Brookite, a sometimes under evaluated TiO2polymorph

Some of the advancements concerning the study of phase-pure brookite and, especially, brookite-containing TiO2 mixed phases are reviewed. Relevance is given to their prospective photocatalytic applications, where the (positive) effect of the presence of brookite has been demonstrated, especially when solar light is concerned. From the literature, it emerges that, besides the band gap determination, which still requires more detailed studies (band gap values in a wide range are reported), the roles of brookite-containing heterojunctions, of the surface properties (i.e. acidity, redox behaviour, and the presence of coordinatively unsaturated sites), of the particular crystalline structure and of brookite influence on the anatase to rutile transition are crucial for its applications in the field of (solar) photocatalysis and electrocatalysis, but also electrochemical applications (i.e. Li batteries). The need emerges for a deeper understanding of the physico-chemical phenomena underlying their (recently demonstrated) capacity of stabilizing photogenerated electron/hole pairs. In perspective, the development of green synthesis methods to tailor the surface and structural properties of phase-pure brookite and brookite-containing mixed phases could extend their photo- and electrochemical applications

Effects of the Brookite Phase on the Properties of Different Nanostructured TiO2 Phases Photocatalytically Active Towards the Degradation of N-Phenylurea

Different sol-gel synthesis methods were used to obtain four nanostructured mesoporous TiO2 samples for an efficient photocatalytic degradation of the emerging contaminant N-phenylurea under either simulated solar light (1 Sun) or UV light. Particularly, two TiO2 samples were obtained by means of as many template-assisted syntheses, whereas other two TiO2 samples were obtained by a greener template-free procedure, implying acidic conditions and, then, calcination at either 200 °C or 600 °C. In one case, anatase was obtained, whereas in the other three cases mixed crystalline phases were obtained. The four TiO2 samples were characterized by X-ray powder diffraction (followed by Rietveld analysis); Transmission Electron Microscopy; N2 adsorption/desorption at −196 °C; Diffuse Reflectance UV/Vis spectroscopy and ζ-potential measurements. A commercial TiO2 powder (i. e., Degussa P25) was used for comparison. Differences among the synthesized samples were observed not only in their quantitative phase composition, but also in their nanoparticles morphology (shape and size), specific surface area, pore size distribution and pHIEP (pH at isoelectric point), whereas the samples band-gap did not vary sizably. The samples showed different photocatalytic behavior in terms of N-phenylurea degradation, which are ascribed to their different physico-chemical properties and, especially, to their phase composition, stemming from the different synthesis conditions

Solid-state ion exchange of Fe in small pore SSZ-13 zeolite: Characterization of the exchanged species and their relevance for the NOx SCR reaction

Solid state ion exchange was performed for the successful introduction of Fe cations in the small pore CHA structured SSZ-13 zeolite. The produced catalysts were characterized by IR and UV-Vis spectroscopies and thermally programmed reaction techniques to probe the Fe sites formed during the exchange and the catalytic activity for the NOx SCR reaction. The results indicate that highly dispersed and heterogeneous Fe sites are formed, and the type depends on the Al distribution in the zeolite. Dimeric Fe species are formed preferentially at the start of the exchange on the 6- and 8-member rings that contain at least two Al exchange sites and once these sites are fully saturated the Fe is exchanged as isolated cations

Red light-emitting Carborane-BODIPY dyes: Synthesis and properties of visible-light tuned fluorophores with enhanced boron content

A small library of 2,6- and 3,5-distyrenyl-substituted carborane-BODIPY dyes was efficiently synthesized by means of a Pd-catalyzed Heck coupling reaction. Styrenyl-carborane derivatives were exploited as molecular tools to insert two carborane clusters into the fluorophore core and to extend the π-conjugation of the final molecule in a single synthetic step. The synthetic approach allows to increase the molecular diversity of this class of fluorescent dyes by the synthesis of symmetric or asymmetric units with enhanced boron content. The structural characterization and the photoluminescence (PL) properties of synthesized dyes were evaluated, and the structure/properties relationships have been investigated by theoretical calculations. The developed compounds exhibit a significant bathochromic shift compared to their parent fluorophore scaffolds, and absorption and emission patterns were practically unaffected by the different substituents (Me or Ph) on the Ccluster atom (Cc) of the carborane cage or the cluster isomer (ortho- or meta-carborane). Remarkably, the presence of carborane units at 2,6-positions of the fluorophore produced a significant increase of the emission fluorescent quantum yields, which could be slightly tuned by changing the Cc-substituent and the carborane isomer, as well as introducing ethylene glycol groups at the meso-position of the BODIPY