• Energy Research

The underwater ultrasound power measurement has become necessary due to the rapid development of sonochemistry and sonocatalysis. This article presents construction of novel triboelectric nanogenerator (TENG) and its application for a detection of ultrasonic waves in water. The device was 3D printed using widely available and cost-effective materials. TENG consisted of the device housing and movable polymer pellets confined between flat electrodes. The device housing and pellets were 3D printed via stereolithography (SLA) and fused deposition modelling (FDM) methods, respectively. The pellets moved periodically driven by the ultrasonic waves leading to generation of an alternating voltage signal. The electric response of TENG was calibrated using a commercially available ultrasonic power sensor. The open-circuit voltage output of TENG was registered in different sections of the ultrasonic bath in order to determine the distribution of the acoustic power. TENG electric responses were analyzed by applying the fast Fourier transform (FFT) and fitting the theoretical dependence to experimental data. The main peaks in the frequency spectra of the voltage waveforms corresponded to the fundamental excitation frequency of the ultrasonic bath. TENG device, presented in this paper, can be successfully applied as a self-powered sensor for detection of ultrasonic waves. It enables precise control of the sonochemical process and reduction of power losses of the ultrasonic reactor. 3D printing technology has been confirmed to be fast, easy, and scalable method of fabrication of the ultrasonic sensors.

The dynamic development of flexible wearable electronics creates new possibilities for the production and use of new types of sensors. Recently, polymer nanocomposites have gained great popularity in the fabrication of sensors. They possess both the mechanical advantages of polymers and the functional properties of nanomaterials. The main drawback of such systems is the complexity of their manufacturing. This article presents, for the first time, fabrication of an antimony sulfoiodide (SbSI) and polyurethane (PU) nanocomposite and its application as a piezoelectric nanogenerator for strain detection. The SbSI/PU nanocomposite was prepared using simple, fast, and efficient technology. It allowed the obtainment of a high amount of material without the need to apply complex chemical methods or material processing. The SbSI/PU nanocomposite exhibited high flexibility and durability. The microstructure and chemical composition of the prepared material were investigated using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), respectively. These studies revealed a lack of defects in the material structure and relatively low agglomeration of nanowires. The piezoelectric response of SbSI/PU nanocomposite was measured by pressing the sample with a pneumatic actuator at different excitation frequencies. It is proposed that the developed nanocomposite can be introduced into the shoe sole in order to harvest energy from human body movement.

Self-powered sensor development is moving towards miniaturization and requires a suitable power source for its operation. The piezoelectric nanogenerator (PENG) is a potential candidate to act as a partial solution to suppress the burgeoning energy demand. The present work is focused on the development of the PENG based on flexible polymer-ceramic composite films. The X-ray spectra suggest that the BTO particles have tetragonal symmetry and the PVDF-BTO composite films (CF) have a mixed phase. The dielectric constant increases with the introduction of the particles in the PVDF polymer and the loss of the CF is much less for all compositions. The BTO particles have a wide structural diversity and are lead-free, which can be further employed to make a CF. An attempt was made to design a robust, scalable, and cost-effective piezoelectric nanogenerator based on the PVDF-BTO CFs. The solvent casting route was a facile approach, with respect to spin coating, electrospinning, or sonication routes. The introduction of the BTO particles into PVDF enhanced the dielectric constant and polarization of the composite film. Furthermore, the single-layered device output could be increased by strategies such as internal polarization amplification, which was confirmed with the help of the polarization-electric field loop of the PVDF-BTO composite film. The piezoelectric nanogenerator with 10 wt% BTO-PVDF CF gives a high electrical output of voltage 7.2 V, current 38 nA, and power density of 0.8 μW/cm2 at 100 MΩ. Finally, the energy harvesting using the fabricated PENG is done by various actives like coin dropping, under air blowing, and finger tapping. Finally, low-power electronics such as calculator is successfully powered by charging a 10 μF capacitor using the PENG device.

For the first time, a composite of ferroelectric antimony sulfoiodide (SbSI) nanowires and non-ferroelectric titanium dioxide (TiO2) nanoparticles was applied as a pyroelectric nanogenerator. SbSI nanowires were fabricated under ultrasonic treatment. Sonochemical synthesis was performed in the presence of TiO2 nanoparticles. The mean lateral dimension da = 68(2) nm and the length La = 2.52(7) µm of the SbSI nanowires were determined. TiO2 nanoparticles served as binders in the synthesized nanocomposite, which allowed for the preparation of dense films via the simple drop-casting method. The SbSI–TiO2 nanocomposite film was sandwiched between gold and indium tin oxide (ITO) electrodes. The Curie temperature of TC = 294(2) K was evaluated and confirmed to be consistent with the data reported in the literature for ferroelectric SbSI. The SbSI–TiO2 device was subjected to periodic thermal fluctuations. The measured pyroelectric signals were highly correlated with the temperature change waveforms. The magnitude of the pyroelectric current was found to be a linear function of the temperature change rate. The high value of the pyroelectric coefficient p = 264(7) nC/(cm2·K) was determined for the SbSI–TiO2 nanocomposite. When the rate of temperature change was equal dT/dt = 62.5 mK/s, the maximum and average surface power densities of the SbSI–TiO2 nanogenerator reached 8.39(2) and 2.57(2) µW/m2, respectively.

The ferroelectric‐semiconductor behavior of antimony sulfoiodide (SbSI) has opened up the material as a base for energy‐harvesting devices. Specifically, SbSI has drawn much attention for pyroelectric energy harvesting and thermal sensing with outstanding electrothermal properties. This work investigates the thermistor properties of an SbSI material and presents the development of an SbSI nanorod/Kapton‐based triboelectric nanogenerator (TENG) for effective energy harvesting and temperature sensing. The TENG based on SbSI/ Kapton operating in vertical contact separation mode delivers a peak‐to‐peak voltage of 90 V and a current of 1510 nA, respectively. Introducing SbSI nanorods for TENG opens the possibility of extending the conventional triboelectric series. The electrical and dielectric properties of the SbSI nanorods are investigated. SbSI exhibits a highly linear temperature coefficient of resistance (TCR) of −0.026 °C−1, making it an excellent candidate material for a thermistor. In addition, the material exhibits an excellent thermal sensitivity (β20/80 = 1612.1 K). For demonstration, the SbSI thermistor is connected with TENG, and the outputs at various temperatures are analyzed for self‐powered temperature sensing. This capability allows for efficient temperature monitoring without relying on external power sources, advancing remote, and autonomous sensing applications.

Piezoelectric nanogenerators are dependent on a piezoelectric material for the conversion of mechanical stress into useful electrical energy.

Metal–organic frameworks (MOFs) have emerged as a transformative class of materials in materials science and chemistry due to their exceptional porosity and structural tunability. Composed of metal ions or clusters intricately coordinated with organic ligands, MOFs form highly ordered 3D networks with well‐defined pores and channels. These unique characteristics enable precise customization of pore size, shape, and functionality through the selection of appropriate metal ions and ligands, unlocking diverse applications across multiple fields. This review provides a comprehensive exploration of MOFs, focusing on their synthesis, structural properties, and versatility. Key areas of discussion include MOFs’ potential for catalytic activity, gas storage, sensing, and drug delivery. Of particular importance is their transformative role in environmental remediation, energy storage, and biomedical applications, demonstrating their adaptability to modern challenges. However, significant barriers such as scalability, long‐term stability, and economic viability must be addressed to enable widespread adoption. By detailing state‐of‐the‐art advancements, this review highlights MOFs’ unparalleled ability to achieve precision and efficiency in targeted applications, offering valuable insights for emerging researchers. The findings underscore MOFs’ pivotal role in addressing contemporary scientific and industrial challenges, paving the way for innovative solutions in energy, environment, and health.