Flexible Films Research Articles

Passive bionic motion of a flexible film in the wake of a circular cylinder: chaos and periodicity, flow–structure interactions and energy evolution

The self-sustained interactions between a flexible film and periodic vortices epitomize the spirit of fish swimming and flag flapping in nature, involving intricate patterns of flow–structure coupling. Here, we comprehensively investigate the multiple coupling states of a film in the cylinder wake mainly with experiments, complemented by theoretical solutions and nonlinear dynamical analyses. Four regimes of film motion states are identified in the parameter space spanned by the reduced velocity and the length ratio. These regimes are (i) keeping stationary, (ii) deflection flutter, (iii) hybrid flutter and (iv) periodic large-amplitude flapping, each governed by a distinct coupling mechanism, involving regular and irregular Kármán vortices, local instability of the elongated shear layers and 2P mode vortex shedding. The film futtering in regimes (ii) and (iii) is substantiated to be chaotic and bears a resemblance to the ‘entraining state’ of fish behind an obstacle in the river. The periodic flapping in regime (iv) manifests itself in an amalgam of standing and travelling waves, and has intrinsic relations to the ‘Kármán gaiting’ of fish in periodic vortices. With the spatiotemporal reconstruction for the periodic flapping, we procure the energy distributions on the film, revealing the energy transfer processes between the film and the large-scale vortices. The findings unequivocally indicate that the flow–structure interaction during the energy-release stage of the film is more intense than that during the energy-extraction stage. Given the similarities, the mathematical and physical methods presented in this work are also applicable to the research on biological undulatory locomotion.

Largely Enhanced Thermoelectric Performance of Flexible Ag2Se Film by Cationic Doping and Dual-Phase Engineering.

Recent studies have shown that silver selenide is a promising thermoelectric material at room temperature. Herein, flexible films with a nominal composition of (Ag1-xCux)2Se are prepared by a simple and efficient one-pot method combined with vacuum-assisted filtration and hot pressing. The thermoelectric properties of the films are regulated by both cationic doping and a dual-phase strategy via a wet chemical method. As the x increases, not only Cu is doped into the Ag2Se, but different new phases (CuAgSe and/or CuSe2) also appear. The (Ag1-xCux)2Se film with x = 0.02 composed of Cu-doped Ag2Se and CuAgSe shows a high PF of ∼2540 μW m-1 K-2 (ZT ∼ 0.90) and outstanding flexibility at room temperature. The high thermoelectric properties of the film are due to the effect of Cu doping and the CuAgSe phase, including the increase in electrical conductivity caused by doping, the enhanced phonon scattering at the Ag2Se/CuAgSe interface, and the interaction between the energy filtering effect and the doping effect. In addition to the high output performance (PDmax = 28.08 W m-2, ΔT = 32.2 K), the flexible device assembled with the (Ag0.98Cu0.02)2Se film also has potential applications as a temperature sensor.

Multifunctional composite flexible films of hydroxypropyl cellulose and silver nanowires

Flexible wearable devices have aroused attentions since the booming flexible electronic technologies, as well as the requirements for improved comfortableness and real-time monitoring for complex motion state of human body. Developing a flexible integrated wearable device with multi functions provides a promising route for next-generation wearable devices. Meanwhile, transparency and biocompatibility are also considered a lot. Herein, hydroxypropyl cellulose/silver nanowires (HPC/AgNWs) flexible composite films were fabricated with a facile two-step method. The fabricated composite films exhibited sufficient transparency and mechanical strength. More importantly, the HPC/AgNWs composite films afforded good motion sensing performances with current sensitivity as high as 350 %. It can accurately identify different bending angles and frequencies, and remained stable for more than 1000 bending cycles. Apart from being employed as motion sensors, the fabricated HPC/AgNWs could be also used for electrical heating and electromagnetic shielding. The films could be heated to more than 60°C at 3.0 V in 57 seconds, and the electromagnetic shielding efficiency reached more than 99.9 %. This study contributed a feasible strategy for the preparation of multifunctional flexible films which are expected to be further applicated in the field of wearable devices.

High-Performance W-Doped Bi0.5Sb1.5Te3 Flexible Thermoelectric Films and Generators.

Bi-Sb-Te-based thermoelectric materials have the best room-temperature thermoelectric properties, but their inherent brittleness and rigidity limit their application in the wearable field. In this study, W-doped p-type Bi0.5Sb1.5Te3 (W-BST) thin films were prepared using magnetron sputtering on polyimide substrates to create thermoelectric generators (TEGs). Bending tests showed that the thin film has excellent flexibility and mechanical durability, meeting the flexible requirements of wearable devices. W doping can significantly increase the carrier concentration, Seebeck coefficient, and electrical conductivity of BST thin films. At 300 K, the power factor of the W-BST film is 2.25 times higher than that of the undoped film, reaching 13.75 μW cm-1 K-2. First-principles calculations showed that W doping introduces significant impurity peaks in the bandgap, in which W d electrons remarkably hybridize with the Sb and Te p electrons, leading to an improved electrical conductivity of BST films. Furthermore, W doping significantly reduces the work function of BST films, thereby improving the carrier mobility. A TEG module fabricated from four layers of W-BST thin films achieved a maximum output power density of 6.91 mW cm-2 at a temperature difference of 60 K. Application tests showed that the flexible TEG module could power a portable clock using the temperature difference between body temperature and room temperature. At a medium temperature of 439 K, the assembled TEG module can provide a stable output voltage of 1.51 V to power a LED. This study demonstrates the feasibility of combining inorganic thermoelectric materials with flexible substrates to create high-performance flexible TEGs.

Largely enhanced Piezoelectric-Fenton capability in rationally designed PVDF/Fe2O3 flexible porous film

The burgeoning piezocatalysts have attracted huge attentions due to their ability to convert natural mechanical energy to degrade water pollutants. However, traditional powder-based piezocatalysts still face an inevitable bottleneck of the secondary pollution because of the diffusion of nanoparticles during the piezocatalysis process. In this work, novel porous polymer-based composite films combining Fenton fillers (α-Fe2O3) and ferroelectric polymer (polyvinylidene fluoride, PVDF) are prepared by rationally designed solution-casted method with a sacrificial “hard template” of table salt. The as-prepared porous PVDF/Fe2O3 film exhibits superior decomposition efficiency of organic pollutants under ultrasonication. Particularly, the easily recyclable porous film with optimized composition and spatial structure offers an ultrahigh rate constant of 0.0498 min−1, which means it can degrade 94.8% rhodamine B (RhB) in 60 min, exceeding that of most reported polymer-based piezocatalysts. Additionally, it has a comprehensive decomposition effect on dyes, antibiotics and natural water with a good cycle performance. The outstanding degradation performance is attributed to the massive hydroxyl radical generated from the enhanced Piezoelectric-Fenton effect, which is ascribed to the synergistic effect of improved piezoelectricity in PVDF, enhanced hydrophilicity and optimized spatial structures in the porous composite films.

Femtosecond Laser-induced Nanoparticle Implantation into Flexible Substrate for Sensitive and Reusable Microfluidics SERS Detection

Abstract Surface-enhanced Raman spectroscopy (SERS) microfluidic system, which enables rapid detection of chemical and biological analytes, offers an effective platform to monitor various food contaminants and disease diagnoses. The efficacy of SERS microfluidic systems is greatly dependent on the sensitivity and reusability of SERS detection substrates to ensure repeated use for prolonged periods. This study proposed a novel process of femtosecond laser nanoparticle array (NPA) implantation to achieve homogeneous forward transfer of gold NPA on a flexible polymer film and accurately integrated it within microfluidic chips for SERS detection. The implanted Au-NPA strips show a remarkable electromagnetic field enhancement with the factor of 9×108 during SERS detection of malachite green (MG) solution, achieving a detection limit lower than 10 ppt, far better than most laser-prepared SERS substrates. Furthermore, Au-NPA strips show excellent reusability after several physical and chemical cleaning, because of the robust embedment of laser-implanted NPA in flexible substrates. To demonstrate the performance of Au-NPA, a SERS microfluidic system is built to monitor the online oxidation reaction between MG/NaClO reactants, which helps infer the reaction path. The proposed method of nanoparticle implantation is more effective than the direct laser structuring technique. It provides better performance for SERS detection, robustness of detection, and substrate flexibility and has a wider range of applications for microfluidic systems without any negative impact.

A Tunable Hydrophilic-Hydrophobic, Stimulus Responsive, and Robust Iridescent Structural Color Bionic Film with Chiral Photonic Crystal Nanointerface.

Bio-inspired in nature, using nanomaterials to fabricate the vivid bionic structural color and intelligent stimulus responsive interface as smart skin or optical devices are widely concerned and remain a huge challenge. Here, the bionic flexible film is designed and fabricated with chiral nanointerface and tunable hydrophilic-hydrophobic by the ultrasonic energy perturbation strategy and crosslinking of the cellulose nanocrystals (CNC). An intelligent nanointerface with adjustable hydrophilic and hydrophobic properties is constructed by the supramolecular assembly using a smart ionic liquid molecule. The bionic flexible film possessed the variable hydrophilic-hydrophobic, stimulus responsive, and robust iridescent structural color. The reflective wavelength and the helical pitch of the film can be easily modulated through the ultrasonic energy perturbation strategy. The bionic flexible film by covalent cross-linking has excellent robustness, good elasticity and flexibility. The tunable brilliant structural color of the chiral nanointerface is attributed to the surface charge change of the CNC photonic crystal, which is disturbed by ultrasonic energy perturbation. The bionic flexible film with tunable structure color has intelligent hydrophilic and hydrophobic stimulus response properties. The chiral bionic materials have potential applications in smart skin, optical devices, bionic materials, robots, anti-counterfeiting, colorful displays, and stealth materials.

Physicochemical and thermal characterization of the edible shellac films incorporated with oleic acid to enhance flexibility, water barrier and retard aging

In this work, shellac plasticized with oleic acid was solvent cast to prepare the flexible and water-resistant film for packaging applications. The films were prepared with varying amounts of oleic acid and studied in detail for appearance, surface morphology, thermal, chemical, barrier, mechanical, and robustness. The surface morphology confirmed the smooth surface of films up to SH-OA20 (100:20 w/w; shellac: oleic acid). Fourier-transform infrared spectroscopy confirmed that oleic acid reduced the hydrogen bonding of the shellac matrix to provide a plasticization effect. Also, the thermal analysis showed a reduction in the melting enthalpy. Moreover, the plasticized films had a better barrier to water vapor due to increased smoothness and reduction in brittleness. Adding oleic acid also increased the elongation at break up to 40 % without any changes in tensile strength. The flexibility of the films increased with the oleic acid content, making them resistant to burst, crumbling, bending, rolling, and stretching. Oleic acid also showed the retardation of aging and thermal aging of shellac. In the future, the long-term stability and migration of the films can be investigated.

Multifunctional wearable Spider-Silk Inspired fabric for personal protection in extreme environments

Personal protective equipment (PPE) plays a vital role in healthcare, industry, and military settings, offering essential protection against various environmental hazards. However, the growing environmental challenges and demand for multifunctional integration make developing PPE that outperforms traditional single-function equipment a significant challenge. Herein, we present a flexible and wearable sandwich-structured film, fabricated by integrating an MXene core layer with Gd(OH)3/TPU outer layers through electrospinning and vacuum filtration process, simultaneously offering neutron and electromagnetic interference (EMI) shielding, energy harvesting, and thermal management. Mimicking spider silk's crystalline and amorphous regions, the outer layers integrate Gd(OH)3 nanorods into TPU nanofibers, thereby enhancing hydrogen bonding and achieving a high tensile strength of 22.94 MPa. Extensive hydrogen-bonding interactions firmly bind the MXene conductive core layer to the gadolinium-rich magnetic outer layers, providing excellent neutron (μ = 22.95 cm−1) and EMI shielding (SE = 35.1 dB). Additionally, the film also functions as a triboelectric nanogenerator (TENG), capturing kinetic energy to power low-voltage electronic devices, reducing reliance on external power in harsh settings. Remarkably, its superior Joule heating capability rapidly reaches various temperature (up to 78.5 ℃) by regulating external voltage to meet diverse user requirements. This study paves the way for future advancements in the realm of multifunctional PPE.

Tailoring the Holocellulose Fiber/Acrylic Resin Composite Interface with Hydrophobic Carboxymethyl Cellulose to Enhance Optical and Mechanical Properties.

Interface engineering is essential for cellulosic fiber-reinforced polymer composites to achieve high strength and toughness. In this study, carboxymethyl cellulose (CMC) functionalized with hydrophobic quaternary ammonium ions (QAs) were utilized to modify the interface between holocellulose fibers (HF) and acrylic resin. The wet HF/CMC papers were prepared by vacuum filtration, akin to papermaking, followed by cationic ion exchange with different hydrophobic QAs. Subsequently, the modified papers were dried, impregnated with an acrylic resin monomer, and cured to produce transparent composite films. The effect of the hydrophobic QA moieties on the structure and optical and mechanical properties of the HF/CMC/acrylic resin composites were investigated. The composite film with cetyltrimethylammonium (CTA)-functionalized CMC showed high optical transmittance (87%) with low haze (43%), while the composite film with phenyltrimethylammonium (PTMA)-functionalized CMC demonstrated high Young's modulus of 7.6 GPa and high tensile strength of 180 MPa. These properties are higher than those of the composites prepared through covalent interfacial modification strategies. The results highlighted the crucial role of hydrophobic functionalized CMCs in facilitating homogeneous resin impregnation in the HF fiber network, producing a composite with enhanced interfacial adhesion strength, increased optical transparency, and mechanical strength. This facile use of hydrophobic CMCs as interfacial compatibilizers provides an energy-efficient route for preparing transparent, thin, and flexible composite films favorable in optoelectronic applications.

Domain wall current, ferroelectric, and piezoelectric properties of flexible SrBi2Ta2O9 thin films affected by the distribution of a-oriented domains and c-oriented domains

We investigated the ferroelectric, piezoelectric, and domain wall current properties affected by the distribution of a-oriented domains and c-oriented domains in flexible SrBi2Ta2O9 (SBT) thin films on flexible Pt/mica substrates. On the flexible Pt/mica substrates, the SBT thin films with a mixed crystallinity of a-oriented and c-oriented crystallinities exhibited the domain structures mixed with a-oriented domains and c-oriented domains. The SBT thin films with excellent a-oriented crystallinity showed improved ferroelectric and piezoelectric properties due to the polar axis perpendicular to the c-axis. In particular, 90o domain walls composed of a-domain and c-domain have larger domain wall currents than 180o domain walls composed of c-domains, which increases the leakage current of the SBT thin films.

Enhancing the piezoelectric coefficient of SrTiO3 nanocubes and PVDF film deposited by supersonic spraying for energy-harvesting nanogenerators

Many perovskites and their piezoelectric composites have been investigated for harvesting ambient mechanical energy over the past two decades; however, the prospects for their commercialization appear remote because of several practical challenges. Therefore, highly scalable supersonic cold-spraying technology was used to fabricate flexible piezoelectric films of poly(vinylidene fluoride) (PVDF) and a novel perovskite SrTiO3 (ST). Substantial shear stress was exerted on PVDF during cold spraying owing to the hydrothermally synthesized SrTiO3 nanocubes and supersonic velocity, and the resulting film delivered an effective piezoelectric coefficient (69.6 pm·V−1) as confirmed by piezo-response force microscopy. As a result, the piezoelectric nanogenerator yields a maximum power of 130 µW at a load resistance of 0.9 MΩ. The composite film exhibited durability for 21,000 tapping cycles with 20 N applied force and 7 Hz frequency. The flexibility endurance was confirmed from 3000 bending cycles. PENG attached to knee delivered 1 and 2.3 V on bending to 45 and 90°, respectively. After electrical poling, the PENG was subjected to a 20 N tapping force that yielded a piezopotential of 31 V. To the best of our knowledge, this is the first time piezoelectricity was obtained using an ST/PVDF composite via mechanical energy harvesting. The flexible PENG film deposited by cold-spraying shows good potential for wearable self-powered devices.

Design of CuS composite carbon-based Ni Al-LDH multifunctional phase change composite with electromagnetic shielding performance and heat storage capacity

CuS-based composites are widely used in the fields related to photothermal energy storage and electromagnetic shielding and are excellent candidates for composites with phase change materials. To meet the requirements of micro-integration and electromagnetic resistance of electronic products and optimize the thermal management of electronic products, it is necessary to prepare new flexible composite phase change materials. In this paper, through the design of MPC@Ni Al-LDH/CuS double-layer structure, two-step vacuum filtration method is used, and the highly conductive materials CuS and MPC are introduced into the manufacture of PCM films. With the help of Ni Al-LDH, flame retardancy is introduced. The electromagnetic wave absorption performance is enhanced, and the existence of nano-cellulose (CNF) makes the film have excellent mechanical properties. Ni Al-LDH/MPC and CuS substrates with stable and high mechanical properties are prepared by ultrasonic treatment. According to scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), differential scanning calorimetry (DSC) and thermogravimetry (TG) characterizations, PEG successfully entered the MPC/CuS skeleton by vacuum filtration, and flexible phase change composite bilayers (MLPC) were obtained. Due to the synergistic effect of structure and components, the obtained composite film has many different excellent functions. Specifically, when MPC@Ni Al-LDH is 15 wt%, the phase transition enthalpy, thermal conductivity, electromagnetic shielding, and electrical conductivity are 146.8 J/g, 1.07 W/m·K, 38.8 dB and 126.4 S/m, respectively. The 3600 s infrared temperature measurement results show that the sample has stable thermal properties. Due to the presence of CuS, when MPC@Ni Al-LDH is 5 wt%, its absorbance can be kept at 1.51 L/(g·cm), and its photothermal conversion efficiency can reach 90.6 %. The MPC/CuS structure in the composite film provides many heat transfer channels, which reduces the phonon scattering in the heat transfer process and significantly increases thermal conductivity. Therefore, this multifunctional flexible phase change film can be used in photothermal conversion devices and for thermal management of electronic equipment, and it has broad application prospects in wearable equipment design due to its excellent electromagnetic shielding ability and infrared thermal stealth ability.

Synthesis of novel Stachytarpheta jamaicensis flower liked hexagonal boron nitride nanoribbons (SJF-BNNBs) to efficiently improve the thermal/mechanical/electrical properties of flexible polyimide films

Heat dissipation has become a bottleneck restricting large-scale integration and flexible electronic technologies. This study reports a novel fabrication strategy to prepare flexible stachytarpheta jamaicensis flower-like hexagonal boron nitride nanoribbons (SJF-BNNBs) and their composite films with polyimide (PI). The effect of synthesis conditions on the morphology of SJF-BNNBs was investigated, and the growth mechanism was proposed. The in-plane and through plane thermal conductivities of the 4 wt% SJF-BNNBs/PI composite film reach 5.98 W m−1 K−1 and 0.79 W m−1 K−1, which are 3047 % and 316 % higher than those of the pure PI film, respectively. The in-plane and through plane thermal conduction enhancement efficiencies reach 761.8 % and 78.9 %, respectively. The tensile strength of the composite film is 61.7 % higher than that of pure PI, and maintains excellent electrical insulating and thermal stability properties. Infrared imaging tests verified the excellent heat dissipation performance of the composite film as a thermal interface material and a flexible copper clad laminate substrate, where the operating temperature of device could be reduced by 17.3 °C. To the best of our knowledge, SJF-BNNBs outperform the most efficient thermally conductive electrically insulating filler and are to break the overcome of polymer composites in heat dissipation applications.

Towards the fabrication of flexible thin film CdTe solar cells: The significance of substrate surfaces

Thin film CdTe solar cells have been recognized as reliable alternative for the manufacture of cheap photovoltaic solar cells of the future, due to its excellent absorber characteristics and simple, low-cost manufacturability. However, for the attainment of higher cell performances, additional studies are needed to increase cell efficiency through further development of better quality films and new fabrication processes. In the substrate-structured CdTe thin film solar cells, the CdTe absorber layer is deposited directly onto the substrate or through a back contact layer. But the quality of deposited film is believed to depend on the type and smoothness of the substrate. In this work CdTe was deposited on different substrates by RF sputtering and the effects on the deposited films were studied in terms of their structural and morphological forms. The substrates used were: pure molybdenum sheets (Mo), molybdenum-sputtered on molybdenum (Mo/Mo), molybdenum-sputtered polyimide (PI/Mo) and molybdenum-sputtered glass (glass/Mo). The characterization tools used included XRD, SEM and AFM. The results showed that all surfaces produced uniform, compact and pinhole-free films; however, those on smoother surfaces produced larger as-deposited grain sizes of up to1.7μm as against 1.3 for rougher surfaces. Non-uniformities such as overgrowth and voids were observed, but only films on PI showed evidence of cracking and peel-offs.

Visible-light photoelectric performance and bending stability of flexible LaCoO3/Mica thin films

New energy sources such as solar energy have been developed and utilized due to the shortage of non-renewable energy, and photoelectric materials have attracted more attention, accordingly. Moreover, flexible optoelectronic devices are crucial in the fields of wearable artificial intelligence, portable energy, and smart medical care. At present, photoelectric devices based on traditional perovskite cobalt oxide rigid films have problems such as inability to bend and deformation, which limits their application environment. Here, natural mica with atomically flat surface, high thermal stability, high transparency and good mechanical flexibility was selected as the substrate for preparing a series of LaCoO3 flexible photoelectric films. These films exhibit excellent photoelectric properties and flexible properties. More importantly, the flexible film still has fast response speed and reproducible light response after 500 bending cycles. It reveals that all-inorganic perovskite LaCoO3 is a promising candidate for designing high-performance, flexible and wearable optoelectronic devices.

A dual function flexible sensor for independent temperature and pressure sensing

Temperature and pressure sensing are two primary goals of bionic electronic skin. In this work, we developed a dual function flexible sensor, which achieved independent temperature and pressure sensing, with easy fabrication and without complicate signal decoupling. For this sensor, two flexible films with conductively bionic microstructure on the surface are combined face to face, which were replicated from rose petal and mulberry leaf. Ti3C2Tx nanoflakes were mixed with PEDOT: PSS as conductive layer and thermoelectric layer, and the performance of which can be optimized by regulating the concentration of Ti3C2Tx. The principles for temperature and pressure sensing are thermoelectric and piezo-resistive respectively, which are isolated by structure design. The change of contact area and resistance between the two micro-structured layers upon pressure determines the pressure response of the device. The thermoelectric response in one layer realizes the temperature sensing. The metallic conductivity of Ti3C2Tx is insensitive to temperature, leading to the invariable electric response to pressure upon varied temperature. The microstructure buffers most of the pressure, which keeps the substrate unchanged and results in the independent thermoelectric response upon varied pressure. This dual function sensor shows robust and repeatable response, and exhibits great application potential in flexible electronics

Chitosan-based nanocomposite films with carnauba wax, rosin resin, and zinc oxide nanoparticles

This work aimed to develop edible emulsion-based barriers in the form of chitosan composite films, with a focus on assessing the impacts of carnauba wax, rosin resin, and zinc oxide nanoparticles on their properties. Six films were produced by casting using chitosan as polymer base and glycerol as plasticizer. Acetic acid and polysorbate 80 were also used to facilitate the dissolution and mixing of the components. The six filmogenic solutions contained chitosan at 1.2% w/v, wax or resin content with 0 or 0.6% m/v and ZnO with 0 or 0.05% m/v. The dried films were characterized according to their chemical, barrier, mechanical, thermal and optical properties. All treatments resulted in flexible films. Chitosan films appeared smoother and more uniform under SEM imaging, while carnauba wax films displayed roughness due to their hydrophobic nature. Wax and resin films were less transparent and water soluble than the chitosan-only films. On the other hand, the addition of ZnO in the formulations increased the solubility of the films. The sorption degree was in line with the solubility results, i.e., films with ZnO presented higher sorption degree and solubility values. All treatments showed low or non-light UV transmission, indicating that the films provide good barrier to UV light. In the visible light region, films of resin with ZnO showed the lowest transmittance values, hence offering a good barrier to visible light. Among the evaluated films, chitosan, and resin films with ZnO nanoparticles were more rigid and resistant to deformation. Overall, films produced with rosin resin and ZnO nanoparticles showed potential improvements in barrier, mechanical, thermal, and optical properties, mainly due to their low water solubility, good UV protection and low permeability to water vapor and oxygen, which are suitable for using in formulations, intended to produce edible films and coatings

Improved dielectric and energy storage capacity of PVDF films via incorporating wide-bandgap silicon oxide decorated graphene oxide

In this work, wide-bandgap silicon oxide decorated graphene oxide (GO@SiO2) hybrid was simply synthesized by in-situ hydrothermal method. The obtained GO@SiO2 as a filler was then introduced into poly (vinylidene fluoride) (PVDF) matrix to prepare GO@SiO2/PVDF composite dielectric films via solution casting method. A comprehensive dielectric and energy storage capacity of PVDF based dielectric films were simultaneously achieved, indicating synergistic enhancement of GO and SiO2. For the 0.2 wt% GO@SiO2/PVDF system, a relatively high dielectric constant (ɛ' = 12.9), an enhanced breakdown strength (404.9 kV mm−1) and an improved discharged density (5.7 J cm−3) were obtained, being 153 %, 111 % and 148 % higher than those of neat PVDF, respectively. Such study provided a new strategy in obtaining flexible and large energy storage dielectric films.

PZT thick film element balancing flexibility with piezoelectricity fabricated by electrohydrodynamics jet printing used for micro power generator

In this paper, a novel flexible piezoelectric thick-film generator is proposed to address the challenges caused by flexible deformation and high piezoelectricity. This improves the output charge of the generator, which breaks the limitation imposed by the rigid and brittle nature of traditional piezoelectric bulks on elastic strain and piezoelectric performance. Additionally, the low piezoelectric coefficient of piezoelectric polymer-based piezoelectric generators is also resolved. Given the high thickness precision of electrohydrodynamic jet printing technology, the facile production of 10-μm thick film components is achieved through a process of printing and layer-by-layer accumulation on a flexible substrate, which ensures the flexible deformation and piezoelectric characteristics of the functional film. To ensure that AC is converted into stable DC output, a bipolar charge collection circuit is developed. The printed thick film produces an excellent performance in surface uniformity and smoothness. Notably, the piezoelectric constant d33 is measured to be approximately 80 pC/N, which is five times higher than the d33 value of flexible PVDF films. Additionally, the strength of adhesion between the printed thick film and the flexible substrate is remarkably high, reaching up to 20 N, which is an order of magnitude higher than the magnetron sputtering method. In a single cycle, the forward charge output reaches an impressively high level of 260 nC, which is approximately thirteen times the charge transfer capability of PVDF flexible generator. Furthermore, a bipolar charge collection circuit is applied to convert AC into DC effectively. This increases the output voltage from 2 V to 4 V. The illumination of commercial electronic screens and 39 LED lights demonstrates the applicability of micron-scale jet-printed thick films in micro-energy harvesting.