Self-powered Electronic Devices Research Articles

Optimization of Thermoelectric Performance of Ag2Te Films via a Co-Sputtering Method.

Providing self-powered energy for wearable electronic devices is currently an important research direction in the field of thermoelectric (TE) thin films. In this study, a simple dual-source magnetron sputtering method was used to prepare Ag2Te thin films, which exhibit good TE properties at room temperature, and the growth temperature and subsequent annealing process were optimized to obtain high-quality films. The experimental results show that films grown at a substrate temperature of 280 °C exhibit a high power factor (PF) of ~3.95 μW/cm·K2 at room temperature, which is further improved to 4.79 μW/cm·K2 after optimal annealing treatment, and a highest PF of ~7.85 μW/cm·K2 was observed at 200 °C. Appropriate annealing temperature effectively increases the carrier mobility of the Ag2Te films and adjusts the Ag/Te ratio to make the composition closer to the stoichiometric ratio, thus promoting the enhancement of electrical transport properties. A TE device with five legs was assembled using as-fabricated Ag2Te thin films. With a temperature difference of 40 K, the device was able to generate an output voltage of approximately 14.43 mV and a corresponding power of about 50.52 nW. This work not only prepared a high-performance Ag2Te film but also demonstrated its application prospects in the field of self-powered electronic devices.

Flexible Organic Molecular Single Crystal-Based Triboelectric Device as a Self-Powered Tactile Sensor.

Triboelectric nanogenerators (TENGs) have proven to be effective at converting mechanical energy into electrical power, making them a viable technology for operating self-powered electronic devices used in medical diagnostics and environmental monitoring. In the present study, we demonstrate the utility of the flexible single crystals of an organic compound for the fabrication of a TENG as a self-powered tactile sensor. Triboelectrification was attained in single crystals as a result of surface functionalization with positively and negatively charged moieties, viz. Zn2+ and F-, respectively, which resulted in a variable surface potential and reversible adhesion through electrostatic interaction and induction phenomena. TENG incorporating the single crystals showed an output voltage of 2.4 V, a current density of ∼2.2 μA/m2, and a power density of ∼850 mW/m2 and was capable of charging commercial capacitors thereby ensuring its ability to be used as a self-powered touch sensor. Capitalizing on these features, a self-powered tactile sensor was fabricated to demonstrate limb movements. The excellent mechano-electric sensitivity (∼102 mV/kPa until 6 kPa range) and response time (∼38 ms) establish the viability of flexible organic single crystals for mechanical energy harvesting and biosensing applications that could pave the way for their utilization as biomedical wearable devices.

Self-powered wearable remote control system based on self-adhesive, self-healing, and tough hydrogels

The advent of the fifth-generation mobile communication network era induces a great potential for the design and development of self-powered wearable electronic devices. Hydrogels, as a typical material for flexible electrodes, have been widely employed in self-powered wearable electronic devices. However, the hydrogel-based triboelectric nanogenerator (H-TENG) is usually compromised by the challenges in data collection, operational stability, and manufacturability due to the unstable combination between the friction layer and the electrode layer, the occurrence of hydrogel damage during prolonged operation, and also the difficulty of machining sticky hydrogel electrodes. In the present study, a composite hydrogel composed of acrylamide, crotonyl alcohol, and 4-carboxyphenylboronic acid was synthesized via ultraviolet crosslinking, which was specially developed for H-TENG and wearable wireless remote control interface, featuring with excellent stretchability and mechanical strength as well as self-healing and self-adhesive properties. The open-circuit voltage of the H-TENG prepared with the hydrogel reached up to 165 V, and the output voltage remained almost unchanged following 10,000 cycles of compression test. Additionally, a wearable wireless remote control system was designed that could accurately control the multiple appliances and adjust different working modes using the H-TENG. Consequently, the development of the H-TENG and wearable wireless remote control system has the potential to provide a new methodology for the application of next-generation wearable devices in various areas, such as smart homes, as a representative example.

V2CTx MXene interspersed PVDF electrospun nanofibers based piezoelectric nanogenerator for self-powered electronic devices and mechano-electrodeposition

Rapid advancement of 2D materials has spurred extensive research into MXenes, given their remarkable properties applicable in fields like energy storage, catalysis, and energy harvesting. MXenes, notably Ti3C2, hold promise for self-powered sensors such as piezoelectric nanogenerators, yet exploration of other variants is limited. This study presents a Piezoelectric Nanogenerator (PENG) composed of electrospun nanofibers fabricated from a composite of PVDF/ V2CTx MXene. V2CTx MXene synthesis involves hydrothermal synthesis followed by an acid etching process. These composite electrospun nanofibers, deposited onto a copper sheet, serve as the PENG, generating 124 V (open-circuit) and 2.2 µAmps (short-circuit) with manual single-finger tapping. Additionally, the PENG's versatility is demonstrated through its ability to facilitate the electrodeposition of ZnO thin films and power various small-scale electronic gadgets. Mechanical stability analysis over 3000 cycles underscores the device's robustness, indicating potential for enhanced self-powered sensing technology in nanogenerator applications and prompting further exploration of MXene variants.

Enhanced Performance of a Self-Powered Au/WSe2/Ta2NiS5/Au Heterojunction by the Interfacial Pyro-phototronic Effect.

The growing need for wearable electronics and self-powered electronic devices has driven the successful development of self-powered two-dimensional (2D) photodetectors using the photovoltaic effect of Schottky and p-n junctions. However, there is an urgent need to develop multifunctional photodetectors capable of harvesting energy from different sources to overcome their limitations in efficiency and cost. While the pyro-phototronic effect has been shown to effectively influence optoelectronic processes in heterojunctions, the number of reported two-dimensional heterojunctions exhibiting interfacial pyroelectricity is still limited, and the responsivity and detectivity based on such heterojunctions tend to be low. In this study, a photodetector based on an Au/WSe2/Ta2NiS5/Au heterojunction was designed and fabricated. By harnessing the interfacial pyro-phototronic effect arising from the built-in electric fields at the Au/WSe2 Schottky junction and WSe2/Ta2NiS5 heterojunction, the photodetector exhibits a broadband response range of 405-1064 nm, with approximately 12 times enhancement in output current compared to solely relying on the photovoltaic effect. Under 660 nm light irradiation, the self-powered photodetector exhibits a responsivity of 121 mA/W, an external quantum efficiency of 22.64%, and a specific detectivity of 2 × 1012 Jones. Notably, its pyroelectric coefficient exceeds 8 × 103 μC·m-2·K-1. These findings pave the way for effectively detecting weak light and temperature variation while presenting a new strategy for developing high-performance photodetectors utilizing the interfacial pyro-phototronic effect.

Super-strain, high sensitivity, and multi-responsive flexible sensor based on nanocellulose hydrogels

The application of flexible sensors based on conductive hydrogels in human motion monitoring has been widely studied. Here, a facile one-pot method is proposed to prepare nanocellulose/polyacrylamide/sodium alginate hydrogel (CNWs/SA/PAM). The resulting CNWs/SA/PAM hydrogel has exceptional mechanical properties (7850 %, 1.3 MPa) and high sensitivity (14200 %, GF=3.6, 68 ms). The nanocellulose crystals (CNWs) are bent and entangled with the backbone of the polyacrylamide/sodium alginate (PAM/SA) hydrogel network, effectively transferring external mechanical forces to the entire physical and chemical cross-linking domains. This feature considerably improves the tensile strength, strain sensing range, and sensitivity of the hydrogel. The CNWs/SA/PAM hydrogel exhibits a sensitive response to water molecules and temperature-stimulated shape memory behaviour and can act as a programmable deformation actuator. The hydrogel sensor can detect and monitor subtle human motion signals in a timely and accurate manner. It is designed as a single-electrode friction nanogenerator insole (insole-TENG) that can monitor the large motion states of the human body in real time and can be efficiently used for small self-powered electronic devices. This study will shed some light on developing cellulose hydrogels in multifunctional human motion health detection sensors, soft-actuated robots, and self-powered applications for small electronic devices.

Enhancing output performance of triboelectric nanogenerators with ZnFe2O4 nanoparticles in biodegradable polylactic acid for sustainable energy harvesting

ABSTRACT The development of triboelectric nanogenerators (TENGs) using sustainable materials addresses the global electronic waste issue. This research focuses on fabricating a TENG device with biodegradable polylactic acid (PLA) as the tribopositive material and polytetrafluoroethylene (PTFE) as the tribonegative material. ZnFe2O4 nanoparticles are incorporated into the PLA matrix to enhance surface charge density and synthesised via a simple combustion method. PLA-ZnFe2O4 composite films were prepared by solvent casting with varying nanofiller content (0.25, 0.45, 0.65, and 0.85 g). Prepared composites were characterised by Powder X-ray Diffraction (PXRD) for crystalline nature and phase purity, Fourier Transform Infrared Spectroscopy (FTIR) for vibrational analysis, and Scanning Electron Microscopy (SEM) for surface morphology. The inclusion of ZnFe2O4 nanoparticles improves TENG output performance, with a maximum output voltage of 18.4 V and a current of 1.57 µA observed for a PLA (poly(lactic acid)) composite with 39.39% nanoparticle content. Electrical studies on the optimised device show successful charging of various capacitors and powering 20 LEDs and a calculator. Body movements like walking and jumping were also tested to measure voltage and current outputs. These findings highlight new possibilities for developing smart, self-powered electronic devices.

Nanocellulose and multi-walled carbon nanotubes reinforced polyacrylamide/sodium alginate conductive hydrogel as flexible sensor

Conductive hydrogels have been widely applied in human–computer interaction, tactile sensing, and sustainable green energy harvesting. Herein, a double cross-linked network composite hydrogel (MWCNTs/CNWs/PAM/SA) by constructing dual enhancers acting together with PAM/SA was constructed. By systematically optimizing the compositions, the hydrogel displayed features advantages of good mechanical adaptability, high conductivity sensitivity (GF = 5.65, 53 ms), low hysteresis (<11 %), and shape memory of water molecules and temperature. The nanocellulose crystals (CNWs) were bent and entangled with the backbone of the polyacrylamide/ sodium alginate (PAM/SA) hydrogel network, which effectively transferred the external mechanical forces to the entire physical and chemical cross-linking domains. Multi-walled carbon nanotubes (MWCNTs) were filled into the cross-linking network of the hydrogel to enhance the conductivity of the hydrogel effectively. Notably, hydrogels are designed as flexible tactile sensors that can accurately recognize and monitor electrical signals from different gesture movements and temperature changes. It was also assembled as a friction nanogenerator (TENG) that continuously generates a stable open circuit voltage (28 V) for self-powered small electronic devices. This research provides a new prospect for designing nanocellulose and MWCNTs reinforced conductive hydrogels via a facile method.

A flexible silicone tube arrangement structure triboelectric nanogenerator for tennis training monitoring

As the Internet of Things (IoTs) rapidly gain popularity, the demand for self-powered flexible electronic devices is continuously rising, particularly in the intelligent sports field. Hence, we introduced a silicone tube-based triboelectric nanogenerator (ST-TENG) designed for mechanical energy harvesting and tennis training monitoring. The ST-TENG, with its innovative tubular structure, effectively harvests low-frequency mechanical energy and converts it into electrical energy. At a working frequency of 6 Hz, the ST-TENG achieved an open-circuit voltage (Voc) of 122.51 V, a short-circuit current (Isc) of 15.05 µA, and a transfer charge (Qsc) of 33.74 nC. The ST-TENG demonstrates high sensitivity and accuracy in capturing subtle motion details, providing comprehensive data on various aspects of an athlete’s performance. The ST-TENG demonstrated excellent responsiveness to pressure and bending, making it suitable for real-time motion monitoring in tennis. Integrating the ST-TENG into the clothing and equipment of tennis players effectively monitored wrist, waist, and foot movements, providing detailed motion data. This research paves the way for developing highly efficient, self-powered wearable sensors that can significantly enhance the accuracy and sustainability of real-time athletic training monitoring.

Tough and temperature-tolerance cellulose/polyacrylic acid/bentonite hydrogel with high ionic conductivity enables self-powered triboelectric wearable electronic devices

Solid-state zinc-ion hybrid supercapacitors (ZHSCs) featuring hydrogel electrolytes have become ideal for large-scale flexible energy storage. However, existing polyacrylic acid (PAA) hydrogel electrolytes often lack the combined traits of ionic conductivity, mechanical robustness, and temperature tolerance. Herein, a versatile PAA-based hydrogel electrolyte (ACBH-Zn) containing a ZnCl2-cellulose solution and bentonite (BT) is delivered, facilitated by cooperative coordination bonds and hydrogen bonds. The coordination bonds between Zn2+ and −COOH of PAA, in conjunction with cellulose and BT, alongside the abundant hydrogen bonds within cellulose and PAA, are conducive to upgrading mechanical strength and ionic conductivity, while the BT's lamellar structure further provides sufficient ion migration channels. Consequently, the ACBH-Zn showcases exceptional mechanical properties, satisfying ionic conductivity (88.9 mS cm−1), and excellent temperature tolerance at −60 °C (30.3 mS cm−1). The ACBH-ZHSC, when assembled, attains a remarkable maximum energy density (323.4 Wh kg−1), maintaining an impressive capacity retention rate (92 %) even after undergoing 10,000 cycles at 10.0 A g−1. Furthermore, the assembled self-powered triboelectric wearable electronic device effectively converts mechanical energy from human movement into electrical energy, enabling efficient storage and utilization, and offering promising insights into the application of flexible wearable devices.

Flexible PVDF/BST nanocomposites for mechanical energy harvesting application

The development of a piezoelectric generator (PEG) that exhibits improved durability, stability, and enhanced output performance continues to be a crucial objective for self-powered and wearable electronic devices. In this study, a PEG was constructed using nanocomposite films composed of sol-gel derived Barium Strontium Titanate (BST) filler embedded within a Polyvinylidene fluoride (PVDF) matrix. This flexible polymer matrix structure is selected for its exceptional performance, flexibility, and cost-efficiency, making it ideal for advanced piezoelectric applications. Homogeneous nanocomposite films of PVDF-BST with different proportions of BST were fabricated using the solution casting method. Integrating BST filler into the PVDF matrix significantly enhances the nucleation of the electroactive β-phase, thereby improving the dielectric and ferroelectric properties, which vary according to the volume fraction of BST used. Specifically, the PVDF-BST composite containing 10 % BST (PB10) exhibited the highest electroactive β-phase content at 41.8 %, and demonstrated an energy storage density of 0.8 J/cm³ with an efficiency of 73.9 %. The dielectric constant at room temperature is seen to rise from 23 in pure PVDF to 132 in the PB20 composition at 1 kHz. The open-circuit voltage (Voc) of the PEG was recorded by exerting a periodic force on its surface. Notably, the PB10 variant achieved the highest peak-to-peak open-circuit voltage, reaching 28 V. Additionally, PB10 produced an open-circuit voltage of 22 V in response to finger tapping, highlighting its suitability for applications in touch and pressure sensing.

Unveiling the potential of Ag2S-based full-inorganic flexible thermoelectric devices for temperature sensors

Thermoelectric sensors, which are capable to convert temperature gradients into electrical signals, hold promise for use in wearable body-temperature monitors and self-powered electronic devices. However, traditional flexible thermoelectric devices constructed with organic materials have been hampered by their low energy conversion efficiency, largely stemming from the lack of ideal materials and optimized device geometry. In this study, we utilize state-of-the-art Ag2S-based inorganic materials and fine-tune the geometric parameters of full-inorganic flexible thermoelectric devices through finite element simulation. Our research reveal that these geometric parameters significantly impact the output performance of the flexible thermoelectric device. With the temperature difference set up as 25 K, the optimized device demonstrates a notable performance enhancement, particularly in terms of power density, which is 84 % higher compared to the pre-optimization state. This work introduces a novel approach for enhancing the performance of full-inorganic flexible thermoelectric devices, and also delves into the potential application of this technology in the realm of respiratory monitoring, underscoring its significance and promising prospects.

High Performance Piezoelectric Nanogenerators Based on Polyvinylidene Fluoride-Graphene Nanoribbon Composite Thin Films.

In this study, a highly efficient, sensitive, and lightweight piezoelectric nanogenerator (PENG) is developed using graphene nanoribbons (GNRs) incorporated into the polyvinylidene fluoride (PVDF) matrix. Unzipping multi-walled carbon nanotubes is an effective and scalable strategy for synthesizing graphene nanoribbons. The synthesized GNRs are employed to prepare nanometer-scale piezoelectric polymer composite films showing higher piezoelectric performance than neat PVDF. The impact of GNR concentration in the PVDF matrix on the electroactive phase content and piezoelectric properties of the composites is systematically investigated. X-ray diffraction (XRD) and Fourier-transformed infrared spectroscopy (FT-IR) analysis demonstrate an increase in the electroactive β and γ phases of PVDF by incorporating GNRs in the composites. With the optimized concentration of GNRs (1 wt%), the fabricated piezoelectric device can generate open-circuit voltage and an output power density of 26V and 16.52 µWcm2, respectively. It is also found that the PVDF-GNR 1 nanogenerator can be used to generate electrical power by converting mechanical energy from different human activities such as wrist bending, palm tapping, and toe tapping. The findings indicate that (PVDF-GNR 1) PENGcan be applied in self-powered portable and wearable electronic devices.

Development of Highly Flexible Piezoelectric PVDF-TRFE/Reduced Graphene Oxide Doped Electrospun Nano-Fibers for Self-Powered Pressure Sensor.

The demand for self-powered, flexible, and wearable electronic devices has been increasing in recent years for physiological and biomedical applications in real-time detection due to their higher flexibility and stretchability. This work fabricated a highly sensitive, self-powered wearable microdevice with Poly-Vinylidene Fluoride-Tetra Fluoroethylene (PVDF-TrFE) nano-fibers using an electrospinning technique. The dielectric response of the polymer was improved by incorporating the reduced-graphene-oxide (rGO) multi-walled carbon nano-tubes (MWCNTs) through doping. The dielectric behavior and piezoelectric effect were improved through the stretching and orientation of polymeric chains. The outermost layer was attained by chemical vapor deposition (CVD) of conductive polymer poly (3,4-ethylenedioxythiophene) to enhance the electrical conductivity and sensitivity. The hetero-structured nano-composite comprises PVDF-TrFE doped with rGO-MWCNTs over poly (3,4-ethylenedioxythiophene) (PEDOT), forming continuous self-assembly. The piezoelectric pressure sensor is capable of detecting human physiological vital signs. The pressure sensor exhibits a high-pressure sensitivity of 19.09 kPa-1, over a sensing range of 1.0 Pa to 25 kPa, and excellent cycling stability of 10,000 cycles. The study reveals that the piezoelectric pressure sensor has superior sensing performance and is capable of monitoring human vital signs, including heartbeat and wrist pulse, masticatory movement, voice recognition, and eye blinking signals. The research work demonstrates that the device could potentially eliminate metallic sensors and be used for early disease diagnosis in biomedical and personal healthcare applications.

A piezoelectric-triboelectric-electromagnetic tri-hybrid energy harvester with dual-frequency-up-conversion mechanism for ultralow-frequency rotational motion

Rotational energy harvesting under ultralow frequencies has always been a great challenge. A piezoelectric-triboelectric-electromagnetic tri-hybrid energy harvester (THEH) with dual-frequency-up-conversion mechanism for ultralow-frequency rotational motion is proposed in this paper. The integration of two piezoelectric nanogenerators (PENG), two triboelectric nanogenerators (TENG), and one electromagnetic generator (EMG) further improves the power output. PENG and TENG can operate at a higher frequency through the magnetic coupling and impact of the center magnet. In the process, the center magnet also causes EMG to generate electricity. The three modules are coupled together by the center magnet to harvest energy continuously. This paper studies the performance of THEH at 0–2.6 Hz and the effects of the key parameter. The maximum average output is obtained as 2.38 mW, 1.3 mW, and 13.3 μW for the PENG, EMG, and TENG components at 1.2 Hz, respectively. Furthermore, a tri-channel power management method is proposed to integrate three modules’ energy in THEH. Some THEH-based self-powered electronic devices are demonstrated, which shows THEH’s great potential for rotational energy harvesting.

Ultra-light, ultra-resilient and ultra-flexible, multifunctional composite carbon nanofiber aerogel for physiological signal monitoring and hazard warning in extreme environments

The emergence of multimodal wearable flexible self-powered electronic devices undoubtedly plays a positive role in areas such as healthcare and energy. However, the preparation of three-dimensional elastic bodies suitable for humidity, temperature, and pressure sensing often involves complex fabrication processes, internal network discontinuities, and difficulties in achieving applications in extreme environments. In this paper, a one-step preparation of three-dimensional fluffy and interlayer porous nanofiber precursors is achieved using direct electrostatic spinning technology. Subsequently, high-temperature calcination and in situ polymerization processes were used to obtain multifunctional composite carbon nanofiber aerogels (MCCNA), which are characterized by ultra-lightness, super elasticity, three-dimensional fluffiness, and interlayer porousness, and are suitable for extreme environments. The ultra-light (53.67 mg cm−3) MCCNA can accurately detect humidity signals over an extremely wide range (10 %RH to 95 %RH), with a minimum temperature response time of 0.5 K. Its pressure response time is only 20 ms, and even after 5000 cycles of pressure loading, it still maintains a stable electrical signal response. Most notably, through demonstration, MCCNA can monitor the actions of firefighters in high-temperature and complex situations such as fires. Furthermore, it can monitor and provide high-temperature warnings for the temperature thresholds in the microenvironment of firefighting suits. The developed self-powered flexible wearable electronic device holds outstanding prospects for applications in healthcare, energy, and extreme conditions.

Innovative Integration of Triboelectric Nanogenerators into Signature Stamps for Energy Harvesting, Self-Powered Electronic Devices, and Smart Applications

In this manuscript, we present a novel approach for integrating Triboelectric Nanogenerators (TENGs) into signature stamps, termed Stamp TENG (S-TENG). We have modified a commercially available stamp holder to integrate triboelectric layers for multiple applications like effective energy harvesting, sensing, and embedded electronics for data prediction. S-TENG has been further explored in remote monitoring systems for elderly individuals and for gathering real-time statistics regarding persons or events at specific locations. The S-TENG is fabricated using FEP and Al as functional layers. It demonstrates an output voltage of 310 V, a current of 165 μA, and a power density of 14.8 W/m2. The simplicity of the S-TENG’s design is noteworthy. Its ability to generate energy through simple, repetitive stamping actions, which anyone can perform without specialized training, stands out as a key feature. The device is also designed for ease of use, being handheld and user-friendly. Its flexible and adaptable structure ensures that individuals with varying physical capabilities can comfortably operate it. An impressive capability of the TENG is its ability to illuminate 320 LEDs with each stamp press momentarily. Furthermore, using energy management circuits, the S-TENG can power small electronic gadgets such as digital watches and thermometers for a few seconds. In addition, when integrated with electronics, the S-TENG shows great potential in data prediction for various practical applications.

Supercapacitors and triboelectric nanogenerators based on electrodes of greener iron nanoparticles/carbon nanotubes composites

The development of supporting materials based on carbon nanotubes (CNTs) impregnated with iron nanoparticles via a sustainable and green synthesis employing plant extract of Punica granatum L. leaves was carried out for the iron nanoparticle modification and the following impregnation into the carbon nanotubes composites (CNT-Fe) that were also coated with polypyrrole (CNT-Fe + PPy) for use as electrode for supercapacitor and triboelectric nanogenerators. The electrochemical characterization of the materials by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) assays revealed that the CNT-Fe + PPy gave rise to better performance due to the association of double-layer capacitance behavior of carbon derivative in association with the pseudocapacitance contribution of PPy resulting in an areal capacitance value 202 mF/ cm2 for the overall composite. In terms of the application of electrodes in triboelectric nanogenerators, the best performance for the composite of CNT-Fe + PPy was 60 V for output voltage and power density of 6 μW/cm2. The integrated system showed that the supercapacitors can be charged directly by the nanogenerator from 0 to 42 mV in 300 s. The successful green synthesis of iron nanoparticles on CNT and further PPy coating provides a feasible method for the design and synthesis of high-performance SCs and TENGs electrode materials. This work provides a systematic approach that moves the research front forward by generating data that underpins further research in self-powered electronic devices.

A high performance triboelectric nanogenerator using assembled sugar naphthalimides for self-powered electronics and sensors

A new class of N-glycosyl naphthalimide ricinoleate (NGNR) amphiphiles were generated using environmentally friendly reaction conditions in good yields. To investigate the potential applications of NGNR amphiphiles within the realm of supramolecular materials, molecular self-assembly experiments were conducted extensively across a diverse range of solvents and oils and observed the gel formation. Molecular-level interactions and assembly patterns were investigated by employing FTIR, SAXRD, UV–vis, and fluorescence spectroscopy, and a plausible assembly mechanism was proposed. The morphology of the supramolecular architecture was identified by scanning electron microscopy. Additionally, rheological studies provided insight into these soft materials' strength and processability. Further, in the process of fabricating a triboelectric nanogenerator (TENG) device, silicone rubber serves as an electron acceptor and assembled NGNR serves as an electron donor. The developed TENG demonstrated a significant improvement in performance over TENG made with amorphous NGNR, with output voltage, current, and power density of 410 V, 100 µA, and 5.1 W/m2, respectively, highlighting the importance of the assembly process. Furthermore, TENG is used to continuously power up small electronic device (calculator), which is useful in building self-powered electronic devices. Lastly, due to its high sensitivity and stability, the TENG was used to detect the humidity of the environment in the food processing, textile, and agriculture sectors. The change in TENG response is notably significant up to 70 % relative humidity (RH). This work showcases the development of self-powered humidity sensors.

Finite Element Analysis and Design of a Flexible Thermoelectric Generator with a Rhombus Gap Structure.

Flexible thermoelectric generators (f-TEGs) offer an opportunity to realize wearable, self-powered electronic devices. A typical f-TEG consists of flexible electrodes and rigid thermoelectric (TE) legs in a flexible package. In the realm of f-TEGs utilizing flexible electrodes and TE cuboids, our unwavering objective lies in the attainment of enhanced flexibility and elevated energy conversion efficiency. In this paper, we employ a quasi-three-dimensional thermal model to design an f-TEG with a rhombus gap structure (E/A-RhTEG) with its optimized performance validated by simulation and experiment. Additionally, the lateral and vertical thermal resistances are introduced to further explain the optimizing principle in the f-TEG's output performance. Compared with the conventional TEG with a rectangular air gap structure (E/A-ReTEG), E/A-RhTEG demonstrates improved energy conversion efficiency to some extent. Simulation results indicate that the output power and energy conversion efficiency of a 25-np-pair E/A-RhTEG at a 30 K temperature gradient reach 8.45 mW and 2.55%, which represent a performance improvement of 3.09 and 6.28%, respectively, compared to E/A-ReTEG. To further elucidate the optimization principle in the performance of f-TEGs, additional considerations are given to the lateral and vertical resistances. In this study, E/A-RhTEG comprising 25 np pairs is fabricated utilizing TE cuboids. Experimental findings indicate that E/A-RhTEG exhibits a voltage output of 127.07 mV when subjected to a temperature difference of 30 K, which demonstrates a performance enhancement of 4.06% compared to E/A-ReTEG. Furthermore, this study also demonstrates its implementation when wrapped around a curved surface and successfully achieves a self-powered device system after device performance optimization.