The method of electrospinning was used to create nanofibers made of cellulose acetate (CA) and essential oils (EOs). CA polymer at 15% w/v was dissolved in acetone and then 1% or 5% v/v of EOs was added to the polymer solution. The utilized essential oils were rosemary and oregano oils. Then, the CA/EOs in acetone solution were electrospun, creating micro/nanofibers, approximately 700–1500 nm in diameter. Raman spectroscopy was used to detect the attachment of the EOs in the CA electrospun fibers (ESFs). Scanning electron microscopy was used to study the morphology, topography and dimensions of the ESFs. The formed CA/EOs ESFs are found to have good antimicrobial properties against three common microbial species, frequently found in difficult to treat infections: Bacteria species Staphylococcus aureus, Escherichia coli and the yeast Candida albicans. ESFs with 5% v/v oregano oil with respect to the initial solution, showed the best antimicrobial and anti-biofilm effects due to the potency of this EO against bacteria and fungi, especially for Escherichia coli and Candida albicans. This work describes an effective and simple method to prepare CA/EOs ESFs and opens up many new applications of micro/nanofibers such as improved antimicrobial wound dressings, anti-biofilm surfaces, sensors and packaging alternatives.

Copper nanoparticles have been synthesized in ethylene glycol (EG) using copper sulphate as a precursor and vanadium sulfate as an atypical reductant being active at room temperature. We have described a technique for a relatively simple preparation of such a reagent, which has been electrolytically produced without using standard procedures requiring an inert atmosphere and a mercury cathode. Several stabilizing agents have been tested and cationic capping agents have been discarded owing to the formation of complex compounds with copper ions leading to insoluble phases contaminating the metallic nanoparticles. The elemental copper nanoparticles, stabilized with polyvinylpyrrolidone (PVP) and sodium dodecyl sulphate (SDS), have been characterized for composition by energy dispersive X-ray spectroscopy (EDS), and for size by dynamic light scattering (DLS), and transmission electron microscopy (TEM), giving a size distribution in the range of 40–50 nm for both stabilizing agents. From a methodological point of view, the process described here may represent an alternative to other wet-chemical techniques for metal nanoparticle synthesis in non-aqueous media based on conventional organic or inorganic reductants.

An innovative approach for the fabrication of hybrid photocatalysts on a solid porous polymeric system for the heterogeneous photocatalytic degradation of organic pollutants is herein presented. Specifically, gold/zinc oxide (Au/ZnO)-based porous nanocomposites are formed in situ by a two-step process. In the first step, branched ZnO nanostructures fixed on poly(methyl methacrylate) (PMMA) fibers are obtained upon the thermal conversion of zinc acetate-loaded PMMA electrospun mats. Subsequently, Au nanoparticles (NPs) are directly formed on the surface of the ZnO through an adsorption dipping process and thermal treatment. The effect of different concentrations of the Au ion solutions to the formation of Au/ZnO hybrids is investigated, proving that for 1 wt % of Au NPs with respect to the composite there is an effective metal–semiconductor interfacial interaction. As a result, a significant improvement of the photocatalytic performance of the ZnO/PMMA electrospun nanocomposite for the degradation of methylene blue (MB) and bisphenol A (BPA) under UV light is observed. Therefore, the proposed method can be used to prepare flexible fibrous composites characterized by a high surface area, flexibility, and light weight. These can be used for heterogeneous photocatalytic applications in water treatment, without the need of post treatment steps for their removal from the treated water which may restrict their wide applicability and cause secondary pollution.

In this work, we report the synthesis of an active material for supercapacitors (SCs), namely α-Fe₂O₃/carbon composite (C-Fe₂O₃) made of elongated nanoparticles linearly connected into a worm-like morphology, by means of electrospinning followed by a calcination/carbonization process. The resulting active material powder can be directly processed in the form of slurry to produce SC electrodes with mass loadings higher than 1 mg cm⁻² on practical flat current collectors, avoiding the need for bulky porous substrate, as often reported in the literature. In aqueous electrolyte (6 M KOH), the so-produced C-Fe₂O₃ electrodes display capacity as high as ~140 mAh g⁻¹ at a scan rate of 2 mV s⁻¹, while showing an optimal rate capability (capacity of 32.4 mAh g⁻¹ at a scan rate of 400 mV s⁻¹). Thanks to their poor catalytic activity towards water splitting reactions, the electrode can operate in a wide potential range (−1.6 V–0.3 V vs. Hg/HgO), enabling the realization of performant quasi-symmetric SCs based on electrodes with the same chemical composition (but different active material mass loadings), achieving energy density approaching 10 Wh kg⁻¹ in aqueous electrolytes.

Light emitting diodes (LED) based on halide perovskite nanocrystals (NC) have received widespread attention in recent years. In particular, LEDs based on CsPbBr₃ NCs were the object of special interest. Here, we report for the first time green LED based on CsPbBr₃ NCs treated with ammonium thiocyanate solution before purification with polar solvent. The champion device fabricated based on the treated CsPbBr₃ NCs showed high efficiency and high stability during operation as well as during storage. A study on morphology and current distribution of NC films under applied voltages was carried out by conductive atomic force microscopy, giving a hint on efficiency roll-off. The current work provides a facile way to treat sensitive perovskite NCs and to fabricate perovskite NC-based LED with high stability. Moreover, the results shed new light on the relation between film morphology and device performance and on the possible mechanism of efficiency roll-off in NC LED.

Titanium dioxide nanocrystals (TiO₂ NCs), through their photocatalytic activity, are able to generate charge carriers and induce the formation of various reactive oxygen species (ROS) in the presence of O₂ and H₂O. This special feature makes TiO₂ an important and promising material in several industrial applications. Under appropriate antioxidant balancing, the presence of ROS is crucial in plant growth and development, therefore, the regulated ROS production through the photocatalytic activity of TiO₂ NCs may be also exploited in the agricultural sector. However, the effects of TiO₂ NCs on plants are not fully understood and/or phase-pure TiO₂ NCs are rarely used in plant experiments. In this work, we present a phase-selective synthesis of TiO₂ NCs with anatase and rutile crystal phases. The nanomaterials obtained were characterized by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy, and electron paramagnetic resonance spectroscopy (EPR). In field experiments, Vitis vinifera cv. Cabernet Sauvignon leaves developed under natural sunlight were treated with aqueous dispersions of TiO₂ NCs at concentrations of 0.001, 0.01, 0.1, and 1 w/v%. The effect of the applied nanocrystals was characterized via leaf photochemistry, mineral nutrient contents, and pyridoxine levels. We found that stress responses of grapevine to anatase and rutile NCs treatments are different, which can be related to the different ROS profiles of the two polymorphs. Our results indicate that TiO₂ NCs may be utilized not only for direct pathogen inactivation but also for eliciting plant defense mechanisms.