New nanostructured hybrid membranes for gas separation have been prepared and characterized for the first time in the literature by using a block copolymer, poly(styrene-b-butadiene-b-styrene) (SBS), and aminated SBA-15. Short mesopore channels, platelet SBA-15 particles with a high surface density of 3-aminopropyl grafts (3.8 nm⁻²) and modest surface area reduction (45%) were prepared, characterized and used as a filler. The gas transport characterization of the hybrid membranes indicates that with a 10 wt% content of aminated filler, outstanding performances in terms of selectivity and permeability for the CH₄/N₂ and the CO₂/N₂ gas pairs can be obtained. In particular, the CH₄/N₂ ideal selectivity of 7.3 is higher than the values of the existing block co-polymers used for this separation and of mixed matrix membranes described to date in the literature. Membranes with such a high separation factor may enable the exploitation of natural gas with high N₂ content and increase the amount of methane that can be economically recovered. The combination of the CO₂/N₂ ideal selectivity of 53 with a CO₂ permeability of 173 Barrer demonstrates that the new hybrid membranes prepared in this study deserve further attention as a practical commercial solution also for the post-combustion capture of carbon dioxide. Finally, the small and flat particles dispersed in the polymer lend themselves to the fabrication of thin industrial membranes with enhanced productivity.

We report on our latest studies on alignment of chromonic liquid crystals, a special class of molecules which recently attracted the attention of researchers. In particular, we show a detailed study of planar anchoring of disodium cromoglycate (DSCG) and, for the first time in the literature, a stable homeotropic alignment, achieved using a surface property of the alignment layer, i.e. the hydrophobicity. Excellent candidates from this point of view are pure polybutadiene (PB) and polydimethylsiloxane (PDMS). In fact, for the former the homeotropic anchoring stabilizes after one day, while for the latter stabilization occurs soon after cooling from the isotropic phase. After a long time both types of alignments (planar and homeotropic) evolve into thermodynamically stable configurations, i.e. ribbon structures. An explanation of the behaviour is given.

A two-fold active control of the plasmonic resonance of randomly distributed gold nanoparticles (GNPs) has been achieved. GNPs have been immobilized on an Indium Tin Oxide (ITO) coated glass substrate and then covered with a liquid crystalline compound. The system has been investigated by means of atomic force and scanning electron microscopy, revealing the presence of isolated and well distributed GNPs. The application of an external electric field to the sample has a two-fold consequence: the re-orientation of the hybrid-aligned liquid crystal layer and the formation of a carrier accumulation layer in the proximity of the ITO substrate. The refractive indices of both liquid crystal and accumulation layers are influenced by the applied field in a competitive way and produce a “dancing behavior” of the GNP's plasmonic resonance spectral position.

Large shifts in the plasmonic resonances of a thin film of gold nanorods (GNRs) are induced through the modulation of the local refractive index of the neighboring dielectric medium. This change is enabled through light-induced surface reorientation of a nematic liquid crystal in contact with a nanometer-thin photoalignment layer coating the GNR film. The presence of isolated and well distributed GNRs, both before and after the photoalignment layer deposition, is shown through atomic force and scanning electron microscopy. Exposure of the photoalignment layer to polarized light is shown to reorient aligned nematic liquid crystal molecules to an orthogonal direction, thereby changing the local refractive index of the medium in close proximity to the GNR film. This large change in the local dielectric strength is shown to cause a broad red shift of the localized plasmonic longitudinal resonance and almost no shift in the local transverse resonance. The ability to remotely and quickly change the plasmonic properties of this GNR system marks a breakthrough towards the realization of all-optical plasmonic and photonic devices such as plasmonic colour filters.