RESUMEN
The great potential of K1/2Bi1/2TiO3 (KBT) for dielectric energy storage ceramics is impeded by its low dielectric breakdown strength, thereby limiting its utilization of high polarization. This study develops a novel composition, 0.83KBT-0.095Na1/2Bi1/2ZrO3-0.075 Bi0.85Nd0.15FeO3 (KNBNTF) ceramics, demonstrating outstanding energy storage performance under high electric fields up to 425 kV cm-1: a remarkable recoverable energy density of 7.03 J cm-3, and a high efficiency of 86.0%. The analysis reveals that the superior dielectric breakdown resistance arises from effective mitigation of space charge accumulation at the interface, influenced by differential dielectric and conductance behaviors between grains and grain boundaries. Electric impedance spectra confirm the significant suppression of space charge accumulation in KNBNTF, attributable to the co-introduction of Na1/2Bi1/2ZrO3 and Bi0.85Nd0.15FeO3. Phase-field simulations reveal the emergence of a trans-granular breakdown mode in KNBNTF resulting from the mitigated interfacial polarization, impeding breakdown propagation and increasing dielectric breakdown resistance. Furthermore, KNBNTF exhibits a complex local polarization and enhances the relaxor features, facilitating high field-induced polarization and establishing favorable conditions for exceptional energy storage performance. Therefore, the proposed strategy is a promising design pathway for tailoring dielectric ceramics in energy storage applications.
RESUMEN
It is an urgent need to develop lead-free piezoelectric energy harvesters (PEHs) to address the energy dilemma and meet environmental protection requirements. However, the low output power densities limit further promotion of lead-free PEHs for use in daily life. Here, an entropy-increasing strategy is proposed to achieve an increased output power density of 819 µW/cm3 in lead-free potassium sodium niobate (KNN)-based piezoceramics by increasing the configuration entropy and realizing nearly two times the growth compared with low-entropy counterparts. Evolution of the energy-harvesting performance with increasing configuration entropy is demonstrated systematically, and the excellent energy-harvesting properties achieved are attributed to the enhanced lattice distortion, the flexible polarization configuration, and the high-density randomly distributed nanodomains with the entropy-increasing effect. Moreover, excellent vibration fatigue resistance and variable temperature output power characteristics were also realized in the PEH prepared by the proposed entropy-increasing material. The significant enhancement of the comprehensive energy-harvesting performance demonstrates that the construction of KNN-based ceramics with high configuration entropy represents an effective and convenient strategy to enable design of high-performance piezoceramics and thus promotes the development of advanced PEHs.
RESUMEN
Although the ability to convert biomechanical vibrations into electric energy has been demonstrated in organic-inorganic piezocomposites, it is challenging to improve their piezoelectric properties owing to insufficient electric field poling. Here, we propose a facile and effective approach to enhance the poling efficiency of a barium calcium zirconate titanate/polydimethylsiloxane (BCZT/PDMS) composite by introducing copper nanowires (Cu NWs) to tune the resistivity of the PDMS matrix. The Cu NW-modified PDMS weakens the resistivity mismatch between the BCZT filler and the PDMS matrix, allowing a higher poling electric field to be applied to the BCZT filler during poling. As a result, the BCZT/Cu-PDMS piezocomposite exhibited a high piezoelectric quality factor (d33 × g33) of 2.58 pm2/N, which was about 7 times higher than that of BCZT/PDMS (d33 × g33 = 0.38 pm2/N). Moreover, BCZT/Cu-PDMS showed a much higher power density (3.18 µW/cm2) and a faster charging capability. This composite approach of introducing metal nanowires can be considered as a generic poling-improvement method that can be extended to other organic-inorganic piezocomposite systems.
RESUMEN
The internal electric field within a piezoelectric material can effectively inhibit the recombination of photogenerated electron-hole pairs, thus serving as a means to enhance photocatalytic efficiency. Herein, we synthesized a Na0.5Bi4.5Ti4O15 (NBT) catalyst by the hydrothermal method and optimized its catalytic performance by simple high-voltage poling. When applying light and mechanical stirring on a 2 kV mm-1 poled NBT sample, almost 100% of Rhodamine B solution could be degraded in 120 min, and the reaction rate constant reached as high as 28.36 × 10-3 min-1, which was 4.2 times higher than that of the unpoled NBT sample. The enhanced piezo-photocatalytic activity is attributed to the poling-enhanced internal electric field, which facilitates the efficient separation and transfer of photogenerated carriers. Our work provides a new option and idea for the development of piezo-photocatalysts for environmental remediation and pollutant treatment.
RESUMEN
The rapid development of flexible micropower electronics has aided the opportunity for the broader application of flexible piezoelectric composites (PCs) but has also led to higher requirements for their power generation. Among them, 0-3 PCs with embedded zero-dimension piezoparticle fillers, although low cost and easy to prepare, suffer from suboptimal output performance because of inherent structural defects. In this work, the voltage output was increased from 3.4 to 12.7 V under a force of 7 N, through first-step regulation by aligning the KNbO3 (KN) particles in the polydimethylsiloxane (PDMS) matrix; then, a significantly enhanced current output (from 0.7 to 4.5 µA) through second-step regulation by introducing copper nanorods (Cu NRs) interspersed in the gaps between the KN chains. Consequently, the proposed PC exhibits much higher power density, 37.3 µW/cm2, than that of random KN/PDMS and thus shows good potential for high-performance, flexible piezoelectric energy harvesters.
RESUMEN
Piezoelectric energy harvesters (PEHs) with piezoceramics as the core can convert low-frequency vibration energy that is ubiquitous in the environment into electrical energy and are at the frontier of research in the field of energy. The high piezoelectric charge coefficient (d) together with the large piezoelectric voltage coefficient (g) are essential for enhancing the energy harvesting performances of PEHs working on a nonresonant state. However, conventional doping and solid solution design strategies lead to the same increase or decrease trend of d and dielectric permittivity ε, making it difficult to obtain a high g value because g = d/ε. Herein, exceptionally well-balanced performances of high d and large g are achieved simultaneously in modified Pb(Zr, Ti)O3(PZT)-based ceramics via a multiscale heterogeneity strategy, which involves coordination among the defect dipole, hierarchical domain, and composite. The electromechanical parameters of the optimal specimen are not only superior to those of many state-of-the-art commercial counterparts but also exhibit good thermal stability. Most importantly, the assembled PEH with the optimal specimen shows excellent variable temperature power generation characteristics. This work provides a paradigm for building PEH material through a multiscale heterogeneity strategy, expected to benefit a wide range of electromechanical coupling materials.
RESUMEN
Based on the strong demand for self-powered wearable electronic devices, flexible piezoelectric energy harvesters (FPEHs) have recently attracted much attention. A polymer-based piezocomposite is the core of an FPEH and its transduction coefficient (d33×g33) is directly related to the material's power generation capacity. Unfortunately, the traditional 0-3 type design method generally causes a weak stress transfer and poor dispersion of the filler in the polymer matrix, making it difficult to obtain a high d33×g33. In this work, a unique interconnected skeleton design strategy has been proposed to overcome these shortcomings. By using the freeze-casting method, an ice-templated 2-2 type composite material has been constructed with the popular piezoelectric relaxor 0.2Pb(Zn1/3Nb2/3)O3-0.8Pb(Zr1/2Ti1/2)O3 (PZN-PZT) as the filler and PDMS as the polymer matrix. Both the theoretical simulation and the experimental results revealed a remarkable enhancement in the stress transfer ability and piezoelectric response. In particular, the 2-2 type piezocomposite has an ultrahigh transduction coefficient of 58 213 × 10-15 m2 N-1, which is significantly better than those of previously reported composite materials, and even textured piezoceramics. This work provides a promising paradigm for the development of high-performance FPEH materials.
RESUMEN
In order to achieve a high-performance flexible piezoelectric energy harvester (FPEH), a unique sandwich structure, that is, a PVDF film filled with FeTiNbO6 (FTN) semiconductor particles as an intermediate layer and a pure PVDF film as an upper and lower barrier layer, has been designed, and the corresponding PVDF-FTN/PVDFx-PVDF (P-FTNx-P) compact composite has been prepared by hot-pressing technology. The special sandwich structure combined with the introduction of FTN particles is beneficial to enhance the interfacial polarization and the content of the electroactive phase in PVDF. Together with the maximum piezoelectric voltage coefficient and the moderate Young's modulus, the P-FTN15%-P FPEH exhibited the optimal energy-harvesting performance with a high power density of 110 µW/cm3 and a large charge density of 75 µC/m2 in cantilever mode. The outstanding design in this work is expected to provide a new way for the development of high-performance FPEH materials.
RESUMEN
Flexible piezocomposites have emerged as promising materials for highly durable wearable devices. Here, we propose a new design strategy, namely particle alignment engineering, to develop high performance flexible piezocomposites by dielectrophoresis (DEP). An ultrahigh piezoelectric voltage coefficient (g33) of 600 × 10-3 V m N-1 is achieved by a composite of (Ba0.85Ca0.15)(Ti0.90Zr0.10)O3 (BCZT) particles aligned in a polydimethylsiloxane (PDMS) matrix. To the best of our knowledge, this g33 value is by far the highest ever achieved in piezocomposites. The significantly improved poling electric voltage applied to the BCZT particles and hugely enhanced stress-transfer capability of the aligned composite synergistically contribute to the record-high piezoelectric response in flexible piezocomposites. The fabricated flexible piezoelectric touch sensor and wearable keyboard possess an excellent sensitivity and cycling stability, which demonstrate a promising strategy for exploring high performance piezocomposites for flexible device application.
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In this study, (Ba0.85Ca0.15)(Ti0.9Zr0.1)O3 (BCTZ) lead-free ceramics with enhanced energy density were prepared by two-step sintering. All ceramics fall into the rhombohedral-orthorhombic-tetragonal (R-O-T) phase boundary near room temperature, and a dense microstructure with an intermediate grain size was observed. The enhanced piezoelectric and energy harvesting properties were attained over a wide grain size range of 10-15 µm, benefiting from the construction of the R-O-T phase boundary. Most interestingly, the maximum values of d33 and d33 × g33 (530 pC N-1 and 9720 × 10-15 m2 N-1) can be achieved at 1500/1350 °C with a grain size of 13.7 µm. The interpretation of the underlying mechanism related to domain and defect engineering has been investigated systematically. Furthermore, a high output power of 99 µW and an energy conversion efficiency of 10% were obtained at a simple cantilever energy harvester fabricated from a 1500/1350 °C specimen under an acceleration of 1.0g, making the current system very promising for piezoelectric energy harvesting applications.
RESUMEN
In this work, a paraelectric complex perovskite Ba(Zn1/3Nb2/3)O3 (BZN) was introduced into the morphotropic boundary composition (Bi0.5Na0.5)0.93Ba0.07TiO3 (BNBT) to modulate the phase structure and electrical properties as well as the field-induced strain behavior. Using a columbite route, the ceramics with pure perovskite structure were successfully fabricated. The structure and electrical measurements showed that the introduction of BZN into BNBT results in the decrease of the rhombohedrality 90-γ, and promotes the evolution from ferroelectric to antiferroelectric (AFE) relaxor. Besides, the introduction of BZN induces the volume increase and dimension reduction of the nanosized AFE relaxor domains. A large field-induced strain of 0.39% with good stability against frequency, field, and temperature was obtained at the BNZ addition of composition x = 0.01, which locates at the critical composition boundary between ferroelectric state and AFE relaxor state.
RESUMEN
BaTiO3/polyvinylidene fluoride (BT/PVDF) is the extensive reported composite material for application in modern electric devices. However, there still exists some obstacles prohibiting the further improvement of dielectric performance, such as poor interfacial compatibility and low dielectric constant. Therefore, in depth study of the size dependent polarization and surface modification of BT particle is of technological importance in developing high performance BT/PVDF composites. Here, a facile molten-salt synthetic method has been applied to prepare different grain sized BT particles through tailoring the calcination temperature. The size dependent spontaneous polarizationof BT particle was thoroughly investigated by theoretical calculation based on powder X-ray diffraction Rietveld refinement data. The results revealed that 600 nm sized BT particles possess the strong polarization, ascribing to the ferroelectric size effect. Furthermore, the surface of optimal BT particles has been modified by water-soluble polyvinylprrolidone (PVP) agent, and the coated particles exhibited fine core-shell structure and homogeneous dispersion in the PVDF matrix. The dielectric constant of the resulted composites increased significantly, especially, the prepared composite with 40 vol % BT loading exhibited the largest dielectric constant (65, 25 °C, 1 kHz) compared with the literature values of BT/PVDF at the same concentration of filler. Moreover, the energy storage density of the composites with tailored structure was largely enhanced at the low electric field, showing promising application as dielectric material in energy storage device. Our work suggested that introduction of strong polarized ferroelectric particles with optimal size and construction of core-shell structured coated fillers by PVP in the PVDF matrix are efficacious in improving dielectric performance of composites. The demonstrated approach can also be applied to the design and preparation of other polymers-based nanocomposites filled with ferroelectric particles to achieve desirable dielectric properties.