A layer of silver nanoplates, specifically synthesized with the desired localized surface plasmon resonance (LSPR) features, was grafted on amino-functionalized bulk glass surfaces to impart a double antibacterial action: (i) the well-known, long-term antibacterial effect based on the release of Ag⁺; (ii) an “on demand” action which can be switched on by the use of photo-thermal properties of silver nano-objects. Irradiation of these samples with a laser having a wavelength falling into the so called “therapeutic window” of the near infrared region allows the reinforcement, in the timescale of minutes, of the classical antibacterial effect of silver nanoparticles. We demonstrate how using the two actions allows for almost complete elimination of the population of two bacterial strains of representative Gram-positive and Gram-negative bacteria.

Nanocrystals of Cs₂SnX₆ (X = Cl, Br, Br_0.5I_0.5, and I) have been prepared by a simple, optimized, hot-injection method, reporting for the first time the synthesis of Cs₂SnCl₆, Cs₂SnBr₆, and mixed Cs₂Sn(I_0.5Br_0.5)₆ nanocrystalline samples. They all show a cubic crystal structure with a linear scaling of lattice parameter by changing the halide size. The prepared nanocrystals have spherical shape with average size from 3 to 6 nm depending on the nature of the halide and span an emission range from 444 nm (Cs₂SnCl₆) to 790 nm (Cs₂SnI₆) with a further modulation provided by mixed Br/I systems.

Historically, photonic crystals have been made of inorganic high refractive index materials coupled to air voids to maximize the dielectric contrast and in turn the light confinement. However, these systems are complex, costly, and time-demanding, and the fabrication processes are difficult to scale. Polymer structures promise to tackle this issue thanks to their easy solution and melt processing. Unfortunately, their low dielectric contrast limits their performance. In this work, we propose a concise but exhaustive review of the common polymers employed in the fabrication of planar 1D photonic crystals and new approaches to the enhancement of their dielectric contrast. Transfer matrix method modeling will be employed to quantify the effect of this parameter in standardized structures and to propose a new polymer structure for applications dealing with light management.

In this study, an innovative microfluidics-based method was developed for one-step synthesis of hyaluronic acid (HA)-based nanoparticles (NPs), by exploiting polyelectrolytic interactions between HA and chitosan (CS), in order to improve reliability, reproducibility and possible scale-up of the NPs preparation. The on-chip synthesis, using a staggered herringbone micromixer, allowed to produce HA/CS NPs with tailored-made size and suitable for both parenteral (117.50 ± 4.51 nm) and loco-regional (349.15 ± 38.09 nm) administration, mainly composed by HA (more than 85% wt) with high negative surface charge (< −20 mV). HA/CS NPs were successfully loaded with a challenging water-insoluble molecule, Everolimus (EVE), an FDA- and EMA-approved anticancer drug able to lead to cell cycle arrest, reduced angiogenesis and promotion of apoptosis. HA/CS NPs resulted to be massively internalized in CD44+ human mesenchymal stem cells via CD44 receptor-mediated endocytosis. HA/CS NPs selectiveness towards CD44 was highlighted by blocking CD44 receptor by anti-CD44 primary antibody and by comparison to CS-based NPs cellular uptake. Eventually, high effectiveness in inhibiting cell proliferation was demonstrated on-chip synthetized EVE loaded HA/CS NPs by tracking in vitro DNA synthesis.

Photonic technologies are nowadays dominated by highly performing inorganic structures that are commonly fabricated via lithography or epitaxial growths. Unfortunately, the fabrication of these systems is costly, time consuming, and does not allow for the growth of large photonic structures. All-polymer photonic crystals could overcome this limitation thanks to easy solubility and melt processing. On the other hand, macromolecules often do not offer a dielectric contrast large enough to approach the performances of their inorganic counterparts. In this work, we demonstrate a new approach to achieve high dielectric contrast distributed Bragg reflectors with a photonic band gap that is tunable in a very broad spectral region. A highly transparent medium was developed through a blend of a commercial polymer with a high refractive index inverse vulcanized polymer that is rich in sulfur, where the large polarizability of the S–S bond provides refractive index values that are unconceivable with common non-conjugated polymers. This approach paves the way to the recycling of sulfur byproducts for new high added-value nano-structures.

Chiral metal halides are promising materials for nonlinear optics and spin-selective devices. Typically, chirality is introduced via large chiral organic cations, leading to low-dimensional structures and limitations in charge transport. Here, we design a family of chiral metal halides based on the relatively small ditopic R/S-3-aminoquinuclidine (3-AQ) cation, forming an (R/S-3AQ)-Pb₂Br₆ structure closely related to the 3D corner-sharing octahedral network of perovskites. The resulting material exhibits a direct bandgap, isotropic band structure, and fully 3D photoexcitation. Circular dichroism confirms a chiral anisotropy factor consistent with theoretical predictions. Moreover, the material displays a Rashba effect in the conduction band, which is attributed to spin-orbit coupling and the lack of inversion symmetry. Offering rich chemical tunability and efficient 3D charge transport, this new class of chiral semiconductors provides a promising platform for advancing nonlinear optoelectronic and spintronic devices.