Photodegradation Efficiency Research Articles

Utilizing waste corn straw to photodegrade methyl orange and methylene blue: Photothermal effect of biochar enhances photodegradation efficiency

The burning of corn straw will cause serious air pollution, and the utilization of corn straw can avoid the burning of corn straw and reduce environmental pollution. The pyrolysis of corn straw into biochar (BC) is a promising approach to apply corn straw in environmentally sustainable development. Dye wastewater such as methyl orange (MO) and methylene blue (MB) is a pollution that poses a threat to human health and the environment. Herein, biochar/TiO2 (BC/TiO2) and biochar/ZnO (BC/ZnO) were prepared by pyrolysis of corn straw for the photodegradation of MO and MB in water. The MO removal rates of BC/TiO2 and BC/ZnO are up to 83.3 % and 76.2 %, respectively, and the MB removal rates of BC/TiO2 and BC/ZnO are 78.6 % and 71.4 %, respectively. The photothermal effect of BC improves the surface temperature of photocatalysts and promotes the separation and transfer of photogenerated electron-hole pairs, enhancing the photodegradation of MO and MB efficiencies. Three-dimensional (3D) FDTD simulations were performed to investigate the mechanism of photothermal effect in BC/TiO2 and BC/ZnO. This work provides a promising approach to the utilization of corn straw.

Construction of AgI/PCN-224 Z-scheme heterojunction for efficient photocatalytic degradation of tetracycline hydrochloride: Pathways, mechanism and theoretical calculations

The construction of heterojunction structures is pivotal in enhancing carrier separation and photocatalytic activity. Hence, AgI/PCN-224 (APN-x composites) Z-scheme heterojunctions were successfully synthesised using an in-situ precipitation method. The direction of electron migration and the band structures of APN-x were comprehensively investigated using a combination of experimental approaches and density functional theory (DFT) calculations. Owing to the extensive visible-light absorption capabilities of PCN-224 and the high efficiency of photogenerated carrier separation in the Z-scheme heterojunction, the optimally developed APN-3 photocatalyst demonstrated exceptional photodegradation efficiency for tetracycline hydrochloride (TCH). The removal rate of TCH by APN-3 within 120 min reached 91.56%, approximately 4.64 times higher than that achieved by pure AgI. The photocatalytic degradation mechanism was explored using free radical trapping experiments, electron spin resonance (ESR) technology and band structure analysis. Degradation pathways and intermediate products were investigated using liquid chromatography–tandem mass spectrometry (LC–MS).

Synergistic enhancement of simazine degradation using ZnO nanosheets and ZnO/GO nanocomposites: A sol-gel synthesis approach

This study aims to optimize the synergistic effect in photocatalytic processes by facilitating the accumulation of graphene oxide (GO) layers onto ZnO nanoparticles, thereby achieving close contact between the two materials, leveraging the high surface-to-volume ratio and efficient charge transport pathways inherent in ZnO nanosheets. The performance of ZnO nanosheets in the photocatalytic degradation of Simazine was investigated, with the aim of further enhancing the performance of the best-performing sample through GO decoration. Accordingly, ZnO nanosheets were obtained by the sol-gel method using different concentration of zinc acetate hexahydrate as a zinc source. According to the obtained results, it was observed that the sample prepared with a concentration of 0.44 M zinc precursor salt exhibited the best performance with a degradation rate of 67 %. In order to improve the performance of the sample prepared under this condition, graphene oxide (GO) was integrated into ZnO nanosheets to form a ZnO/GO nanocomposite structure. This composite structure achieved a photodegradation efficiency of 85 % for Simazine. The data obtained showed that the use of GO-based ZnO nanocomposites can improve charge separation, light absorption, charge transport and photo-oxidation of organic pollutants.

MoSe2 with Ultra-Fine Pt Decoration for Efficient Photodegradation

Transition metal dichalcogenides are widely studied for their photocatalytic ability due to the adjustable bandgap, high carrier mobility and possibility of foreign-element doping. In this work, multilayer molybdenum diselenide (MoSe2) was decorated with ultra-fine Pt nanoparticles through the mild hydrothermal method. MoSe2-Pt nanocomposites were synthesized and showed good structural and chemical stabilities. The incorporation of Pt nanoparticles provides plenty of active sites for MoSe2. The dominant Pt particle sizes are 1.8 nm, 1.8 nm, and 1.9 nm for the three synthesized samples, respectively. The mean crystal sizes of Pt (111) were calculated from X-ray diffraction patterns and we found that they were in accordance with the particle sizes. Both the particle sizes and mean crystal sizes are related to the synthesis conditions. X-ray photoelectron spectroscopy (XPS) characterizations revealed the formation of Se–Pt bonding. The relative contents of Pt–Se bonding were also calculated from XPS results, and they show the same trends as the optical absorption properties. Combining the XPS and optical absorption results, the effects of Se–Pt bonding during the photo-related process could be further confirmed. By degrading methylene blue (MB) under visible light, the synthesized nanocomposites proved promising for application in real-case degradation of organic pollutants. The sample synthesized with a moderate content of MoSe2 exhibited the best photodegradation efficiency, which could be explained by the maximum Pt-Se contents. Based on the experimental findings, we proposed a possible photodegradation mechanism.

Polyaniline-supported g-C3N4/ZnO/Ag2CrO4 composite for photodegradation of methylene blue under visible light irradiation

Organic dyes are a major source of environmental pollution from different industries. To remove these recalcitrant, a novel ternary g-C3N4/ZnO/Ag2CrO4 and its polyaniline-supported (PANI) composites were synthesized using an “in situ” oxidative polymerization approach. XRD, SEM, UV–Vis DRS, and PL techniques were utilized to characterize the as-prepared composites. The photocatalytic efficiency was evaluated using a model organic pollutant, methylene blue (MB), and samples of the effluent of the textile industry. The as-synthesized ternary g-C3N4/ZnO/Ag2CrO4 (ZT3= 87.87 %) composite showed better photocatalytic performance than the single (5 %) and binaries (15–25 %) counterparts for MB degradation. The influence of various experimental settings on the photodegradation of MB dye was examined and these were an initial dye amount of 10 ppm, photocatalyst load of 0.15 g/L, and pH 10. Under optimized conditions, PANI-supported g-C3N4/ZnO/Ag2CrO4 composite (PAST) demonstrated substantial degradation efficiency (97.5 %). The reusability study of the spent catalyst revealed a reduced efficiency from 97.5 to 78.5 % photodegradation of MB after four successive cycles, demonstrating the photocatalyst's stability and efficiency. According to the study on the effect of scavengers, h+ plays a significant part in the discoloration of MB. The PAST photocatalyst outperformed the MB discoloration (97.5 %) and adequate degradation for real textile effluent samples (77.7 %) collected from Hawassa textile industries. The photodegradation efficiency result of this study demonstrated that PANI-supported g-C3N4/ZnO/Ag2CrO4 might serve as an advantageous photocatalyst for the efficient removal of MB and other dyes under visible light irradiation at the optimum conditions. The total estimated cost analysis of synthesis and photocatalytic degradation using Polyaniline-supported g-C3N4/ZnO/Ag2CrO4 composite found that it was quite affordable, costing around $5 per 1,000 L of wastewater treatment.

Novel CQDs/BiOI Microspheres with Gradient Oxygen Vacancies for Efficient Photocatalytic Performance Boosting by the Synergism of Reactive Oxygen and Iodine Species

AbstractThe synergy of reactive oxidative species (ROSs: ⋅OH, ⋅O2− and 1O2) and reactive iodine species (RISs: ⋅I and ⋅I2−) is conclusive to driving organic pollutant degradation in various aquatic environments. Over the past years, rational design of Vis‐NIR responsive photocatalyst with enhanced photocatalytic performance has attracted drawing attention. Herein, CQDs/BiOI composites with up‐conversion photoluminescence (UCPL) properties and oxygen vacancies was constructed for tetracycline (TC) and oxytetracycline (OTC) degradation. The apparent kinetic constant of the 4‐CQDs/BiOI is 2.13 and 2.38 times on pure BiOI. The excellent photodegradation efficiency can be attributed to the enhanced light absorption originated from the up‐conversion property and improved charge separation efficiency. Furthermore, the iodine free radicals (⋅I) and superoxide free radicals (⋅O2−) played a crucial role in the photodegradation procedure. I− from BiOI could be partially oxidized to form ⋅I. At the same time, the electron capture traps formed by Oxygen vacancies can promote the production of ⋅O2−. Remarkably, the removal efficiency of TC and OTC was still maintained at 80 % by 4‐CQDs/BiOI under different water quality conditions due to the synergy of ⋅O2− with ⋅I. This work sheds light on a new treatment for the synergistic degradation of pollutants in complex water by RISs and ROSs.

Basic magnesium sulfate@TiO2 composite for efficient adsorption and photocatalytic degradation of 4-dodecylmorpholine in brine

More than 70% of the potash fertilizer globally is produced by the froth flotation process, in which 4-dodecylmorpholine (DMP) serves as a reverse flotation agent. As the potash fertilizer production rapidly rises, the increased DMP levels in discharged brine pose a threat to the production of high-value chemicals. In this paper, composite particles of basic magnesium sulfate@TiO2 (BMS@TiO2) were prepared using a simple and mild loading method. These particles were utilized for the adsorption and photocatalytic degradation of DMP in brine. Compared with normal powdered materials, the granular BMS@TiO2 in this study can be easily separated from liquid, and the degradation intermediates will not enter the brine without causing secondary pollution. BMS@TiO2 consists of 5·1·7 phase (5Mg(OH)2·MgSO4·7H2O) whisker clusters embedding 2.3% TiO2. The adsorption equilibrium of DMP on BMS@TiO2 particles was achieved through hydrogen bonding and pore interception with the adsorption capacity of approximately 5 mg g−1 after 6 h. The photodegradation efficiency of DMP adsorbed on BMS@TiO2 reached about 92% within 16 h, which is compared with that of pure TiO2 nanoparticles. Additionally, excellent stability and recyclability of BMS@TiO2 were also observed in five cycle tests of adsorption and photocatalytic degradation of DMP, and the possible photocatalytic degradation pathways and mechanism of DMP are proposed following molecular electrostatic potential analysis. This work provides a sustainable and environmentally friendly approach for eliminating organic micropollutants from water environments.

Synthesis and application of Cu-CaTiO3-GO ternary composite: A new visible-light active multifunctional photocatalyst efficient towards antibiotic cefixime degradation and H2 evolution reaction

To combat the issues of energy scarcity and environmental pollution, a visible-light responsive, ternary photocatalyst (Cu-CaTiO3-GO) was fabricated, by photo-depositing Cu nanoparticles over a CaTiO3-GO binary composite. The physicochemical characteristics of Cu-CaTiO3-GO were investigated using XRD, HR-TEM, FE-SEM, EDS-mapping XPS, Raman, FT-IR, BET, EIS, UV–vis DRS, and PL techniques. In comparison with pristine CaTiO3, and binary composites (Cu-CaTiO3, CaTiO3-GO), the ternary hybrid exhibited superior photocatalytic activity for H2generation as well as antibiotic cefixime (CFX) degradation. Under LED light, the rate of H2 generation over Cu-CaTiO3-GO accumulated to 57.69 mmolh−1, while the photodegradation efficiency for CFX reached 94.1 % in 100 min with 53.4 % of TOC removal. The upgraded performance is credited to synergistic effects of Cu NPs (SPR effect), CaTiO3 (specialized cuboid-like morphology), and GO (high conductivity), co-existing in the trio-hybrid, which resulted in a greatly increased surface area, an expanded spectral response range, a stronger adsorption property, efficient charge migration and separation extent. Ternary catalyst performed well even in the 4 recycling tests (retaining 79.4 % CFX removal and 52.51 mmolh−1 H2 evolution efficiency). In Cu-CaTiO3-GO system, the electron transport channel (Cu → CaTiO3 → GO) with adequate band potentials effectively supports both photocatalytic oxidation and reduction. Photoelectrons are enriched and transferred by plasmonic Cu, and then captured by GO, an e- sink. This maximizes composite photo redox capability, rapidly generating active radicals (OH), and (O2-), degrading CFX to simpler molecules and reducing proton to H2. The effectiveness of Cu-CaTiO3-GO was even tested in the real water matrices. Besides, degradation intermediates of CFX were elucidated using LC-MS, and the decomposition pathway was suggested. Finally, the probable photocatalytic reaction mechanism was deduced for both the degradation and H2 generation processes. The current study proposes a non-noble transition metal-based perovskite-type photocatalytic material for both clean energy generation and wastewater treatment.

A Novel Z-type 0D/2D BiOCl/NiAl-LDH heterojunction for photodegradation of multiple antibiotics in industrial wastewater: Degradation pathways and toxicity analysis

In this paper, two metal compounds were combined and successfully prepared a Z-type BiOCl/NiAl-LDH(B/NL) heterojunction for the degradation of various antibiotics in industrial wastewater under visible light. The optical properties and photocatalytic activity of B/NL can be adjusted by varying the amount of NiAl-LDH. In the simulated degradation of tetracycline (TC) under visible light, B/NL-11 showed the best photodegradation efficiency, with a degradation rate of 92.57 % within 100 min. By using catalytic materials to degrade industrial wastewater, the degradation rate of tetracycline antibiotics (tetracycline, oxytetracycline) is more than 70 %, and the degradation rate of quinolone antibiotics (ciprofloxacin, norfloxacin) is more than 50 %. Mineralization process of the B/NL-11 system to degrade antibiotics in industrial wastewater was evaluated by 3D EMMS technology, and the degradation pathways were analyzed by LC-MS. The toxicity of the intermediate products produced is much lower than that of the pollutants themselves, and there is no secondary pollution. The degradation activity of BiOCl/NiAl-LDH is due to the construction of heterojunction adds many active sites, and the formed band structure promotes the efficient separation and transfer of photogenerated electron-holes. The free radical trapping experiment proved that h+, ∙O2−, ∙OH was the main active substance in the degradation process, and finally proposed the Z-type heterojunction mechanism.

Protonated g-C3N4/oxygen-doped g-C3N4 S-scheme homojunction fabricated by electrostatic self-assembly for photocatalytic hydrogen evolution and tetracycline hydrochloride degradation

S-scheme photocatalytic systems with high redox ability and separation efficiency of photoexcited charge carriers supply considerable prospects for environmental optimization and sustainable energy development. However, coupling well-suited reduction and oxidation components for target reactions remains a challenge worth exploring. Herein, an efficient S-scheme system for H2 generation and tetracycline hydrochloride (TCH) photodegradation based on protonated g-C3N4 (PCN) coupling with oxygen-doped g-C3N4 (OCN) is fabricated via a facile electrostatic self-assembly strategy. Intimate interfacial interactions originating from the ultrathin nanostructure and staggered energy band arrangement for the S-scheme charge transfer pathway provide compelling advantages for the highly efficient separation of photoinduced electron-hole pairs in the as-designed PCN/OCN homojunction. The in-situ irradiated X-ray photoelectron spectroscopy (ISI-XPS) techniques and electron paramagnetic resonance (EPR) measurements are applied to confirm the successful construction and the validity of the S-scheme charge transfer pathway. The obtained PCN/OCN composites with optimal ratio achieve a decent H2 generation rate of 6184.7 μmol g−1 h−1 outpacing the single PCN by approximately 4.8-fold, and 90.5 % TCH photodegradation efficiency is also realized within 90 min. This work provides a delicate fresh round of elevation for the exploration of an effective photocatalytic system.

Facile synthesis of nano CeO2/sepiolite composite as visible-light-driven photocatalyst for rapid tetracycline removal

A novel CeO2/sepiolite (CeO2/SEP) composite with sepiolite as the support of CeO2 was successfully prepared using a simple ammonia precipitation method for the photocatalytic degradation of tetracycline (TC) by loading CeO2 nanoparticles on sepiolite. The analytical results showed that CeO2/SEP had good crystallization, and CeO2 nanoparticles were deposited on the surface of fibrous sepiolite. The composite photocatalyst with 50 % CeO2 loading presented the highest tetracycline degradation efficiency (92.7 %), and the reaction rate constant was 4.88 times greater than that of pure CeO2. In addition, quenching experiments showed that the main reactive active species included photogenerated holes (h+) and superoxide radical anions(O2·-).Furthermore, the enhanced photodegradation mechanisms and the possible degradation pathways of TC were also systematically discussed. The investigating results show that the enhanced photocatalytic performance was mainly due to the uniform attachment of CeO2 with smaller particle size on the surface of sepiolite, which increased the specific surface area of the photocatalyst and promoted the redox cycle of Ce3+/Ce4+ to generate more reactive free radicals. It can be concluded that this study offers a new potential option for efficient photodegradation of antibiotics in wastewater based on the visible-light-driven mineral based photocatalyst.

Accelerated photodegradation of T-2 toxin over magnetic recyclable ZnO/CaFe2O4 nanocomposite with a p-n based Z-scheme heterojunction architecture

T-2 toxin (T-2), one of the most toxic mycotoxins, has drawn extensive attention due to its universality and persistence in food and the environment. In this study, a novel magnetic ZnO/CaFe2O4 nanocomposite with a p-n based Z-scheme heterojunction was successfully constructed by a hydrothermal method for efficient photodegradation of T-2 toxin. The optimal cubic structure of ZnO/CaFe2O4 endows it with excellent photocatalytic efficiency in removing T-2 toxin, such that near-total degradation was achieved with an exceptionally high mineralization value (64 %) after 180 min of UV radiation. This efficacy was attributed not only to the abundant reaction sites on the binary composites, but also its Z-scheme heterojunction promoting the electron-hole (e−-h+) separation and hence favors redox processes. The OH played a major role in the photodegradation, and the decomposition pathway of T-2 was proposed based on the results of UHPLC-Q-TOF-MS/MS data and density functional theory (DFT) calculations. This work provided a green approach for removing the refractory natural pollutants.

Effect of Heating Power on The Synthesis of Titanium Dioxide Particles by Direct Heating Method for Photodegradation of Methylene Blue Solution

Dyes are extensively used in the textile industry. Untreated dye-containing wastewater is hazardous to humans and the environment. Advanced oxidation processes (AOPs) based on heterogeneous TiO2photocatalyst is a technology that has been proven successful for effluent treatment. Nevertheless, use of TiO2 photocatalyst in particles form could result in loss of TiO2 photocatalyst over time during effluent treatment. Immobilization of TiO2 photocatalyst on substrates could address this problem. In this study, a method called direct heating (DH) was devised to deposit TiO2 particles on kanthal wires to prevent the particles from being washed away during effluent treatment. This method has low equipment cost and short synthesis duration when compared to others. The TiO2 particles synthesized at 50 W in 15 min gave the best photodegradation efficiency, which was 36.3 % under 90 mins of UV light irradiation. It contained a mixture of anatase (22.5 %) and brookite (77.5 %), with an average particle size of 139.34 ± 15.89 nm. The TiO2 particles had high surface coverage on kanthal wire with little agglomeration. The current work presents a captivating and low-cost setup, providing easy control over synthesis conditions and scaling potential for immobilizing TiO2 particles on the kanthal wires.

Fabrication of Catechol Sensitized Hollow Microspheres ZnTiO3/TiO2/ZnO for the Photodegradation of Methylene Blue

AbstractDesigning new materials that can be used to treat environmental pollutants is one of the prime focuses of chemical science. Here, an unprecedented photocatalytic material with high activity of catechol sensitized ZnTiO3/TiO2/ZnO hollow microspheres was synthesized by hydrothermal method. The structure and properties of the composite photocatalyst were analyzed by various testing methods. The photocatalytic activity was evaluated by using methylene blue (MB) as the target degradation substance. The results demonstrated that catechol (CA) sensitized ZnTiO3/TiO2/ZnO photocatalyst is a hollow microsphere with a diameter of 1–1.5 mm, the CA molecules are covalently bonded to the ZnTiO3/TiO2/ZnO surface, and the composite photocatalyst has good light absorption and carrier separation performance. Under the condition of irradiation for 90 min, the degradation rate of the composite photocatalyst for MB was higher than that of ZnTiO3/TiO2/ZnO. When the loading amount of CA was 0.6 wt%, the degradation rate of CA/ZnTiO3/TiO2/ZnO for MB was as high as 98.28 %, and the reaction rate constant was up to 4.35×10−2 min−1. A reasonable mechanism of photocatalytic degradation of pollutants by catechol as sensitizer on ZnTiO3/TiO2/ZnO was proposed. This study provides a theoretical reference for efficient photodegradation of pollutants in the environment.

Enhancing charge transfer in 0D/2D cobalt sulfide/boron-doped graphitic carbon nitride heterojunction photocatalyst for degradation of organic pollutants under LED illumination

Semiconductor-based photocatalytic processes are widely applied as ecofriendly technology for degrading organic pollutants. Establishing photocatalytic heterojunctions with Z-type photocarriers transfer pathways is projected to be a superb strategy to enhance photocatalytic behavior. In this paper, novel and stable (0D/2D) heterojunctions of CoS-embedded boron-doped g-C3N4 (CoS/BCN) with a high rate of charges transfer/separation were assembled for degradation of malachite green dye (MG). The CoS/BCN photocatalyst achieves a photodegradation efficiency of 96.9 % within 1 h of LED illumination, which is 2.5 and 1.4-fold enhancement compared with bare g-C3N4 and BCN, respectively. Besides, the results of species-trapping trials exhibited that •O2− and at a lower degree, photogenerated holes were mainly in charge of the boosted performance. In light of the above results of the trapping experiments, the charge transfer mechanism was discussed, and the Z-form heterojunction between BCN and CoS was taken as the reason for enhancing the photocatalytic efficiency. The stability of the CoS/BCN hybrid was also checked, showing excellent photostability performance after five degradation rounds.

Experimental and numerical study of photocatalysis in Taylor photoreactors with carbon-quantum-dots/BiOCl as catalysts

A comprehensive CFD model considering the photo radiation, discrete phase dispersion, flow behaviors and photoreactions was built for Taylor‐Couette reactors (TCRs). The carbon quantum dots (CQDs) modified BiOCl composites which were responsive to visible light were synthesized and used as the catalysts for photodegradation of organic pollutants. The degradation kinetic parameters were obtained experimentally. The validated model was used to investigate the effects of the key parameters of TCRs such as rotation speed, light intensity and catalyst properties. The interactions among the photo radiation field, catalyst distribution, flow field, and degradation efficiency were discussed. The results showed the addition of 8 ωt % CQDs/BiOCl enhanced the degradation efficiency to 97% as compared to pure BiOCl, while the catalyst dosage had a limited impact on degradation performance. This work provides engineering insights in the CQDs-based photocatalysis, and the proposed model can serve as an effective tool for the design and scale-up of the TCRs.

Visible Light-Induced Photocatalytic Degradation of Methylene Blue Using Copper-Doped Carbon Dots One-Step Derived from CCA-Wood

Developing novel eco-friendly broad-spectrum visible light photocatalysts for dye removal is one of the urgent problems for water treatment. Here, copper-doped carbon dots (CDs) were reported to be directly fabricated from chromated copper arsenate (CCA) wood waste for the photocatalytic degradation of the methylene blue dye. The properties of the resulting CDs were thoroughly characterized and analyzed, preceding an investigation into the adsorption kinetics of dye degradation. The kinetic study showed that reactant concentration was the rate-limiting factor. The obtained CDs showed a 151 mg/g photocatalytic degradation capacity. Comparing pure CDs to CDs/TiO2 composites, the former demonstrated higher photodegradation efficiency. This superiority can be attributed to the synergistic action of adsorption and photocatalytic degradation working in tandem. This study prepared Cu doped CDs and elucidated the photocatalysis mechanism of methylene blue degradation by CDs. The photodegradation of organic dyes through CDs derived from waste CCA wood emerges as an eco-friendly, facile, and highly efficient method.

Fabrication of Ag-decorated La0.9Ag0.1FeO3 for efficient photocatalytic degradation of tetracycline under visible light with the assistance of water oxidation

The photocatalytic conversion of molecular O2 into reactive oxygen species, such as superoxide radicals (·O2-), has become the focus in the oxidative removal of organic pollutants. Nevertheless, the inefficient light absorption, limited adsorption of O2, and the fast recombination rate of photo-induced electron-hole pairs considerably impede the conversion efficiency of the photocatalysts. Herein, we report the synthesis of Ag@LAFO photocatalyst, which contains Ag nanoparticles (NPs)-decorated LAFO (Ag-substituted LaFeO3), to enhance the photodegradation efficiency of tetracycline (TC) with the assistance of water oxidation. Structural and spectroscopic analyses confirmed the successful decoration of Ag NPs on LAFO, which was prepared by substituting 10 % La with Ag. The efficiency of TC photocatalytic degradation rate of Ag@LAFO is 76.25 %, which is 6.1-fold higher than that of pure LFO (12.41 %). The trapping experiment of active radicals verified that ·O2- was crucial in the decomposition of TC molecules and was continuously supplied by the reduction of O2 molecules supported by photocatalytic water oxidation. Moreover, the Ag NPs in Ag@LAFO were found to be crucial for boosting the capture of photo-induced electrons and the activation of adsorbed O2. This study offers a new perspective on the conversion of O2 to ·O2- with the assistance of photocatalytic water oxidation for photocatalytic degradation of organic pollutants.

BiOBr/Cu2S p-n heterojunction for efficient photodegradation of ciprofloxacin and tetracycline under visible light

With the increasing needs of people for a better life, the problem of water resources pollution has attracted wide attention. The construction of p-n heterojunction is an effective strategy to promote the removal of pollutants by photocatalysts. In this work, a series of BiOBr/Cu2S heterojunction photocatalysts with mass ratios of Cu2S have been synthesized successfully by a hydrothermal method combined with grinding method for photocatalytic degradation of tetracycline (TC) and ciprofloxacin (CIP). The results showed that BiOBr/Cu2S exhibited superior photodegradation efficiency of TC and ciprofloxacin CIP than BiOBr and Cu2S monomers. When the mass ratio of Cu2S is 0.15 %, the visible degradation of CIP and TC are 79.2 % in 90 min and 88.5% in 60 min. In addition, the effects of different inorganic ions and pH value on the photocatalytic performance of BiOBr/Cu2S were investigated. It was proved that superoxide free radical (•O2-) was the main active species by free radical trapping experiment. The photocatalytic degradation process was further evaluated by total organic carbon and mass spectrometry tests. This work provides a feasible construction strategy for photocatalysts with potential application in water resources pollutants.

CdIn2Se4@chitosan heterojunction nanocomposite with ultrahigh photocatalytic activity under sunlight driven photodegradation of organic pollutants

This research focused on synthesizing a CdIn2Se4@Ch nanocomposite by doping CdIn2Se4 into chitosan using a photolysis assisted ultrasonic process. The aim was to enhance the photodegradation efficiency of ofloxacin and 2,4-dichlorophenoxyacetic acid under sunlight. The synthesized CdIn2Se4@Ch nanocomposite was investigated via different techniques, including XRD, XPS, FTIR, TEM, DSC, TGA, UV–Vis and PL. The study also investigated the influence of various reaction parameters, including the effects of inorganic and organic ions. The synthesized nanocomposite demonstrated exceptional efficiency, achieving 86 % and 95 % removal rates, with corresponding rate constants of 0.025 and 0.047 min-1. This performance surpasses that of CdIn2Se4 by approximately 1.35 and 2.25 times, respectively. The values of COD were decreased to 78 and 86 % for ofloxacin and 2,4-dichlorophenoxyacetic, while the TOC values decreased to 71 and 84 %, respectively, from their premier values. The improvement in performance is associated with the introduction of CdIn2Se4 into chitosan, resulting in the self-integration of Cd into the catalyst. This creates a localized accumulation point for electrons, enhancing the efficiency of charge separation and further reducing the surface charge of chitosan. Experimental evidence suggests that superoxide and hydroxyl radicals play a significant role in the photodegradation of pollutants. Additionally, the nanocomposite exhibits excellent stability and can be reused up to five times, indicating remarkable stability and reusability of the developed photocatalyst.