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.

Nanoparticles (NPs) are excellent antibacterial agents due to their ability to interact with microorganisms at the cellular level. However, their antimicrobial capacity can be limited by their tendency to agglomerate. Functionalizing NPs with suitable ligands improves their stability and dispersion in different media and enhances their antibacterial activity. The present work studied the functionalization of SiO₂ NPs using the sonochemical method and the Influence of organic ligands on antimicrobial activity (AA). The organic ligands studied were citric acid (CA) and monoethanolamine (MEA). X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) results confirmed the amorphous structure of SiO₂ NPs and their functionalization. Thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS) showed that functionalization with MEA (SiO₂-MEA NPs) is more favored compared to AC (SiO₂-CA NPs), and the organic ligand content was 34.42% and 28.0%, respectively. Fourier-transform infrared spectroscopy (FTIR) and RAMAN spectroscopy results confirmed the functionalization of NPs through the presence of carboxyl and amino groups. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), and zeta potential results showed that functionalization of SiO₂ NPs helped to improve their dispersion and prevent their agglomeration. Furthermore, the results of antibacterial activity against Staphylococcus aureus and Escherichia coli showed that the functionalization provided a significant improvement in the antibacterial activity (AA) of the SiO₂ NPs, where the SiO₂-CA NPs showed the highest activity, with a 99.99% inhibition percentage at concentrations of 200 ppm against both E. coli and S. aureus strains. The AA is maintained at high concentrations of 1200 ppm, which is essential in applications requiring high percentages of biocidal NPs, such as marine coatings.

Weeds decrease yield in crops through competition for water, nutrients, and light. Due to the circumstances mentioned above and the challenge of the emergence of herbicide-resistant weeds, developing sustainable alternatives becomes imperative. Plant extracts formulated into nano- and micro-encapsulates (NPs) emerge as a viable option for weed management. The objectives of this study were to identify phytochemical compounds within the ethanolic extracts of Carya illinoinensis, Ruta graveolens, and Solanum rostratum; determine their pre-emergence herbicidal activity on the indicator plants Sorghum bicolor and Phaseolus vulgaris; produce and characterize NPs with plant extracts; and assess their phytotoxicity under greenhouse conditions. The extracts were provided by Greencorp Biorganiks de México. Phytochemicals were identified through colorimetric assays and HPLC-MS, while pre-emergence tests were conducted in vitro, assessing concentrations of 12.5, 25, and 50% for each extract. NPs were synthesized using the ionotropic pre-gelation method, with size, zeta potential, and encapsulation efficiency (EE) being characterized. Finally, post-emergence tests were carried out in a greenhouse with seedlings. Compounds belonging to the hydroxycinnamic acid, flavonol, methoxyflavonol, hydroxybenzoic acid, methoxyflavone, tyrosol, stilbene, and lignan families were identified in all extracts. The pre-emergence herbicidal activity was observed for all extracts, with germination percentages ranging from 0 to 41% in both indicator plants. NPs exhibited sizes between 290 and 345 nm, zeta potentials ranging from −30 to −35 mV, and EE up to 94%. Finally, enhanced herbicidal activity was observed with plant extract NPs, with the species S. bicolor being more susceptible. NPs containing plant extracts are a viable option for bioherbicide production; however, continued research is necessary to refine formulations and enhance efficacy.

This work biosynthesized poly(γ-glutamic acid) (γ-PGA) produced by Bacillus licheniformis ATCC-9945a. This material was utilized to prepare electrospun nanofibers with solutions of 10% polyvinyl alcohol (PVA) (w/v) mixed with γ-PGA at 5 and 10% w/v, intended as a wound dressing for diabetic foot treatment. These solutions were loaded with chlorogenic acid (CGA), an active hypoglycemic agent. Morphological analysis showed a decrease in size of the fibers with the combination of PVA/γ-PGA compared to pure PVA nanofibers, which was attributed to the hydrogen bonding interactions between the glutaraldehyde vapors, γ-PGA, and PVA that permitted nanofiber cross-linking and allowed CGA release. The in vitro release analysis showed that the PVA membranes reached 28% delivery after the first 24 h. Notably, the nanofiber mat with PVA blended with 5% γ-PGA reached 57% delivery, and the PVA nanofiber with 10% γ-PGA reached 66% release after the same amount of time. The rate constant for the release kinetics showed that PVA with 5% γ-PGA had a higher value than that of the other samples, reaching saturation first.