The perovskite film is the core of a perovskite solar cell (PSC), and its quality is crucial for the performance of such devices. The morphology, crystallinity, and surface coverage of the perovskite layer greatly affect the power conversion efficiency (PCE), hysteresis, and long-term stability of PSCs. The incorporation of appropriate solvent additives in the perovskite precursor solution is an effective strategy to control the film morphology and reduce the defects and grain boundaries. However, the commonly used solvent additives are environmentally harmful and highly toxic. In this work, α-terpineol (a nontoxic, eco-friendly, and low-cost monoterpene alcohol) is employed for the first time as an alternative green solvent additive to improve the quality of one-step solution-processed CH₃NH₃PbI_3–xCl_x films and to restrain nonradiative recombination in the corresponding devices. An in-depth investigation of the physicochemical effects induced by such a high-boiling-point, polar protic solvent when incorporated into a conventional perovskite solvent system is provided. The collected data demonstrate that the addition of a precise amount of α-terpineol can generate uniform and highly crystalline perovskite films with improved photovoltaic performances. Through this approach, the PCE of planar n–i–p PSCs is boosted up to 17.5% (against 16.1% of the top control device) with reduced hysteresis and enhanced ambient stability.

Focusing on the interplay between interface chemistry, electrochemistry, and integrated electronics, we show a novel low-cost and flexible biosensing platform for continuous glucose monitoring. The amperometric biosensing system features a planar three-electrode structure on a plastic substrate, and a wireless NFC-powered electronic system performing sensor analog front-end (AFE), A/D conversion, digital control, and display tasks. The working electrode is made of electropolymerized poly(3,4-ethylenedioxythiophene) (PEDOT) film onto an Au/PET electrode followed by immobilization of cross-linked glucose oxidase by glutaraldehyde. The advantages offered by such a device, including low-cost materials and instrumentation as well as the good sensitivity of 9.24 μA/(mM · cm2) are promising tools for point-of-care monitoring. It is demonstrated that the devices are good candidates for the development of advanced sensing approaches based on the investigation of the noise produced during operation (Fluctuation Enhanced Sensing).

A polybutyleneadipate-co-butylenetherephthalate (PBAT) sample, commercially known as Ecoflex^®, was processed via melt extrusion with CaCO₃ nanoparticles coated with a hydrophobic coating. Blown films of PBAT and two composites with nanofiller (2% and 5%wt) were prepared and degradation tests in soil at 30 °C up to 180 days were carried out with weight loss measurements. Furthermore, biodegradation test according to ISO 14851 was carried out at 30 °C. The effect of CaCO₃ on soil burial degradation was assessed by surface wettability and SEM. ATR-FTIR and XPS analyses highlighted chemical modifications induced by soil degradation. CaCO₃ nanoparticles decreased surface wettability and discouraged the disintegration in soil. Interestingly, SEM images after soil degradation highlighted in the nanocomposite films selective zones of disintegration. XPS showed an increasing peak area C 1s ratio of C–O to C=O with degradation time. Moreover, after the soil burial test, carbonyl index determined by ATR-FTIR increased in both nanocomposites. In fact, the addition of CaCO₃ leads to a rise in the carbonyl zone due to the presence of the carbonate group. Remarkably, FTIR data after soil degradation showed an enrichment of the aromatic content, a preferential cleavage and erosion of the aliphatic moiety in PBAT films, amplified by the presence of the CaCO₃ nanofiller.