Charge Pumping Strategy for Rotation and Sliding Type Triboelectric Nanogenerators

Triboelectric nanogenerator (TENG) is an emerging approach for harvesting energy from the living environment. But its performance is limited by the maximum density of surface charges created by contact electrification. Here, by rationally designing a synchronous rotation structure, a charge pumping strategy is realized for the first time in a rotary sliding TENGs, which is demonstrated to enhance the charge density by a factor of 9, setting up a record for rotary TENGs. The average power is boosted by more than 15 times compared with normal TENGs, achieving an ultrahigh average power density of 1.66 kW m^?3, under a low drive frequency of 2 Hz. Moreover, the charge pumping mechanism enables decoupling of bound charge generation and the severity of interfacial friction in the main TENG, allowing surface lubricants to be applied for suppressing abrasion and lowering heat generation. The adaptability of the strategy to rotation and sliding type TENGs in low‐frequency agitations provides a breakthrough to the bottleneck of power output for mechanical energy harvesting, and should have a great impact on high‐power TENG design and practical applications in various fields.     

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.     

Multilayered‐Electrode‐Based Triboelectric Nanogenerators with Managed Output Voltage and Multifold Enhanced Charge Transport

The open‐circuit voltage of a triboelectric nanogenerator (TENG) increases with the tribo‐charge density and the separated distance between two tribo‐surfaces, which can reach several thousand volts and is much higher than the working voltage required by most electrical devices and energy storage units. Therefore, improving the effective efficiency of TENGs requires reducing the output voltage and enhancing the transferred charges. Here, a multilayered‐electrode‐based TENG (ME‐TENG) is developed in which the output voltage can be managed by controlling the charge flow in a process of multiple (N) steps, which results in N times lower voltage but N times higher total charge transport. The ME‐TENG is demonstrated to work in various modes, including multichannel, single‐channel, and double‐tribo‐surface structures. The effects of insulator layer thickness and total layer number on the output voltage are simulated by the finite element method. The output voltage can be modulated from 14 to 102 V by changing the insulator layer number between two adjacent working electrodes, based on which the 8‐bit logic representations of the characters in the ACSII code table are demonstrated. The ME‐TENG provides a novel method to manage the output power and has potential applications in self‐powered sensors array and human–machine interfacing with logic communications.     

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.     

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.     

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.     

A New Single-Electrode Generator for Water Droplet Energy Harvesting with A 3 mA Current Output

Triboelectric nanogenerators (TENGs) based on water droplets can harvest water kinetic energy using triboelectrification and electrostatic induction mechanisms. However, the development of traditional liquid–solid TENGs (L–S TENGs) is severely limited due to their low-performance output and high device encapsulation requirements for preparation technology. In this work, a single-electrode mode droplet-based TENG (D-TENG) is devised to effectively harvest water kinetic energy by optimizing the interface contact behavior of droplets, increasing the short-circuit current (I_SC) of one drop of water from microamperes to milliamperes levels. In the D-TENG configuration, the electrode is positioned above the dielectric rather than at the bottom, allowing efficient utilization of generated friction charges and reducing the dissipation of these charges, thereby enhancing the output performance of the TENG. The influencing factors and operational mechanisms of D-TENG are studied to obtain optimized working conditions to improve its output performance. Under optimal conditions, the D-TENG can saturate the charge of the PTFE surface with only 8 droplets, achieving an I_SC of up to 3.51 mA and an output voltage (V_O) of 298.27 V. This work provides a convenient method for efficiently harvesting water kinetic energy based on interfacial behavior control.     

Direct‐Current Triboelectric Nanogenerator Realized by Air Breakdown Induced Ionized Air Channel

The air breakdown phenomenon is generally considered as a negative effect in previous research on triboelectric nanogenerators (TENGs), which is always accompanied by air ionization. Here, by utilizing the air breakdown induced ionized air channel, a direct‐current triboelectric nanogenerator (DC‐TENG) is designed for harvesting contact‐separation mechanical energy. During working process, the charges first transfer from bottom to top electrodes through an external circuit in contact state, then flow back via the ionized air channel created by air breakdown in the separation process. So a unidirectional flow of electrical charges can be observed in the external circuit. With repeating contact‐separation cycles, continuous pulsed DC output through the external circuit can be realized. This working mechanism was verified by real‐time electrode potential monitoring, photocurrent signal detection, and controllable discharging observation. The DC‐TENG can be used for directly and continuously charging an energy storage unit and/or driving electronic devices without using a bridge rectifier. Owing to its simplicity in structure, the mechanism is further applied to fabricate the first flexible DC‐TENG. This research provides a significant fundamental study for DC‐TENG technology and may expand its application in flexible electronics and flexible self‐charging power systems.     

High Permittivity CaCu3Ti4O12 Particle‐Induced Internal Polarization Amplification for High Performance Triboelectric Nanogenerators

Here, a composite material based on the butylated melamine formaldehyde (BMF) and high permittivity CaCu₃Ti₄O₁₂ (CCTO) particles as a triboelectric dielectric material for stable high output triboelectric nanogenerators (TENGs) is proposed. CCTO particles, which have the high permittivity of 7500, can potentially result in the formation of strong internal polarization into the dielectric material under the electric field from triboelectric charges. As a consequence, the charge induction on the bottom electrode is enhanced thereby increasing the triboelectric output performance. A rotation‐type freestanding mode TENG based on BMF–CCTO 1 wt% composite material demonstrates high performance power output of a root‐mean‐square voltage and current density with 268 V and 25.8 mA m^?2, respectively. The strategy of incorporating the high permittivity CCTO particles can be universally applied to any triboelectric polymer matrix in order to enhance the output performance of TENGs.     

Multidirection and Multiamplitude Triboelectric Nanogenerator Composed of Porous Conductive Polymer with Prolonged Time of Current Generation

In this work, a sponge structure triboelectric nanogenerator (TENG) named as porous conductive polymer (PCP)‐TENG, is demonstrated. The measured volume charge density of PCP‐TENG is reached to 60 mC m^?3 by utilizing wide inner surface of the sponge structure as contact surface. Moreover, the PCP‐TENG generates a continuous sinusoidal‐like alternative current. Notably, the PCP‐TENG can effectively harvest vibrational mechanical energy from various directions and amplitudes. With these characteristics, the PCP‐TENG can be implemented in a wide variety of settings, such as inside of a tire. It is confirmed that the PCP‐TENG generates electrical power for operating a commercial light‐emitting diode and a humidity sensor even under small deformation of the tire.     

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.     

Addressing Triboelectric Nanogenerator Impedance for Efficient CO2 Utilization

Reducing the impedance of a triboelectric nanogenerator (TENG) without power loss is crucial for enhancing its energy conversion efficiency and overall performance. In this paper, a novel signal management structure, based on a newly designed sliding-mode TENG, aimed at effectively reducing impedance by converting narrow, instantaneous signals into broader ones is presented. This transformation is accomplished by adding a grounded electrode connected to a high-inductive inductor and fine-tuning the parasitic capacitance of the dielectric material. Utilizing a highly resistive material like P(VDF–TrFE), a significant improvement in the TENG's performance is achieved, resulting in an increase of output power to 0.352 mW and a decrease in impedance from 3.2 to 0.3 MΩ. This results in a threefold increase in charging speed, which can be attributed to the reduced charge loss and improved matching at lower impedance. Based on these promising findings, the enhanced TENG is successfully connected to power a system for electrochemical CO₂ reduction for CO production. This system effectively reduces the required electrochemical reduction potential by ≈15% under real environments.     

Boost the Performance of Triboelectric Nanogenerators through Circuit Oscillation

Triboelectric nanogenerator (TENG) which harvests ubiquitous ambient mechanical energy is a promising power source that can meet the distributed energy demand in the internet of things, wearable electronics, etc. However, the available output of TENG is severely limited by the saturated polarized charge density, small intrinsic capacitance, and large matching impedance. Herein, an effective power management strategy is proposed that flips the free charges on the conductive layer through a controlled LC oscillating circuit composed of the diode, switch, inductor, and the intrinsic capacitor of TENG. In this way, the equivalent charge density reaches a level higher than the saturated polarized charge density. The simulation and experiments show that the limit of energy output can be exceeded under arbitrary load resistance, especially for the low‐impedance common electronics. It is believed that such a general, low‐cost, and highly effective strategy can further broaden the applications of TENG devices across the fields and probably be a new performance evaluation standard for TENG.     

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.     

Boosting Ion Diffusion and Charge Transfer by Zincophilic Accordion Arrays to Achieve Ultrafast Aqueous Zinc Metal Batteries

A key challenge to apply aqueous zinc metal batteries (AZMBs) as next-generation energy storage device is to improve the rechargeability at high current densities, which is needed to circumvent slowly ion diffusion in anode and sluggish charge transfer of Zn²⁺. Herein, a zincophilic accordion array derived from MOF is developed as zinc host for simultaneously boosted ion diffusion and charge transfer. The designed host is prepared by etching and disproportionation reactions, the abundant zincophilic Sn sites with nano-size uniform disperse on accordion arrays nanosheets (Sn-AA). Then a composite Zn anode (Sn-AA@Zn) is obtained by compacting Sn-AA host with zinc power (Zn-P). The Sn-AA@Zn anode has an ultra-low activation energy (37.1 kJ mol⁻¹) and nucleation overpotential (10 mV), achieving fast charge transfer of Zinc deposition. In addition, the cycle life of the symmetric cell with Sn-AA@Zn anode exceeds 13 000 cycles at 50 mA cm⁻², which is 32 times than that of the Zn-P anode. And the full cell with Sn-AA@Zn anode and MnO₂ cathode maintains a capacity of 122 mAh g⁻¹ after 5000 cycles at 5 Ag⁻¹. Hopefully, the 3D anode based on Sn-AA@Zn accordion array and Zn-P has significantly improved the rechargeability of AZMB at high current density.     

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.     

Local Charge Distribution Engineered by Schottky Heterojunctions toward Urea Electrolysis

Urea electrooxidation with favorable thermodynamic potential offers great promise for decoupling H₂/O₂ evolution from sluggish water splitting, and simultaneously mitigating the problem of urea‐rich water pollution. However, the intrinsically slow kinetics of the six‐electron transfer process impels one to explore efficient catalysts in order to enable widespread use of this catalytic system. In response, taking CoS₂/MoS₂ Schottky heterojunctions as the proof‐of‐concept paradigm, a catalytic model to modulate the surface charge distribution for synergistically facilitating the adsorption and fracture of chemical group in urea molecule is proposed and the mechanism of urea electrooxidation at the molecular level is elucidated. Based on density functional calculations, the self‐driven charge transfer across CoS₂/MoS₂ heterointerface would induce the formation of local electrophilic/nucleophilic region, which will intelligently adsorb electron‐donating/electron‐withdrawing groups in urea molecule, activate the chemical bonds, and thus trigger the decomposition of urea. Benefiting from the regulation of local charge distribution, the constructed Schottky catalyst of CoS₂‐MoS₂ exhibits superior urea catalytic activities with a potential of 1.29 V (only 0.06 V higher than the thermodynamic voltage of water decomposition) to attain 10 mA cm^?2 as well as robust durability over 60 h. This innovational manipulation of charge distribution via Schottky heterojunction provides a model in exploring other highly efficient electrocatalysts.     

Spatial Charge Storage within Honeycomb‐Carbon Frameworks for Ultrafast Supercapacitors with High Energy and Power Densities

Carbon‐based supercapacitors store charge through the adsorption of electrolyte ions onto the carbon surface. Therefore, it would be more attractive for the enhanced charge storage if the locations for storing charge can be extended from carbon surface to space. Here, a novel spatial charge storage mechanism based on counterion effect from Fe(CN)₆^3? ions bridged by oxygen groups and confined into honeycomb‐carbon frameworks is presented, which can provide additionally spatial charge storage for electrical double‐layer capacitances in a negative potential region and pseudocapacitances from Fe(CN)₆^3?/Fe(CN)₆^4? in a positive potential region. More importantly, an ultrafast supercapacitor based on this novelty carbon can be charged/discharged within 0.7 s to deliver both high specific energy of 15 W h kg^?1 and ultrahigh specific power of 79.1 kW kg^?1 in 1 m Na₂SO₄ electrolyte, much higher than those of previously reported asymmetric supercapacitors in aqueous electrolytes, as well as excellent cycling stability. These features suggest a new generation of ultrafast asymmetric supercapacitors as novel high‐performance energy storage devices.