In this study, molybdenum disulfide (MoS₂) decorated on graphitic carbon nitride (g-C₃N₄) heterostructure catalysts at various weight ratios (0.5%, 1%, 3%, 10%, w/w) were successfully prepared via a two-step hydrothermal synthesis preparation method. The properties of the synthesized materials were studied by X-ray diffraction (XRD), attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FT-IR), UV–Vis diffuse reflection spectroscopy (DRS), scanning electron microscopy (SEM) and N₂ porosimetry. MoS₂ was successfully loaded on the g-C₃N₄ forming heterojunction composite materials. N₂ porosimetry results showed mesoporous materials, with surface areas up to 93.7 m²g⁻¹, while determined band gaps ranging between 1.31 and 2.66 eV showed absorption over a wide band of solar light. The photocatalytic performance was evaluated towards phenol oxidation and of Cr(VI) reduction in single and binary systems under simulated sunlight irradiation. The optimum mass loading ratio of MoS₂ in g-C₃N₄ was 1%, showing higher photocatalytic activity under simulated solar light in comparison with bare g-C₃N₄ and MoS₂ for both oxidation and reduction processes. Based on scavenging experiments a type-II photocatalytic mechanism is proposed. Finally, the catalysts presented satisfactory stability (7.8% loss) within three catalytic cycles. Such composite materials can receive further applications as well as energy conversion.

Photocatalysis is a prominent alternative wastewater treatment technique that has the potential to completely degrade pesticides as well as other persistent organic pollutants, leading to detoxification of wastewater and thus paving the way for its efficient reuse. In addition to the more conventional photocatalysts (e.g., TiO₂, ZnO, etc.) that utilize only UV light for activation, the interest of the scientific community has recently focused on the development and application of visible light-activated photocatalysts like g-C₃N₄. However, some disadvantages of g-C₃N₄, such as the high recombination rate of photogenerated charges, limit its utility. In this light, the present study focuses on the synthesis of WO₃ fibers/g-C₃N₄ Z-scheme heterojunctions to improve the efficiency of g-C₃N₄ towards the photocatalytic removal of the widely used insecticide clothianidin. The effect of two different g-C₃N₄ precursors (urea and thiourea) and of WO₃ fiber content on the properties of the synthesized composite materials was also investigated. All aforementioned materials were characterized by a number of techniques (XRD, SEM-EDS, ATR-FTIR, Raman spectroscopy, DRS, etc.). According to the results, mixing 6.5% ^W/_W WO₃ fibers with either urea or thiourea derived g-C₃N₄ significantly increased the photocatalytic activity of the resulting composites compared to the precursor materials. In order to further elucidate the effect of the most efficient composite photocatalyst in the degradation of clothianidin, the generated transformation products were tentatively identified through UHPLC tandem high-resolution mass spectroscopy. Finally, the detoxification effect of the most efficient process was also assessed by combining the results of an in-vitro methodology and the predictions of two in-silico tools.

In this study, the aqueous photolytic degradation of the neonicotinoid pesticide clothianidin was studied in suspensions and aqueous extracts of hydrochar produced from olive kernels. A slight and nonsignificant decrease in the photodegradation rate of clothianidin in aqueous extracts of hydrochar (HCw) with an initial concentration of hydrochar ranged from 50 to 400 mg L⁻¹ (rate constants ranged between k = 0.0034 and 0.0039 min⁻¹) was observed in comparison to the respective rate in the bi-distilled water (k = 0.0040 min⁻¹). On the contrary, in the presence of hydrochar suspensions (HCp), a significant decrease was observed for 50 mg L⁻¹ hydrochar particle concentration (k = 0.020 min⁻¹), while for higher concentrations (100 to 400 mg L⁻¹), rate constants increased but with nonsignificant differences compared with the kinetics followed in the absence of them. Generally, the photodegradation rate of clothianidin, in the presence of HCw and HCp, is reduced compared to the photodegradation rate in bi-distilled aqueous solutions, except in the case of the aqueous suspension with an HCp concentration of 200 mg L⁻¹. The transformation products (TPs) of clothianidin formed in the photolytic degradation processes were identified using ultrahigh-performance liquid chromatography coupled with accurate high-resolution mass spectrometry technique (UHPLC-LTQ-ORBITRAP). The formation profiles of TPs varied according to the matrix showing different degrees of participation of direct and indirect (photosensitized) phototransformation pathways. Photolytic degradation of clothianidin takes place mainly through denitration, hydroxylation and dechlorination pathways. Finally, the toxicity of the identified TPs was studied using the Vibrio fischeri bioassay. Toxicity was slightly reduced after 300 min of irradiation while maximum value was observed after 180–240 min of irradiation showing the formation of more toxic TPs along the photochemical degradation.

Conventional carbon-based electrodes like graphene are limited by costly, energy-intensive synthesis that rely on non-renewable precursors, challenging their scalability. While biomass-derived carbons (biochar) are a promising green alternative, achieving state-of-the-art performance typically requires chemical activation. Developing high-performance biochar through simple, scalable, and green pathways therefore remains a key challenge. In this work, we present a comprehensive physicochemical characterization of activation-free biochar derived from walnut, carob, rice husk and coffee via simple pyrolysis. Surface area, porosity and structural disorder were systematically analyzed to identify the key parameters governing ion interaction and charge storage. The results reveal a strong dependence of biochar properties on biomass type, with pronounced differences in accessible porosity and defect density. Among the materials studied, walnut-derived biochar combined a high specific surface area (1146 m²/g) with a high degree of structural disorder, highlighting the critical role of defects in enhancing ion adsorption and charge-transfer processes. Electrochemical measurements illustrated the functional implications of these intrinsic characteristics. Overall, this work demonstrates that carefully selected, unprocessed biomass can serve as a direct, low-cost source of functional carbon electrodes, providing insight into the parameters that dictate their electrochemical behavior and enable broader functional potential.