Developing a low-cost and highly efficient semiconductor photocatalyst for the decomposition of organic pollutants and antibiotics is highly desirable. Herein, FeOOH nanosheets were prepared using a liquid-phase stirring technique and combined with ZnCdS (ZCS) nanoparticles to construct FeOOH/ZCS nanocomposite photocatalysts. The photocatalytic efficiency of the FeOOH/ZCS nanocomposite was evaluated for the decomposition of various pollutants, including rhodamine B, methylene Blue, and tetracycline. The FeOOH/ZCS nanocomposite exhibited significantly higher photocatalytic performance for the decomposition of various organics. Moreover, the optimized FeOOH/ZCS retained more than 90% of its initial photocatalytic activity even after five successful runs. Radical quenching test and electron spin resonance (ESR) analysis revealed that hydroxyl radicals (•OH) play a dominant role for the decomposition of organics. The FeOOH/ZCS Z-scheme heterojunction significantly facilitates higher charge transfer efficiency and the generation of reactive radicals, resulting in excellent photocatalytic degradation performance. This work offers a new approach to synthesis FeOOH-based photocatalyst for the elimination of organics and antibiotics in water.

In this study, S-doped graphitic carbon nitride (S-C3N4) was prepared using the high-temperature polymerization method, and then S-C3N4/AgCdS heterojunction photocatalyst was obtained using the chemical deposition method through loading Ag-doped CdS nanoparticles (AgCdS NPs) on the surface of S-C3N4. Experimental results show that the AgCdS NPs were evenly dispersed on the surface of S-C3N4, indicating that a good heterojunction structure was formed. Compared to S-C3N4, CdS, AgCdS and S-C3N4/CdS, the photocatalytic performance of S-C3N4/AgCdS has been significantly improved, and exhibits excellent photocatalytic degradation performance of Rhodamine B and methyl orange. The doping of Ag in collaboration with the construction of a Z-scheme heterojunction system promoted the effective separation and transport of the photogenerated carriers in S-C3N4/AgCdS, significantly accelerated its photocatalytic reaction process, and thus improved its photocatalytic performance.

Carbon felt was used as the anode and WO3/MoS2/FTO (fluorine-doped tin oxide) was used as the photocathode in a photocatalytic microbial fuel cell (PMFC). The photoelectric performance of the WO3/MoS2/FTO photocathode and the removal efficiency of methylene blue (MB) and Cr(VI) mixed pollutants were systematically investigated in the cathode chamber. The results showed that after 12 h of light irradiation in the PMFC with WO3/MoS2/FTO as the photocathode, the removal rates of MB and Cr(VI) were 84.56 and 68.11 %, respectively, which were much higher than those using WO3/FTO as a photocathode (55.57 % and 45.26 %, respectively). The corresponding maximum output power was 33.14 mW/m2, which was 1.85 times that of the WO3/FTO photocathode PMFC. These results can be attributed to the fact that WO3 is an n-type semiconductor and MoS2 is a p-type semiconductor. Analysis of trapping experiments showed that the composite of WO3 and MoS2 formed a Z-scheme heterojunction, which improved the separation efficiency of the photoelectric carriers and enhanced the pollutant removal efficiency of the photocathode. PMFCs are a new and environment-friendly technology for removing pollutants thereby providing an experimental basis for future engineering applications.

Antibiotics cannot be effectively removed by traditional wastewater treatment processes, and have become widespread pollutants in various environments. In this study, a Z-type heterojunction photo-catalyst Pg-C3N4 (PCN)/Nitrogen doped biochar (N-Biochar)/BiVO4 (NCBN) for the degradation of norfloxacin (NOR) was prepared by the hydrothermal method. The specific surface area of the NCBN (42.88 m2/g) was further improved compared to BiVO4 (4.528 m2/g). The photo-catalytic performance of the catalyst was investigated, and the N-Biochar acted as a charge transfer channel to promote carrier separation and form Z-type heterojunctions. Moreover, the NCBN exhibited excellent performance (92.5%) in removing NOR, which maintained 70% degradation after four cycles. The main active substance of the NCBN was •O2-, and the possible degradation pathways are provided. This work will provide a theoretical basis for the construction of heterojunction photo-catalysts.

Efficient separation of electron-hole pairs remains pivotal in optimizing photogenerated carrier functionality across diverse catalytic and optoelectronic systems. This study presents the fabrication of a novel hollow direct Z-scheme photocatalyst, ZnO/TiO2. A thorough analysis encompassing various techniques such as Ultraviolet-Visible Spectroscopy (UV-Vis), X-ray Diffraction (XRD), Transmission electron Microscopy (TEM), Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric Analysis (TGA), and Energy-Dispersive X-ray Spectroscopy (EDX) provided detailed insights into the complex material characteristics of the ZnO/TiO2 heterojunction catalyst. The findings revealed coexisting anatase TiO2 and wurtzite ZnO phases, each retaining distinct attributes within the nanocomposites (NCs) structure. The study showcased the photocatalytic efficacy of ZnO/TiO2-NCs in decomposing Methylene Blue and Acridine Orange under UV irradiation, correlated with their underlying structures. Enhanced degradation of these dyes resulted from the establishment of a direct Z-scheme heterojunction between ZnO and TiO2. Employing Density Functional Theory (DFT) using Quantum ESPRESSO, this research analyzed phase diagrams and band structures, elucidating electronic properties and structural correlations. The study characterized a ZnO/TiO2 composite, revealing a band gap of 3.1-3.3 eV through UV-Visible spectroscopy and confirming its formation without impurity phases via XRD analysis. TEM and EDX showed uniform element dispersion (Zn: 27%, Ti: 29.62%, C: 5.03%, O: 38.35%). Computational analysis using DFT indicated a reduction in stable phases with increasing temperature. Enhanced dye degradation was observed (MB: 88.9%, AO: 84%), alongside significant antibacterial activity. In the future we predict that research will focus on development of scaled up production and photocatalytic activity through surface modification, while unveiling mechanistic insights and environmental applicability for multifunctional use in water treatment and antibacterial applications, leading to further advancement of the field.

Water pollution has becoming an increasingly serious issue, and it has attracted a significant amount of attention from scholars. Here, in order remove heavy metal hexavalent chromium (Cr (VI)) from wastewater, graphitic carbon nitride (g-C3N4) was modified with molybdenum disulfide (MoS2) at different mass ratios via an ultrasonic method to synthesize g-C3N4/MoS2 (CNM) nanocomposites as photocatalysts. The nanocomposites displayed efficient photocatalytic removal of toxic hexavalent chromium (Cr (VI)) from water under UV, solar, and visible light irradiation. The CNM composite with a 1:2 g-C3N4 to MoS2 ratio achieved optimal 91% Cr (VI) removal efficiency at an initial 20 mg/L Cr (VI) concentration and pH 3 after 120 min visible light irradiation. The results showed a high pH range and good recycling stability. The g-C3N4/MoS2 nanocomposites exhibited higher performance compared to pure g-C3N4 due to the narrowed band gap of the Z-scheme heterojunction structure and effective separation of photo-generated electron-hole pairs, as evidenced by structural and optical characterization. Overall, the ultrasonic synthesis of g-C3N4/MoS2 photocatalysts shows promise as an efficient technique for enhancing heavy metal wastewater remediation under solar and visible light.

In the presented work, heterostructured nanocomposites based on g-C3N4 and PrFeO3 with different mass content of PrFeO3 (0-10 wt%) were prepared by ultrasonic processing to study their photocatalytic activity in the process of antibiotic degradation under visible light. The study of phase composition, structural, morphological and textural characteristics carried out by powder X-ray diffraction, scanning electron microscopy and adsorption-structural analysis confirmed the presence of two phases - graphite-like C3N4 and orthorhombic PrFeO3 with average crystallite sizes of 5 and 21 nm and mesoporous structure with specific surface area of 57.2-68.6 m2/g and average pore size of 20 nm. The measured values of the forbidden bandwidth for the obtained nanocomposites were ∼3 eV, indicating potential activity under visible light irradiation. The efficiency of antibiotic removal under visible light was evaluated in the degradation of TCHCl. It was found that 5 % PrFeO3 content was optimal and increased the TOF by 5 times compared to pure g-C3N4. The results of photocatalytic test with absorbers showed that photocatalysis occurs by Z-scheme mechanism. The results obtained allow us to consider this nanocomposite as an effective and stable photocatalyst for pharmaceutical wastewater treatment.

Porous carbon nitride/bismuth oxychloride (PCN/BiOCl-x) polymer-based heterojunction photocatalysts were successfully synthesized via a simple in situ hydrothermal method. A PCN/BiOCl heterojunction with rich chlorine defects is prepared by adjusting the chlorine content of the BiOCl unit in the heterojunction by changing the solvent. The as-prepared catalysts were characterized via BET, SEM, TEM, XRD, XPS and optical testing, and they were used for a photocatalytic amine oxidation reaction. The results indicated that the catalytic performance of the PCN/BiOCl heterojunction was significantly enhanced due to the rich chlorine vacancies in the samples. The enhanced catalytic activity may be attributed to the Z-scheme heterojunction, abundant chlorine defects and large specific surface area. At the same time, the catalyst circulation experiment shows that the PCN/BiOCl heterojunction has good circulation performance.

Z-scheme Bi2MoO6/Bi5O7I heterojunction was constructed by an in situ solvothermal method, which was composed of Bi2MoO6 nanosheets growing on the surface of Bi5O7I microrods. The antibacterial activities under illumination towards Escherichia coli (E. coli) were investigated. The Bi2MoO6/Bi5O7I composites exhibited more outstanding antibacterial performance than pure Bi2MoO6 and Bi5O7I, and the E. coli (108 cfu/mL) was completely inactivated by BM/BI-3 under 90 min irradiation. Additionally, the experiment of adding scavengers revealed that h+, •O2- and •OH played an important role in the E. coli inactivation process. The E. coli cell membrane was damaged by the oxidation of h+, •O2- and •OH, and the intracellular components (K+, DNA) subsequently released, which ultimately triggered the apoptosis of the E. coli cell. The enhanced antibacterial performance of Bi2MoO6/Bi5O7I heterojunction is due to the formation of Z-scheme heterojunction with the effective charge transfer via the well-contacted interface of Bi2MoO6 and Bi5O7I. This study provides useful guidance on how to construct Bi5O7I-based heterojunction for water disinfection with abundant solar energy.

Building heterojunctions is a promising strategy for the achievement of highly efficient photocatalysis. Herein, a novel SnIn4S8@ZnO Z-scheme heterostructure with a tight contact interface was successfully constructed using a convenient two-step hydrothermal approach. The phase composition, morphology, specific surface area, as well as photophysical characteristics of SnIn4S8@ZnO were investigated through a series of characterization methods, respectively. Methylene blue (MB) was chosen as the target contaminant for photocatalytic degradation. In addition, the degradation process was fitted with pseudo-first-order kinetics. The as-prepared SnIn4S8@ZnO heterojunctions displayed excellent photocatalytic activities toward MB degradation. The optimized sample (ZS800), in which the molar ratio of ZnO to SnIn4S8 was 800, displayed the highest photodegradation efficiency toward MB (91%) after 20 min. Furthermore, the apparent rate constant of MB photodegradation using ZS800 (0.121 min-1) was 2.2 times that using ZnO (0.054 min-1). The improvement in photocatalytic activity could be ascribed to the efficient spatial separation of photoinduced charge carriers through a Z-scheme heterojunction with an intimate contact interface. The results in this paper bring a novel insight into constructing excellent ZnO-based photocatalytic systems for wastewater purification.