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[Display omitted] Semiconductors, such as metal oxides and metal sulfides (MS X), are widely investigated as effectively catalytic materials to convert carbon dioxide (CO 2) and water into chemicals under simulated solar light. These valuable investigations might address both the energy crisis and climate change in our modern society. Herein, a novel strategy to construct leaf-like heterojunctions of V S -ZnIn 2 S 4 /TiN-x is reported. The new semiconductor heterojunctions were then applied to photoelectrocatalytic CO 2 reduction, achieving excellent performance (formate formation rate of 1173.2 μM h−1 cm−2) attributed to the plant cell-like morphology and enhanced electron mobility from the heterojunction interfaces to the active sites on the surface. Our findings suggest that titanium nitride (TiN) with good conductivity can improve the photoelectrocatalytic ability of MS X through heterojunction construction. The photocathode V S -ZnIn 2 S 4 /TiN-3 exhibits 81.0 % selectivity toward C2 products by optimizing the material structure and reaction conditions. According to the systematic investigation of operando Fourier transform infrared (FTIR) spectra, common intermediates such as *COO−, *COOH, * C O, *CHO, *COCHO, and *COCH 3 reported in the literature were carefully verified. Among these, the carbene specie serve as the key intermediate responsible for generating other intermediates and resulting in all products. [ABSTRACT FROM AUTHOR]

With growing environmental concerns and the need for sustainable energy, multifunctional materials that can simultaneously address water treatment and clean energy production are in high demand. In this study, we developed a cost-effective method to synthesize zinc oxide (ZnO) nanowires via the anodic oxidation of zinc foil. By carefully controlling the anodization time, we optimized the Zn/ZnO-5 min electrode to achieve impressive dual-function performance in terms of effective photoelectrocatalysis for water splitting and waste water treatment. The electrode exhibited a high photocurrent density of 1.18 mA/cm2 at 1.23 V vs. RHE and achieved a solar-to-hydrogen conversion efficiency of 0.55%. A key factor behind this performance is the presence of surface defects, such as oxygen vacancies (OVs), which enhanced charge separation and boosted electron transport. In tests for waste water treatment, the Zn/ZnO-5 min electrode demonstrated the highly efficient degradation of methylene blue (MB) dye, with a reaction rate constant of 0.4211 min−1 when exposed to light and a 1.0 V applied voltage significantly faster than using light or voltage alone. Electrochemical analyses, including impedance spectroscopy and voltammetry, further confirmed the superior charge transfer properties of the electrode under illumination, making it an excellent candidate for both energy conversion and pollutant removal. This study highlights the potential of using simple anodic oxidation to produce scalable and efficient ZnO-based photocatalysts. The dual-function capability of this material could pave the way for large-scale applications in renewable hydrogen production and advanced waste water treatment, offering a promising solution to some of today's most pressing environmental and energy challenges. [ABSTRACT FROM AUTHOR]

Heterojunction formation between BiVO4 nanomaterials and benchmark semiconductor photocatalysts has been keenly pursued as a promising approach to improve charge transport and charge separation via interfacial electron transfer for the photoelectrocatalytic degradation of recalcitrant pharmaceutical pollutants. In this work, a heterostructured TiO2/Mo-BiVO4 bilayer photoanode was fabricated by the deposition of a mesoporous TiO2 overlayer using the benchmark P25 titania catalyst on top of Mo-doped BiVO4 inverse opal films as the supporting layer, which intrinsically absorbs visible light below 490 nm, while offering improved charge transport. A porous P25/Mo-BiVO4 bilayer structure was produced from the densification of the inverse opal underlayer after post-thermal annealing, which was evaluated on photocurrent generation in aqueous electrolyte and the photoelectrocatalytic degradation of the refractory anti-inflammatory drug ibuprofen under back-side illumination by visible and UV–Vis light. Significantly enhanced photoelectrochemical performance on both photocurrent density and pharmaceutical degradation was achieved for the bilayer structure with respect to the additive effect of the constituent layers, which was related to the improved light harvesting arising from the backscattering by the mesoporous TiO2 layer in combination with the favorable charge transfer at the TiO2/Mo-BiVO4 interface. [ABSTRACT FROM AUTHOR]

In this study, seeded zinc oxide (Z-ZnO) thin films were fabricated by a two-step electrochemical deposition process. Different annealing temperatures (300, 400, 500, and 600 °C) were investigated to determine the most effective temperature for the photocatalytic activity. Comprehensive analyses were conducted using X-Ray Diffraction (XRD), scanning electron microscopy (SEM), and UV–visible spectrophotometry. The XRD results confirmed the formation of a wurtzite hexagonal structure, with the highest crystallinity observed at 400 °C. The lowest band gap value, 3.29 eV, was also recorded for Z-ZnO thin film annealed at 400 °C. SEM images revealed that the thin film treated at 400 °C exhibited a well-defined and uniform structure, contributing to its enhanced properties. The photocatalytic efficiency of ZnO (without seeding layer) and Z-ZnO thin films annealed at 400 °C was evaluated through the degradation of tetracycline hydrochloride (TCH) to prove the effect of the presence of a primary seeding layer on ZnO 400 °C thin film efficiency. The degradation efficiency of ZnO thin film without seeding layer was 69.8%. By applying a seeding layer in Z-ZnO 400 °C thin film, the degradation efficiency has been increased to 75.8%. On the other hand, Z-ZnO 400 °C thin film achieved a high degradation efficiency of 82.6% over 300 min in the photoelectrocatalytic system. The obtained Z-ZnO thin films annealed at 400 °C are highly effective photocatalysts and photoelectrocatalysts, offering a significant potential for the degradation of pharmaceuticals and other pollutants in water. [ABSTRACT FROM AUTHOR]