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This study aims to elucidate the possible application of cobalt aluminate nanoparticles (CoAl 2 O 4) as a photocatalyst for the removal of organic dyes. The sol-gel method was employed to synthesise Nd x /CoAl 2 O 4 nanoparticles with varying weight percentages (x = 0.0, 0.2, 0.4, and 0.6 wt %). The experimental investigation focused on the photocatalytic destruction of colour, employing a visible light irradiation source. The structural and optical properties of the synthesised nanoparticle were examined through various analytical techniques, including X-Ray Diffraction (XRD), Ultra Violet-Diffuse Reflectance Spectroscopy (UV-DRS), Scanning Electron Microscopy (SEM), Energy-Dispersive X-ray spectroscopy (EDX), Tunnelling Electron Microscopy (TEM), and X-ray Photoelectron Spectroscopy (XPS). The cubic spinel structure was confirmed through the study of the X-ray diffraction (XRD) pattern of the Nd x /CoAl 2 O 4 nanoparticles. For the compositions x = 0.0, 0.2, 0.4, and 0.6, the nanoparticles exhibited average crystallite sizes of 23.73, 22.99, 21.69, and 21.65 nm, respectively. The synthesised nanoparticle exhibited heterogeneous photocatalytic potential when employed as a model pollutant for the oxidative destruction of crystal violet dye. The experimental findings validated that the CoAl 2 O 4 nanoparticle exhibited a dye degradation rate of 64 % during a 100-min timeframe. Additionally, the 0.6 wt % Nd CoAl 2 O 4 nanoparticle shows a quick dye degradation rate of 91 % for crystal violet dyes when exposed to visible light sources. Hence, the synthesised nanoparticle exhibits catalytic activity and holds potential for utilisation in the treatment of hazardous contaminants in industrial wastewater. [ABSTRACT FROM AUTHOR]

Environmental remediation evinces sensitive detection and elimination of contaminants from the environment. Recent investigations delineate nanomaterials as potentially useful agents in environment remediation. In this investigation, we have developed multifunctional CdO‐ZnO nanocomposite (NCs) for efficient degradation of organic dyes and sensitive detection of nitrite ions which also exhibits excellent luminescence and antioxidant properties. The CdO‐ZnO NCs were developed through a facile method which improved the yield quantity by decreasing the energy consumption there by reducing the cost. Thus synthesized CdO‐ZnO NCs were characterized through X‐ray diffraction, FT‐IR, SEM, TEM, EDX studies. These studies confirmed the successful formation of CdO‐ZnO composite and the average particle size of the NCs was found to be ~50 nm. Selective reduction of harmful industrial organic dyes from the water bodies is one of the important aspects of water pollution. As prepared CdO‐ZnO NCs degraded the MB dye completely in 30 min under visible light irradiation. The effect of various parameters such as catalytic load, dye concentration and pH on the degradation of dye was assessed and the NCs exhibited maximum degradation efficiency at 25 mg of catalytic load and alkaline pH of 11. The photoluminescence studies reveal that the NCs have inherent excellent luminescence property by exhibiting the emission band at 277 and 282 nm. From electrochemical studies, the CdO‐ZnO NCs proclaimed magnificent nitrite sensing property with the LOD value of 9.8 μM. Additionally, antioxidant studies disclosed that NCs remarkably scavenged the DPPH free radicals with IC50 value of 249 μg/mL. Thus, this study establishes simple method for the development of efficient mixed oxide material CdO‐ZnO for multifunctional properties that could find industrial applications. [ABSTRACT FROM AUTHOR]

Organic dyes that absorb light in the visible to near‐infrared region have garnered significant interest, owing to their extensive utility in organic photovoltaics and various biomedical applications. Aza‐boron‐dipyrromethene (Aza‐BODIPY) dyes are a class of chromophores with impressive photophysical properties such as tunable absorption from the visible region towards near infrared (NIR) region, high molar absorptivity, and fluorescence quantum yield. In this review, we discuss the developments in the aza‐BODIPYs, related to their synthetic routes, photophysical properties and their applications. Their design strategies, modifications in chemical structures, mode/position of attachment, and their impact on photo‐physical properties are reviewed. The potential applications of aza‐BODIPY derivatives such as organic solar cells, photodynamic therapy, boron‐neutron capture therapy, fluorescence sensors, photo‐redox catalysis, photoacoustic probes and optoelectronic devices are explained. [ABSTRACT FROM AUTHOR]

We have demonstrated a single‐crystal‐to‐single‐crystal (SCSC) transformation from a two‐dimensional noninterpenetrated layer to a microporous three‐dimensional fourfold interpenetrated MOF. The centrosymmetric [Co2(μ2‐OH)(EIBA)3]n (SNUT‐25) transforms into a microporous [Co(EIBA)2]n (SNUT‐26), which is triggered by the reaction time with DMF that acts as a structure‐directing agent (HEIBA = 4‐(2‐ethyl‐1H‐imidazol‐1‐yl)benzoic acid; DMF = N,N′‐dimethylformamide). Despite the distinct structure and coordination arrangements of SNUT‐25 in contrast to SNUT‐26, both Co‐MOFs were synthesized using the same ligand. Fascinatingly, upon introducing a specific quantity of DMF combined with a negligible proportion of nitric acid, SNUT‐25 will progressively and completely transform into SNUT‐26. Under the synergistic induction of solvent molecules and temperature, SNUT‐25 changed from the original two‐dimensional layered structure to the three‐dimensional pore structure of SNUT‐26. In addition, SNUT‐25 and SNUT‐26 are efficient photocatalysts for the degradation of organic dye methyl blue (MB) under visible light irradiation. Surprisingly, the degradation rates of both SNUT‐25 and SNUT‐26 can reach over 96%. In addition, SNUT‐25 and SNUT‐26 also exhibited high electrocatalytic oxygen evolution reaction. [ABSTRACT FROM AUTHOR]

An efficient removal of the photocatalysts used in the decontamination of water is crucial after its application beside its expected visible light sensitive activities. This study presents the synthesis of magnetically separable CuFe2O4 nanoparticles (CFNPs) with enhanced photoactivity under AM 1.5 G sunlight. A simple two-step process involving co-precipitation and hydrothermal treatment is employed, with subsequent annealing at temperatures from 200 °C to 1000 °C to synthesize the CFNPs. The characteristic features of the highest photoactive tetragonal phase of CFNP are confirmed by powder XRD studies with Rietveld refinement. This scheme strategically controls the growth of a highly photoactive tetragonal phase with predominant (224) facets over other less active facets in cubic CuFe2O4. Mott–Schottky analysis confirms the p -type semiconducting nature of CFNPs. A favourable direct optical band gap of 1.73 eV, as well as photoluminescence emission quenching for visible photons, show that the (224) oriented CFNPs are good photocatalysts in the visible spectrum with demonstrated organic dye degradations, including methylene blue and others. A density functional theory-based approach validates that the adsorption of such dye is thermodynamically more favourable on (224) facets of CuFe2O4 to facilitate the redox action by the excitons. [ABSTRACT FROM AUTHOR]

Well-constructed photocatalysts with efficient catalytic activity have attracted much attention due to their efficient visible-light absorption and superior charge separation capability. Visible-light responsive Cu 3 Mo 2 O 9 nanoparticles are synthesized utilising a simple and environmentally friendly green combustion process with Butea monosperma leaf extract as a reducing agent. X-ray diffraction pattern confirms the formation of orthorhombic crystal structure of Cu 3 Mo 2 O 9 NPs corresponding to space group Pnma (62). Furthermore, the synthesized NPs were characterized using FTIR, UV-DRS, PL, SEM and TEM studies. It was found that the direct energy band gap was 2.29 eV. Through photodegradation in the presence of visible light, the dye-sorbed photocatalyst exhibited excellent results. The sorbents have also been examined for recycling, and it has been observed that they maintain their effectiveness even after multiple successive runs. These substances therefore appear to have potential as efficient industrial dye wastewater remediators. Moreover, the high intensity emission in the green zone is amply confirmed by the photoluminescence emission spectra and CIE coordinates. The Latent fingerprints (LFP) are visible with the application of the powder dusting process. The synthesized CMO nanoparticles exhibit ridge patterns that are well-resolved and useful for identifying unique LFP. [ABSTRACT FROM AUTHOR]

The combination of visible light, a renewable and green energy source, and rose bengal, a non‐toxic organic dye as a photoredox catalyst, is an easy and efficient method for synthesizing 3,4‐dihydropyrimidin‐2(1H)‐ones/thiones in EtOH at ambient temperature in very short reaction time. The present work offers simple operation, easy workup, rapid conversion, and excellent product yields, while accommodating a wide range of substrates. Rose bengal‐based photocatalytic approach permits foremost sustainability, which delivers economic and environmental rewards. [ABSTRACT FROM AUTHOR]

Comprehensive strategies with the development of advanced materials are required for the remediation of water and land pollution to protect the environment and human health. In this regard, iron oxide catalysts are recognized as preferable catalysts for the heterogeneous photo-Fenton process, which is an efficient technique for degrading organic pollutants in waste water. The present study discusses the photocatalytic performance of iron oxide-based catalysts synthesized from industrial waste red mud for methylene blue degradation under visible light irradiation. XRD studies confirmed the formation of a pure α-Fe2O3 (hematite) phase, whereas the doping of iron oxide with Mn, Cu, and Ce was ascertained by XPS analysis. 3 wt% Cu doped iron oxide with a TOC value of ∼84.7% showed the best removal efficacy to the tune of ∼91% within 60 min of visible light irradiation. Impedance data supports the enhanced charge separation in metal doped α-Fe2O3, which improves the photocatalytic performance. A similar trend was observed in photo-electrochemical (PEC) properties, where Cu doped Fe2O3 showed 2 times higher photocurrent than the bare one. Based on scavenging tests, electrons and hydroxyl radicals (˙OH) were shown to be major players in the photodegradation of pollutants under visible light. A probable mechanism explaining the enhanced e−/h+ pair separation and migration was proposed by examining electrochemical properties. This work has significant implications for wastewater treatment with the efficient use of industrial waste red mud as a cost-effective resource. [ABSTRACT FROM AUTHOR]

Herein, a Bi2S3/Cu2S was successfully synthesized via a simple one-step wet impregnation process. The compositional behavior and electrical and optical properties of photocatalysts were investigated in detail. Photocatalytic technology has shown great promise in wastewater treatment, splitting water to hydrogen, and converting CO2 to fuel. Researchers or scientist are attempting to design sulfate-based heterojunction photocatalytic systems in order to develop novel photocatalysts with excellent performance. Photodegradation of methylene blue (MB) dye and tetracycline (TC) drug under visible light irradiation was used to assess the photocatalytic activity of as-prepared samples. As a result, 2:1% wt of Bi2S3/Cu2S heterostructure composite revealed superior visible light degradation performing of MB dye, and TC drug efficiency as 90.2% and 87.5%, respectively. The prepared hybrid photocatalyst has demonstated a potential for use in the photocatalytic degradation of antibiotic durgs and dyes, indicating a promissing future for its application. [ABSTRACT FROM AUTHOR]

The release of industrial effluents into fresh water is a major contributor of water contamination. Therefore, it is highly desirable to develop a viable solution to this alarming issue to improve the quality of clean water. To enhance the photocatalytic efficiency and hence utilization ratio of CuO, a series of CuO–FeSe2 composites with different varying contents of FeSe2 were prepared through facile synthetic methods. X-ray diffraction (XRD) and energy-dispersive X-rays (EDX) analysis verified that the samples were successfully prepared without any contaminating phases. The average crystallite sizes of CuO and FeSe2 were computed to be 29 and 21 nm respectively. For the CuO–FeSe2 composites, the crystallite sizes varied between 25 and 27 nm. The morphology of CuO was comprised of needle-shaped structures, whereas that of FeSe2 was observed to be flower-shaped structures comprising of irregular crystals. A red shift in the bandgap of CuO–FeSe2 composites was observed with the increase in FeSe2 concentration. The prepared photocatalysts were utilized to evaluate their efficiency under visible light against Rhodamine B (RhB). Among all the prepared composites, CuO–75% FeSe2 revealed a remarkable performance and degraded 96% RhB in 180 min. Rate constants for the degradation of the dye were determined by applying the Langmuir–Hinshelwood model. [ABSTRACT FROM AUTHOR]

Fabrication of efficient perovskite photo-Fenton catalytic systems is recognized as an effective strategy for clean water production. However, modifying perovskite catalysts effectively remains a formidable challenge. In this study, we prepared Bi-doped LaFeO 3 photo-Fenton catalysts using a facile microwave-assisted method. Various characterization techniques confirmed the successful formation of these Bi-doped LaFeO 3 perovskite materials. The photo-Fenton activity of the Bi-doped LaFeO 3 perovskite materials with varying Bi content was assessed by monitoring the degradation of methylene blue (MB) dye solution. Remarkably, the optimized Bi-doped LaFeO 3 (referred to as LBFO3) catalyst achieved approximately 93.64% degradation of MB within 100 min of visible light exposure, demonstrating exceptional efficacy in treating wastewater containing organic dye pollutants. The enhanced photocatalytic activity of the LBFO3 perovskite materials arises from the incorporation of Bi, leading to an expanded optical absorption range, increased specific surface area, and enhanced separation and migration of photo-generated carriers. Importantly, the LBFO3 photo-Fenton system exhibited remarkable stability during four successive cycling treatments, indicating promising practical applications. Additionally, quenching experiments were conducted to elucidate electron transfer in the LBFO3 catalyst related to the photo-Fenton degradation mechanism of MB. This study might pave the way toward designing novel perovskite based photo-Fenton systems for highly efficient degradation of waterborne contaminants. [ABSTRACT FROM AUTHOR]

In this paper, three-dimensional TiO2 nanoflowers (NFs) were prepared by a facile hydrothermal method, and Ag3PO4 was grown in situ following alkali treatment to design and synthesize a Ag3PO4/OH/TiO2 catalyst with excellent photocatalytic activity under visible light. The test results show that the photocatalytic degradation performance of TiO2 NFs after alkali treatment and Ag3PO4 loading is significantly improved. This is because the alkali treatment and the introduction of Ag3PO4 can provide a large amount of –OH, which can be converted to ˙OH under UV irradiation, followed by an increase in the number of active radicals to enhance the photocatalytic degradation performance. Meanwhile, the introduction of Ag3PO4 can effectively improve the light absorption ability of the photocatalyst. Moreover, the in situ growth of Ag3PO4 on TiO2 NFs can construct a high-quality Ag3PO4/TiO2 heterojunction to promote the charge separation and transport. Therefore, the degradation rate of Ag3PO4/OH/TiO2 can reach 90% after 30 min for degrading 3 mg L−1 RhB under visible light. The Ag3PO4/OH/TiO2 photocatalyst designed in the present work provides a new tool for the degradation of organic dyes. [ABSTRACT FROM AUTHOR]

In this work, a composite ZnO/MoS2/AuNPs supported on carbon fiber cloth (CFC) was prepared by progressively growing ZnO nanorods array, MoS2 nanosheets and AuNPs on CFC for sensitive SERS detection and efficient photocatalytic degradation of organic dye pollutants. The ZnO/MoS2 heterojunctions showed a significant CM effect and further decorating AuNPs with EM effect improved the detection limit of crystal violet (CV) from 10–6 to 10–13 M. The composite can be used for qualitative SERS detection of CV or Nile blue in standard solution or real samples with high stability and good stability. The enhancement mechanisms of CFC/ZnO/MoS2 and CFC/ZnO/MoS2/AuNPs were discussed based on corresponding characterizations and calculations. The composite also showed efficient photocatalysis for dye degradation. The ZnO/MoS2 heterojunction played a key role in enhancing the charge separation rate and improving the photocatalytic performance. The materials achieved degradation efficiencies of 71.4% for CV (1.5 × 10–5 M) after 60 min irradiation under visible light. The active radical species were investigated and possible degradation approach were proposed. Such composite with both SERS enhancement and visible light photodegradation ability has great promise in environment monitoring and remediation. [ABSTRACT FROM AUTHOR]

Over the past few years, organic chemistry has used the organic dye rose bengal's ability to absorb visible light. In present‐day research, the innovation of environmentally friendly processes for carbon‐carbon/carbon‐heteroatoms (Nitrogen, Oxygen, Sulphur, and Phosphorus) bond formation has great importance. The photocatalyzed cross‐dehydrogenative coupling (CDC) reactions using rose bengal (RB) is a promising technique for creating carbon‐carbon/carbon‐heteroatom bonds directly from readily available compounds. Our review focuses on the current advancement in rose bengal that uses photocatalyzed carbon‐carbon/carbon‐heteroatom bond‐making reactions to synthesize various important organic molecules via CDC reactions. [ABSTRACT FROM AUTHOR]

Bismuth oxybromide (BiOBr) nanoflowers were anchored onto kaolinite nanosheets via a calcination method. Assisted by characterization methods including XRD, SEM, and XPS, the microstructures of photocatalysts were comparatively investigated. The findings revealed a close integration of BiOBr nanoflowers with kaolinite, resulting in a gradual phase transition and augmented surface oxygen. Furthermore, the photocatalytic performance was assessed by investigating the degradation of organic dyes under visible light irradiation. Notably, the experimental results demonstrated that the degradation efficiencies of BiOBr/kaolinite composites were higher than that of pure BiOBr. The ⋅O2− was proven to be the major active radical in the photocatalytic process. This study presents a straightforward approach for fabricating BiOBr‐based photocatalysts, showcasing their enhanced performance in organic dye degradation under visible light. [ABSTRACT FROM AUTHOR]

This study aimed to synthesize a new magnetic photocatalytic nanosystem composed of Ag-CuFe2O4@rGO and to investigate its photodegradation efficiency for two organic pollutants of methylene blue (MB) 4-nitrophenol (4-NP) under visible light irradiation. The synthesized Ag-CuFe2O4@rGO nanocomposites were fully characterized by XRD, TEM, HRTEM, XPS, FTIR, UV and PL analysis which shows well controlled small sized (∼ 10 nm from Scherrer formula) CuFe2O4 NPs with dense and compact loading over rGO sheets. XRD results reveal that cubic spinel structure of CuFe2O4 with nanoparticles (5–10 nm) in shape, which is uniformly, decorated on the surface of the rGO sheets. The band gap energy values of CuFe2O4, Ag-CuFe2O4 and Ag-CuFe2O4@rGO nanoparticles are calculated as 2.76, 2.27 and 2.03 eV, respectively. After incorporation of Ag and rGO into CuFe2O4, the specific surface area was significantly improved to 154 m2/g for Ag-CuFe2O4@rGO nanocomposite. Upon inclusion of the photocatalysts, photodegradation efficiency increased and the Ag-CuFe2O4@rGO composite showed the highest efficiency towards MB (99.5%) and 4-NP (88.7%) followed by the Ag-CuFe2O4. With addition of rGO, the electron-hole recombination declines, thus resulting in a more optimum photocatalytic performance. The rate constant of Ag-CuFe2O4@rGO composite was found to be 0.0985 min−1 for MB and 0.0542 min−1 for 4-NP, respectively. Moreover, the effect of pH, catalyst dosage, and long term stability was thoroughly determined. The improved performance could be attributed to the positive synergistic effect between CuFe2O4 nanoparticles and rGO. The samples were further evaluated by EIS and dynamic photoresponse in order to identify the charge transfer efficiency. The improved photocatalytic mechanism was also explained briefly. [ABSTRACT FROM AUTHOR]

Safranine-catalyzed oxidative cyclization reaction of substituted 2-aminobenzamides and aldehydes utilizing oxygen as a green oxidant under visible light conditions at room temperature has been developed. Good to excellent yields of the desired quinazolinone products were achieved. Furthermore, the presented procedure illustrates the applicability of gram scale reactions. [ABSTRACT FROM AUTHOR]

This article discusses the use of photoredox catalysts in organic synthesis, specifically focusing on the activation of inert C-H bonds through hydrogen atom transfer. The authors examine the synthesis of carboxylic acid derivatives using a homemade reactor and various organic photocatalysts. They analyze the effects of different substituents on the reactivity of aldehydes and discuss the factors that influence the reaction outcome. The study also explores the photocatalytic aerobic photooxidation of benzaldehyde to benzoic acid using different organic dyes as photocatalysts, finding that 2-chloroanthraquinone under home white-light lamps resulted in efficient conversion. The study provides insights into the photocatalytic activity of anthraquinones and offers guidelines for reproducibility and further exploration of environmentally friendly methodologies. [Extracted from the article]

In the present study, the synthesis of metal organic framework (MOF) template-derived materials is reported. Cubic Fe2O3·TiO2 material was synthesized by using Prussian blue as the sacrificed template and aqueous soluble TiOSO4 as a TiO2 precursor. The obtained material was characterized by Fourier transform infrared (FT-IR) and Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet visible diffuse reflectance spectroscopy (UV-Vis DRS), and nitrogen adsorption/desorption isotherms. The characterization confirmed the existence of cubic α-Fe2O3 core and anatase TiO2 shell in the composite. Furthermore, the appearance of TiO2 shell has significantly enhanced the Brunauer–Emmett–Teller (BET) surface area yet still retained small bandgap energy of around 2.0 eV. This material was employed to degrade chosen organic dyes, including cationic dyes and anionic dye, in a heterogeneous photo-Fenton like system. The experimental results showed that this material exhibited higher adsorption and degradation capacity toward cationic dyes than anionic dye. The fitting of experimental data into two kinetic models revealed that the removal of the dyes can be better described by Langmuir-Hinshelwood model. The recyclability of the catalyst was also examined. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: A photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic dye photocatalysts. Broad substrate scope and high functional group tolerance were demonstrated by more than 50 examples. The reaction provides a novel and efficient method for the synthesis of polyfunctionalized pyrroles under very mild metal‐free conditions without other additives. [ABSTRACT FROM AUTHOR]

This study reports magnetic graphene oxide composite microspheres (MGO) were firstly synthesized via one step miniemulsion polymerization. α-FeOOH rods were then loaded onto MGO via a facile hydrothermal method to prepare α-FeOOH@MGO, which was served as the photocatalyst for the Fenton reaction. Subsequently, the properties of the resulting α-FeOOH@MGO were characterized by FT-IR, XRD, SEM, VSM and UV-vis DRS analysis methods. The influence of various parameters was investigated, such as dye type, dye concentration, H2O2 dosage, catalysts dosage and pH of MO solution during heterogeneous photo-Fenton processes. Under visible light irradiation, the degradation rate of MO, MB and CR could reach 99.96%, 98.47% and 99.97% in 40 min, respectively. Six cycle experiments confirmed that the α-FeOOH@MGO possessed a satisfied stability and recycling ability. In addition, the photocatalytic reaction mechanism was also revealed by the Mott-Schottky plot, band structure and trapping experiments of active species. [ABSTRACT FROM AUTHOR]

A novel metal-free and environment-friendly approach for synthesizing biologically important moieties, benzothiazoles and benzimidazoles, under visible light irradiation using photocatalyst Eosin Y, ethanol:water as a green solvent and atmospheric air as an oxidant has been developed. Using an organic dye, Eosin Y, provided a mild and economical catalytic system to synthesize a series of benzothiazoles and benzimidazoles in good to excellent yields. Besides, the photocatalytic system does not require an additional oxidant, which is good for the environment. This method has several advantages, including the absence of metals, low cost, environmental friendliness, green solvent, non-toxicity, ease of handling, and renewable energy sources such as visible light. [ABSTRACT FROM AUTHOR]

A visible‐light‐mediated cycloaddition of azobenzenes and nonstabilized azomethine ylides has been developed to access 1,2,4‐triazolidines. With readily available organic dye rose bengal as a photocatalyst and alkyl tertiary amines as precursors for azomethine ylides, the reaction proceeded smoothly under visible light irradiation at room temperature, affording various 4‐alkyl‐1,2‐diaryl‐1,2,4‐triazolidines with yields of up to 96%. Preliminarily mechanistic studies suggest that the nonstabilized azomethine ylides are formed in situ through photoredox catalysis. [ABSTRACT FROM AUTHOR]

The construction of photocatalysts with a Z-scheme heterojunction is considered to be a superior strategy for improving photocatalytic activity. In this study, a photocatalyst (PI/TiC/TiO2) with a Z-scheme heterojunction was fabricated, in which polyimide (PI) and TiO2 were used as the organic/inorganic semiconductor photocatalyst and TiC acted as the transmission bridge for electrons between PI and TiO2. In the self-made air flow photocatalytic reactor, the photocatalytic degradation efficiencies of organic dyes by PI/TiC/TiO2 increased with the increase of both the concentration and diffusion rate of O2. The degradation efficiencies of RhB and MB by PI/TiC/TiO2 reached 93.87% and 90.96%, respectively, within 90 min of visible light exposure, showing its outstanding photocatalytic performance. The mechanism analysis indicated that the Z-scheme heterojunction in PI/TiC/TiO2 facilitated the separation and migration of photoexcited charges while retaining stronger redox capabilities for charge carriers. This study provides an insight into the construction of visible light responsive organic/inorganic photocatalysts with Z-scheme heterojunctions for organic pollution treatment applications. [ABSTRACT FROM AUTHOR]

The development of photocatalysts for organic degradation is a hot research topic. In this study, CdZnS was selected as the carrier, and ZIF-8 was combined with it to explore the photocatalytic performance of the composite. In addition, the compound material, CdZnS@ZIF-8, was used as a photocatalyst for the decomposition of methylene blue dye, and the performance of pure CdZnS and pure ZIF-8 was compared. The photocatalytic efficiency of CdZnS@ZIF-8 was significantly higher than that of the other two. In the experimental reaction, the amount of catalyst was 0.04 g, the pH value was 7, the initial concentration of methylene blue aqueous solution was 20 mg/L, and the degradation of methylene blue in 50 mL aqueous solution could reach 99.5% under visible light irradiation for 90 min, showing excellent photocatalytic efficiency in the visible light range. It demonstrated excellent photocatalytic function in the visible light region, and the electron transfer phenomenon at the interface occurred in the het-junction and the separation of the photo-generating electron–hole as an electron acceptor of ZIF-8 further promoted the photocatalytic effect. [ABSTRACT FROM AUTHOR]

Industrial effluents are a leading major threat for water contamination, subsequently which results in severe health associated risks. Hence, purifying wastewater before releasing into the water resources is essential to avoid contamination. In this study, ZnO/Cu-DPA nano-composites were prepared by altering the percentage of Cu-DPA (20%, 30%, 40%, and 50% which are denoted to be ZnO/20%Cu-DPA, ZnO/30%Cu-DPA, ZnO/40%Cu-DPA and ZnO/50%Cu-DPA) using a simple mechanical grinding process. Several spectroscopic studies were employed such as electron paramagnetic analysis (EPR), powdered X-ray diffractometer (PXRD), UV–Vis absorbance spectroscopy, Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscope to characterize these nano-composites. The photo-catalytic activities of the prepared nano-composites were studied by degrading MB under visible light irradiation. ZnO, ZnO/20%Cu-DPA, ZnO/30%Cu-DPA, ZnO/40%Cu-DPA and ZnO/50%Cu-DPA degradation efficiencies were determined to be 71.8, 78.5, 77.1, and 66.1%, respectively. Among the composite catalysts, the ZnO/20%Cu-DPA coupled system are demonstrated the best efficiency (87%) for photo-degradation of MB within 80 min when exposed to visible light. The ZnO/Cu-DPA nano-composites had a greater MB photodegradation efficiency than pristine ZnO owing to p-n heterojunction in the linked system. Under visible light irradiation, the ZnO/20%Cu-DPA catalysed the conversion of dissolved O2 to hydroxyl radicals (OH·), triggering the reduction of MB. This suggests that ·OH is the primary specific active radical involved in the photo-catalytic decomposition of MB. Furthermore, EPR analysis indicates the existence of ·OH in the photo-catalytic system. The proposed nano-composites (ZnO/20%Cu-DPA) reusability was investigated across three cycles as the most efficient photo-catalyst. The results show that, the ZnO/Cu-DPA nano-catalyst is a potential candidate for the remediation of dirty water. [ABSTRACT FROM AUTHOR]

The development of fluorophores with photoemission beyond 1000 nm provides the opportunity to develop novel fluorescence microscopes sensitive to those wavelengths. Imaging at wavelengths beyond the visible spectrum enables imaging depths of hundreds of microns in intact tissue, making this attractive for volumetric imaging applications. Here, a novel shortwave‐infrared line‐scan confocal microscope is presented that is capable of deep imaging of biological specimens, as demonstrated by visualization of labeled glomeruli in a fixed uncleared kidney at depths beyond 400 µm. Imaging of brain vasculature labeled with the near‐infrared organic dye indocyanine green, the shortwave‐infrared organic dye Chrom7, and rare earth‐doped nanoparticles is also shown, thus encompassing the entire spectrum detectable by a typical shortwave‐infrared sensitive InGaAs detector. [ABSTRACT FROM AUTHOR]

Some organic dyes and photosensitizers with strong visible absorption can behave as photo‐responsive oxidase mimics. However, the relationship between the photo‐oxidase activity and molecular structure remains unclear to date. In this work, a new type of photosensitizer with the characteristics of molecular rotors, namely DPPy, served as the molecular scaffold for further investigation. To adjust the photocatalytic oxidation ability, DAPy and CBPy were designed and synthesized based on the enhancement and diminishment of the intramolecular charge transfer (ICT) process, respectively. Kinetic studies revealed that DAPy and CBPy both exhibited highly efficient photo‐activated oxidase‐like activity with 3,3′,5,5′‐tetramethylbenzidine (TMB) as the substrate, which were in good accordance with their molecular engineering to promote either type I or type II reactive oxygen species (ROS) generation. Impressively a colorimetric method based on the visible light induced oxidase‐like activity of molecular rotors was developed to determine the environmental temperature for the first time. Both DAPy and CBPy showed distinct sensitivities toward temperature as compared with several molecular rotors based on the typical fluorimetric detection. This work provides a new strategy for the application of molecular rotors to overcome the non‐emissive challenge in temperature sensing. [ABSTRACT FROM AUTHOR]

In this work, cobalt activated TiO2 photocatalyst have been successfully prepared on graphene oxide (GO) using simple and cost‐effective method to prepare Co‐TiO2/GO nanocomposites for the photocatalytic treatment of methylene blue (MB), representative organic dye, under visible light irradiation. The as‐prepared samples were characterized by X‐ray diffraction (XRD), High resolution transmission electron microscope (HRTEM), X‐ray photoelectron spectroscopy (XPS), UV‐vis diffused reflectance spectra (DRS), Raman spectroscopy and photoluminescence spectroscopy (PL). The characterization results confirmed that Co‐TiO2 catalyst is decorated on the graphene oxide. The photocatalytic efficiency of Co‐TiO2/GO for the degradation of MB was also improved by changing the proportion between Co‐TiO2 and GO. Highest photocatalytic activity was observed for Co‐TiO2 loaded with 5 wt % GO (88.7 %) compared with neat Co‐TiO2 (43.4 %) after 180 min of visible light irradiation. Furthermore, degradation by products was analyzed on Quadrupole Time‐of‐Flight Liquid Chromatography/Mass Spectroscopy (QTOF/LCMS) and the possible degradation pathway was proposed. It is investigated that the Co‐TiO2/GO nanocomposite has potential use in the catalytic degradation of organic contaminants under visible light irradiation. [ABSTRACT FROM AUTHOR]

Here, the zinc sulfide–copper sulfide (ZnS–CuS) nanocomposites have been synthesized using immersing thin layers of ZnS in 0.5 (M) Copper (II) chloride solution at low temperature by a simple and cost-effective chemical bath deposition (CBD) method. The immersion time of ZnS thin films in copper (II) chloride solution was investigated based on the structural, morphological, optical and optical catalytic activity of the prepared layers. The results of X-ray diffraction (XRD) and transmission electron microscopy (TEM) confirmed the formation of CuS: ZnS nanolayers consists of nanocrystals with an approximate diameter of less than 10 nm during the immersion time of 1 min. The particles forming the layers are dense and have good adhesion to the substrate. The energy gap of the layers decreases with increasing copper, which can lead to phase formation. Their significant photocatalytic activities in the photodegradation of Rhodamine B (RhB) dye in aqueous media have been considered, because ZnS:CuS nanocomposite thin films showed light catalytic activity in the RhB degradation in presence of visible radiation, so that the percentage of dye degradation is decreased by increasing the amount of copper and the duration of exposure to visible light due to slowing down the recombination rate of electron–hole pairs. While investigating the optical catalytic activity of the layers, there was no need to homogenize and centrifuge the solution to separate the nanoparticles from it. The main aim of this study is consideration of the effects of CuS amount on the photocatalytic activity of ZnS–CuS nanocomposite under the CBD method of synthesis condition. [ABSTRACT FROM AUTHOR]

The problem of industrial dyes depollution has pushed the scientific research community to identify novel photocatalysts with high performance. Herein, new photocatalysts composed of BaTiO3, BaTi0.96Cu0.04O3, BaTi0.96Cu0.02V0.02O3 and BaTi0.96Cu0.02Nb0.02O3 powders were prepared by solid-state reaction. The structural analysis of the samples confirmed the formation of the BaTiO3 structure. The splitting of (002) and (200) planes verified the formation of the tetragonal phase. The XRD peaks shifted, and the unit cell volume expansion verified the substitution of the Ti4+ site by Cu2+, V4+ and Nb5+ ions. The morphological measurements showed that the addition of (Cu, V) and (Cu, Nb) ions changes the particles' morphology of BaTiO3, reducing its grains size. After the incorporation of (Cu, V) and (Cu, Nb) ions, the band gap of BaTiO3 was reduced from 3.2 to 2.84 and 2.72 eV, respectively. The modification of BaTiO3 by (Cu, Nb) ions induced superior photocatalytic properties for methyl green and methyl orange with degradation efficiencies of 97% and 94% during 60 and 90 min under sunlight irradiation, respectively. The total organic carbon results indicated that the BaTi0.96Cu0.02Nb0.02O3 catalyst has a high mineralization efficiency. In addition, it possesses a high stability during three cycles. The high photodegradation efficiency of Bi0.96La0.02Gd0.02FeO3 was related to the wide-ranging visible light absorption. [ABSTRACT FROM AUTHOR]

Photocatalytic dye degradation is an energy-saving, environmentally friendly and sustainable way of managing potentially toxic wastewater from the textile industry. PbTiO3 was prepared using a solid-state reaction method, and an optimal ratio of PbTiO3/TiO2/g-C3N4 photocatalyst was synthesized using the sol-gel method to test its ability to decompose organic dyes. Methylene blue (MB) was selected as a target dye to test the photocatalytic effects. SEM results showed that the synthesis of a PbTiO3/TiO2/g-C3N4 photocatalyst yielded a unique nano structure with many surface pores. UV-Vis analysis demonstrated that the novel composite photocatalyst had higher visible light absorption, and a reduced energy gap. Experimental results showed that of the samples tested, PTO/TO/CN 1.0 showed the best photocatalytic effect on the removal of MB. Under visible light, the removal rate of MB by PTO/TO/CN 1.0 was up to 98.79%. The novel PTO/TO/CN 1.0 photocatalyst exhibited relatively high MB adsorption and had a high photocatalytic ability. [ABSTRACT FROM AUTHOR]

Unique nonlinear optical properties for converting low-energy incident light into high-energy radiation enable up-conversion materials to be employed in photocatalytic systems. An efficient near-infrared (NIR) response photocatalyst was successfully fabricated through a facile two-step method to load BiOBr on the Nd3+, Er3+@NaYF4 (NE@NYF) up-conversion material. The NE@NYF can transform NIR into visible and UV light and promote charge–energy transfer in the semiconductor. Consequently, the as-obtained photocatalysts exhibit excellent photodegradation performance for rhodamine B dye (RhB) and tetracycline (TC) organic pollutants. About 98.9% of the RhB was decomposed within 60 min with the 20% NE@NYF-B sample, outperforming the pristine BiOBr (61.9%). In addition, the 20% NE@NYF-B composite could decompose approximately 72.7% of the organic carbon during a 10 h reaction, which was almost two-fold more than that of BiOBr. Meanwhile, a possible charge transfer mechanism is proposed based on the recombination of electron–hole pairs and reactive oxygen species. This work provides a rational hybrid structure photocatalyst for improving photocatalytic performance in the broadband spectrum and provides a new strategy for NIR light utilization. [ABSTRACT FROM AUTHOR]

The functionalized NiFe‐LDH with photosensitized GQDs were synthesized through the hydrothermal route by differing the amount of GQDs solution and studied its efficacy towards the mineralization of textile dyes under visible light. The synthesized samples were characterized by XRD, FESEM, HRTEM, DRUV‐Vis, RAMAN, XPS, and BET. The combined effect of the hexagonal carbon lattice in GQD and open layered porous structure of NiFe‐LDH nanosheets results in the contraction of the lattice. Different reactive and conventional dyes were taken as representative dyes to evaluate the activity of the as‐synthesized photocatalysts. The enhanced electron absorption/donor effect between GQDs and NiFe‐LDH, and the growth of oxygen‐bridged Ni/Fe−C moieties enable the composite to exhibit better photocatalytic activity. Both photocatalytic activity and characterization results confirmed that the GQD@NiFe‐LDH nanocomposite heterostructure synthesized at 160 °C by taking 10 mL of GQDs aqueous solution named GNFLDH10 has a higher degree of crystallinity and has the best photocatalytic efficiency compared to other reported visible light catalysts. Specifically, the above optimized GQD@NiFe‐LDH photocatalyst is capable of photo‐mineralizing 50 ppm of Reactive Green in 20 min, Reactive Red in 20 min, and Congo Red in 25 min respectively following a direct Z‐scheme mechanism with substantial reusability. [ABSTRACT FROM AUTHOR]

Advance the photo-activity of the nano-sized ZnO photocatalyst is an essential factor in remediation of environmental pollution caused by industrial-organic dyes. Blends of transition elements including Mn, Fe and Co ions were employed to modify the energy gap and the visible absorption state tail of ZnO as well as inhibit the charge carriers recombination by their flexible oxidation states. Five nanocatalysts composed of ZnO, Zn0.97Mn0.015Fe0.015O, Zn0.97Mn0.015Co0.015O, Zn0.97Fe0.015Co0.015O and Zn0.97Mn0.01Fe0.01Co0.01O were simply synthesized. All the prepared compositions have a single phase of ZnO wurtzite structure. Both compositions of Zn0.97Fe0.015Co0.015O and Zn0.97Mn0.01Fe0.01Co0.01O have high sensitive responses to visible light spectrum owing to band gap reduction and formation of absorption state tails. The SEM images demonstrated that the kind of the transition metal blends added to ZnO powder have a significant effect on its morphology. Remarkably, the addition of (Fe, Co) mixture to ZnO powder leads to formation of homogenous rods structure besides very fine spherical particles. All modified ZnO samples revealed enhanced photocatalytic activity but Zn0.97Fe0.015Co0.015O powder possesses the greatest efficiency (98%) for 25 ppm Reactive Yellow 145 dye in 75 min of solar illumination with acceptable stability. In addition, Zn0.97Fe0.015Co0.015O catalyst revealed high photo-removal activity for 25 ppm Rhodamine B and malachite green with measured efficiencies of 94 and 91% in 75 min, respectively. The suitable catalyst dose was identified to be 0.04 g (100 mL solution) and the main effective radicals are the hydroxyl (·OH) species. [ABSTRACT FROM AUTHOR]

Remediation of organic dyes from wastewater in textile industries is a big challenge to decreasing water pollution. This study was aimed at the preparation of ZnO nanoparticles (NPs) and their application as a photocatalyst for the degradation of methylene blue (MB), sunfix red (SR) and real textile wastewater (RTW) under both UV and visible irradiations. The ZnO NPs were synthesized with a green Thymus vulgaris leaf extract-supported approach following the calcination process. 50 mg L−1 MB and 50 mg L−1 SR dyes were completely photodegrade under UV irradiation after only 20 and 45 minutes, respectively, in the presence of 1.0 mg/mL ZnO NPs. When they are exposed to visible light, the degradation efficiency reached 91 and 75% within 60 and 120 min, respectively. Photocatalytic measurements of RTW depict that 95% (within 60 min under UV illumination) and 79% (within 90 min under visible illumination) were degraded, respectively. The enhanced photodegradation can be attributed to the narrowing of the bandgap of the ZnO NPs, high crystallinity and nearly hexagonal morphology with an average size of 20–30 nm. The present results show that ZnO NPs could potentially be applied for high-efficiency degradation of organic dyes and RTW under both UV and visible light irradiation. We report for the first time, Thymus vulgaris leaf extract–assisted synthesis of ZnO nanoparticles (NPs) has been applied as a photocatalytic dye and RTW degradation. Second, our synthesis approach is more facile and simple than the previous method where complex hydrothermal or solvothermal methods have been applied, which leads to a complex preparation procedure. We systematically prepared ZnO materials in taking account into the variable Thymus vulgaris/ZnO precursor ratio, different calcination temperature and time and in detail, their photocatalytic activity has been fully investigated. [ABSTRACT FROM AUTHOR]

Metal ion doping is the most widely used means to improve the photocatalytic performance of semiconductor materials, which can adjust the band gap, broaden the range of optical response and construct impurity levels. The high efficiency modified NaTaO3 perovskite catalyst with good structural and catalytic properties was synthesized by a simple hydrothermal reaction method. A variety of analysis and testing techniques, such as XRD, SEM, DRS, XPS and EPR, were used to analyze the structure properties of the prepared materials. The results show that the influence mechanism of different metal introduction on the structure and properties of the NaTaO3 perovskite was different. Metal doping promoted the bond angle of Ta-O-Ta close to 180°, which restrains the recombination of the photogenerated electron-holes in the crystal. As Ce is introduced into the perovskite, the CeO2 forms and agglomerates around the perovskite, which improves the electron transport performance. With the narrower band gap, the Ce-modified perovskite shows that the degradation rate of ARS is 84% after 180 min of photoreaction. The species of h+, O2− and ·OH play different roles in improving the performance of the photocatalytic degradation process. [ABSTRACT FROM AUTHOR]

Wastewater remediation is a major issue that threatens the ecosystem and health of human population and hence deserves our undivided attention. Dye effluents, in particular those comprising organic colourants from a number of industrial sites, are a major source of wastewater pollution that poses serious dangers to human health and the environment today. Therefore, the goal of this study is to eliminate these coloured effluents, which are present in substantial amounts in wastewater, either singly or in mixtures. In this respect, we present an easy sol-gel synthesis of CoFe 2- x Cr x O 4 (x = 0, 0.2, 0.4, 0.6, 0.8, and 1) nano-ferrites for use as efficient photocatalysts. P-XRD technique was used for the confirmation of cubic spinel nanostructures having crystallite sizes in the nano-regime. Also, the optical band gap values resulted from Tauc plot indicates that incorporation of Cr3+ significantly reduces the band gap values. All the Co–Cr nano photocatalysts can be easily separable using an external magnet as indicated by the magnetic studies. For exploring the photocatalytic activity by photo-fenton process, we chose Rhodamine-B (RhB) as a model dye pollutant. Surprisingly, Cr3+ substitution into cobalt ferrite resulted in a dramatic transformation of the inert CoFe 2 O 4 into a highly visible light active photocatalyst for organic pollutant degradation. The CoFeCrO 4 nanocatalyst showed excellent results for the removal of RhB i.e., 99% removal in 30 min as compared to the CoFe 2 O 4 which was found to be inactive for the degradation. As a result of these exciting photocatalytic results, we were further encouraged to extend the degradation of a few other organic dye contaminants such methylene blue (MB), methyl orange (MO) and the mixture all three dyes (RhB + MB + MO). It was found that CoFeCrO 4 photocatalyst efficiently and swiftly degrades all three dye contaminants individually or in mixture with excellent recyclability and durability. [ABSTRACT FROM AUTHOR]

In this work, photocatalytic materials constituted by Cr-doped TiO2 (Cr-TiO2) decorated with noble metals show high effectiveness in the mineralization of Acid Orange 7 (AO7) and in the disinfection of real river water. The materials were firstly obtained by sol-gel method to get Cr-TiO2 that was subsequently modified by photochemical deposition of Ag or Pd nanoparticles (Ag/Cr-TiO2, Pd/Cr-TiO2). Chemical-physical characterization results evidenced that the noble metals were homogeneously distributed on the Cr-TiO2 surface. By using Pd(0.25%)/Cr-TiO2, the AO7 discoloration efficiency was about 91.4% after only 60 min of visible irradiation, which can be due to the lowest band gap of this material. Moreover, nitrates, chlorides, total hardness, and coliform bacteria content significantly decreased after the treatment of real river water samples (that is contaminated by industrial and domestic effluents) under UV and visible light irradiation in the presence of TiCrOx decorated with noble metals. One hundred percent of elimination rate for E. coli, total coliforms, and other enterobacteriaceae (without regrowth) was achieved by using Ag/Cr-TiO2 as photocatalyst. [ABSTRACT FROM AUTHOR]

In this study, the Mg2+-doped anatase TiO2 phase was synthesized via the solvothermal method by changing the ratio of deionized water and absolute ethanol Vwater/Vethanol). This enhances the bleaching efficiency under visible light. The crystal structure, morphology, and photocatalytic properties of Mg-doped TiO2 were characterized by X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, N2 adsorption-desorption, UV-Vis spectroscopy analysis, etc. Results showed that the photocatalytic activity of the Mg2+-doped TiO2 sample was effectively improved, and the morphology, specific surface area, and porosity of TiO2 could be controlled by Vwater/Vethanol. Compared with the Mg-undoped TiO2 sample, Mg-doped TiO2 samples have higher photocatalytic properties due to pure anatase phase formation. The Mg-doped TiO2 sample was synthesized at Vwater/Vethanol of 12.5:2.5, which has the highest bleaching rate of 99.5% for the rhodamine B dye during 80 min under visible light. Adding Mg2+-doped TiO2 into the phase-separated glaze is an essential factor for enhancing the self-cleaning capability. The glaze samples fired at 1180 °C achieved a water contact angle of 5.623° at room temperature and had high stain resistance (the blot floats as a whole after meeting the water). [ABSTRACT FROM AUTHOR]

This is due to the fact that TiO2 has the wide energy gap and short life and its photocatalytic active only under ultraviolet light, and so its application is greatly limited. TiO2 can form a heterojunction if combined with other semiconductors to enhance its photocatalytic ability under visible light. In this study, a TiO2/Bi2SiO5 photocatalyst with n–n heterojunction was successfully synthesized by the sol–gel method and hydrothermal method. Eggshell waste has long been used as fertilizer to grow plants or food additives for livestock, or as an adsorbent in metal ions and organic dyes. Using eggshell as a carrier of photocatalyst can possibly reduce its cracking of the substrate. The photocatalyst was deposited on eggshell powder by solid state dispersion (SSD). It was analyzed for the adsorption and degradation of methylene blue by various compositions of the photocatalysts and eggshell powder under visible light. The results demonstrated that the ratio of TiO2/Bi2SiO5: eggshell powder at 1:1 could have the best removal ability. To better facilitate the recovery of the photocatalyst from the aqueous solution, we used the techniques of electrostatic spraying and electrospinning to prepare nylon 6,6 nanofiber membranes with various composite photocatalyst (TiO2/Bi2SiO5/Eggshell/Nylon 6,6 NFM). The nanofiber membrane degraded 98% of methylene blue after 30 min of dark adsorption and 1 h of visible light irradiation. [ABSTRACT FROM AUTHOR]

[Display omitted] The exploration of emerging photocatalysts like covalent organic frameworks (COFs) is an essential but challenging endeavor to find sustainable solutions for selective organic transformations. Anthraquinones are envisaged to construct COFs for visible light photocatalysis because their derivatives are employed industrially as oxidation catalysts or organic dyes. Herein, an anthraquinone COF, TpAQ-COF, is successfully constructed with 1,3,5-triformylphloroglucinol (Tp) and 2,6-diaminoanthraquinone (AQ). Then, the selective oxidation of amines over TpAQ-COF is implemented. Amines can be effectively converted into corresponding imines over TpAQ-COF powered with green light and oxygen, during which superoxide radical anion is discerned as the pivotal reactive oxygen species. This work suggests that COFs could inherit the advantages of molecular building blocks for selective reactions powered with broad visible light. [ABSTRACT FROM AUTHOR]

Textile wastewater becomes the primary root of environmental pollution due to the rapid infection rates of freshwater, subsurface water, soil, and air. Due to the high absorption abilities of UV and visible light, polymer nanocomposite photocatalyst films (PNPFs) are recognized as potential candidates for textile wastewater treatment. Here, we developed novel cobalt monoxide (CoO)/polyaniline (PANI) PNPFs with high photocatalytic efficiency and stability. The photocatalytic efficiencies of PANI/CoO films were estimated utilizing the degradation of organic dyes and real-textile wastewater (RTW) under various lighting conditions. PANI/CoO PNPF completely decomposed methylene blue and RTW samples in 30 and 45 min under UV light illumination, respectively. We found that the CoO nanoparticles doubled the PANI's photocatalytic decomposition rate. However, under visible light irradiation, their photocatalytic efficiencies almost halved. Moreover, PANI/CoO PNPF exhibited excellent photocatalytic stability by maintaining the photocatalytic performance for up to five cycles with over 95% removal efficiency. This study yielded an efficient and alternative polymer nanocomposite to decompose wastewater sources contaminated with various textile dyes and may be examined for industrial-scale applications in the future. [ABSTRACT FROM AUTHOR]

MIL-101(Cr)@TiO2 core-shell composite material was synthesized via the hydrothermal method, where MIL-101(Cr) served as the core and TiO2 acted as the shell. SEM results revealed that the metal-organic framework core effectively prevented the aggregation of TiO2 nanoparticles and facilitated their dispersion. Characterization techniques such as XRD, XPS, and TGA were utilized to confirm the successful loading of TiO2 onto MIL-101(Cr) and its excellent thermal stability. MIL-101(Cr)@TiO2 was employed in photocatalytic degradation of dye pollutants and vehicle exhaust, and the potential degradation mechanisms were investigated in detail. The results showed that MIL-101(Cr)@TiO2 exhibited excellent photocatalytic degradation performance towards dye pollutants, with degradation efficiencies of 91.7% and 67.8% achieved for MB and RhB, respectively, under visible light irradiation for 90 min. Furthermore, the photocatalytic degradation of automobile exhaust revealed that the MIL-101(Cr)@TiO2 composite material also exhibited degradation effects on NOx, CO, and HC. The degradation efficiency for NO reached 24.2%, indicating its broader applicability. [ABSTRACT FROM AUTHOR]

Ag-ZnO/MWCNT composites were obtained by microwave-assisted, varying-charge synthesis of multiwalled carbon nanotubes (MWCNT). The structural, morphological and optical properties were characterized by: XRD, SEM, TEM, Physisorption of N2 and UVVis. The incorporation of Ag ions and MWNTC caused changes in the structure tension and in the average crystallite size of ZnO. The micrographs revealed that ZnO agglomerates were distributed on the MWNTC and that Ag particles were deposited on the surface of the heterostructure, thus the energy gap decreased. The percentages of degradation of methylene blue were 98 and 75% under ultraviolet and visible radiation, respectively, in the Ag-ZnO/CNT composites. [ABSTRACT FROM AUTHOR]

By employing a photoredox catalyst which is an affordable organic dye, we present a simple and efficient visible light induced, eco‐friendly and metal‐free quinoline derivative synthesis. The current strategy is the first to utilize visible light to induce quinoline by tandem reactions through the formation of CN and CC bonds, resulting in high yields of products under relatively moderate reaction conditions. Inexpensive, short response time, admirable atom economy, easy work‐up and wide substrate scope are some of the primary advantages of the current approach. [ABSTRACT FROM AUTHOR]

In the past decades, great efforts have been made to develop novel visible‐light photocatalysts to achieve high photocatalytic efficiency by utilizing visible light, the largest proportion of solar energy. As a new type of photocatalyst materials, all‐inorganic lead‐free halide double perovskites have begun to attract widespread interest. Herein, double perovskite Cs2AgBiCl6 was developed into a visible‐light photocatalyst for degrading organic dyes. Cs2AgBiCl6 was prepared by the hydrochloric acid precipitation and anti‐solvent recrystallization methods, respectively, and was used to degrade organic dyes under visible light. Samples prepared by the anti‐solvent recrystallization method are smaller than those prepared by the hydrochloric acid precipitation method, which can degrade 95.7 % of Sudan III in 10 min and show excellent photocatalytic activity. The cyclic experiments demonstrate that Cs2AgBiCl6 has a good cycle stability. Moreover, Cs2AgBiCl6‐AS also exhibits good photocatalytic degradation ability for Methyl red and Malachite green. These distinctive results indicate that Cs2AgBiCl6 may be a promising material for developing novel, high‐efficient and stable visible‐light photocatalysts. [ABSTRACT FROM AUTHOR]

This article addresses the synthesis of Fe3+ doped TiO2 nanoparticles with variations of molar concentrations of Fe3+ and their adequate use as potential photocatalysts for Photocatalysis applications. Synthesized photocatalysts were characterized thoroughly by different analytical techniques in terms of morphological, chemical, structural, crystalline, optical, electronic structure, surface area etc properties. The occurrence of red shift phenomenon of the energy band gap attributes to the transfer of charges and transition between the d electrons of dopant and conduction band (CB) or valence band (VB) of TiO2. The doping of Fe3+ ions generates more trap sites for charge carriers with the surface trap sites. Thorough experimental conclusions revealed that the Fe3+ ions necessarily regulate the catalytic property of TiO2 nanomaterial. The obtained total degradation efficiency rate of Methylene Blue (MB) was 93.3% in the presence of 0.1 M Fe3+ in the host material and for Malachite Green Oxalate the efficiency was 100% in the presence of 0.05 M and 0.1 M Fe3+in the host material. In both the cases the total visible light irradiation time was 90 min. The adsorption properties of the photocatalysts have been also performed in a dark for 90 min in the presence of MB dye. However, till now there are hardly reported photocatalysts which shows complete degradation of these toxic organic dyes by visible light driven photocatalysis. of potential values of valence and conduction band shows the production of active oxidizing species for hydrogen yield and the possible mechanism of the Schottky barrier has been proposed. A schematic diagram of visible light driven Photocatalysis has been pictured showing degradation activity of Fe3+-TiO2 catalysts sample. [ABSTRACT FROM AUTHOR]

It is a great challenge to develop photocatalysts for the degradation of organic pollutants in the aqueous environment, especially those with excellent catalytic performance under visible light conditions. In this work, using graphene oxide (GO) as an electron shuttle agent and carrier, a hybrid of ZIF-8/NH2-MIL-125(Ti) and GO (ZIF-8/NH2-MIL-125(Ti)/GO) was prepared by a simple two-step solvothermal method. The morphology, structure, and combination of the synthesized catalysts were studied. The results showed that graphene oxide and ZIF-8 formed an in situ load on NH2-MIL-125(Ti). The construction of hybrid materials significantly improved the catalytic activity of NH2-MIL-125(Ti) in the visible light range. The degradation activity of the synthesized catalyst was further tested with reactive red dye. The results showed that the catalyst exhibited excellent catalytic removal efficiency for active red, with a degradation rate of 99.8% within 2 h. The prepared hybrid materials have good application prospects in the field of organic pollutant treatment in water. [ABSTRACT FROM AUTHOR]

In this paper, we present the first attempt to evaluate the role of carboxymethyl cellulose (CMC) as a chelating agent in the sol–gel auto-combustion method of producing barium hexaferrite (BaFe12O19). We also report the application of the system as a photocatalyst for dye degradation. The formation, morphology, and crystalline structure of the synthesized nanoparticles are determined using XRD, SEM, EDS, VSM, FTIR, and TEM techniques. High efficiency under visible light, with a band gap of 1.62 eV and a BET surface of 17.93 m2/g, has been observed for the BaFe12O19 catalyst. The operating parameters, such as reaction time, initial dye concentration, light intensity, reusability, and dye type, are studied. Degradation rates as high as 98.26% (Kapp = 0.082 min–1) and 89.07% (Kapp = 0.0743 min–1) were obtained for cases of methylene blue and malachite green under conditions of visible light irradiations when BaFe12O19 was used. The BaFe12O19 catalyst has been shown to exhibit a high degradation performance for cationic dyes. Furthermore, BaFe12O19 magnetic nanoparticles show excellent reusability for dye degradation because the photocatalyst did not exhibit a significant decrease in its activity even after five runs (81.56%). As a result, the current study confirmed that photocatalytic degradation was a promising technology for saving water and treating wastewater formed from textile dye industries. The technique can be used to study the efficiency of photocatalytic degradation and understand the process of recycling waste effluents under conditions of minimized water use. [ABSTRACT FROM AUTHOR]