RESUMEN

Integrating flexible piezoelectric nanogenerators (PENGs) into wearable and portable electronics offers promising prospects for motion monitoring. However, it remains a significant challenge to develop environmentally friendly PENGs using biodegradable and cost-effective natural polymers for mechanical energy harvesting and self-powered sensing. Herein, reduced graphene oxide (rGO) and barium titanate (BTO) were introduced into regenerated cellulose pulp to fabricate a composite porous film-based PENG. The incorporation of rGO not only increased the electrical conductivity of the porous film but also enhanced the dispersibility of BTO. Moreover, the unique pore structure of the composite porous film improved the polarization effect of the air inside the pores, thereby greatly boosting the overall piezoelectric performance. The piezoelectric coefficient of the resulting composite porous film reaches up to 41.5 pC·N-1, which is comparable to or higher than those reported in similar studies. Consequently, the PENG assembled from this cellulose/rGO/BTO composite porous film (CGB-PENG) achieved an output voltage of 47 V, a current of 4.6 µA, and a power density of 30 µW·cm-2, approximately three times the output voltage and ten times the power density of similar studies. This work presents a feasible approach for the fabrication of high-performance cellulose-based PENGs derived from recycled waste cotton textiles.

RESUMEN

Sleep plays a role in maintaining our physical well-being. However, sleep-related issues impact millions of people globally. Accurate monitoring of sleep is vital for identifying and addressing these problems. While traditional methods like polysomnography (PSG) are commonly used in settings, they may not fully capture natural sleep patterns at home. Moreover, PSG equipment can disrupt sleep quality. In recent years, there has been growing interest in the use of sensors for sleep monitoring. These lightweight sensors can be easily integrated into textiles or wearable devices using technology. The flexible sensors can be designed for skin contact to offer continuous monitoring without being obtrusive in a home environment. This review presents an overview of the advancements made in flexible sensors for tracking body movements during sleep, which focus on their principles, mechanisms, and strategies for improved flexibility, practical applications, and future trends.

Asunto(s)

RESUMEN

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 ß 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 26 V 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) PENG can be applied in self-powered portable and wearable electronic devices.

RESUMEN

Organic piezoelectric nanogenerators (PENGs) are attractive in harvesting mechanical energy for various self-powering systems. However, their practical applications are severely restricted by their low output open circuit voltage. To address this issue, herein, we prepared two two-dimensional (2D) covalent organic frameworks (COFs, CityU-13 and CityU-14), functionalized with fluorinated alkyl chains for PENGs. The piezoelectricity of both COFs was evidenced by switchable polarization, characteristic butterfly amplitude loops, phase hysteresis loops, conspicuous surface potentials and high piezoelectric coefficient value (d33). The PENGs fabricated with COFs displayed highest output open circuit voltages (60 V for CityU-13 and 50 V for CityU-14) and delivered satisfactory short circuit current with an excellent stability of over 600 seconds. The superior open circuit voltages of CityU-13 and CityU-14 rank in top 1 and 2 among all reported organic materials-based PENGs.

RESUMEN

Amidst the growing challenge of meeting global energy demands with conventional sources, self-powered devices offer promising solution. Flexible and stretchable electronics are pivotal in wearable technology, enhancing the scope and functionality of these devices. This study employs potassium sodium niobite-lithium antimonate (K0.5Na0.5NbO3-LiSbO3) nanoparticles as fillers in polyvinylidene fluoride (PVDF) to fabricate piezoelectric thin films. These films are integrated with fabric-based electrodes to develop high-performance, flexible self-powered sensors. The sensor comprises a fabric-based electrode with polypyrrole (PPy) coated on plain nylon fabric, a 0.93KNN-0.07LS/PVDF composite piezoelectric thin film, and a protective PET layer. Results demonstrate that the 0.93KNN-0.07LS/PVDF-PPy/nylon composite sensors exhibit a stable piezoelectric output. Under 6 Hz and 10 N excitation, the piezoelectric output reaches approximately 6.1 V upon pressing. Additionally, the device shows good linear sensitivity in the 2-20 N pressure range and produces clear, regular output waveforms under cyclic pressures of varying frequencies and amplitudes, indicating excellent response repeatability. Even after extensive bending, twisting, and 5000 pressing cycles, the sensors maintain considerable cyclic stability, demonstrating high durability. These tests collectively indicate that the developed sensors possess high sensitivity, flexibility, durability, stability, and significant self-powered potential. This research provides a reference for the next generation of textile-based electrodes and offers potential strategies for flexible, wearable applications.

RESUMEN

Self-powered sensors have the potential to enable real-time health monitoring without contributing to the ever-growing demand for energy. Piezoelectric nanogenerators (PENGs) respond to mechanical deformations to produce electrical signals, imparting a sensing capability without external power sources. Textiles conform to the human body and serve as an interactive biomechanical energy harvesting and sensing medium without compromising comfort. However, the textile-based PENG fabrication process is complex and lacks scalability, making these devices impractical for mass production. Here, we demonstrate the fabrication of a long-length PENG fiber compatible with industrial-scale manufacturing. The thermal drawing process enables the one-step fabrication of self-poled MoS2-poly(vinylidene fluoride) (PVDF) nanocomposite fiber devices integrated with electrodes. Heat and stress during thermal drawing and MoS2 nanoparticle addition facilitate interfacial polarization and dielectric modulation to enhance the output performance. The fibers show a 57 and 70% increase in the output voltage and current compared to the pristine PVDF fiber, respectively, at a considerably low MoS2 loading of 3 wt %. The low Young's modulus of the outer cladding ensures an effective stress transfer to the piezocomposite domain and allows minute motion detection. The flexible fibers demonstrate wireless, self-powered physiological sensing and biomotion analysis capability. The study aims to guide the large-scale production of highly sensitive integrated fibers to enable textile-based and plug-and-play wearable sensors.

RESUMEN

Flexible, air permeable and elastic self-powered sensors for human motion monitoring and assisted medical rehabilitation have recently become a hot research topic. However, most current piezoelectric sensors can not account for many characteristics. Addressing this challenge, an all-textile piezoelectric sensor (ATPS) based on 3D structured knitted fabric electrodes is reported. The ATPS consists of a piezoelectric element polyvinylidene fluoride nanofiber membrane, flexible knitted fabric electrodes, and an elastic self-adhesive bandage. Based on the flexible and efficient knitting technology, the sensor has the advantages of low cost, flexibility, simple structure, and convenient large-area manufacturing. Experimental and finite element simulation results show that the knitting pattern of fabric electrodes can enhance the piezoelectric output of ATPS. The optimal ATPS has a high voltage response sensitivity of up to 0.68 V/kPa. The proposed ATPS responds to a wide range of input forces from 0.098 to 724 N in self-powered mode, verifying its feasibility as a tactile sensor for human motion detection and recognition (throat swallowing, wrist bending, elbow bending, knee bending, walking slowly, running fast) and as a pressure sensor (Morse code, digit recognition) and demonstrating its potential for motion tracking, medical rehabilitation, and human-computer interaction.

Asunto(s)

RESUMEN

Flexible electrospun fiber-based piezoelectric nanogenerator (PENG) has attracted a lot of interest due to its ability of generating electrical energy from mechanical energy sources. The present work aims to improve the piezoelectric output of PENG devices based on electrospun polyvinylidene fluoride (PVDF) doped with nickel oxide nanoparticles (NiO NPs) in different concentrations (2, 4, 6, 8 and 10 wt.-%). Crystalline phase changes and ß-crystalline content in electrospun fibers were evaluated using XRD and FTIR-ATR, respectively. Surface morphology and surface roughness of the electrospun fibers were observed using FE-SEM and AFM, respectively. The hydrophobic nature of the fibers was analyzed using a wettability test. PENG output voltage and short-circuit current performance of neat PVDF and PVDF doped with NiO (PN) composite electrospun fibers were calculated using a customized variable-pressure setup with an optimized force of 1.0 kgf and 1.0 Hz frequency. Neat PVDF-based PENG exhibited only 1.7 V and 0.7 µA, whereas, PVDF doped with 6 wt.-% NiO NP (PN-6) based PENG generated a high output voltage of 5.5 V and 1.83 µA current. The optimized PN-6 PENG device is demonstrated for use in wearable devices towards identifying certain body movements like tapping, wrist movement, walking and running.

RESUMEN

Challenges such as poor dispersion and insufficient polarization of BaTiO3 (BTO) nanoparticles (NPs) within poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)) composites have hindered their piezoelectricity, limiting their uses in pressure sensors, nanogenerators, and artificial sensory synapses. Here, we introduce a high-performance piezoelectric nanocomposite material consisting of P(VDF-TrFE)/modified-BTO (mBTO) NPs for use as a self-activating component in a piezotronic artificial mechanoreceptor. To generate high-performance piezoelectric nanocomposite materials, the surface of BTO is hydroxylated, followed by the covalent attachment of (3-aminopropyl)triethoxysilane to improve the dispersibility of mBTO NPs within the P(VDF-TrFE) matrix. We also aim to enhance the crystallization degree of P(VDF-TrFE), the efficiency characteristics of mBTO, and the poling efficiency, even when incorporating small amounts of mBTO NPs. The piezoelectric potential mechanically induced from the P(VDF-TrFE)/mBTO NPs nanocomposite was three times greater than that from P(VDF-TrFE) and twice as high as that from the P(VDF-TrFE)/BTO NPs nanocomposite. The piezoelectric potential generated by mechanical stimuli on the piezoelectric nanocomposite was utilized to activate the synaptic ionogel-gated field-effect transistor for the development of self-powered piezotronics artificial mechanoreceptors on a polyimide substrate. The device successfully emulated fast-adapting (FA) functions found in biological FA mechanoreceptors. This approach has great potential for applications to future intelligent tactile perception technology.

RESUMEN

Piezoelectric poly(vinylidene fluoride) (PVDF) and its copolymer, poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)), have attracted considerable attention due to their potential in flexible, biocompatible energy harvesting and sensing devices. However, their limited piezoelectric performance hinders their widespread application. Inspired by the concept of morphotropic phase boundary (MPB) prevalent in high-performance piezoelectric ceramics, we successfully constructed MPB in the piezoelectric polymer P(VDF-TrFE) through size-dependent interface effects. We provided direct structural evidence using atomic force microscopy-infrared spectroscopy (AFM-IR) and significantly improved the piezoelectric performance of P(VDF-TrFE). The emergence of MPB is attributed to the interface effect induced by electrostatic interactions between ZnO fillers and the -CH2, -CF2, and -CHF groups in P(VDF-TrFE). This interaction drives a concomitant competition between the all-trans ß phase (normal ferroelectric) and the 3/1 helical phase (relaxor), resulting in enhanced piezoelectric responses in the transition region. By coupling the MPB effect with a porous structure, we developed a piezoelectric nanogenerator (PENG) that surpasses the electrical output limitation of current P(VDF-TrFE)-based PENGs. The fabricated PENG exhibits superior piezoelectric outputs (6.9 µW/cm2), impressive pressure sensitivity (2.3038 V/kPa), ultrafast response time (4.3 ms), and recovery time (46.4 ms)─notably, without the need for additional poling treatment. In practical applications, the constructed PENG can efficiently generate characteristic signals in response to various human movements and harvest biomechanical energy. This work offers insight into utilizing interface-induced MPB and proposes a simple, scalable approach for developing high-performance self-polarized piezoelectric polymer films for self-powered sensing systems toward human-machine interaction.

RESUMEN

In recent years, portable and wearable personal electronic devices have rapidly developed with increasing mass production and rising energy consumption, creating an energy crisis. Using batteries and supercapacitors with limited lifespans and environmental hazards drives the need to find new, environmentally friendly, and renewable sources. One idea is to harness the energy of human motion and convert it into electrical energy using energy harvesting devices-piezoelectric nanogenerators (PENGs), triboelectric nanogenerators (TENGs) and hybrids. They are characterized by a wide variety of features, such as lightness, flexibility, low cost, richness of materials, and many more. These devices offer the opportunity to use new technologies such as IoT, AI or HMI and create smart self-powered sensors, actuators, and self-powered implantable/wearable devices. This review focuses on recent examples of PENGs, TENGs and hybrid devices for wearable and implantable self-powered systems. The basic mechanisms of operation, micro/nano-scale material selection and manufacturing processes of selected examples are discussed. Current challenges and the outlook for the future of the nanogenerators are also discussed.

RESUMEN

Piezoelectric nanogenerator (PENG) produces stable electrical signals in response to external mechanical stimuli and holds promise in the fields of flexible sensors and smart wearable devices. In practice, a high-performance PENG with a straightforward structure and exceptional reliability is deeply desired. This study optimally synthesizes piezoelectric composites comprising polyvinylidene fluoride (PVDF) incorporated with barium titanate (BTO) nanoparticles (NPs) and fabricated a PENG with heightened sensitivity by using the electrospinning technique. The polar ß-phase content of the dual-optimized BTO-PVDF (barium titanate and polyvinylidene fluoride) electrospun fiber reaches up to 82.39%. In the bending mode, it achieves a remarkable maximum open-circuit voltage of 19.152 V, a transferred charge of 8.058 nC, and an output voltage per unit area of 2.128 V cm- 2. Under vertical pressure conditions, the BP-PENG exhibits an impressive voltage of 12.361 V while the force is 2.156 N, demonstrating a notable pressure sensing sensitivity of 5.159 V kPa-1, with an excellent linear relationship. Furthermore, the BP-PENG displays sensitive sensing features in monitoring hand movements. The sensitive response and high performance make it promising for applications in human motion monitoring and smart wearable devices.

Asunto(s)

RESUMEN

The human body is a source of multiple types of energy, such as mechanical, thermal and biochemical, which can be scavenged through appropriate technological means. Mechanical vibrations originating from contraction and expansion of the radial artery represent a reliable source of displacement to be picked up and exploited by a harvester. The continuous monitoring of physiological biomarkers is an essential part of the timely and accurate diagnosis of a disease with subsequent medical treatment, and wearable biosensors are increasingly utilized for biomedical data acquisition of important biomarkers. However, they rely on batteries and their replacement introduces a discontinuity in measured signals, which could be critical for the patients and also causes discomfort. In the present work, the research into a novel 3D-printed wearable energy harvesting platform for scavenging energy from arterial pulsations via a piezoelectric material is described. An elastic thermoplastic polyurethane (TPU) film, which forms an air chamber between the skin and the piezoelectric disc electrode, was introduced to provide better adsorption to the skin, prevent damage to the piezoelectric disc and electrically isolate components in the platform from the human body. Computational fluid dynamics in the framework of COMSOL Multiphysics 6.1 software was employed to perform a series of coupled time-varying simulations of the interaction among a number of associated physical phenomena. The mathematical model of the harvester was investigated computationally, and quantification of the output energy and power parameters was used for comparisons. A prototype wearable platform enclosure was designed and manufactured using fused filament fabrication (FFF). The influence of the piezoelectric disc material and its diameter on the electrical output were studied and various geometrical parameters of the enclosure and the TPU film were optimized based on theoretical and empirical data. Physiological data, such as interdependency between the harvester skin fit and voltage output, were obtained.

RESUMEN

Piezoelectric nanogenerators (PENGs) with molybdenum disulfide (MoS2) monolayers have been intensively studied owing to their superior mechanical durability and stability. However, the limited output performance resulting from a small active area and low strain levels continues to pose a significant challenge that should be overcome. Herein, we report a novel strategy for the epoch-making output performance of a PENG with a MoS2 monolayer by adopting the additive strain concentration concept. The simulation study indicates that strain in the MoS2 monolayer can be initially augmented by the wavy structure resulting from the prestretched poly(dimethylsiloxane) (PDMS) and is further increased through flexural deformation (i.e., bending). Based on these studies, we have developed concentrated strain-applied PENGs with MoS2 monolayers. The wavy structures effectively applied strain to the MoS2 monolayer and generated a piezoelectric output voltage and current of around 580 mV and 47.5 nA, respectively. Our innovative approach to enhancing the performance of PENGs with MoS2 monolayers through the artificial dual strain concept has led to groundbreaking results, achieving the highest recorded output voltage and current for PENGs based on two-dimensional (2D) materials, which provides unique opportunities for the 2D-based energy harvesting field and structural insight into how to improve the net strain on 2D materials.

RESUMEN

Energy storage devices such as supercapacitors (SCs), if equipped with built-in energy harvesters such as piezoelectric nanogenerators, will continuously power wearable electronics and become important enablers of the future Internet of Things. As wearable gadgets become flexible, energy items that can be fabricated with greater compliance will be crucial, and designing them with sustainable and flexible strategies for future use will be important. In this review, flexible supercapacitors designed with built-in nanogenerators, mainly piezoelectric nanogenerators, are discussed in terms of their operational principles, device configuration, and material selection, with a focus on their application in flexible wearable electronics. While the structural design and materials selection are highlighted, the current shortcomings and challenges in the emerging field of nanogenerators that can be integrated into flexible supercapacitors are also discussed to make wearable devices more comfortable and sustainable. We hope this work may provide references, future directions, and new perspectives for the development of electrochemical power sources that can charge themselves by harvesting mechanical energy from the ambient environment.

RESUMEN

One of the recent innovations in the field of personalized healthcare is the piezoelectric nanogenerators (PENGs) for various clinical applications, including self-powered sensors, drug delivery, tissue regeneration etc. Such innovations are perceived to potentially address some of the unmet clinical needs, e.g., limited life-span of implantable biomedical devices (e.g., pacemaker) and replacement related complications. To this end, the generation of green energy from biomechanical sources for wearable and implantable bioelectronic devices gained considerable attention in the scientific community. In this perspective, this article provides a comprehensive state-of-the-art review on the recent developments in the processing, applications and associated concerns of piezoelectric materials (synthetic/biological) for personalized healthcare applications. In particular, this review briefly discusses the concepts of piezoelectric energy harvesting, piezoelectric materials (ceramics, polymers, nature-inspired), and the various applications of piezoelectric nanogenerators, such as, self-powered sensors, self-powered pacemakers, deep brain stimulators etc. Important distinction has been made in terms of the potential clinical applications of PENGs, either as wearable or implantable bioelectronic devices. While discussing the potential applications as implantable devices, the biocompatibility of the several hybrid devices using large animal models is summarized. This review closes with the futuristic vision of integrating data science approaches in developmental pipeline of PENGs as well as clinical translation of the next generation PENGs. STATEMENT OF SIGNIFICANCE: Piezoelectric nanogenerators (PENGs) hold great promise for transforming personalized healthcare through self-powered sensors, drug delivery systems, and tissue regeneration. The limited battery life of implantable devices like pacemakers presents a significant challenge, leading to complications from repititive surgeries. To address such a critical issue, researchers are focusing on generating green energy from biomechanical sources to power wearable and implantable bioelectronic devices. This comprehensive review critically examines the latest advancements in synthetic and nature-inspired piezoelectric materials for PENGs in personalized healthcare. Moreover, it discusses the potential of piezoelectric materials and data science approaches to enhance the efficiency and reliability of personalized healthcare devices for clinical applications.

Asunto(s)

RESUMEN

A significant driving force for the fabrication of IoT-compatible smart health gear integrated with multifunctional sensors is the growing trend in fitness and the overall wellness of the human body. In this work, we present an autonomous motion and activity-sensing device based on the efficacious nucleation of the polar ß-phase in an electroactive polymer. Representatively, we investigate the nucleating effect of TiO2 nanoparticles on weight-modulated PVDF-HFP films (PT-5, PT-10, and PT-15) and subsequently prototype a sensing device with the film that demonstrates superior ß-phase nucleation. The PT-10 film, with an optimal polar ß-phase, shows the highest remnant polarization (2Pr) and energy density of 0.36 µC/cm2 and 22.3 mJ/cm3, respectively, at 60 kV/cm. The films mimic a high pass filter at frequencies above 10 KHz with very low impedance and high ac conductivity values. The frequency-dependent impedance studies reveal an effective interfacial polarization between TiO2 nanoparticles and PVDF-HFP, explicitly observed in the low-frequency region. Consequently, the sensor fabricated with PT-10 as the sensing layer exhibits ultralow frequency detection (25 Hz) resulting from the blood flow muscle oxygenation. The device successfully senses voluntary joint movements of the human body and actively tracks a range of motions, from brisk walking to running. Additionally, through repetitive human finger-tapping motion, the nanogenerator lights up multiple light-emitting diodes in series and charges capacitors of varying magnitudes under 50 s. The real-time human motion sensing and movement tracking modalities of the sensor hold promise in the arena of smart wearables, sports biomechanics, and contact-based medical devices.

RESUMEN

In addition to the superior electrical and optoelectronic attributes, ultrathin two-dimensional transition metal dichalcogenides (TMDCs) have evoked appreciable attention for their piezoelectric properties. In this study, we report, the piezoelectric characteristics of large area, chemically exfoliated TMDCs and their heterostructures for the first time, as verified by piezoelectric force microscopy measurements. Piezoelectric output voltage response of the MoS2-WSe2heterostructure piezoelectric nanogenerator (PENG) is enhanced by ∼47.5% if compared with WSe2and ∼29% if compared to MoS2PENG, attributed to large band offset induced by heterojunction formation. This allows the scalable fabrication of self-powered energy harvesting PENGs, which can overcome the various shortcomings of complicated synthesis processes, complex fabrication steps, low yield, and poor stability. The fabricated flexible, self-powered MoS2-WSe2heterostructure nanogenerator exhibits piezoelectric output ∼46 mV under a strain of ∼0.66% yielding a power output ∼12.3 nW, which offers better performance than other two-dimensional material based piezoelectric devices and also reveals the ability of bio-mechanical energy harvesting. This cost effective approach to fabricate eco-friendly MoS2-WSe2based fatigue free, superior performance piezoelectric-nanogenerators can be utilized to evolve flexible energy harvesting devices and may also be attractive as a self-powered, smart wearable sensor devices.

RESUMEN

The main challenges impeding the widespread use of organic-inorganic lead halide perovskites in modern-day technological devices are their long-term instability and lead contamination. Among other environmentally convivial and sustainable alternatives, Cs2SnX6 (X = Cl, Br, and I) compounds have shown promise as ambient-stable, lead-free materials for energy harvesting, and optoelectronic applications. Additionally, they have demonstrated tremendous potential for the fabrication of self-powered nanogenerators in conjunction with piezoelectric polymers like polyvinylidene-fluoride (PVDF). We report on the fabrication of composites constituting solvothermally synthesized Cs2SnX6 nanostructures and PVDF. The electroactive phases in PVDF were boosted by the incorporation of Cs2SnX6, leading to enhanced piezoelectricity in the composites. First-principles density functional theory (DFT) studies were carried out to understand the interfacial interaction between the Cs2SnX6 and PVDF, which unravels the mechanism of physisorption between the perovskite and PVDF, leading to enhanced piezoresponse. The halide ions in the inorganic Cs2SnX6 perovskites were varied systematically, and the piezoelectric behaviors of the respective piezoelectric nanogenerators (PENGs) were investigated. Further, the dielectric properties of these halide perovskite-based hybrids are quantified, and their piezoresponse amplitude, piezoelectric output signals, and charging capacity are also evaluated. Out of the several films fabricated, the optimized Cs2SnI6_PVDF film shows a piezoelectric coefficient (d33) value of ∼200 pm V-1 and a remanent polarization of ∼0.74 µC cm-2 estimated from piezoresponse force microscopy and polarization hysteresis loop measurement, respectively. The optimized Cs2SnI6_PVDF-based device produced an instantaneous output voltage of ∼167 V, a current of ∼5.0 µA, and a power of ∼835 µW across a 5 MΩ resistor when subjected to periodic vertical compression. The output voltage of this device is used to charge a capacitor with a 10 µF capacitance up to 2.2 V, which is then used to power some commercial LEDs. In addition to being used as a pressure sensor, the device is employed to monitor human physiological activities. The device demonstrates excellent operational durability over a span of several months in an ambient environment vouching for its exceptional potential in application to mechanical energy harvesting and pressure sensing applications.

RESUMEN

Piezoelectric nanogenerator (PENG) for practical application is constrained by low output and difficult polarization. In this work, a kind of flexible PENG with high output and self-polarization is fabricated by constructing CsPbBr3 -Ti3 C2 Tx heterojunctions in PVDF fiber. The polarized charges rapidly migrate to the electrodes from the Ti3 C2 Tx nanosheets by forming heterojunctions, achieving the maximum utilization of polarized charges and leading to enhanced piezoelectric output macroscopically. Optimally, PVDF/4wt%CsPbBr3 /0.6wt%Ti3 C2 Tx -PENG exhibits an excellent voltage output of 160 V under self-polarization conditions, which is higher than other self-polarized PENG previously. Further, the working principle and self-polarization mechanism are uncovered by calculating the interfacial charge and electric field using first-principles calculation. In addition, PVDF/4wt%CsPbBr3 /0.6wt%Ti3 C2 Tx -PENG exhibits better water and thermal stability attributed to the protection of PVDF. It is also evaluated in practice by harvesting the energy from human palm taps and successfully lighting up 150 LEDs and an electronic watch. This work presents a new idea of design for high-performance self-polarization PENG.

Asunto(s)