The vapor-phase deposition of triethoxy(octyl)-silane and 1H,1H,2H,2H-perfluoroctyltriethoxysilane on silica substrates was studied at different temperatures (70−150°C). An original combination of spectroscopic ( 13 C and 29 Si solid state NMR, FTIR), electrochemical (CV, EIS), and surface (surface free energy determinations, AFM) characterization techniques was adopted to shed light on the role played by the alkylsilane structure and deposition temperature on the resulting layer. As for the unfluorinated molecule, both wettability and ion permeability displayed a bell-shaped curve with respect to the functionalization temperature. Spectroscopic techniques showed similar trends in the functionalization degree and suggested the formation of oligomers/polymers covalently attached to the surface. 29 Si NMR proved that higher functionalization temperatures increase lateral polymerization across the alkylsilane layer. Conversely, the wettability was almost invariant with the functionalization temperature for the fluorinated analogue. However, electrochemical and spectroscopic results had a significant dependence on the functionalization conditions, even more marked than for the unfluorinated alkylsilane. The higher thermal reactivity of fluorinated molecules led to vertical polymerization, as supported by very high water contact angles, diffusion components in EIS, and a lower degree of covalent bonding with the surface. Optimal deposition conditions were identified at 100 and 90°C for the unfluorinated and fluorinated alkylsilane, respectively.

Selecting the proper doping strategy is essential to controlling the photocatalytic activity of TiO 2 -based nanomaterials. In this work, we compare impregnation and bulk synthesis methods for feeding titania nanocrystals with either Nb or Ta as transition metal dopant and N as nonmetal codopant.The resulting photocatalytic efficiency was tested toward ethanol degradation under either UV or simulated solar irradiation. Microstructure, morphology, and electronic properties at various length scales were deeply investigated and compared with DFT simulations. Instead, under UV irradiation, impregnated samples performed better than bulk synthesis ones, with Ta-doped powders being more efficient than Nb-doped and undoped TiO 2 . Under simulated solar irradiation, bulk synthesis Nbdoped materials were the most active ones, while all the impregnated samples were even less performing than the undoped TiO 2 reference. On the basis of XPS, EPR, DRS, and XRPD results, such differences were attributed to the bulk synthesis approach producing a more homogeneous distribution of guest dopants within the grains, in conjunction with a higher amount of intrinsic defects (such as O vacancies). Implications of these findings on the engineering of efficient titania photocatalysts are discussed.

Pharmaceutics and personal care products (PPCPs) are raising growing concern due to their widespread usage and resistance to conventional remediation techniques. Several of them raise significant health and environmental concerns, especially when present in complex mixtures. Due to their chemical resistance, Advanced Oxidation Processes (AOPs) are needed for their complete removal from surface and wastewaters. In the present work, photocatalysis by titanium dioxide (TiO) under UV and simulated solar irradiation was adopted to degrade tetracycline hydrochloride, paracetamol, caffeine and atenolol, both as single pollutants and in mixtures. All molecules showed high removal and mineralization degrees. Moreover, no interference effects decreased the efficiency of the processes in the case of pollutant mixtures, achieving 60% of mineralization after 6 h. An immobilized TiO system was also developed by depositing titania on titanium meshes. A 50% mineralization degree of the pollutant mixture was obtained after 6 h, revealing a suitable efficiency for field applications. Eventually, the impact of the matrix composition on the photocatalytic efficiency was investigated by studying the reaction both in simulated drinking water and in commercial bottled mineral water. The scavenger role played by HCO species appears to be dominant in inhibiting the mineralization.

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