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Diphenylalanine (FF) is a piezoelectric material that is widely known for its high piezoelectric constant, self-assembly characteristics, and ease of manufacture. Because of its biocompatible nature, it is useful for implantable applications. However, its use in real applications is challenging because it degrades too easily in the body due to its solubility in water (0.76 g/mL). Upon incorporation of hydrophobic and biocompatible porphyrins into the FF, the degradability of the piezoelectric FF and their piezoelectric nanogenerators (PENGs) is controlled. Porphyrin-incorporated FFs are also formed as piezoelectric nanostructures well aligned on the substrate through self-assembly, and their piezoelectric properties are comparable to those of FF. The FF-based PENG degrades in only 5 min, whereas the FF-porphyrin-based PENG produces a stable output for15 min in phosphate-buffered saline. This strategy for realizing biodegradable functional materials and devices with tunable degradation rates in the body can be applied to many implantable electronics.

Triboelectric nanogenerators have garnered significant attention as alternative power sources for wearable electronics owing to their simple structure, easy fabrication, low cost, and superior power output. In this study, a transparent, stretchable, and attachable triboelectric nanogenerator (TENG) is built with an advanced power output using plasticized polyvinyl chloride (PVC)-gel. The PVC-gel exhibit very high negative triboelectric properties and electrically insulating PVC became an electrically active material. It is found that a single layer of PVC-gel can act as a dielectric and as a conducting layer. The PVC-gel based single layer of triboelectric nanogenerator (S-TENG) creates output signals of 24.7 V and 0.83 µA, i.e., a 20-fold enhancement in the output power compared to pristine PVC-based TENGs. In addition, the S-TENG can stably generate output voltage and current under stretching condition (80%). The S-TENG can be implemented as a tactile sensor that can sense position and pressure without combining multiple elements or electrode grid patterns. This study provides new applications of power sources and tactile sensors in wearable electronics.

Triboelectrification is a phenomenon that generates electric potential upon contact. Here, we report a viral particle capable of generating triboelectric potential. M13 bacteriophage is exploited to fabricate precisely defined chemical and physical structures. By genetically engineering the charged structures, we observe that more negatively charged phages can generate higher triboelectric potentials and can diffuse the electric charges faster than less negatively charged phages can. The computational results show that the glutamate-engineered phages lower the LUMO energy level so that they can easily accept electrons from other materials upon contact. A phage-based triboelectric nanogenerator is fabricated and it could produce ∼76 V and ∼5.1 μA, enough to power 30 light-emitting diodes upon a mechanical force application. Our biotechnological approach will be useful to understand the electrical behavior of biomaterials, harvest mechanical energy, and provide a novel modality to detect desired viruses in the future.

Solid-state batteries with nonflammable inorganic solid electrolytes provide a fundamental solution for resolving safety concerns. Li7La3Zr2O12 (LLZO) has been considered as a promising candidate for solid electrolytes, due to its high Li+ conductivity and chemical/electrochemical compatibility with Li metal. However, LLZO electrolytes are known to react with H2O and CO2 to form lithium carbonates (Li2CO3) on the surface when exposed to the ambient air, resulting in the significant degradation in Li+-conduction properties. Herein, we propose an effective approach for improving the air-stability of LLZO via hydrophobic polymer encapsulation. For encapsulation of LLZO powders, polyurethane-based polymers are designed and synthesized to have high hydrophobicity and ionic conductivity by engineering soft segment and hydrophobic chain extender. Bare LLZO and polymer-encapsulated LLZO (P-LLZO) powders are subjected to accelerated durability tests (ADTs) in which the concentrations of O2, H2O, and CO2 are precisely controlled to promote the interfacial reactions. Surface characterization studies reveal that the polymer encapsulation of LLZO effectively mitigates the interfacial degradation (Li2CO3 formation) by preventing the direct contact between LLZO and H2O/CO2. Furthermore, a biphasic solid electrolyte (BSE) fabricated using ADT-tested P-LLZO powders exhibits higher ionic conductivity as compared with that of BSE with ADT-tested LLZO, proving the efficacy of the polymer encapsulation. The findings of this study would be essential in understanding the role of interfacial engineering in mitigating the degradation of Li+-conduction properties and developing highly conductive and stable LLZO solid electrolytes.

As the internet of things (IoT) era approaches, various sensors, and wireless electronic devices such as smartphones, smart watches, and earphones are emerging. As the types and functions of electronics are diversified, the energy consumption of electronics increases, which causes battery charging and maintenance issues. The piezoelectric nanogenerator (PENG) received great attention as an alternative to solving the energy issues of future small electronics. In particular, polyvinylidene fluoride (PVDF) piezoelectric polymer-based PENGs are strong potential candidate with robust mechanical properties and a high piezoelectric coefficient. In this review, we summarize the recent significant advances of the development of PVDF-based PENGs for self-powered energy-harvesting systems. We discuss the piezoelectric properties of the various structures of PVDF-based PENGs such as thin film, microstructure, nanostructure, and nanocomposite.

M13 bacteriophage (phage) nano- and microfibers were fabricated using electrospinning. Using liquid crystalline suspension of the phage, we successfully fabricated nano- and microscale pure phage fibers. Through a near field electrospinning process, we fabricated the desired phage fiber pattern with tunable direction and spacing. In addition, we demonstrated that the resulting phage fibers could be utilized as an electrostatic-stimulus responsive actuator. The near field electrospinning would be a very useful tool to design phage-based chemical sensors, tissue regenerative materials, energy generators, metallic and semiconductor nanowires in the future.

Despite their high power density, aqueous-based electric double-layer capacitors (EDLCs) possess relatively low energy density due to the limitation of potential window (~1.0 V) and low specific capacitance of active materials. To increase the energy density without sacrificing the power density, it is highly desired to achieve a simultaneous improvement of both specific capacitance and potential window of EDLCs. However, this remains a major challenge that is not been solved up to date. This work demonstrates that by inserting a polarized-polyvinylidene fluoride (PVDF) ferroelectric layer underneath the graphene, a simultaneous enhancement of both areal capacitance and potential window is achieved, in which the areal capacitance increases from 5.5 to 7.5 μF/cm2 (i.e., 36%) (or 55 F/cm3 to 75 F/cm3 in terms of volumetric capacitance), and the potential window expands from 1.0 V to 1.5 V. This results in a threefold increase in the areal energy density of the capacitor. The enhancement in capacitance can be explained by the Gouy–Chapman–Stern model. The widening of potential window is due to the shift of the Fermi level of graphene caused by the doping effect of the polarized-PVDF layer.

Biomolecular piezoelectric materials are considered a strong candidate material for biomedical applications due to their robust piezoelectricity, biocompatibility, and low dielectric property. The electric field has been found to affect tissue development and regeneration, and the piezoelectric properties of biological materials in the human body are known to provide electric fields by pressure. Therefore, great attention has been paid to the understanding of piezoelectricity in biological tissues and its building blocks. The aim herein is to describe the principle of piezoelectricity in biological materials from the very basic building blocks (i.e., amino acids, peptides, proteins, etc.) to highly organized tissues (i.e., bones, skin, etc.). Research progress on the piezoelectricity within various biological materials is summarized, including amino acids, peptides, proteins, and tissues. The mechanisms and origin of piezoelectricity within various biological materials are also covered.

With the development of technology, electronic devices are becoming more miniaturized and multifunctional. With the development of small electronic devices, they are changing from the conventional accessory type, which is portable, to the patchable type, which can be attached to a person's apparel or body, and the eatable/implantable type, which can be directly implanted into the human body. In this regard, it is necessary to address various technical issues, such as high-capacity/high-efficiency small-sized battery technology, component miniaturization, low power technology, flexible technology, and smart sensing technology. In addition, there is a demand for self-powered wireless systems in particular devices. A piezoelectric/triboelectric nanogenerator (PENG/TENG) can generate electric energy from small amounts of mechanical energy such as from blood flow and heartbeats in the human body as well as human movement, so it is expected that it will enable the development of self-powered wireless systems. Due to their unique properties, such as flexibility, transparency, mechanical stability, and nontoxicity, 2D materials are optimal materials for the development of implantable and patchable self-powered nanodevices in the human body. In this Review, the studies related to patchable and implantable devices for the human body using PENGs/TENGs based on 2D materials are discussed.

Controlling the shape, geometry, density, and orientation of nanomaterials is critical to fabricate functional devices. However, there is limited control over the morphological and directional characteristics of presynthesized nanomaterials, which makes them unsuitable for developing devices for practical applications. Here, we address this challenge by demonstrating vertically aligned and polarized piezoelectric nanostructures from presynthesized biological piezoelectric nanofibers, M13 phage, with control over the orientation, polarization direction, microstructure morphology, and density using genetic engineering and template-assisted self-assembly process. The resulting vertically ordered structures exhibit strong unidirectional polarization with three times higher piezoelectric constant values than that of in-plane aligned structures, supported by second harmonic generation and piezoelectric force microscopy measurements. The resulting vertically self-assembled phage-based piezoelectric energy harvester (PEH) produces up to 2.8 V of potential, 120 nA of current, and 236 nW of power upon 17 N of force. In addition, five phage-based PEH integrated devices produce an output voltage of 12 V and an output current of 300 nA, simply by pressing with a finger. The resulting device can operate light-emitting diode backlights on a liquid crystal display. Our approach will be useful for assembling many other presynthesized nanomaterials into high-performance devices for various applications.

Next-generation memory and energy harvesting devices require a higher output performance for charging lectric devices. Generally, it is very limited to control charge transfer through triboelectricity in triboelectric materials. Here, using ferroelectric polarization, it is found that both the amount and direction of charge transfer in triboelectric materials can be controlled. The ferroelectric-dependent triboelectricity in a ferroelectric co-polymer film is explored using atomic force microscopy (AFM). Ferroelectric surfaces are rubbed with the AFM tip after poling with positive and negative bias voltages to achieve a triboelectric effect. The surface potential of the positively (negatively) poled area becomes smaller (larger) after rubbing the film surface with the AFM tip. Furthermore, the power output from the triboelectric nanogenerator is dependent on the ferroelectric polarization state. The results indicate that the amount and direction of the charge transfer in triboelectricity can be controlled by the ferroelectric polarization state.

Piezoelectric materials are excellent generators of clean energy, as they can harvest the ubiquitous vibrational and mechanical forces. We developed large-scale unidirectionally polarized, aligned diphenylalanine (FF) nanotubes and fabricated peptide-based piezoelectric energy harvesters. We first used the meniscus-driven self-assembly process to fabricate horizontally aligned FF nanotubes. The FF nanotubes exhibit piezoelectric properties as well as unidirectional polarization. In addition, the asymmetric shapes of the self-assembled FF nanotubes enable them to effectively translate external axial forces into shear deformation to generate electrical energy. The fabricated peptide-based piezoelectric energy harvesters can generate voltage, current, and power of up to 2.8 V, 37.4 nA, and 8.2 nW, respectively, with 42 N of force, and can power multiple liquid-crystal display panels. These peptide-based energy-harvesting materials will provide a compatible energy source for biomedical applications in the future.

Currently, integration of energy harvesting and storage devices is considered to be one of the most important energy-related technologies due to the possibility of replacing batteries or at least extending the lifetime of a battery. This review aims to describe current progress in the various types of energy harvesters, hybrid energy harvesters, including multi-type energy harvesters with coupling of multiple energy sources, and hybridization of energy harvesters and energy storage devices for self-powered electronics. We summarize research on recent energy harvesters based on the piezoelectric, triboelectric, pyroelectric, thermoelectric, and photovoltaic effects. We also cover hybrid cell technologies to simultaneously generate electricity using multiple types of environmental energy, such as mechanical, thermal, and solar energy. Energy harvesters based on the coupling of multiple energy sources exhibit enhancement of power generation performance with synergetic effects. Finally, integration of energy harvesters and energy storage devices is introduced. In particular, self-charging power cells provide an innovative approach to the direct conversion of mechanical energy into electrochemical energy to decrease energy conversion loss.

Transparent and flexible (TF) microheaters are required in wearable devices, labs-on-chip, and micro-reactors. Nevertheless, conventional microheaters are rigid or opaque or both. Moreover, the resistances of conventional metallic microheaters are too low to be effectively powered by wearable energy harvesters. Here, we demonstrate the first TF microheaters by taking advantage of chemical vapor deposition (CVD)-grown graphene heating tracks and of a hexagonal boron nitride (h-BN) sheet for passivation; the h-BN sheet increases the maximum temperature by ~80%. Our TF microheaters show excellent temperature uniformity and can reach temperatures above 200 °C in just 4 s, with power consumption as low as 39 mW. Additionally, since the CVD-graphene sheet resistance is orders of magnitude higher than that of typical metallic heaters, our devices can be effectively powered by wearable energy harvesters. As a proof-of-concept, we demonstrate the first self-powered, wearable microheater which achieves a temperature increase of 8 °C when operated by a sound driven textile-based triboelectric nanogenerator. This is a key milestone towards next generation microheaters with applications in portable/wearable personal electronics, wireless health, and remote and mobile environmental sensors.

Here micropatterned poly(vinylidenefluoride-co-trifluoroethylene) (P(VDF-TrFE)) films-based piezoelectric nanogenerators (PNGs) with high power-generating performance for highly sensitive self-powered pressure sensors are demonstrated. The microstructured P(VDF-TrFE)-based PNGs reveal nearly five times larger power output compared to a flat film-based PNG. The micropatterning of P(VDF-TrFE) polymer makes itself ultrasensitive in response to mechanical deformation. The application is demonstrated successfully as self-powered pressure sensors in which mechanical energy comes from water droplet and wind. The mechanism of the high performance is intensively discussed and illustrated in terms of strain developed in the flat and micropatterned P(VDF-TrFE) films. The impact derived from the patterning on the output performance is studied in term of effective pressure using COMSOL multiphysics software.

The search for harvesting both the mechanical and solar energies from a single hybrid system is of significant value and represents a new trend in energy harvesting technologies. This single hybrid system can utilize both the energy sources easily available from nature and most importantly it is clean and sustainable. It is a novel technique involving completely different physical principles utilized for scavenging different types of energies. This report presents studies of a hybrid power generator made a direct-current piezoelectric nanogenerator based on ZnO nanosheets and a bulk heterojunction organic solar cell based on an inverted structure. The device shows much larger electric power output compared to its two individual power output components, which facilitates more effective multi-type energies harvesting and clarifies a mechanism for realizing multi-functional energy devices.

In this work, a sulfur (S) vacancy passivated monolayer MoS

Piezoelectric semiconductor materials have emerged as the most attractive material for nanogenerator (NG)-based prototype applications, such as piezotronics, piezophotonics and energy harvesting, due to the coupling of piezoelectric and semiconducting dual properties. Understanding the mechanisms for high power generation, charge transport behavior, energy band modulations, and role of depletion width in piezoelectric semiconducting p–n junction, through piezoelectric charges developed by external mechanical strains, are essential for various NGs. Here, we demonstrate enhancement of the output power of one-dimensional zinc oxide (ZnO) nanowires (NWs)-based NG using a p-type semiconductor polymer, by controlling their energy band at depletion width in the piezoelectric semiconducting p–n junction interface and native defects presented in as-grown ZnO NWs. The piezoelectric output performance from the P3HT-coated ZnO NWs-based NG was several times higher than that from the pristine ZnO NWs-based NG, under application of the same vertical compressive strain. Holes from the p-type P3HT polymer significantly reduced the piezoelectric potential screening effect caused by free electrons in ZnO. Theoretical investigations using COMSOL multiphysics software were also carried out, in order to understand the improvement in the performance of surface passivated ZnO NWs-based NG, in terms of free carriers concentration and holes diffusion, due to the formation of p–n junction at the interface of ZnO and P3HT, and depletion width change.

Piezoelectric materials are excellent generators of clean renewable energy because they can convert ubiquitous vibration and mechanical power into electrical energy. Although traditional piezoelectric materials such as lead zirconate titanate (PZT), lithium niobate, gallium nitride, and barium titanate are practical for energy generation, their fabrication frequently requires environmentally harmful components and/or energy processes. Recent studies on environmental friend biomolecular piezoelectric materials such as amino acids, peptides, proteins, and viruses have great attention because they are applicable to bioelectronics and biomedical applications. Compared with inorganic and synthetic counterparts, however, biomolecular piezoelectric materials have not been extensively studied for general piezoelectric applications because the piezoelectric response of the major piezoelectric components (d33, d31, d11) are weak. Furthermore, the difficulty of fabricating unidirectionally polarized biomolecular piezoelectric structures that can efficiently convert mechanical energy into electrical energy has been a major obstacle to the realization of robust piezoelectric energy generators. In this talk, I will introduce recent research on strategies and methods for synthesizing and controlling large-scale aligned various biomolecule piezoelectric materials. The orientation and polarization directions of these materials were controlled using biomimetic self-assembly process which is low cost and environmentally friend process. Furthermore, the energy generators based on the biomolecular piezoelectric materials were demonstrated.

Here, we report the synthesis of lead-free single-crystalline two-dimensional (2D) vanadium(V)-doped ZnO nanosheets (NSs) and their application for high-performance flexible direct current (DC) power piezoelectric nanogenerators (NGs). The vertically aligned ZnO nanorods (NRs) converted to NS networks by V doping. Piezoresponse force microscopy studies reveal that vertical V-doped ZnO NS exhibit typical ferroelectricity with clear phase loops, butterfly, and well-defined hysteresis loops with a piezoelectric charge coefficient of up to 4 pm/V, even in 2D nanostructures. From pristine ZnO NR-based NGs, alternating current (AC)-type output current was observed, while from V-doped ZnO NS-based NGs, a DC-type output current density of up to 1.0 μAcm(-2) was surprisingly obtained under the same vertical compressive force. The growth mechanism, ferroelectric behavior, charge inverted phenomena, and high piezoelectric output performance observed from the V-doped ZnO NS are discussed in terms of the formation of an ionic layer of [V(OH)4(-)], permanent electric dipole, and the doping-induced resistive behavior of ZnO NS.

Here we report a new type of stretchable transparent piezoelectric nanogenerator (NG) using an organic piezoelectric material consisting of poly(vinylidene fluoride trifluoroethylene) [P(VDF-TrFE)] sandwiched with mobility-modified chemical vapor deposition-grown graphene electrodes by ferroelectric polarization into P(VDF-TrFE). This new type of NG has a very high sensitivity and mechanical durability with fully flexible, rollable, stretchable, foldable, and twistable properties. We also investigated the mobility-modified graphene electrodes with ferroelectric P(VDF-TrFE) remnant polarization, and a mechanism is proposed for switching the mobility of the carriers by the ferroelectric remnant polarization. Upon exposure to the same input sound pressure, the measured output performance of the stretchable NG with a thin polydimethylsiloxane stretchable rubber template is up to 30 times that of a normal NG with a plastic substrate. Upon exposure to an air flow at the same speed, the measured output voltage from the stretchable NG is about 8 times larger than that of the normal NG.

Recently, piezoelectricity has been observed in 2D atomically thin materials, such as hexagonal-boron nitride, graphene, and transition metal dichalcogenides (TMDs). Specifically, exfoliated monolayer MoS

We report the synthesis of KNbO(3) nanowires (NWs) with a monoclinic phase, a phase not observed in bulk KNbO(3) materials. The monoclinic NWs can be synthesized via a hydrothermal method using metallic Nb as a precursor. The NWs are metastable, and thermal treatment at ∼450 °C changed the monoclinic phase into the orthorhombic phase, which is the most stable phase of KNbO(3) at room temperature. Furthermore, we fabricated energy-harvesting nanogenerators by vertically aligning the NWs on SrTiO(3) substrates. The monoclinic NWs showed significantly better energy conversion characteristics than orthorhombic NWs. Moreover, the frequency-doubling efficiency of the monoclinic NWs was ∼3 times higher than that of orthorhombic NWs. This work may contribute to the synthesis of materials with new crystalline structures and hence improve the properties of the materials for various applications.