Ricerc@Sapienza

Photo-anisotropic properties of a particular command layer for Liquid Crystals (LCs), based on azo-benzene material, are exploited to control the photo-thermal response of a single layer of homogeneously and uniformly distributed Au nanoparticles, immobilised on a glass substrate. Experiments demonstrate that the intrinsic anisotropy of materials can influence the photo-thermal response of plasmonic systems. Indeed, the resonant absorption of radiation by plasmonic subunits is followed by a noticeable increase of their temperature.

A thermoresponsive large-area plasmonic architecture, made from randomly distributed gold nanoparticles (GNPs) located at the substrate interface of a cholesteric liquid crystal (CLC) cell, is fabricated and thoroughly characterized. A photo-thermal heating effect due to the localized plasmonic resonance (LPR) mechanism is generated by pumping the GNP array with a resonant light beam. The photo-induced heat, propagating through the CLC layer, induces a gradual phase transition from the cholesteric to isotropic phase.

Dynamic diffraction gratings that are hidden in the field-off state are fabricated utilizing a room-temperature photocurable liquid crystal (LC) monomer and nematic LC (NLC) using holographic photopolymerization techniques. These holographic LC polymer-dispersed LCs (HLCPDLCs) are hidden because of the refractive index matching between the LC polymer and the NLC regions in the as-formed state (no E-field applied).

Natural Mg-rich lucchesiite was thermally treated in air and hydrogen atmosphere up to 800 °C to study potential changes in Fe-, Mg- and Al ordering over the octahedrally coordinated Y- and Z-sites, and to explore possible applications to intracrystalline geothermometry based on tourmaline. Overall, the experimental data (structural refinement, Mössbauer, infrared and optical absorption spectroscopy) show that thermal treatment of lucchesiite results in an increase of Fetotcontents at Z balanced by an increase of Mg and Al at Y.

Abstract.: In recent years, technologies revolving around the use of lyophobic nanopores gained considerable attention in both fundamental and applied research. Owing to the enormous internal surface area, heterogeneous lyophobic systems (HLS), constituted by a nanoporous lyophobic material and a non-wetting liquid, are promising candidates for the efficient storage or dissipation of mechanical energy.

In this contribution we explore by means of experiments, theory, and molecular dynamics the effect of pore morphology on the spontaneous extrusion of nonwetting liquids from nanopores. Understanding and controlling this phenomenon is central for manipulating nanoconfined liquids, e.g., in nanofluidic applications, drug delivery, and oil extraction.

We investigated by a multi-analytical approach (Brillouin scattering, X-ray diffraction and electron microprobe) the dependence of the elastic properties on the chemical composition of six spinels in the series (Mg1−x,Fex)Al2O4(0 ≤ x ≤ 0.5). With the exception of C12, all the elastic moduli (C11, C44, KS0and G) are insensitive to chemical composition for low iron concentration, while they decrease linearly for higher Fe2+content. Only C12shows a continuous linear increase with increasing Fe2+across the whole compositional range under investigation.

Twenty natural spinel single crystals displaying colors almost representative for the entire spinel variability were investigated by electron microprobe and UV–VIS–NIR–MIR and FTIR spectroscopies. Eight of them, selected among the Fe-bearing ones, were also analyzed by X-ray diffraction, and five by Mössbauer spectroscopy to obtain information on the oxidation state and site distribution of Fe.

Here we discuss the incorporation of Cr(III) as dopant in the spinel lattice of the NiCo2O4cubic phase and its beneficial effect on the electro-catalytic activity of this material in aprotic Li-O2cells. To this aim, we synthesized highly porous carbon-free self-standing electrodes constituted by nanostructured undoped and Cr-doped NiCo2O4grown on open nickel mesh. These materials were characterized by X-ray diffraction, field emission scanning electron microscopy coupled with energy dispersive spectroscopy, transmission electron microscopy and X-ray photoelectron spectroscopy.