achieves a high recognition accuracy of 96.15 % for 10 different hand sign languages.

Printed-scalable microstructure BaTiO3/ecoflex nanocomposite for high-performance triboelectric nanogenerators and self-powered human-machine interaction

Triboelectric sensing technology reinforced with deep learning algorithm has shown significant potentials in the fields of sophisticated wearable devices and Internet of Things (IoT) applications. Herein, we present a large-scale and printable nanocomposite film for high-performance microstructured BaTiO3/Ecoflex triboelectric nanogenerator (MBE-TENG) and demonstrate its applications in deep-learning assisted self-powered sensing and human-machine interaction. The MBE-TENG device achieves a short-circuit current of 1.46 μA, an open-circuit voltage of 144 V, and a transfer charge density of 6.62 nC/cm². Additionally, the MBE-TENG device can charge a 10 μF capacitor from 0 to 2 V within 200 seconds, illuminate over 70 commercial LEDs, and power a digital calculator. Based on the MBE-TENG, a sensory array keyboard is demonstrated to wirelessly control the movement of a smart car via Bluetooth communication. Furthermore, a smart tactile sensing glove is developed by combining the MEB-TENG, residual neural network and convolutional block attention module, realizing the facile recognition on six different objects with a high accuracy of 96.33 %. This work presents a scalable fabrication for microstructured triboelectric layer and highlights the versatility and efficiency of TENG sensing technology when combined with advanced neural networks and embedded systems, paving the way for innovative development in human-machine interaction, personalized healthcare, and intelligent control interfaces.

Self-healable, recyclable, and mechanically robust vitrimer composite for high-performance triboelectric nanogenerators and self-powered wireless electronics

With growing concerns about sustainability, there has been significant research interest in fabricating triboelectric nanogenerators (TENGs) from materials capable of self-repair. Here, we presented a novel polyimine/graphite polypropylene (PI/GP) vitrimer composite as a tribo-positive material for harvesting biomechanical energy. The PI/GP exhibited mechanical robustness, self-healing properties after damage, and recyclability through physical or chemical methods. The GP provided a high dielectric constant, charge transport paths, and desirable surface roughness, resulting in an outstanding TENG performance at an optimized addition level of 30 wt% in the composite (PI/GP30). Under a force of 15 N and a frequency of 6 Hz, the PI/GP30 TENG generated a power density of 2571 mW/m². Moreover, a PI/GP30 TENG device with an area of 49 cm2 was able to generate a remarkable output voltage of nearly 1325 V, at a frequency of 6 Hz and under a vertical force of 15 N. Additionally, the PI/GP30 TENG device produced a peak-to-peak voltage of 1250 V, and an outstanding current of around 2 mA by hand tapping with a force of 35–40 N. The PI/GP30 TENG was utilized for real-life applications, including a triboelectric watchband for a self-powered watch, and wireless data transmission. Furthermore, the PI/GP30 TENG demonstrated excellent self-healing and recyclability, and these properties were examined in a mousepad power generator. This study highlights the excellent promise of PI/GP vitrimer composite for fabricating high-performance, mechanically robust, self-healable, and recyclable TENGs, enabling their applications in green biomechanical power generators and wearable and wireless communication devices.

Thermal-driven self-healing and recyclable thermosetting polyurethane resins for energy harvesting

Improving the mechanical properties, self-healing capabilities, and recyclability of friction layer materials is crucial for the advancement of high-performance triboelectric nanogenerators (TENG). In this study, self-healing cross-linked polyurethanes were synthesized through the prepolymer technique, employing the Diels-Alder (D-A) reaction between the furan ring and Bismaleimide (BMI). The tensile strength of PU film with 10 wt% MBI is 54 MPa, and the shape recovery rate is 96.99 %. Moreover, it exhibits excellent self-healing and recyclable characteristics. Surface cracks can be healing within 10 min under heat, reshaped through hot pressing, while retaining 93.3 % of its mechanical properties. Additionally, the 2 cm × 2 cm area PU-based TENG can generate a short-circuit current, open-circuit voltage, transferred charge, and power density of 3.6 μA, 89 V, 29 nC, and 2.5 W/m2, respectively, at a frequency of 1 Hz. Futhermore, the self-healing efficiency of mechanical properties and the triboelectric output performances were found to reach 93.3 % and 98 %, respectively, after reprocessing. This study introduces a promising method for enhancing self-healing, shape memory characteristics, and the design of wearable TENG devices.

Highly Porous, Ultralight, Biocompatible Silk Fibroin Aerogel-Based Triboelectric Nanogenerator.

This study presents the fabrication of an ultralight, porous, and high-performance triboelectric nanogenerator (TENG) utilizing silk fibroin (SF) aerogels and PDMS sponges as the friction layer. The transition from two-dimensional film friction layers to three-dimensional porous aerogels significantly increased the specific surface area, offering an effective strategy for designing high-performance SF aerogel-based TENGs. The TENG incorporating the porous SF aerogel exhibited optimal output performance at a 3% SF concentration, achieving a maximum open circuit voltage of 365 V, a maximum short-circuit current of 11.8 μA, and a maximum power density of 7.52 W/m2. In comparison to SF-film-based TENGs, the SF-aerogel based TENG demonstrated a remarkable 6.5-fold increase in voltage and a 4.5-fold increase in current. Furthermore, the power density of our SF-based TENG surpassed the previously reported optimal values for SF-based TENGs by 2.4 times. Leveraging the excellent mechanical stability and biocompatibility of TENGs, we developed an SF-based TENG self-powered sensor for the real-time monitoring of subtle biological movements. The SF-based TENG exhibits promising potential as a wearable bioelectronic device for health monitoring.

High-performance triboelectric nanogenerator based on biocompatible electrospun polycaprolactone nanofiber and counter convex PDMS for low-frequency mechanical energy harvesting

High-performance triboelectric nanogenerator based on biocompatible electrospun polycaprolactone nanofiber and counter convex PDMS for low-frequency mechanical energy harvesting

Phosphorus-Doped g-C3N4 Induces Self-Polarization PVDF for High-Performance Triboelectric Nanogenerator As Wearable Power Sources

In recent years, the requirement for wearable electronic energy has become increasingly popular, which can be seen from the creation of numerous energy harvesters and storage devices. Among them, a new type of energy harvesting technology named triboelectric nanogenerator (TENG) has gradually matured for nearly ten years. Increasing the output performance by enhancing the surface charge of the TENG is what most researchers have focused on recently. There are several ways such as changing the surface structures, improving the dielectric constant and spontaneous polarization, which is related to this work. Some papers mention that filling nanoparticles or adding 2-dimensional material will induce PVDF self-polarization to the beta phase, making it a highly electronegative state. Moreover, adding high electronegative atoms will also change the state of the PVDF. Therefore, we synthesize the PVDF film by adding phosphorus-doped g-C3N4 (PCN) in order to enhance the output performance. By introducing the P atom into the matrix of g-C3N4 via an annealing process, the P atom in g-C3N4 not only increases the electronegativity of the film surface but also induces PVDF to a polarized crystal b phase for absorbing more positive charges. Consequently, the TENG with PVDF/PCN displays a remarkable improvement in output performance compared to the pristine PVDF-based TENG with more than a 100 V increase. Furthermore, the flexibility and durability of PVDF/PCN thin film have the potential to be widely used in self-powered wearable sources. Figure 1

β-enhanced humidity robust high performance triboelectric nanogenerator for energy harvesting and sensors

Limited output current and harsh environmental conditions are big challenges to harvesting electrical energy from triboelectric nanogenerators (TENG) in sensing applications. One contributing factor to this issue is matching the density of state between two layers of TENG for maximum charge transfer. To ensure a stable output performance, a superhydrophobic interface between the TENG's two layers has been achieved by applying a novel fluorescence enhanced hexamethyldisiloxane (HMDSO) dielectric barrier discharge (DBD) plasma. The plasma coating not only improve the hydrophobicity but also the interface contacts between the two layers of TENG and therefore a maximum charge transfer and ultra-high current density are obtained. The plasma treatment increases the surface roughness and introduces functional groups such as amino (-NH2), hydroxyl (-OH), and siloxane (-Si-O-Si) on the PMMA film, which increases the electron affinity difference between the two layers, increases humidity resistance. The modified TENG generates a maximum stable output voltage of 1400 V and a maximum current of 125 µA with a power density of 55 W/m2, which is significantly higher than those reported in previous studies. Therefore, the TENG has been used as a self-powered droplet detector with an ultra-fast response time of 1.8 ms and has the potential to be used as a self-powered humidity sensor.

Fully wood-based high-performance triboelectric nanogenerator for smart home

Fully wood-based high-performance triboelectric nanogenerator for smart home

Shape memory behavior of polyethylene-foam-based nanocomposite for sustainable triboelectric nanogenerators

Durable self-powering electronic devices need high-performance triboelectric nanogenerators (TENGs) with shape memory capabilities. A novel porous shape memory polymer nanocomposite that includes polyethylene foam (PEF) with switching molecules and graphitic carbon nitride nanosheets is designed to create a robust, high-performance TENG. This nanocomposite shows outstanding thermal-actuated shape recovery capabilities by heating at 70 °C. Although the TENG initially excels in output performance (1840 V voltage, 79.66 mW.cm‐2 power density), prolonged harsh conditions cause nanocomposite deformation and performance decline. However, heating the nanocomposite to 70 °C fully restores the TENG’s original performance. Besides, the COMSOL Multiphysics simulation of TENG aligns with the experimental results. Furthermore, two TENG application scenarios are demonstrated: self-charging humidity sensing (where TENG’s output performance is humidity-sensitive and decreases as humidity rises) and powering electronic devices (where TENG turns on commercial LEDs, powers a smartwatch, and charges capacitors). Therefore, this TENG may open new possibilities for future self-powered electrical devices and sensors.

In-situ amino-functionalized and reduced graphene oxide/polyimide composite films for high-performance triboelectric nanogenerator

As a promising sustainable power source in intelligent electronics, Triboelectric Nanogenerators (TENGs) have garnered widespread interest, with various strategies explored to enhance their output performance. However, most optimization methods for triboelectric materials have focused solely on tuning chemical compositions or fabricating surface microstructures. Here, we have prepared amino-functionalized reduced graphene oxide (FRGO)/polyimide (PI) composite films (PI-FRGO) via in-situ polymerization, aimed at enhancing PI materials’ nanotribological power generation performance. By varying the doping levels of amino groups and controlling the FRGO proportion during synthesis, we can explore the optimal FRGO/PI composite film ratio. At a p-Phenylenediamine: reduced Graphene Oxide (PPDA: RGO) ratio of 1:1 and an FRGO addition of 0.1 %, the output electrical performance peaks with a voltage of 58 V, a charge of 33 nC and a current of 12 μA, nearly 2 times that of a pure PI film. We have fabricated a TENG with an optimally formulated PI-FRGO composite to explore its application potential. Under a 10 MΩ external load resistance, the TENG can deliver a power density of 3.5 mW/m2 and can be powering small devices. This work presents new effective strategies to significantly enhance TENG output performance and promote their widespread application.

Antagonistic strategy for enhanced performance polyimide-based triboelectric nanogenerators and wireless self-powered sensors in extremely harsh environments

Triboelectric nanogenerators (TENGs) offer promising green energy solutions for portable microelectronics in the Internet of Everything era. However, their practical applications are limited by low electrical output and stability in harsh environments. This study introduces an innovative antagonistic strategy to enhance TENG performance and stability using thermo-stable polyimide with customizable porous structures (ip-PI). By employing antagonistic solubility, we create ip-PI using chloroform as a solvent for PI and acetone as a solvent for the Poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-co-HFP) template, whereas they both act as nonsolvents for their respective counterparts. Additionally, microbeads-patterned chitosan (mb-CS) is rationally designed and fabricated as morphologically and electrically antagonistic counter surfaces for ip-PI. The resulting antagonist-inspired TENG (AI-TENG) constructed from ip-PI and mb-CS achieves a remarkable average power density of 4 W·m−2, presenting an outstanding 200-fold increase in power compared to TENG made from unstructured flat surfaces. Furthermore, the ip-PI demonstrates excellent temperature resistance, enabling the TENG to operate at extremely high temperatures up to 250 °C, with promising durability of over 10,000 contact-separation cycles. Applications include self-powered machinery condition monitoring sensors and a wireless communication fire forest pre-warning system, showcasing significant advancements in flexible, high-performance TENGs suitable for industrial use in extreme environments.

Durable and High-Performance Triboelectric Nanogenerator Based on an Inorganic Triboelectric Pair of Diamond-Like-Carbon and Glass.

The long-term durability of triboelectric nanogenerators (TENGs) remains a main challenge for practical applications because of inevitable material abrasion and wear, especially for sliding TENGs. Herein, an inorganic triboelectric pair composed of diamond-like carbon (DLC) and glass with excellent durability and triboelectric output for sliding-mode TENGs is proposed. This triboelectric pair possesses a low coefficient of friction and little abrasion and accordingly excellent durability (>500 000cycles). Moreover, compared with the traditional copper-polytetrafluoroethylene (Cu-PTFE)TENG with maximum transferred charges of 50nC, those of the DLC-glass TENG reaches 141nC. Due to the low-friction and high hardness of the triboelectric pair, the output quickly recovers after simply cleaning wear debris. The DLC-glass TENG demonstrates an output power density of 530mWm-2 and a fourfold faster capacitor charging speed than the Cu-PTFE TENG. Compared to the reported durable TENGs via structure optimization and interface lubrication, the DLC-glass TENG shows higher outputs and simpler structure. This DLC-glass pair structure is also introduced into a spherical TENG for blue energy harvesting with excellent durability. The inorganic triboelectric pair with excellent mechanical durability and electrical performance proposed in this work shows huge prospects for practical applications of TENGs.

Unveiling the marine Sargassum horneri material for energy and active sensor devices: Towards multitasking approaches

The quest for a future with greater environmental sustainability has led to a rising focus on investigating innovative methods for energy production and storage. However, marine invasions have steadily increased over the past two centuries, necessitating innovative approaches for the remediation and preservation of oceanic environments. Especially, Sargassum horneri (S. horneri) is a brown algae that causes massive floating macroalgal blooms along the coasts of East Asia. Given these facts, this paper develops high-performance triboelectric nanogenerator (TENG), and electrode material for both supercapacitor and water-splitting devices based on S. horneri. The TENG device, constructed using S. horneri coastal bio-waste collected from Jeju Island, yields impressive results. The output current, voltage and power generated by the S. horneri-based triboelectric nanogenerator (SH-TENG) is around 47 µA, 775 V, and 2880 µW, respectively. The electrochemical analysis of carbon derived from S. horneri reveals an excellent electrode capacitance of 225 F/g at 2.5 mA. Constructing the symmetric supercapacitor device using S. horneri-derived carbon, which shows excellent energy and power densities around 14.85 Wh/kg and 972.22 W/kg, with remarkable cyclic stability of 81.3 % for 5000 GCD cycles at 7 mA. On the other hand, the developed S. horneri electrode demonstrated much-improved activity towards water splitting application, exhibiting overpotentials of 0.101 V and 0.198 V for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) at an applied current density of 20 mA/cm2, respectively. The fabricated sample also demonstrated the lowest Tafel values towards HER (119 mv/dec) and for OER (109 mv/dec). Finally, the time series analysis (TSA) technique was employed for modeling and prediction of capacity retention of the SH//SH supercapacitor and electrochemical potential (E) of SH/NF║SH/NF cell. In both cases, the mean squared error between experimental and predicted data was very small, suggesting the TSA is a powerful statistical technique to model and predict the vial features of the electrochemical devices. Overall, these results suggest that S. horneri-derived carbon presents a viable alternative in the realm of energy storage and harvesting, promising sustainable technological advancements.

Advanced Applications of Porous Materials in Triboelectric Nanogenerator Self-Powered Sensors.

Porous materials possess advantages such as rich pore structures, a large surface area, low relative density, high specific strength, and good breathability. They have broad prospects in the development of a high-performance Triboelectric Nanogenerator (TENG) and self-powered sensing fields. This paper elaborates on the structural forms and construction methods of porous materials in existing TENG, including aerogels, foam sponges, electrospinning, 3D printing, and fabric structures. The research progress of porous materials in improving TENG performance is systematically summarized, with a focus on discussing design strategies of porous structures to enhance the TENG mechanical performance, frictional electrical performance, and environmental tolerance. The current applications of porous-material-based TENG in self-powered sensing such as pressure sensing, health monitoring, and human-machine interactions are introduced, and future development directions and challenges are discussed.

Fast-Curing of Liquid Crystal Thermosets Enabled by End-Groups Regulation and In Situ Monitoring by Triboelectric Spectroscopy.

The development of high-performance polymer is crucial for the fabrication of triboelectric nanogenerators (TENGs) used in extreme conditions. Liquid crystal polyarylate thermosets (LCTs) demonstrate great potential as triboelectric material by virtue of exceptional comprehensive properties. However, there are only a few specific end-groups like phenylethynyl matching the LCT polycondensation temperature (above 300°C). Moreover, the excellent properties of LCTs rely on the crosslinked network formed with long curing time at high temperature, restricting their further application in triboelectric material. Herein, a fast-curing LCT is designed by terminating with 4-maleimidophenol possessing appropriate reactivity. The resultant LCT (MA-LC-MA) exhibits much lower polycondensation temperature (250-270°C) and curing temperature of 300°C within only 1min compared to typical LCTs (cured at 370°C for 1h). Furthermore, the cured MA-LC-MA retains a high glass transition temperature of 135°C, storage modulus of 6MPa even at 350°C, and great electrical output performance. Additionally, triboelectric measurement related to the dielectric properties that vary with crosslinked network is innovatively utilized as an analysis technique of curing progress. This work provides a new strategy to design high-performance TENGs and promotes the development of next generation thermosets in extreme conditions.