Fossil fuels, especially coal, have played a pivotal role in driving technological and economic advancements over the past century, though accompanied by numerous environmental challenges. Rapid progress in green and sustainable energy sources, including tidal, wind, and solar energy, coupled with growing environmental concerns, the conventional coal industry is experiencing a sustained decline in both size and financial viability. This situation necessitates the urgent adoption of advanced approaches to coal utilization. Beyond serving as an energy source, coal and its by-products, known as coal waste, can serve as valuable resources for the development of advanced materials, including photocatalysts. The advancement of photocatalytic materials derived from coal and coal waste can capitalize on these natural carbon and mineral sources, providing a viable solution to numerous environmental challenges. Currently, research in this domain remains in its early stages, with existing studies primarily focusing on specific types of photocatalysts or particular aspects of the fabrication process. Therefore, available coal-based and coal waste-based photocatalytic materials were systematically examined and categorized into six types according to their composition and dimensional/structural characteristics. Each type of photocatalytic material was introduced, along with common fabrication and characterization technologies. Representative works were discussed in detail to highlight the unique features of different types of coal-based and coal waste-based photocatalytic materials. Furthermore, the promising applications of these materials in environmental protection and pollution treatment were summarized, while also addressing the challenges and prospects in this research field. This review comprehensively overviews the fundamental knowledge and recent advancements in photocatalytic materials derived from coal and coal waste, with the goal of catalyzing the development of next generation photocatalysts and contributing to the transformation of the conventional coal industry.

Squaric-acid-linked zwitterionic covalent organic frameworks (Z-COFs), assembled through interlayer interactions, are emerging as potential materials in the field of photocatalysis. However, the study of their interlayer interactions has been largely overlooked. To address this, this work systematically calculated interlayer interactions via density functional theory (DFT) and analyzed the differences in interlayer interactions of different structures of Z-COFs through interlayer slippage, planarity, and an independent gradient model based on the Hirshfeld partition (IGMH). Furthermore, it revealed the relationship between the interactions and the macroscopic photocatalytic carrier transport performance of the material. The results indicated that both preventing interlayer slippage and enhancing planarity can enhance the interlayer interactions of Z-COFs, thereby improving their macroscopic carrier transport performance in photocatalysis.

Urban air pollution is one of the most important environmental problems for human health and several strategies have been developed for its mitigation. The objective of this study is to assess the impact of single and combined mitigation measures on concentrations of air pollutants emitted by traffic at pedestrian level in the same urban environment. The effectiveness of different scenarios of green infrastructure (GI), the implementation of photocatalytic materials and traffic low emission zones (LEZ) are investigated, as well as several combinations of LEZ and GI. A wide set of scenarios is simulated through Computational Fluid Dynamics (CFD) modelling for two different wind directions (perpendicular (0°) and 45° wind directions). Wind flow for the BASE scenario without any measure implemented was previously evaluated using wind-tunnel measurements. Air pollutant concentrations for this scenario are compared with the results obtained from the different mitigation scenarios. Reduction of traffic emissions through LEZ is found to be the most effective single measure to improve local air quality. However, GI enhances the effects of LEZ, which makes the combination of LEZ + GI a very effective measure. The effectiveness of this combination depends on the GI layout, the intensity of emission reduction in the LEZ and the traffic diversion in streets surrounding the LEZ. These findings, in line with previous literature, suggest that the implementation of GI may increase air pollutant concentrations at pedestrian level for some cases. However, this study highlights that this negative effect on air quality can turn into positive when used in combination with reductions of local traffic emissions.

Theoretically, lanthanum can bond with surface oxygens of ZnTiO3 to form La-O-Ti bonds, resulting in the change of both the band structure and the electron state of the surface. To verify this statement, DFT calculations were performed using a model with a dispersed lanthanum atom on the surface (101) of ZnTiO3. The negative heat segmentation values obtained suggest that the incorporation of La on the surface of ZnTiO3 is thermodynamically stable. The bandgap energy value of La/ZnTiO3 (2.92 eV) was lower than that of ZnTiO3 (3.16 eV). TDOS showed that the conduction band (CB) and the valence band (VB) energy levels of La/ZnTiO3 are denser than those of ZnTiO3 due to the participation of hybrid levels composed mainly of O2p and La5d orbitals. From the PDOSs, Bader\'s charge analysis, and ELF function, it was established that the La-O bond is polar covalent. MB adsorption on La/ZnTiO3 (-200 kJ/mol) was more favorable than on ZnTiO3 (-85 kJ/mol). From the evidence of this study, it is proposed that the MB molecule first is adsorbed on the surface of La/ZnTiO3, and then the electrons in the VB of La/ZnTiO3 are photoexcited to hybrid levels, and finally, the MB molecule oxidizes into smaller molecules.

OBJECTIVE: The problem of the development of miniature motors able to move on the air-liquid interface at low Reynolds numbers is a crucial challenge due to dominating role of viscous force. To solve this problem the chemical generation of gas can be used. Generated gas pushes liquid out from the surfer surface, so the resistance force is reduced.
METHODS: Surfer composed of TiO2 nanoparticles and ferromagnetic cobalt microparticles moves at the interface of an aqueous solution of hydrogen peroxide under the action of magnetic force. After irradiation with UV or visible light, the gas cavern is formed at the surfer surface due to photo-catalytic decomposition of hydrogen peroxide. As a result, the area of surfer contact with liquid is reduced.
RESULTS: The resistance force acting on the surfer is reduced due to the liquid pushing out from the surfer surface. This effect is strengthened with the increase in the intensity of gas generation. The resistance force is increased when increasing the liquid viscosity or using a surfactant. The proposed method allows control of the velocity of the motors in a rather wide range by changing the gradient of the magnetic field and parameters of light.

This paper investigates the photocatalytic characteristics of Ag nanowire (AgNW)/TiO2 and AgNW/TiO2/graphene oxide (GO) nanocomposites. Samples were synthesized by the direct coating of TiO2 particles on the surface of silver nanowires. As-prepared AgNW/TiO2 and AgNW/TiO2/GO nanocomposites were characterized by electron microscopy, X-ray diffraction, UV/visible absorption spectroscopy, and infrared spectroscopy. Transmission electron microscope (TEM) images confirmed the successful deposition of TiO2 nanoparticles on the surface of AgNWs. The photocatalytic activity of synthesized nanocomposites was evaluated using Rhodamine B (RhB) in an aqueous solution as the model organic dye. Results showed that synthesized AgNW/TiO2/GO nanocomposite has superior photocatalytic activities when it comes to the decomposition of RhB.

Developing photoelectrochemical (PEC) sensors based on photocatalytic materials has recently attracted great interest as an emerging technology for environmental monitoring. TiO2 P25 is a well-known highly active photocatalyst, cheap, and produced commercially on a large scale. In the current work, a practical and durable TiO2-based PEC sensor has been fabricated by immobilizing TiO2 P25 nanoparticles at disposable screen-printed carbon substrates using drop-casting method. The fabricated PEC sensor has been applied for the anodic-detection and determination of nitrite (NO2-) ions under UV(A) light (LED, 365 nm) using chronoamperometry (CA) and differential pulse voltammetry (DPV). Linear calibration curves were obtained between the photocurrent responses and the concentrations of NO2- ions in the ranges of 0.1-5.0 and 0.5-10 mg L-1 for CA and DPV, respectively. Surprisingly, the detection limits (sensitivities) of the fabricated sensor towards NO2- ions under light were enhanced by a factor of 4.75 (4.1) and 8.3 (37.4) for CA and DPV, respectively, in comparsion with those measured in the dark. It is found that the photo-excitation of TiO2 facilitates the photooxidation of NO2- ions via the photo-generated holes whereas the photogenerated electrons contribute to the enhanced photocurrent and consequently the enhanced detection limit and sensitivity. The fabricated TiO2-based PEC sensor exhibits a good stability, durability, and satisfying selectivity for NO2- ions determination. These results indicate that the TiO2-based PEC sensor fabricated by utilizing cheap and commercially available components has great potential for being transferred from lab-to-factory.

In addition to the most common applications of macroporous film: Supplying a large surface area, PC-FTO (macroporous fluorine-doped tin oxide with photonic crystal structure) can be employed as a template to control the morphologies of WO3 for exposing a more active facet, and enhance the overall photo-electron conversion efficiency for the embedded photoactive materials under changing illumination incidence through refracting and scattering. The optical features of PC-FTO film was demonstrated by DRUVS (diffuse reflectance UV-vis spectra). Plate-like WO3 were directly synthesized inside the PC-FTO film as a control group photoanode, Ag2S quantum dots were subsequently decorated on WO3 to tune the light absorption range. The impact of photonic crystal film on the photoactivity of Ag2S/WO3 was demonstrated by using the photoelectrochemical current density as a function of the incidence of the simulated light source.

The photo-induced reactivity of compounds at the surface of photocatalytic materials is used to maintain the cleanliness of the surface of glass, concretes and paints. A standard method to quantify the photocatalytic self-cleaning (SC) properties of non-transparent materials was recently published. It is based on the covering of the sample surface with a defined amount of dye and on the evaluation of the reflectance spectra of the coloured surface under irradiation. The calibration of the spectral changes allowed the quantification of the surface residual dye and the evaluation of the self-cleaning kinetics. The method was tested on seven white and coloured photocatalytic materials using methylene blue (MB), rhodamine B (RhB) and metanil yellow (MY). The main by-products of the MB photocatalytic degradation at the solid/solid interface were identified, showing that MB degradation in solution follows a path quite different from that at the solid/solid interface. Also MY showed a different order of photoreactivity. Furthermore, experiments at the solid/solid interface are more trustworthy than tests in solution for evaluating the self-cleaning ability. The differences of the photocatalytic phenomena at the solid/solid interface in comparison with the most studied photoactivated processes at the solid/liquid interface are outlined. Furthermore, photocatalytic materials showed selectivity toward some specific dyes. This encourages the use of more than one dye for the evaluation of the self-cleaning ability of a photocatalytic material.

TiO2 is an ideal photocatalyst candidate except for its large bandgap and fast charge recombination. A novel laminated junction composed of defect-controlled and sulfur-doped TiO2 with carbon substrate (LDC-S-TiO2/C) is synthesized using the 2D transition metal carbides (MXenes) as a template to enhance light absorption and improve charge separation. The prepared LDC-S-TiO2/C catalyst delivers a high photocatalytic H2 evolution rate of 333 µmol g-1 h-1 with a high apparent quantum yield of 7.36% at 400 nm and it is also active even at 600 nm, resulting into a 48 time activity compared with L-TiO2/C under visible light irradiation. Further theoretical modeling calculation indicates that such novel approach also reduces activation energy of hydrogen production apart from broadening the absorption wavelength, facilitating charge separation, and creating a large surface area substrate. This synergic effect can also be applied to other photocatalysts\' modification. The study provides a novel approach for synthesis defective metal oxides based hybrids and broaden the applications of MXene family.