Four organotin compounds bearing Schiff bases were prepared via a multicomponent microwave-assisted reaction among 2-hydroxy-1-naphthaldehyde, 2-aminophenol derivatives and the corresponding diorganotin oxide (R₂SnO, R = nBu or Ph), with high yields and a low economic/environmental impact. All of the compounds were fully characterized by NMR (¹H, ¹³C, and ¹¹⁹Sn) spectroscopy, high-resolution mass spectrometry, X-ray diffraction, cyclic voltammetry, UV/Vis spectroscopy, and fluorescence spectroscopy. All of the compounds absorb in the visible region around 480–490 nm, close to the maximum solar emission, with an optical band gap of around 2.3 eV and low fluorescence quantum yields. According to the electrochemical study, they present LUMO values close to that of [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM-C₆₀), a typical electron acceptor organic photovoltaic material. Based on this combined optical/electrochemical study and as it allows the preparation of homogeneous spun films, the n-butyltin complex with carboxylic acid was selected for the investigation of its possible photovoltaic properties in organic solar cells. Charge photogeneration was obtained only using this organotin compound as an electron acceptor material with poly(3-hexylthiophene, P3HT) (typical electron donor material) with an open circuit voltage of 300 mV, a short-circuit current density of 0.11 mA cm⁻² and an efficiency of 5.2 × 10⁻³%. Despite the fact that the efficiency is much lower with respect to the reference device P3HT/PCBM-C₆₀, this preliminary result suggests that, after chemical and device processing optimization, tin complexes with Schiff bases could be applied as electron acceptor materials in organic photovoltaic devices.

The synthesis of reliable, cost-effective, and eco-friendly ZnO piezoelectric nanoparticles (NPs) can contribute to nanotechnology applications in electronics, sensors, and energy harvesting. Herein, ZnO NPs were synthesized using a hydrothermal method under varied reaction times and adding ammonium hydroxide, which provided an advantage of a low-cost, scalable, low-temperature, and environmentally friendly process. Characterization through UV–Vis spectroscopy revealed absorption peaks between 374 and 397 nm, showing a blue shift compared to bulk ZnO (400 nm) attributable to nanoscale dimensions. Transmission Electron Microscopy (TEM) analysis indicated particle dimensions with length and width ranges from 150 to 341 nm and from 83 to 120 nm, respectively. X-ray diffraction (XRD) confirmed high-crystalline quality, with crystallite sizes calculated using the Scherrer equation. In addition, the effective mass model provided an estimated band gap that matched with the reported data. Also, the lattice parameters, interplanar distances, and Zn-O bond lengths were consistent with Joint Committee on Powder Diffraction Standards (JCPDS). Finally, a ZnO NP film was deposited on a steel substrate, which generated a displacement of 150 nm under a square wave voltage of 10 V. The piezoelectric behavior of the synthesized ZnO NPs can be useful for fabrication of piezoelectric nanogenerators. The proposed synthesis can allow ZnO NPs with potential application in electronic devices, energy harvesters, and transducers.

Triboelectric nanogenerators (TENGs) based on organic materials can harvest green energy to convert it into electrical energy. These nanogenerators could be used for Internet-of-Things (IoT) devices, substituting solid-state chemical batteries that have toxic materials and limited-service time. Herein, we develop a portable triboelectric nanogenerator based on dehydrated nopal powder (NOP-TENG) as novel triboelectric material. In addition, this nanogenerator uses a polyimide film tape adhered to two copper-coated Bakelite plates. The NOP-TENG generates a power density of 2309.98 μW·m⁻² with a load resistance of 76.89 MΩ by applying a hand force on its outer surface. Furthermore, the nanogenerator shows a power density of 556.72 μW·m⁻² with a load resistance of 76.89 MΩ and under 4g acceleration at 15 Hz. The output voltage of the NOP-TENG depicts a stable output performance even after 27,000 operation cycles. This nanogenerator can light eighteen green commercial LEDs and power a digital calculator. The proposed NOP-TENG has a simple structure, easy manufacturing process, stable electric behavior, and cost-effective output performance. This portable nanogenerator may power electronic devices using different vibration energy sources.

Hollow ZnO microspheres were successfully synthesized by a hydrothermal method and then functionalized with graphene oxide (GO) flakes, previously obtained through electrochemical oxidation.

The smart healthcare devices connected with the internet of things (IoT) for medical services can obtain physiological data of risk patients and communicate these data in real-time to doctors and hospitals. These devices require power sources with a sufficient lifetime to supply them energy, limiting the conventional electrochemical batteries. Additionally, these batteries may contain toxic materials that damage the health of patients and environment. An alternative solution to gradually substitute these electrochemical batteries is the development of triboelectric energy harvesters (TEHs), which can convert the kinetic energy of ambient into electrical energy. Here, we present the fabrication of a TEH formed by a stainless steel substrate (25 mm × 15 mm) coated with a molybdenum disulfide (MoS₂) film as top element and a polydimethylsiloxane (PDMS) film deposited on indium tin oxide coated polyethylene terephthalate substrate (PET/ITO). This TEH has a generated maximum voltage of 2.3 V and maximum output power of 112.55 μW using a load resistance of 47 kΩ and a mechanical vibration to 59.7 Hz. The proposed TEH could be used to power potential smart healthcare devices.