• Two-faceted (DAP) ― more favorable configuration than single-faceted (OAP) under UV irradiation. • Bare and modified DAP ― efficient charge carriers’ separation under UV irradiation. • Noble metal-modified OAP ― higher activity than respective DAP under vis irradiation. • “Hot” (plasmonic) electron transfer via shallow electron traps in OAP. • Localization of noble metal on DAP – key factor of vis activity.

Developing eco-friendly strategies to produce green fuel has attracted continuous and extensive attention. In this study, a novel gas-templating method was developed to prepare 2D porous S-doped g-C₃N₄ photocatalyst through simultaneous pyrolysis of urea (main g-C₃N₄ precursor) and ammonium sulfate (sulfur source and structure promoter). Different content of ammonium sulfate was examined to find the optimal synthesis conditions and to investigate the property-governed activity. The physicochemical properties of the obtained photocatalysts were analyzed by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), scanning transmission electron microscopy (STEM), specific surface area (BET) measurement, ultraviolet-visible light diffuse reflectance spectroscopy (UV/vis DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy and reversed double-beam photo-acoustic spectroscopy (RDB-PAS). The as-prepared S-doped g-C₃N₄ photocatalysts were applied for photocatalytic H₂ evolution under vis irradiation. The condition-dependent activity was probed to achieve the best photocatalytic performance. It was demonstrated that ammonium sulfate played a crucial role to achieve concurrently 2D morphology, controlled nanostructure, and S-doping of g-C₃N₄ in a one-pot process. The 2D nanoporous S-doped g-C₃N₄ of crumpled lamellar-like structure with large specific surface area (73.8 m² g⁻¹) and improved electron−hole separation showed a remarkable H₂ generation rate, which was almost one order in magnitude higher than that of pristine g-C₃N₄. It has been found that though all properties are crucial for the overall photocatalytic performance, efficient doping is probably a key factor for high photocatalytic activity. Moreover, the photocatalysts exhibit significant stability during recycling. Accordingly, a significant potential of S-doped g-C₃N₄ has been revealed for practical use under natural solar radiation.

A simple, low-cost method was applied to prepare hybrid photocatalysts of copper (I) oxide/titania. Five different TiO₂ powders were used to perform the study of the effect of titania matrix on the photocatalytic and antimicrobial properties of prepared nanocomposites. The photocatalytic efficiency of such a dual heterojunction system was tested in three reaction systems: ultraviolet-visible (UV-Vis)-induced methanol dehydrogenation and oxidation of acetic acid, and 2-propanol oxidation under visible light irradiation. In all the reaction systems considered, the crucial enhancement of photocatalytic activity in relation to corresponding bare titania was observed. The reaction mechanism for a specific reaction and the influence of titania matrix were discussed. Furthermore, antimicrobial (bactericidal and fungicidal) properties of Cu₂O/TiO₂ materials were analyzed. The antimicrobial activity was found under UV, visible and solar irradiation, and even for dark conditions. The origin of antimicrobial properties with emphasis on the role of titania matrix was also discussed.

• Gold-modified octahedral anatase particles (Au/OAPs) with enhanced photocatalytic activity. • Structural/lattice defects as nucleation sites for gold NPs. • Size-controllable gold NPs by photodeposition method in the presence of various hole and electron scavengers. • Enhanced vis-photocatalytic activity with an increase in gold NPs’ size. • Strong enhancement of plasmon resonance for larger gold NPs by 3D-FDTD simulations.

Titania photocatalysts have been intensively examined for both mechanism study and possible commercial applications for more than 30 years. Although various reports have already been published on titania, including comprehensive review papers, the morphology-governed activity, especially for novel nanostructures, has not been reviewed recently. Therefore, this paper presents novel, attractive, and prospective titania photocatalysts, including zero-, one-, two-, and three-dimensional titania structures. The 1D, 2D, and 3D titania structures have been mainly designed for possible applications, e.g., (i) continuous use without the necessity of particulate titania separation, (ii) efficient light harvesting (e.g., inverse opals), (iii) enhanced activity (fast charge carriers’ separation, e.g., 1D nanoplates and 2D nanotubes). It should be pointed out that these structures might be also useful for mechanism investigation, e.g., (i) 3D titania aerogels with gold either incorporated inside the 3D network or supported in the porosity, and (ii) titania mesocrystals with gold deposited either on basal or lateral surfaces, for the clarification of plasmonic photocatalysis. Moreover, 0D nanostructures of special composition and morphology, e.g., magnetic(core)–titania(shell), mixed-phase titania (anatase/rutile/brookite), and faceted titania NPs have been presented, due to their exceptional properties, including easy separation in the magnetic field, high activity, and mechanism clarification, respectively. Although anatase has been usually thought as the most active phase of titania, the co-existence of other crystalline phases accelerates the photocatalytic activity significantly, and thus mixed-phase titania (e.g., famous P25) exhibits high photocatalytic activity for both oxidation and reduction reactions. It is believed that this review might be useful for the architecture design of novel nanomaterials for broad and diverse applications, including environmental purification, energy conversion, synthesis and preparation of “intelligent” surfaces with self-cleaning, antifogging, and antiseptic properties.