High‐Performance Triboelectric Nanogenerators Based on Solid Polymer Electrolytes with Asymmetric Pairing of Ions

In general, various kinds of surface modifications are utilized to enhance the power output performance of triboelectric nanogenerators (TENGs), but they typically have limited stability. Here, a new strategy of adding electrolytes with asymmetric ion pairing to polymer friction layers of TENGs is introduced in order to enhance their triboelectric property. Indeed, Kelvin probe force microscopy (KPFM) measurements show that an addition of phosphoric acid (H₃PO₄ ), an electrolyte with more cations than anions, to polyvinyl alcohol (PVA) can make it one of the most negative triboelectric materials; whereas, an addition of calcium chloride (CaCl₂ ), an electrolyte with more anions than cations, to PVA can make it one of the most positive triboelectric materials. Furthermore, the TENGs based on such solid polymer electrolytes (SPEs) produce significantly higher power output than typical metal‐polymer TENGs. Due to these unique features, SPEs are a promising triboelectric material for realizing high‐performance TENGs for self‐powered small electronics.     

1D Stretchable Block Copolymer Yarn‐Based Energy Harvesters via BaTiO3/Polydimethylsiloxane Composite‐Carbon Conductive Ink

Highly stretchable self‐powered energy sources are promising options for powering diverse wearable smart electronics. However, commercially existing energy sources are disadvantaged by tensile strain limitations and constrained deformability. Here, 1D thread‐based highly stretchable triboelectric nanogenerators (HS‐TENGs), a crucial step toward overcoming these obstacles, are developed based on a highly stretchable coaxial‐type poly[styrene‐b‐isoprene‐b‐styrene] (SIS) elastomer tube. Carbon conductive ink is injected into the SIS tube as a core 1D electrode that remains almost unaffected even under 250% stretching because of its low Young's modulus. To further facilitate power generation by the HS‐TENG, a composite of barium titanate nanoparticles (BaTiO₃ NPs) and polydimethylsiloxane (PDMS) is coated on the initial SIS tube to modulate the dielectric permittivity based on variations in the BaTiO₃ NPs volume ratio. The 1D PDMS/BaTiO₃ NP composite‐coated SIS and a nylon 6‐coated 2D Ni–Cu conductive fabric are selected as triboelectric bottom and top layers, respectively. Woven HS‐TENGs textiles yield consistent power output under various extreme and harsh conditions, including folded, twisted, and washed states. These experimental findings indicate that the approach may become useful for realizing stretchable multifunctional power sources for various wearable electronics.     

A Fully Verified Theoretical Analysis of Contact‐Mode Triboelectric Nanogenerators as a Wearable Power Source

Harvesting mechanical energy from human activities by triboelectric nanogenerators (TENGs) is an effective approach for sustainable, maintenance‐free, and green power source for wireless, portable, and wearable electronics. A theoretical model for contact‐mode triboelectric nanogenerators based on the principles of charge conservation and zero loop‐voltage is illustrated. Explicit expressions for the output current, voltage, and power are presented for the TENGs with an external load of resistance. Experimental verification is conducted by using a laboratory‐fabricated contact‐mode TENG made from conducting fabric electrodes and polydimethylsiloxane/graphene oxide composite as the dielectric layer. Excellent agreements of the output voltage, current, and power are demonstrated between the theoretical and experimental results, without any adjustable parameters. The effects of the moving speed on output voltage, current, and power are illustrated in three cases, that is, the motion with constant speed, the sinusoidal motion cycles, and the real walking cycles by human subject. The fully verified theoretical model is a very powerful tool to guide the design of the device structure and selection of materials, and optimization of performance with respect to the application conditions of TENGs.     

Enhancing the Output Performance of Triboelectric Nanogenerator via Grating‐Electrode‐Enabled Surface Plasmon Excitation

The surface charge density and the output impedance of triboelectric nanogenerators (TENGs) are two critical factors for TENGs to speed up their commercialization, so it is important to explore unique methods to reduce the output impedance and increase the surface charge density. Here, an approach is demonstrated to effectively boost the output performance of TENG while reducing the output impedance of TENGs by utilizing grating‐electrode‐enabled surface plasmon excitation. A sustainable and enhanced output performance of about 40 µA (short‐circuit current) and 350 V (peak‐to‐peak voltage at a resistance of 10 MΩ) is produced via grating‐coupled surface plasmon resonance on the TENG with the aluminum grating electrode in the line density of 600 lines mm^?1, and it delivers a peak output power of 3.6 mW under a loading resistance of 1 MΩ, giving over 4.5‐fold enhancement in output power and a 75% reduction in the output impedance. Finally a self‐powered ultrasonic ranging system is utilized to verify the capability of the TENG in powering portable electrics.     

High‐Output Triboelectric Nanogenerator Based on Dual Inductive and Resonance Effects‐Controlled Highly Transparent Polyimide for Self‐Powered Sensor Network Systems

High‐output triboelectric nanogenerators (TENGs) are demonstrated based on polyimide (PI)‐based polymers by introducing functionalities (e.g., electron‐withdrawing and electron‐donating groups) into the backbone. The TENG based on 6FDA‐APS PI, possessing the most negative electrostatic potential and the low‐lying lowest unoccupied molecular orbital level, produces the highest effective charge density of about 860 µC m^?2 in practical working conditions with the ion injection process. This may be ascribed to the excellent charge‐retention characteristics as well as the enhanced charge transfer capability, which increases the output power by 7 times compared to the commercially available Kapton film‐based TENG. Finally, a 6FDA‐APS‐driven sensor network system is demonstrated, providing the identity of three gases (H₂, CO, and NO₂) by illuminating the light‐emitting diodes within several seconds.     

Microdischarge‐Based Direct Current Triboelectric Nanogenerator via Accumulation of Triboelectric Charge in Atmospheric Condition

Direct conversion of mechanical energy into direct current (DC) by triboelectric nanogenerators (TENGs) is one of the desired features in terms of energy conversion efficiency. Although promising applications have been reported using the triboelectric effect, effective DC generating TENGs must be developed for practical purposes. Here, it is reported that continuous DC generation within a TENG itself, without any circuitry, can be achieved by triggering air breakdown via triboelectrification. It is demonstrated that DC generation occurs in combination with i) charge accumulation to generate air breakdown, ii) incident discharge (microdischarge), and iii) conveyance of charges to make the device sustainable. 10.5 mA m^?2 of output current and 10.6 W m^?2 of output power at 33 MΩ load resistance are achieved. Compared to the best DC generating TENGs ever reported, the TENG in this present study generates about 20 times larger root‐mean square current density.     

Rationally Designed Dual‐Mode Triboelectric Nanogenerator for Harvesting Mechanical Energy by Both Electrostatic Induction and Dielectric Breakdown Effects

With the advantages of its light weight, low cost, and high efficiency especially at low operation frequency, the triboelectric nanogenerator (TENG) is considered to be a potential solution for self‐powered sensor networks and large‐scale renewable blue energy. However, the conventional TENG converts mechanical energy into electrical energy only via either electrostatic induction or electrostatic breakdown. Here, a novel dual‐mode TENG is presented, which can simultaneously harvest mechanical energy by electrostatic induction and dielectric breakdown in a single device. Based on the complementary working mechanism, it achieves a great improvement in the output performance with the sum of two TENGs via a single mechanism and reveals the effect of dielectric layer thickness on the triboelectrification, electrostatic induction, and air breakdown. This study establishes a new methodology to optimize TENGs and provides a new tool to investigate the triboelectrification, electrostatic induction and dielectric breakdown simultaneously.     

A Novel MXene/Ecoflex Nanocomposite-Coated Fabric as a Highly Negative and Stable Friction Layer for High-Output Triboelectric Nanogenerators

The triboelectric material properties and mechanical stability of the contact layer are vital to achieving durable triboelectric nanogenerators (TENGs) with high output performance. Herein, a novel MXene/Ecoflex nanocomposite is introduced as a promising triboelectric material because of its highly negative triboelectric properties and mechanical stability. The MXene/Ecoflex nanocomposite with a fabric-based waterproof TENG (FW-TENG) is fabricated and designed to universally harvest energy from various human motions as well as the natural environment (rain and wind). The fabricated FW-TENG delivers a maximum output peak power of 3.69 mW and a power density of 9.24 W m⁻², respectively, at a matching load resistance of 4.5 MΩ under a frequency of 4.5 Hz and a force of 8 N. Furthermore, the applicability of this device in various products is investigated. The FW-TENG can protect against a crash caused by rainy and humid weather. An FW-TENG-based self-powered smart active device that detects motion on a carpet is demonstrated and is equipped with sleep monitoring motion sensors. The FW-TENG not only has self-powered benefits and excellent mechanical amenability but is also exceptionally reliable and stable against water intrusion, which are important characteristics to realize next-generation wearable/portable technologies.     

Robust Triboelectric Nanogenerator Achieved by Centrifugal Force Induced Automatic Working Mode Transition

Material abrasion in contact‐based freestanding mode‐triboelectric nanogenerators (FS‐TENGs) seriously deteriorates device mechanical durability and electrical stability, which causes TENGs to be only applicable in the harvesting of mechanical energy at low‐frequency. Here, a wide‐frequency and ultra‐robust rotational TENG is reported that is composed of a built‐in traction rope structure and capable of transforming from contact mode to non‐contact mode automatically as driven by the centrifugal force. With optimizing the fixed x and y position on slider and center shaft, respectively, the mode transition threshold speed can be reduced to 225 rpm. Additionally, the automatic working mode transition TENG exhibits excellent electrical stability, which can maintain 90% electric output after over 24 h of continuous operation, while the contact and non‐contact mode TENGs only retain 30% and 2% output, respectively. The high stability and large output density ensure its usage in the fast and effective charging of commercial capacitors or electronics. This work provides a prospective strategy for rotational TENGs to extend the frequency operation region and mechanical durability for practical applications.     

Boosting Power‐Generating Performance of Triboelectric Nanogenerators via Artificial Control of Ferroelectric Polarization and Dielectric Properties

Low output current represents a critical challenge that has interrupted the use of triboelectric nanogenerators (TNGs) in a wide range of applications as sustainable power sources. Many approaches (e.g., operation at high frequency, parallel stacks of individual devices, and hybridization with other energy harvesters) remain limited in solving the challenge of low output current from TNGs. Here, a nanocomposite material system having a superior surface charge density as a triboelectric active material is reported. The nanocomposite material consists of a high dielectric ceramic material, barium titanate, showing great charge‐trapping capability, together with a ferroelectric copolymer matrix, Poly(vinylidenefluoride‐co‐trifluoroethylene) (P(VDF‐TrFE)), with electrically manipulated polarization with strong triboelectric charge transfer characteristics. Based on a contact potential difference study showing that poled P(VDF‐TrFE) has 18 times higher charge attracting properties, a fraction between two components is optimized. Boosting power‐generating performance is achieved for 1130 V of output voltage and 1.5 mA of output current with this ferroelectric composite‐based TNG, under 6 kgf of pushing force at 5 Hz. An enormously faster charging property than traditional polymer film‐based TNGs is demonstrated in this study. Finally, the charging of a self‐powering smartwatch with a charging management circuit system with no external power sources is demonstrated successfully.     

Blue Energy Collection toward All‐Hours Self‐Powered Chemical Energy Conversion

The conversion and transmission of blue energy in the ocean are critical issues. By employing triboelectric nanogenerators (TENGs), blue energy can be harvested but the corresponding electricity transmission and storage are still great challenges. In this work, an automatic high‐efficiency self‐powered energy collection and conversion system is proposed that converts blue energy to chemical energy. A gear‐driven unidirectional acceleration TENG is designed to convert disordered and low‐frequency water wave energy to low voltage and high current DC output. The output bias from the TENG can be used to drive a Ti–Fe₂O₃/FeNiOOH based photoelectrochemical cell under sunlight to produce hydrogen. Moreover, under the situation without sunlight, the self‐powered system can be automatically switched to another working state to charge a Co₃O₄ based lithium‐ion battery. The hydrogen production rate reaches to 4.65 µL min^‐1 under sunlight at the rotation speed of 120 rpm. The conversion efficiency of the whole system is calculated to be 2.29%. The system triggered by photoswitches can automatically switch between two working states with or without sunlight and convert the blue energy to either hydrogen energy or battery energy for easy storage and transmission, which widens the future applications for blue energy.     

Robust Thin Films‐Based Triboelectric Nanogenerator Arrays for Harvesting Bidirectional Wind Energy

Wind‐driven triboelectric nanogenerators (TENGs) play an important role in harvesting energy from ambient environments. Compared to single‐side‐fixed triboelectric nanogenerator (STENG) arrays for harvesting single‐pathway wind energy, double‐side‐fixed triboelectric nanogenerator (DTENG) arrays are developed to harvest bidirectional wind energy. Electrical performances of the STENG and DTENG can be improved due to sticky, abrasive, and electrical properties of the Ti buffer layers among Al, polytetrafluoroethylene (PTFE), and polyimide (Kapton), configuring in triboelectric PTFE/Ti/Al and Al/Ti/Kapton/Ti/Al thin films. Short‐circuit current (I _SC), open‐circuit voltage (V _OC), and frequencies of the STENG and DTENG increase with increasing wind velocity ranging from 9.2 to 18.4 m s²¹, revealing that the moderate I _SC, V _OC, frequencies, and output powers of the STENG and DTENG reach 67 μA, 57 μA, 334 V, 296 V, 173 Hz, 162 Hz, 5.5 mW and 3.4 mW with a matched load of 4 MΩ at airflow rate of 15.9 m s²¹, respectively. Compared with counterparts of the single‐pathway‐harvested STENG arrays, the I _SC, durability, and stability of the bidirectional‐harvested DTENG can be dramatically improved by a 4 3 1 array connected in parallel because of the improved device configuration, stickiness, and abrasion by adhering Ti buffer layers. The durable DTENG arrays present a step toward practical applications in harvesting bidirectional wind energy for self‐powered systems and wireless sensors.     

Robust Swing‐Structured Triboelectric Nanogenerator for Efficient Blue Energy Harvesting

Ocean wave energy is a promising renewable energy source, but harvesting such irregular, “random,” and mostly ultra‐low frequency energies is rather challenging due to technological limitations. Triboelectric nanogenerators (TENGs) provide a potential efficient technology for scavenging ocean wave energy. Here, a robust swing‐structured triboelectric nanogenerator (SS‐TENG) with high energy conversion efficiency for ultra‐low frequency water wave energy harvesting is reported. The swing structure inside the cylindrical TENG greatly elongates its operation time, accompanied with multiplied output frequency. The design of the air gap and flexible dielectric brushes enable mininized frictional resistance and sustainable triboelectric charges, leading to enhanced robustness and durability. The TENG performance is controlled by external triggering conditions, with a long swing time of 88 s and a high energy conversion efficiency, as well as undiminished performance after continuous triggering for 4 00 000 cycles. Furthermore, the SS‐TENG is demonstrated to effectively harvest water wave energy. Portable electronic devices are successfully powered for self‐powered sensing and environment monitoring. Due to the excellent performance of the distinctive mechanism and structure, the SS‐TENG in this work provides a good candidate for harvesting blue energy on a large scale.     

Long‐Lifetime Triboelectric Nanogenerator Operated in Conjunction Modes and Low Crest Factor

The high‐output triboelectric nanogenerator (TENG) is indispensable for its practical applications toward industrial products. However, the electricity loss in simple parallel connection among all units and the typically high crest factor output seriously hamper the practical applications of TENG. Here, a rectified TENG is reported in parallel structure to solve the problem of electricity loss in simple parallel connection. The rotational contact–separation structure with phase difference between rectified TENGs addresses high crest factor output and extends service life of rotational TENG simultaneously. The current crest factor is dramatically decreased to 1.31 in multiple rectifier multiple TENG in parallel (MRM‐TENG), while that of TENG in simple parallel is higher than 6. Meanwhile, the current output can retain up to ≈93% of its initial performance after 7 200 000 rotations under 2.00 r s^?1 of 1000 h. Furthermore, the equivalent current can be in linear growth with low crest factor by making MRM‐TENG in parallel for distributed energy supply without electricity loss. This work may provide a new strategy for TENG in parallel to achieve a low crest factor output and long‐term cycling stability power generation in distributed energy harvesting for large‐scale power application.     

Polymer Nanocomposites with Interpenetrating Gradient Structure Exhibiting Ultrahigh Discharge Efficiency and Energy Density

Poly(vinylidene fluoride) (PVDF) based polymer nanocomposites with high‐permittivity nanofillers exhibit outstanding dielectric energy storage performance due to their high dielectric permittivities and breakdown strength. However, their discharge efficiency is relatively low (usually lower than 70%), which limits their practical applications. Here, polymer nanocomposites with a novel interpenetrating gradient structure are designed and demonstrated by cofilling a PVDF matrix with barium zirconate titanate nanofibers and hexagonal boron nitride nanosheets via modified nonequilibrium processing. The interpenetrating gradient structure is highly effective in breaking the trade‐off between discharge energy density and efficiency of the corresponding nanocomposite, as indicated by the concomitantly enhanced discharge energy density (U _e ≈ 23.4 J cm^?3) and discharge efficiency (η ≈ 83%). The superior performance is primarily attributed to the rational distribution of nanofillers in the polymer matrix, which raises the height of the potential barrier for charge injection at the dielectric/electrode interface, suppresses electric conduction and contributes to enhanced apparent breakdown strength. Meanwhile, the gradient configuration allows higher volume fraction of high‐permittivity nanofillers without compromising the breakdown strength, leading to higher electric polarization compared with the random configuration. This work provides new opportunities to PVDF‐based polymer nanocomposites with high energy density and discharge efficiency for capacitive energy storage applications.     

Ion‐Enhanced Field Emission Triboelectric Nanogenerator

As interest in triboelectric nanogenerators (TENGs) continues to increase, some studies have reported that certain limitations exist in TENG due to high potential difference, resulting in air breakdown and field emission. In addition, with known limitations such as extremely low voltage at low external resistance, a breakthrough is required to overcome the limitations of TENG. Here, a new TENG mechanism is reported, utilizing ion‐enhanced field emission (IEFE). Using a simple IEFE‐inducing layer, which consists of a charge accumulation layer and a metal‐to‐metal contact point, electrons can flow directly to a counter electrode while generating high‐output power. Under vertical contact–separation input, the generated root mean square (RMS) power of IEFE‐TENG is 635% higher compared to conventional TENG. As the fundamental mechanism of the IEFE‐TENG is based on installing this simple IEFE‐inducing layer, the power output of existing TENGs including sliding mode types can be boosted. This new TENG mechanism can be a new standard for metal–metal contact TENGs to effectively amplify the output power and to overcome potential limitations.     

Suppressing Lithium Dendrite Growth via Sinusoidal Ripple Current Produced by Triboelectric Nanogenerators

Lithium metal as an ultimate anode material of future rechargeable batteries may furnish the highest energy density for its pairing cathode, although preventing the growth of lithium dendrites in liquid electrolytes is a major challenge. This work reports that stable lithium metal anodes can be achieved by charging with high‐frequency sinusoidal ripple current generated by rotating triboelectric nanogenerators (R‐TENGs). Compared with constant DC current charging, sinusoidal ripple current charging by R‐TENG improves the uniformity of lithium deposition during cycling test. Consequently, symmetric Li/Li cells exhibit lower overpotential and better cycling stability. In addition, full cells assembled with lithium metal anodes and LiFePO₄ cathodes show considerably improved capacity retention when charged by R‐TENG's sinusoidal ripple current (99.5%) compared to constant current (78.7%) after 200 cycles. The charging strategy device in this work provides a promising direction toward improving the cycle life of Li metal batteries. In addition, the combination of R‐TENGs with Li metal batteries offers an encouraging solution for achieving stable energy supply in self‐powered systems.     

Poly(vinylferrocene)–Reduced Graphene Oxide as a High Power/High Capacity Cathodic Battery Material

The preparation and performance of a new cathodic battery material consisting of a composite of poly(vinylferrocene) (PVFc) and reduced graphene oxide (rGO) is described. It shows the highest charge/discharge efficiency (at a rate of 100 A g^?1) ever reported for ferrocene–polymer materials. The composite allows for specific capacities up to 0.21 mAh cm^?2 (770 mC cm^?2, 29 μm film thickness) at a specific capacity density of 114 mAh g^?1 and less than 5% performance decay over 300 cycles. The composite material is binder free and the charge storing PVFc accounts for 88% of the total weight of the cathodic material. The superb performance is based on (i) perfect self‐assembling of oxidized PVFc on graphene oxide (GO) leading to PVFc@GO, (ii) its stepwise (n steps) transfer onto a current collector (CC) (PVFc@GO)_n@CC (n = drop casting steps), and (iii) the efficient electrochemical transformation of GO into rGO in the composite using viologen as homogeneous electrocatalyst. The self‐assembling step is analyzed by zeta potential and atomic force microscopy (AFM) studies, demonstrating heavy ferrocene loading on GO and a mesoporous composite structure, respectively. Complete GO/rGO transition and quantitative ClO₄ ^? ion breathing of the composite are found by electrochemical quartz crystal microbalance and by electrochemical AFM.     

Dual‐Tube Helmholtz Resonator‐Based Triboelectric Nanogenerator for Highly Efficient Harvesting of Acoustic Energy

An acoustic wave is a type of energy that is clean and abundant but almost totally unused because of its very low density. This study investigates a novel dual‐tube Helmholtz resonator‐based triboelectric nanogenerator (HR‐TENG) for highly efficient harvesting of acoustic energy. This HR‐TENG is composed of a Helmholtz resonant cavity, a metal film with evenly distributed acoustic holes, and a dielectric soft film with one side ink‐printed for electrode. Effects of resonant cavity structure, acoustic conditions, and film tension on the HR‐TENG performance are investigated systematically. By coupling the mechanisms of triboelectric nanogenerator and acoustic propagation, a theoretical guideline is provided for improving energy output and broadening the frequency band. Specifically, the present HR‐TENG generates the maximum acoustic sensitivity per unit area of 1.23 VPa^?1 cm^?2 and the maximum power density per unit sound pressure of 1.82 WPa^?1 m^?2, which are higher than the best results from the literature by 60 and 20%, respectively. In addition, the HR‐TENG may also serve as a self‐powered acoustic sensor.     

Tribovoltaic Effect on Metal–Semiconductor Interface for Direct‐Current Low‐Impedance Triboelectric Nanogenerators

The triboelectric nanogenerator (TENG) is a new energy technology that is enabled by coupled contact electrification and electrostatic induction. The conventional TENGs are usually based on organic polymer insulator materials, which have the limitations and disadvantages of high impedance and alternating output current. Here, a tribovoltaic effect based metal–semiconductor direct‐current triboelectric nanogenerator (MSDC‐TENG) is reported. The tribovoltaic effect is facilitated by direct voltage and current by rubbing a metal/semiconductor on another semiconductor. The frictional energy released by the forming atomic bonds excites nonequilibrium carriers, which are directionally separated to form a current under the built‐in electric field. The continuous average open‐circuit voltage (10–20 mV), short‐circuit direct‐current output (10–20 µA), and low impedance characteristic (0.55–5 kΩ) of the MSDC‐TENG can be observed during relative sliding of the metal and silicon. The working parameters are systematically studied for electric output and impedance characteristics. The results reveal that faster velocity, larger pressure, and smaller area can improve the maximum power density. The internal resistance is mainly determined by the velocity and the electrical resistance of semiconductor. This work not only expands the material candidates of TENGs from organic polymers to semiconductors, but also demonstrates a tribovoltaic effect based electric energy conversion mechanism.