A comprehensive study on the sulfur doping of TiO₂, by means of H₂S treatment at 673 K, has been performed in order to highlight the role of sulfur in affecting the properties of the system, as compared to the native TiO₂. The focus of this study is to find a relationship among the surface, structure, and morphology properties, by means of a detailed chemical and physical characterization of the samples. In particular, transmission electron microscopy images provide a simple tool to have a direct and immediate evidence of the effects of H₂S action on the TiO₂ particles structure and surface defects. Furthermore, from spectroscopy analyses, the peculiar surface, optical properties, and methylene blue photodegradation test of S-doped TiO₂ samples, as compared to pure TiO₂, have been investigated and explained by the effects caused by the exchange of S species with O species and by the surface defects induced by the strong H₂S treatment.

S-doped TiO₂ and hybrid MoS₂/TiO₂ systems have been synthesized, via the sulfidation with H₂S of the bare TiO₂ and of MoO_x supported on TiO₂ systems, with the aim of enhancing the photocatalytic properties of TiO₂ for the degradation of carbamazepine, an anticonvulsant drug, whose residues and metabolites are usually inefficiently removed in wastewater treatment plants. The focus of this study is to find a relationship between the morphology/structure/surface properties and photoactivity. The full characterization of samples reveals the strong effects of the H₂S action on the properties of TiO₂, with the formation of defects at the surface, as shown by transmission electron microscopy (TEM) and infrared spectroscopy (IR), while also the optical properties are strongly affected by the sulfidation treatment, with changes in the electronic states of TiO₂. Meanwhile, the formation of small and thin few-layer MoS₂ domains, decorating the TiO₂ surface, is evidenced by both high-resolution transmission electron microscopy (HRTEM) and UV-Vis/Raman spectroscopies, while Fourier-transform infrared (FTIR) spectra give insights into the nature of Ti and Mo surface sites. The most interesting findings of our research are the enhanced photoactivity of the MoS₂/TiO₂ hybrid photocatalyst toward the carbamazepine mineralization. Surprisingly, the formation of hazardous compounds (i.e., acridine derivatives), usually obtained from carbamazepine, is precluded when treated with MoS₂/TiO₂ systems.

The aim of this work was to investigate how ZnO tetrapod (ZnO-T) morphology, structure, and surface charge properties (i.e. Debye length) influence their UV sensing properties, shedding light on the underlying photoresponse mechanisms. ZnO-Ts were synthesized and centrifuged to obtain three different fractions with tuned morphology, which were characterized by scanning electron microscopy, transmission electron microscopy, and high-resolution transmission electron microscopy microscopies, x-ray diffraction analysis, Brunauer–Emmett–Teller measurements, FTIR and UV–vis spectroscopies. ZnO-T UV sensors were fabricated and tested comparing among ZnO-T fractions and commercial ZnO nanoparticles. ZnO-T photoresponse was mostly influenced by ZnO-T leg diameter, with the optimal value close to the double Debye length. We also demonstrated how fractionating ZnO-Ts for morphology optimization can increased the responsivity by 2 orders of magnitude. Moreover, ZnO-T showed 3 orders of magnitude higher responsivity compared to commercial ZnO nanopowder. These results are beneficial for the engineering of efficient UV sensors and contribute to a deeper understanding the overall mechanism governing UV photoresponse.

This paper reports the synthesis of Fe-titanate nanotubes by means of the conventional ion-exchange method with iron nitrate solutions. As the iron-rich nanotubes were found to contain the catalyst precursor intrinsically dispersed in their structures, the unprecedented possibility of using this kind of materials for building carbon nanostructures, firmly attached at the surface of the forming TiO₂ nanoparticles, was verified. The catalytic decomposition of ethylene, used as a carbon source, was performed at a relatively high temperature (750 °C) when the nanotubes undergo an irreversible phase transformation to form anatase and rutile nanoparticles. Due to the different amounts of Fe ions in the nanotubes, distinct types of carbon/TiO₂ hybrid interfaces were formed, ranging from amorphous (lower Fe³⁺ concentration) to the more crystalline graphitic domains (higher Fe³⁺ concentrations), as documented by the microstructure of the treated samples. The present approach is of potential interest for (photo)catalytic and energy conversion/transport applications.