In a flexible nanocomposite-based nanogenerator, in which piezoelectric nanostructures are mixed with polymers, important parameters to increase the output power include using long nanowires with high piezoelectricity and decreasing the dielectric constant of the nanocomposite. Here, we report on piezoelectric power generation from a lead-free LiNbO₃ nanowire-based nanocomposite. Through ion exchange of ultra-long Na₂Nb₂O₆-H₂O nanowires, we synthesized long (approximately 50 μm in length) single-crystalline LiNbO₃ nanowires having a high piezoelectric coefficient (d ₃₃ approximately 25 pmV^-1). By blending LiNbO₃ nanowires with poly(dimethylsiloxane) (PDMS) polymer (volume ratio 1:100), we fabricated a flexible nanocomposite nanogenerator having a low dielectric constant (approximately 2.7). The nanogenerator generated stable electric power, even under excessive strain conditions (approximately 10⁵ cycles). The different piezoelectric coefficients of d ₃₃ and d ₃₁ for LiNbO₃ may have resulted in generated voltage and current for the e ₃₃ geometry that were 20 and 100 times larger than those for the e ₃₁ geometry, respectively. This study suggests the importance of the blending ratio and strain geometry for higher output-power generation in a piezoelectric nanocomposite-based nanogenerator. PACS 77.65.-j; 77.84.-s; 73.21.Hb

The electric power output of a piezoelectric nanogenerator (PENG) depends on the various physical parameters of the constituent materials, including the piezoelectric coefficient, Young’s modulus, and dielectric constant. Herein, we report the mechanical and electrical properties of a poly(vinylidene fluoride)–BaTiO₃ (PVDF–BTO) composite-based PENG. Variation of the BTO nanoparticle (NP) content enabled the systematic tuning of the physical parameters that are related to power generation in the composite. The Young’s modulus of the PVDF–BTO composite initially increased, and then eventually decreased, with the increasing BTO content, which was probably due to the clustering effect of the high modulus BTO NPs. The dielectric constant of the composite continuously increased as the BaTiO₃ content increased. The piezoelectric outputs were greatly enhanced at 10 wt% of BTO, where the Young’s modulus was the highest. These results indicate that the Young’s modulus plays an important role in the piezoelectric power generation of the composite-based PENGs.

The reversibly stable formation and rupture processes of electrical percolative pathways in organic and inorganic insulating materials are essential prerequisites for operating non-volatile resistive memory devices. However, such resistive switching has not yet been reported for dynamically cross-linked polymers capable of intrinsic stretchability and self-healing. This is attributable to the uncontrollable interplay between the conducting filler and the polymer. Herein, we present the development of the self-healing, stretchable, and reconfigurable resistive random-access memory. The device was fabricated via the self-assembly of a silver-gradient nanocomposite bilayer which is capable of easily forming the metal-insulator-metal structure. To realize stable resistive switching in dynamic molecular networks, our device features the following properties: i) self-reconstruction of nanoscale conducting fillers in dynamic hydrogen bonding for self-healing and reconfiguration and ii) stronger interaction among the conducting fillers than with polymers for the formation of robust percolation paths. Based on these unique features, we successfully demonstrated stable data storage of cardiac signals, damage-reliable memory triggering system using a triboelectric energy-harvesting device, and touch sensing via pressure-induced resistive switching.

While sliding-mode triboelectric nanogenerators (S-TENGs) have been considered as one of the most promising devices for rotational energy harvesting, their inherently poor durability has been a serious bottleneck for applications. Herein, we report a three-dimensional kirigami TENG as a highly efficient and durable rotational energy harvesting device. The kirigami TENG consisted of cube-shaped paper, aluminum (Al) foil electrode and polytetrafluoroethylene (PTFE) polymer film, and converted rotational motion into multiple folding-unfolding vibrations. The rotation-folding (R-F) kirigami TENG generated an open-circuit voltage of 31 V, a short-circuit current of 0.67 μA and an instantaneous power (power density) of 1.2 μW (0.13 μW/cm²) at 200 rpm, which was sufficient to turn on 25 light-emitting diodes and a thermo-hygrometer. The triboelectric outputs of the R-F kirigami TENG were only slightly decreased even after 288,000 continuous rotations, i.e., the output remained at 86% of its initial value. This work demonstrates that an R-F kirigami TENG could be a plausible candidate to efficiently harvest various forms of rotational energy with a long-term durability.