Piezoelectric Coefficient D33 Research Articles

Mn‐doped Pb(In1/2Nb1/2)O3‐Pb(Mg1/3Nb2/3)O3‐PbTiO3 relaxor ferroelectric ceramics for high‐power piezoelectric applications

AbstractAchieving comprehensive improvement in both piezoelectric coefficient (d33) and mechanical quality factor (Qm) has become a key issue in the research of high‐power piezoelectric ceramics. Here, we focused on Mn‐doped Pb(In1/2Nb1/2)O3‐Pb(Sc1/2Nb1/2)O3‐PbTiO3 (PIN‐PSN‐PT) relaxor ferroelectric ceramics, where Mn‐doping is employed to enhance Qm. The effects of doping concentration and PT content on phase structure, ferroelectric, dielectric, and electromechanical properties were systematically studied. The well radius matching between Mn ions and B‐site ions facilitates the ion substitution and significantly increases the concentration of oxygen vacancies, thereby enhancing the domain wall pinning effect. A significantly weakened mutual constraint relationship between d33 and Qm is observed in the 2 mol% Mn‐doped PIN‐PSN‐PT ceramics with tetragonal phase, which exhibits Qm exceeding 3000 while maintaining d33 higher than 320 pC/N and Curie temperature higher than 300°C, leading to the vibration velocity over 1.15 m/s. Rayleigh analysis reveals the higher intrinsic piezoelectric response in high PT components compared to that in low PT components, which was thought to be the origin for the weakened mutual constraint relationship between d33 and Qm in tetragonal Mn‐doped PIN‐PSN‐PT ceramics.

Spatially-resolved in-situ/operando structural study of screen-printed BaTiO3/P(VDF-TrFE) flexible piezoelectric device

The incorporation of lead-free BaTiO3 particles into P(VDF-TrFE) provides a versatile way for tuning dielectric and piezoelectric properties. Screen-printing enables the easy production of flexible capacitors. To prevent particle aggregation, the BaTiO3 particles are functionalized with a surfactant. Initially, 60 % vol. BaTiO3 particles are deposited in the second layer out of three layers. After annealing and cooling, the particle distribution is successfully homogeneous in the whole film. After poling at 80 °C, the relative permittivity and the piezoelectric coefficient d33 significantly increase up to 159 and 8 pC/N respectively. In situ/operando spatially-resolved X-ray techniques allow exploring the structural evolution of the composite device during annealing and during an applied electric field. The application of an electric field leads to the quasi-disappearance of the P(VDF-TrFE) ferroelectric state. As a matter of fact, the interactions between the P(VDF-TrFE) and the surfactant may limit the rotation of P(VDF-TrFE) chains near the particles. Hence, paraelectric polymers could be chosen on a mechanical or economic basis for the matrix in piezoelectric composite devices. Regarding BaTiO3, the lattice strain evolves from an extrinsic strain at RT to an intrinsic strain after annealing and cooling. At the cooled state, the tetragonality c/a is higher than 1.01, leading to improved piezoelectric properties. The increase of the average domain size leads to the increase of the composite permittivity. Finally this knowledge facilitates the development of tailored flexible piezoelectric composite devices.

The electrical properties and in vitro osteogenic properties of 3D‐printed MgO@BT/HA piezoelectric ceramic disk

AbstractThe repair of bone defects from various causes remains a significant challenge in clinical settings. Piezoelectric materials have been demonstrated to promote osteogenic differentiation, among which barium titanate (BT) has been widely reported. Magnesium oxide (MgO) dopants not only enhance the piezoelectric properties but also stimulate the osteogenic and angiogenic properties in stem cells. In this study, a MgO‐modified BT/hydroxyapatite (MgO@BT/HA) piezoelectric ceramic scaffold was constructed using three‐dimensional (3D)‐printed technology. The results indicated that the addition of MgO improved the electrical properties of BT (d33 = 68.26 pC/N), and facilitated an increase in the proportion of HA (30%) while maintaining the piezoelectric coefficient (d33 = 2.04 pC/N) of the ceramic system. Furthermore, under the induction of low‐intensity pulsed ultrasound (LIPUS) stimulation, in vitro biosafety experiments confirmed that MgO@BT/HA exhibits excellent biosafety and promotes the osteogenic differentiation of dental pulp stem cells (DPSCs).

A novel method to fabricate curved piezoelectric composites with high piezoelectric phase volume fraction

Underwater acoustic transducer based on high piezoelectric phase volume fraction, large thickness, large area and curved piezoelectric composites (PC) possess wider beam width, higher source level and better directivity. However, the curved PC with large size is difficult to fabricate. The preparation of curved PC with large size and high piezoelectric phase volume fraction is even more tricky. The reported methods have risks of depolarization, deformation and poor periodicity and are not suitable for preparing PC with high piezoelectric phase volume fraction and large thickness. In this work, we proposed a novel fabrication method of the shaped-mold-assisted dice and fill technology. The 1–3 PC with high piezoelectric ceramic volume fraction of 80 %, thickness of 4.3 mm and area of 340 mm × 77 mm and the 2-2 PC with high piezoelectric ceramic volume fraction of 89.5 %, thickness of 5 mm and area of 262 mm × 20 mm were fabricated. The piezoelectric coefficient d33 and relative constant stress permittivity ε33T/ε0 of 1–3 and 2-2 PCs were comparable to piezoelectric phase itself. In addition, both 1–3 and 2-2 PCs exhibited a favorable performance consistency. This method solved the problem of limited cutting depth of thin blade, realizing PC with the structure of high piezoelectric phase volume fraction (＞ 70 %) and large thickness (＞ 3 mm) and eliminates the risk of depolarization, deformation and poor periodicity. This work enabled the potential for achieving large area, high piezoelectric phase volume and special-shaped PCs, which offers new ideas for designing innovative acoustic transducers and facilitates the progress of acoustic sensing technology.

Realization of ultra-high temperature stability and excellent electrical properties in LTO-based ceramics via A/B-site co-doing

La2Ti2O7 (LTO) ceramics, ideal for ultra-high temperature applications with a Curie temperature near 1460 °C, were previously limited by a low piezoelectric coefficient (d33) of 1.5 pC/N. In this work, the incorporation of Bi3+ and V5+ dopants have been employed to augment the piezoelectric properties of LTO. An enhanced d33 ∼ 4.0 pC/N is achieved in La1.91Bi0.09Ti1.97V0.03O7 (LBTV9) ceramics, while maintaining an ultra-high Curie temperature of 1437 °C. This improvement is attributed to local heterogeneity in the lattice structure induced by the doping. LBTV9 ceramics also exhibit excellent high-temperature stability and insulation properties, maintaining a d33 at 4.0 pC/N after annealing at 1000 °C for 48 h and stabilizing at 4.2 pC/N across temperatures from 200 °C to 1600 °C, with a DC resistivity of 1.7 × 106 Ω·cm at 1000 °C. These enhancements make LBTV9 ceramics suitable for extreme condition applications, thus unlocking new possibilities for their use in ultra-high temperature piezoelectric devices.

Boosting piezoelectric properties of PVDF nanofibers via embedded graphene oxide nanosheets

Tremendous research efforts have been directed toward developing polymer-based piezoelectric nanogenerators (PENG) in a promising step to investigate self-charging powered systems (SCPSs) and consequently, support the need for flexible, intelligent, and ultra-compact wearable electronic devices. In our work, electrospun polyvinylidene fluoride (PVDF) nanofiber mats were investigated while graphene oxide (GO) was added with different concentrations (from 0 to 3 wt.%). Sonication treatment was introduced for 5 min to GO nanosheets before combined PVDF solution. A comprehensive study was conducted to examine the GO incremental effect. Microstructural and mechanical properties were examined using a scanning electron microscope (SEM) and a texture analyzer. Moreover, piezoelectric properties were assessed via various tests including impulse response, frequency effect, d33 coefficient, charging and discharging analysis, and sawyer tower circuit. Experimental results indicate that incorporation of GO nanosheets enhances piezoelectric properties for all concentrations, which was linked to the increase in β phase inside the nanofibers, which has a significant potential of enhancing nanogenerator performance. PVDF-GO 1.5 wt.% shows a notably higher enhancing effect where the electroactive β-phase and γ-phase are recorded to be boosted to ~ 68.13%, as well as piezoelectric coefficient (d33 ~ 55.57 pC/N). Furthermore, increasing impact force encouraged the output voltage. Also noted that the delivered open circuit voltage is ~ 3671 V/g and the power density is ~ 150 µw/cm2. It was observed that GO of concentration 1.5 wt.% recorded a conversion efficiency of ~ 74.73%. All results are in line, showing better performance for PVDF-GO 1.5 wt.% for almost all concentrations.

Piezoelectric Enhancement in P(VDF-TrFE) Copolymer Films via Controlled and Template-Induced Epitaxy.

The surge in wearable electronics and Internet of Things technologies necessitates the development of both flexible sensors and a sustainable, efficient, and compact power source. The latter further challenges conventional batteries due to environmental pollution and compatibility issues. Addressing this gap, piezoelectric energy harvesters emerge as one kind of promising alternative to convert mechanical energy from ambient sources to electrical energy to charge those low-energy-consumption electronic devices. Despite slightly lower piezoelectric performance compared with those inorganic materials, piezoelectric polymers, notably poly(vinylidene fluoride-co-trifluoroethylene) P(VDF-TrFE), offer compelling properties for both flexible mechanical energy harvesting and self-powered strain/stress sensing, though their piezoelectric performance is expected to be further enhanced via varieties of modulation strategies of microstructures. Herein, we reported the controlled epitaxy process of micrometer-thick copolymer films with the cooperation of friction-transferred poly(tetrafluoroethylene) templates and precise modulation of the annealing conditions. Epitaxial P(VDF-TrFE) films present averaged d33 piezoelectric coefficient of -58.2 pC/N between 50 Hz and 1 kHz with good electromechanical and thermal stability. Owing to the nature of anisotropic crystallization, the epitaxial films exhibit an anisotropic transverse piezoelectric property. Epitaxial films were further utilized for mechanical energy harvesting and monitoring of human pulsation and respiration. This study provided a feasible route for the development of high-performance flexible piezoelectric devices to meet the requirement of flexible electronics.

Defect dipole stretching enables ultrahigh electrostrain.

Piezoelectric actuators have been extensively utilized as micro-displacement devices because of their advantages of large output displacement, high sensitivity, and immunity to electromagnetic interference. Here, we propose a straightforward approach to design <110>-oriented defect dipoles by introducing A-site vacancies and oxygen vacancies in (K0.48Na0.52)0.99NbO2.995 ceramics. As a result, we achieve ultrahigh electrostrains of 0.7% at 20 kV cm-1 (with an effective piezoelectric strain coefficient d33* = 3500 pm V-1), outperforming the performance of existing piezoelectric ceramics at the same driving field. The exceptional electrostrain is primarily attributed to the large stretching of defect dipoles when subjected to an applied electric field, a phenomenon that has been experimentally confirmed. Moreover, the strong interaction between these defect dipoles and <110> spontaneous polarizations plays a critical role in minimizing hysteresis and ensuring excellent fatigue resistance. Our findings present a practical and effective strategy for developing high-performance piezoelectric materials tailored for advanced actuator applications.

Quaternary piezoelectric ceramics with ultra-high mechanical quality factor

The development of piezoelectric ceramics with large piezoelectric coefficient (d33), high Curie temperature (TC) and high mechanical quality factor (Qm) is still a key challenge for practical application for high-power device. Herein, a novel quaternary piezoelectric ceramics of (0.125-x) Pb0.98Sr0.02(Mg1/3Nb2/3)O3–0.445PbTiO3–0.43PbZrO3-xPb(Mn1/3Nb2/3)O3 (abbreviated as xPMnN-PSMN-PZT) were prepared by the solid-state sintering method. The hard dopant PMnN induced the morphotropic phase boundary (MPB) of PSMN-PZT into a tetragonal-rich region. In addition, the XPS and EPR analysis proved the existence of a large amount of oxygen vacancies (Vo••) in PMnN-PSMN-PZT ceramic system. The composition near tetragonal-rich MPB region and the appearance of defect dipoles formed a strong coupling effect on the domain wall motion and leaded to an ultra Qm value. The optimum piezoelectric properties were achieved at x = 9 mol% with d33 = 260 pC/N, Qm = 3880, tanδ = 0.009 and TC = 332 °C. A significant internal bias field (Ebias) of 8.83 kV/cm was also observed in 0.09PMnN-PSMN-PZT ceramics. The origin of this excellent piezoelectric properties was explained by the phase structure, piezoelectric and dielectric analysis. This work demonstrated a rational strategy to obtain ultra Qm value for high-power piezoceramics.

Giant field-induced strain with excellent fatigue performance in (Al0.5Nb0.5)4+-modified 0.85Bi0.5Na0.5TiO3-0.11Bi0.5K0.5TiO3-0.04BaTiO3 piezoelectric ceramics

Utilizing a conventional solid-state reaction procedure, (Al0.5Nb0.5)4+-modified 0.85Bi0.5Na0.5TiO3-0.11Bi0.5K0.5TiO3-0.04BaTiO3 (BNKT-BT) samples were synthesized. The impact of (Al0.5Nb0.5)4+ on the crystal structure, ferroelectric, dielectric, and AC impedance properties was systematically investigated. The XRD patterns demonstrate that the crystal structures of all samples exhibit typical pseudo-cubic features. According to the XPS, the doping of (Al0.5Nb0.5)4+ reduces the concentration of oxygen vacancies inside the ceramics, which significantly affects the relaxation properties. This substitution successfully triggers a change from a non-ergodic relaxor (NR) state to an ergodic relaxor (ER) state, which is ascribed to the weakening of the pinning effect of the oxygen vacancies on the polar nanoregions (PNRs). The ceramics exhibit an enormous monopolar strain of 0.468 % under 60 kV/cm, accompanied by an inverse piezoelectric coefficient (d33*) of 780 pm/V, surpassing the performance of numerous other BNT-based piezoelectric ceramics. After 1×104 switching cycles, the strain value changes slightly, indicating excellent fatigue performance. The considerable strain arises from a reversible transformation of the ER phase to the ferroelectric phase induced by an electric field. This research suggests that (Al0.5Nb0.5)4+-doped BNKT-BT ceramics have good prospects for application in actuators and sensors.

Compressive stress reduction in sputter-deposited yttrium aluminum nitride (Y0.2Al0.8N) thin films for BAW resonators with high electromechanical coupling

In the past decade, rare earth elements have found increasing interest in enhancing the piezoelectric coefficient of aluminum nitride (AlN) thin films. Until now, scandium has been the most successful rare earth element to enhance the piezoelectric coefficient (d33) up to 600 %. In this research paper, we present a 250 % increase in d33 to 12.5 pC/N for sputter-deposited yttrium alloyed aluminum nitride (Y0.2Al0.8N) thin films compared to pure AlN. However, this increase in d33 comes with a substantial increase in compressive layer stress well above 1 GPa. Therefore, a chamber pressure sweep technique is introduced, resulting in a 40 % reduction in the stress level without significantly affecting the crystallographic film parameters to facilitate device integration. Even more, high compressive stress in thin films is a critical concern in piezoelectric MEMS devices such as bulk acoustic wave (BAW) resonators, as it can adversely affect the piezoelectric material properties and hence, the electromechanical performance. For this purpose, we demonstrate that the pressure sweep technique improves the electromechanical coupling factor of Y0.2Al0.8N to 7.02 %, being substantially above the reference value of 6.02 % set by pure AlN. In summary, the findings from this study may stimulate further effort to integrate YxAl1-xN thin films in BAW filter devices for future telecommunication applications.

Adaptive ferroelectric states in KNN-based piezoceramics: Unveiling the mechanism of enhancing piezoelectric properties through multiple phase boundary engineering

Developing high-performance lead-free piezoceramics, such as (K,Na)NbO3 (KNN) material, is critical to achieving environmental sustainability in next-generation electromechanical devices. Although substantial advancements have been made in KNN-based ceramics, a general coherent framework is lacking that links microscopic structure to the enhancement of macroscopic properties. Our findings indicate that the enhanced performance of KNN-based ceramics in multiphase coexistence boundaries can be attributed to the formation of self-adjusting nanodomains in response to strong local structural heterogeneity. The self-adjusting behavior of domain structure is an outcome of minimizing the local stress generated by the lattice mismatch within KNN-based ceramics, which conforms to the thermodynamic principles that favor minimizing total free energy. Guided by this strategy, the present work achieves a significant improvement of electromechanical properties, including a piezoelectric coefficient (d33) of ∼585 pC N−1, an electromechanical coupling factor (kp) of ∼62 %, and a figure of merit (d33 × g33) of ∼12.78 ×10−12 m2 N−1. This study offers a new strategy for developing lead-free piezoceramics through dedicated design of novel phase boundaries.

Microwave sintering of CaBi2Nb2O9 ceramics for improved piezoelectric response and electrical resistivity

AbstractCaBi2Nb2O9 (CBN) ceramic is a promising sensing element to convert vibration to electrical signal at temperatures higher than 600°C. However, conventionally sintered ceramics suffer from poor piezoelectric coefficient (d33) and low electrical resistivity (ρdc). Here, we report that CBN ceramics can be prepared by microwave sintering (MS) to mitigate volatilization issue of Bi2O3 and thus suppress the generation of oxygen vacancies usually seen in conventional sintering (CS) as demonstrated by X‐ray photoelectron spectroscopy (XPS) analysis and mass‐loss measurement. As compared to the CS, the MS is more favorable for reducing the sintering time, and obtaining a dense, fine, and uniform grain morphology as revealed by scanning electron microscopy (SEM) characterizations of both surface and interior of the CBN ceramics, leading to an enhancement of 86% and 75% in d33 and ρdc, respectively. Piezoresponse force microscopy (PFM) as combined with Rayleigh law analysis clearly revealed that the enhancement of piezoelectric properties was attributed to the thinner domains, the higher domain wall density, and the enhanced domain wall motion in the MS‐940 samples. This study paves an important road to simultaneously improve both d33 and ρdc in CBN ceramics for developing high‐temperature vibration sensors.

Achieving enhanced piezoelectric properties in BiFeO3-PbTiO3 based ceramics by a synergistic effects of texturing and structure engineering in reactive template grain growth-like process

A synergistic strategy of texturing and structure engineering in reactive template grain growth-like process has been validated on fabricating 0.66Bi0.9Sm0.1FeO3-0.34PbTiO3 piezoelectric ceramics with enhanced properties. A considerable texture degree is successfully obtained by optimizing sintering conditions. The template is fully dissolved into the matrix after sintering, driving a structure transformation from rhombohedral to pseudo-cubic phase. In comparison to its non-textured counterpart, the textured ceramics show a 69 % increase on large-signal piezoelectric coefficient d33* and a 43 % increase on small-signal piezoelectric coefficient d33. Good high temperature piezoelectric performance is also revealed. At 225 °C, the maximum strain and calculated d33* are 0.22 % and 436 pm/V, respectively, which increase by 49 % compared with corresponding parameters at room temperature. The study not only signify a promising strategy to design high performance BFO based functional materials, but also broaden the scope of texture technology in the development of piezoelectric ceramics.

Restraining quenching-induced decline of resistivity in NBT-BFO ceramics by incorporation of BiAlO3

(1-x)Na0.5Bi0.5TiO3-xBiFeO3 (NBT-BFO) is a system with a composition-induced transition from relaxor to ferroelectric. Upon quenching, 0.4NBT-0.6BFO obtain a Td of 640 °C and d33 of 56 pC/N. However, the quenching treatment also causes the reduction of resistivity, which is unfavorable for high-temperature piezoelectric ceramics. The aim of this study is to restrain quenching-induced decline of resistance in NBT-BFO ceramics by doping a small amount of BiAlO3 (BA). For unquenched NBT-BFO-BA, with increasing BA content, the piezoelectric coefficient (d33) decreases slightly, while the resistivity increases. After quenching, both d33 and the depolarization temperature (Td) increase, but more importantly, the resistivity of quenched NBT-BFO-BA is comparable with that of the unquenched samples. This phenomenon is not observed in other quenched samples, and the reason is attributed to the defect dipoles caused by BA. Besides, the enhanced piezoelectric properties and the resistivity can be retained after annealing the quenched samples at 400 °C for 4 h. Thus, this work implies the potential application of NBT-BFO based piezoelectric ceramics at elevated temperatures.

High-precision BaTiO3 piezoelectric ceramics via vat photopolymerization 3D printing

BaTiO3 ceramics with high precision and superior performance are fabricated by vat photopolymerization 3D printing technology. The curing behaviors and photosensitive mechanisms are systematically investigated. Through the optimization of printing parameters, BaTiO3 ceramics with a high relative density of 95 % and few defects are obtained. Notably, the sintered BaTiO3 ceramics exhibit impressive properties, including a high piezoelectric coefficient d33 of 201 pC/N and strong ferroelectric characteristics with a maximum polarization Pmax of 31.4 μC/cm2 and residual polarization Pr of 18.5 μC/cm2. More importantly, a series of complex BaTiO3 structures including the body-centered cubic lattice and triply periodic minimal surface (TPMS) structures are created perfectly with the feature size as fine as 75 μm. Compared with other reported BaTiO3 structures printed by vat photopolymerization and material extrusion technologies, this work realizes a much higher printing resolution. The excellent performance and high precision of these BaTiO3 ceramics make them great potential for practical applications in piezoelectric components.

Thickness and temperature dependence performances for single crystal composites by different polarization conditions

Alternating current polarization (ACP) has been demonstrated to enhance the performance of 1-3 piezoelectric single crystal composites (PSCCs), compared to direct current polarization (DCP). However, the scaling effect and temperature stability of PSCCs under different polarization modes, which are of significance to practical applications, have rarely been studied. Here, we compared and analyzed the thickness and temperature-dependent properties of PSCCs under ACP and DCP. The results indicated that ACP PSCCs have improved piezoelectric, electromechanical coupling, and dielectric properties. There were scaling effects for PSCCs with thickness below 400 μm. Compared to high-thickness PSCCs, the piezoelectric coefficient (d33), free dielectric constant (ε33Tε0) as well as thickness electromechanical coupling factor (kt) of low-thickness samples were inferior and the corresponding performance enhancements under ACP were also relatively low. In contrast, the clamped dielectric constant (ε33Sε0) did not show significant thickness correlation. As for temperature stability, all performances of PSCCs improved with increase in temperature and the performance enhancement with temperature change was not dependent on the polarization conditions. This work provides reference significance of selecting appropriate polarization for PSCCs, thus benefiting the design and preparation for transducers.

Morphotropic phase boundary composition PNN-PZT ceramics and their outstanding electromechanical properties

xPb(Ni1/3Nb2/3)O3-(1-x)Pb(Zr,Ti)O3 (x = 0.12, 0.24, 0.36, 0.42, 0.55 and 0.64) ceramics were prepared using conventional solid-state reaction. The morphotropic phase boundary (MPB) composition region, sintering characteristics and performance parameters of ceramic samples with different PNN compositions were studied. The phase structure, microstructure and electrical properties were characterized in detail. The results show that the Curie temperature (TC) of PNN-PZT ceramics decreases from 324 °C to 44 °C while the piezoelectric coefficient (d33) changes from 43 pC/N to 1170 pC/N with PNN content from 0.12 to 0.64. Interesting phenomena were observed, which can provide useful information for practical applications of PNN-PZT ceramics.

Narrow-Bandgap Tellurium-Based Chiral Hybrid Perovskite Single Crystals with Rashba-Dresselhaus Effect and Piezoelectricity.

Chiral hybrid perovskites have aroused great interest due to their unique versatile properties. However, designing chiral perovskites with narrow bandgaps is challenging, with their electronic properties such as the Rashba-Dresselhaus effect and piezoelectricity remaining unclear. Herein, single crystals of zero-dimensional (0D) tellurium-based chiral hybrid perovskite, (R-/S-α-PEA)2TeI6 and (R-/S-α-PEA)2TeBr6 (PEA = phenylethylammonium), with sizes of over 5 mm are grown by seed-crystal-assisted solution-temperature-lowering. The optical bandgaps are about 1.60 and 2.18 eV for the iodide and bromide analogues, respectively, which are the lowest among various chiral lead-free hybrid perovskites with the same halide ions in the X-site to the best of our knowledge. First-principles calculations reveal that (R-/S-α-PEA)2TeBr6 shows a larger Rashba-Dresselhaus spin-splitting than (R-/S-α-PEA)2TeI6, probably thanks to the greater distortion of [TeBr6] octahedra. Moreover, the piezoelectric coefficients d33 of (R-/S-α-PEA)2TeI6 and (R-/S-α-PEA)2TeBr6 are about 2.6 and 1.8 pC N-1, respectively. This work deepens the understanding of physical properties of 0D tellurium-based chiral perovskites with potential multifunctionality, including spintronic and piezoelectric performances.

Advanced 3D-printed PVDF/BT piezoelectric energy harvester with a bio-inspired 3D structure for a self-powered smart mouse

Piezoelectric polymers such as poly(vinylidene fluoride) (PVDF) exhibit remarkable flexibility, lightweight, durability, and biocompatibility compared to their ceramic counterparts. This unique characteristic makes them highly suitable for harvesting mechanical vibrations. However, conventional manufacturing methods mainly result in two-dimensional (2D) piezoelectric energy harvester (PEHs) structures. This confines the internal stress and, as a result, limits their potential voltage output. This study introduces an innovative bio-inspired three-dimensional (3D) structure crafted through fused deposition modeling (FDM). Barium titanate (BT) nanoparticles were added as piezoelectric fillers to improve the performance of the PEH. The obtained nanocomposite was poled under optimal poling conditions, achieving a β-phase fraction of 95,72 %, a piezoelectric charge coefficient (d33) of 28 pC/N, and a permittivity of 24.2 at 100 Hz. A parametric study was performed through numerical analysis, resulting in an effective and optimized structural configuration. The combined excellent piezoelectric properties of the nanocomposite with the optimized structure enabled the PEH to generate an open-circuit voltage of 30.8 V, enabling it to charge a commercial 1 μF capacitor to 25 V in just 260 s. The bioinspired PEH demonstrates its practical application by powering an innovative device known as the "smart mouse," showcasing its utility and potential in real-world applications.