Hybrid Hemp Particles as Functional Fillers for the Manufacturing of Hydrophobic and Anti-icing Epoxy Composite Coatings.

The development of hydrophobic composite coatings is of great interest for several applications in the aerospace industry. Functionalized microparticles can be obtained from waste fabrics and employed as fillers to prepare sustainable hydrophobic epoxy-based coatings. Following a waste-to-wealth approach, a novel hydrophobic epoxy-based composite including hemp microparticles (HMPs) functionalized with waterglass solution, 3-aminopropyl triethoxysilane, polypropylene-graft-maleic anhydride, and either hexadecyltrimethoxysilane or 1H,1H,2H,2H-perfluorooctyltriethoxysilane is presented. The resulting epoxy coatings based on hydrophobic HMPs were cast on aeronautical carbon fiber-reinforced panels to improve their anti-icing performance. Wettability and anti-icing behavior of the prepared composites were investigated at 25 °C and -30 °C (complete icing time), respectively. Samples cast with the composite coating can achieve up to 30 °C higher water contact angle and doubled icing time than aeronautical panels treated with unfilled epoxy resin. A low content (2 wt %) of tailored HMPs causes an increase of ∼26% in the glass transition temperature of the coatings compared to pristine resin, confirming the good interaction between the hemp filler and epoxy matrix at the interphase. Finally, atomic force microscopy reveals that the HMPs can induce the formation of a hierarchical structure on the surface of casted panels. This rough morphology, combined with the silane activity, allows the preparation of aeronautical substrates with enhanced hydrophobicity, anti-icing capability, and thermal stability.

Tunable Raman Gain in Transparent Nanostructured Glass-Ceramic Based on Ba2NaNb5O15 †.

Stimulated Raman scattering in transparent glass-ceramics (TGCs) based on bulk nucleating phase Ba2NaNb5O15 were investigated with the aim to explore the influence of micro- and nanoscale structural transformations on Raman gain. Nanostructured TGCs were synthesized, starting with 8BaO·15Na2O·27Nb2O5·50SiO2 (BaNaNS) glass, by proper nucleation and crystallization heat treatments. TGCs are composed of nanocrystals that are 10-15 nm in size, uniformly distributed in the residual glass matrix, with a crystallinity degree ranging from 30 up to 50% for samples subjected to different heat treatments. A significant Raman gain improvement for both BaNaNS glass and TGCs with respect to SiO2 glass is demonstrated, which can be clearly related to the nanostructuring process. These findings show that the nonlinear optical functionalities of TGC materials can be modulated by controlling the structural transformations at the nanoscale rather than microscale.

Copper indium sulfide quantum dots in photocatalysis.

Since the advent of photocatalytic technology, scientists have been searching for semiconductor materials with high efficiency in solar energy utilization and conversion to chemical energy. Recently, the development of quantum dot (QD) photocatalysts has attracted much attention because of their unique characteristics: small size, quantum effects, strong surface activity, and wide photoresponse range. Among ternary chalcogenide semiconductors, CuInS2 QDs are increasingly examined in the field of photocatalysis due to their high absorption coefficients, good matching of the absorption range with sunlight spectrum, long lifetimes of photogenerated electron-hole pairs and environmental sustainability. In this review paper, the structural and electronic properties, synthesis methods and various photocatalytic applications of CuInS2 QDs are systematically expounded. The current research status on the photocatalytic properties of materials based on CuInS2 QD is discussed combined with the existing modification approaches for the enhancement of their performances. Future challenges and new development opportunities of CuInS2 QDs in the field of photocatalysis are then prospected.

Redox behavior of potassium doped and transition metal co-doped Ce0.75Zr0.25O2 for thermochemical H2O/CO2 splitting.

CeO2 slow redox kinetics as well as low oxygen exchange ability limit its application as a catalyst in solar thermochemical two-step cycles. In this study, Ce0.75Zr0.25O2 catalysts doped with potassium or transition metals (Cu, Mn, Fe), as well as co-doped materials were synthesized. Samples were investigated by X-ray diffraction (XRD), N2 sorption (BET), as well as by electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) to gain insight into surface and bulk features, which were connected to redox properties assessed both in a thermogravimetric (TG) balance and in a fixed bed reactor. Obtained results revealed that doping as well as co-doping with non-reducible K cations promoted the increase of both surface and bulk oxygen vacancies. Accordingly, K-doped and Fe-K co-doped materials show the best redox performances evidencing the highest reduction degree, the largest H2 amounts and the fastest kinetics, thus emerging as very interesting materials for solar thermochemical splitting cycles.

Interfacial Charge Transfer Complexes in TiO2-Enediol Hybrids Synthesized by Sol-Gel.

Metal oxide-organic hybrid semiconductors exhibit specific properties depending not only on their composition but also on the synthesis procedure, and particularly on the functionalization method, determining the interaction between the two components. Surface adsorption is the most common way to prepare organic-modified metal oxides. Here a simple sol-gel route is described as an alternative, finely controlled strategy to synthesize titanium oxide-based materials containing organic molecules coordinated to the metal. The effect of the molecular structure of the ligands on the surface properties of the hybrids is studied using three enediols able to form charge transfer complexes: catechol, dopamine, and ascorbic acid. For each system, the process conditions driving the transition from the sol to chemical, physical, or particulate gels are explored. The structural, optical, and photoelectrochemical characterization of the amorphous hybrid materials shows analogies and differences related to the organic component. In particular, electron paramagnetic resonance (EPR) spectroscopy at room temperature reveals the presence of organic radical species with different evolution and stability, and photocurrent measurements prove the effective photosensitization of TiO2 in the visible range induced by interfacial ligand-to-metal charge transfer.

ROS-Generating Hyaluronic Acid-Modified Zirconium Dioxide-Acetylacetonate Nanoparticles as a Theranostic Platform for the Treatment of Osteosarcoma.

Materials that are able to produce free radicals have gained increasing attention for environmental and biomedical purposes. Free radicals, such as the superoxide anion (O2•-), act as secondary messengers in many physiological pathways, such as cell survival. Therefore, the production of free radicals over physiological levels has been exploited in the treatment of different types of cancer, including osteosarcoma (OS). In most cases, the production of reactive oxygen species (ROS) by materials is light-induced and requires the use of chemical photosensitisers, making it difficult and expensive. Here, for the first time, we propose photoluminescent hybrid ZrO2-acetylacetonate nanoparticles (ZrO2-acac NPs) that are capable of generating O2•- without light activation as an adjuvant for the treatment of OS. To increase the uptake and ROS generation in cancer cells, we modify the surface of ZrO2-acac NPs with hyaluronic acid (HA), which recognizes and binds to the surface antigen CD44 overexpressed on OS cells. Since these nanoparticles emit in the visible range, their uptake into cancer cells can be followed by a label-free approach. Overall, we show that the generation of O2•- is toxic to OS cells and can be used as an adjuvant treatment to increase the efficacy of conventional drugs.

F-doped ZnO nano- and meso-crystals with enhanced photocatalytic activity in diclofenac degradation.

Diclofenac (DCF), a non-steroidal anti-inflammatory drug, is considered one of the most widespread emerging contaminants. Its incidence in water can favor the growth of drug-resistant bacteria and harm aquatic organisms endangering both the human health and the ecosystem. Advanced oxidation processes (AOPs) based on the action of reactive oxygen species are very effective technologies for the removal of this contaminant from water. In this context, ZnO is one of the most studied semiconductors for photocatalytic water treatment. In this work, the photocatalytic activity of fluorine-doped ZnO nano- and meso-crystals synthesized by a hydrothermal approach is reported, exploring the role of a low F atomic concentration (0.25, 0.5 and 1 at. %) on the degradation of DCF in comparison with bare ZnO. All doped samples show high rates of DCF degradation and mineralization, which were realized primarily thanks to their high efficiency in the generation of hydroxyl radicals (OH). The property-structure-function relationships of the materials are investigated by complementary techniques, such as SEM, XRD, EPR, UV-vis DRS and PL, with the aim to evaluate the role of fluorine in determining their morphological, electronic and optical properties.

Photocatalytic hydrogen evolution by co-catalyst-free TiO2/C bulk heterostructures synthesized under mild conditions.

Hydrogen production by photocatalytic water splitting is one of the most promising sustainable routes to store solar energy in the form of chemical bonds. To obtain significant H2 evolution rates (HERs) a variety of defective TiO2 catalysts were synthesized by means of procedures generally requiring highly energy-consuming treatments, e.g. hydrogenation. Even if a complete understanding of the relationship between defects, electronic structure and catalytic active sites is far from being achieved, the band gap narrowing and Ti3+-self-doping have been considered essential to date. In most reports a metal co-catalyst (commonly Pt) and a sacrificial electron donor (such as methanol) are used to improve HERs. Here we report the synthesis of TiO2/C bulk heterostructures, obtained from a hybrid TiO2-based gel by simple heat treatments at 400 °C under different atmospheres. The electronic structure and properties of the grey or black gel-derived powders are deeply inspected by a combination of classical and less conventional techniques, in order to identify the origin of their photoresponsivity. The defective sites of these heterostructures, namely oxygen vacancies, graphitic carbon and unpaired electrons localized on the C matrix, result in a remarkable visible light activity in spite of the lack of band gap narrowing or Ti3+-self doping. The materials provide HER values ranging from about 0.15 to 0.40 mmol h-1 gcat -1, under both UV- and visible-light irradiation, employing glycerol as sacrificial agent and without any co-catalyst.

Three-year lifetime and regeneration of superoxide radicals on the surface of hybrid TiO2 materials exposed to air.

The generation and stabilization of reactive oxygen species (ROS), including the superoxide radical anion (O2-), have a huge potential in environmental remediation and industrial chemical processes, but they still remain a challenge. Here, we elucidate the formation, stability and reactivity of superoxide radicals spontaneously produced on the surface of a hybrid TiO2-acetylacetonate material exposed to air. EPR spectra reveal an exceptional lifetime (up to three years, in air at room temperature) of the adsorbed O2-, which can also be easily regenerated after its decay. The performances of this material in the degradation of organic pollutants in aqueous solution without any light irradiation indicate a heterogeneous catalytic mechanism, mediated by superoxide radicals, with a synergistic homogeneous action of hydroxyl radicals (OH), which are released in solution, as detected by the EPR spin trapping method. The regeneration ability of the adsorbed superoxide radicals by simple exposure to air counteracts the partial instability in aqueous environment of the organic component of the hybrid structure allowing the catalyst reuse. These structural and functional features joined to the simple preparation route open a new perspective in the field of advanced oxidation processes for hybrid TiO2 materials.