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[Display omitted] • A "Turning waste into treasure" strategy was proposed. • An efficient ARM/NiOOH adsorbent has been successfully prepared. • The adsorption kinetics model has been reasonably established. • 348.0 mg g−1 congo red was adsorbed with a ∼ 100 % adsorption efficiency within 5 min. Extracting functional materials from industrial waste residues to absorb organic dyes can maximize waste reuse and minimize water pollution. However, the extraordinarily low purification efficiency still limits the practical application of this strategy. Herein, the lamellar NiOOH is in-situ anchored on the industrial waste red mud surface (ARM/NiOOH) as an adsorbent to purify organic dyes in wastewater. ARM/NiOOH adsorbent with high specific surface area and porosity provides considerable active sites for the congo red (CR), thereby significantly enhancing the removal efficiency of CR. Besides, we fit a reasonable adsorption model for ARM/NiOOH adsorbent and investigate its adsorption kinetics. Resultantly, ARM/NiOOH adsorbent can remarkably adsorb 348.0 mg g−1 CR within 5 min, which is 7.91 times that of raw RM. Our work provides a strategy for reusing industrial waste and purifying sewage pollution, which advances wastewater treatment engineering. [ABSTRACT FROM AUTHOR]

Dyes can be determined as a substance that creates many environmental issues leading to the death of aquatic life, plants and all living organisms. Dye removal can be done by several physical, chemical and biological methods, including the photocatalytic method. Photocatalysis is a method in which light energy is used to degrade the dye. This technique is low-cost and eco-friendly, and it degrades many harmful substances from organic dyes compared to other techniques. The prime aim of the present work is to degrade the largely used organic dyes such as methylene blue, malachite green and crystal violet using EDTA-doped FeZnS2 and Leishman stain-doped FeZnS2 thin films. The doped FeZnS2 thin films were fabricated using the co-precipitation method. Thin fabricated films are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and UV–Visible spectroscopy (UV). These characterization studies show an active photo response indicating effective dye degradation. Based on the absorption studies of UV spectroscopy measurements after 60 min, the degradation efficiency of methylene blue, crystal violet and malachite green using EDTA-doped FeZnS2 are 76, 85 and 90, respectively. Similarly, the degradation efficiency after 60 min of methylene blue, crystal violet and malachite green using Leishman stain-doped FeZnS2 are 82, 79 and 89, respectively. [ABSTRACT FROM AUTHOR]

Advances in electronics and medical diagnostics have made organic dyes extremely popular as key functional materials. From a practical viewpoint, it is necessary to assess the spectroscopic and physicochemical properties of newly designed dyes. In this context, the condensation of 1,3-dimethylbarbituric acid with electron-rich alkylaminobenzaldehyde derivatives has been described, resulting in a series of merocyanine-type dyes. These dyes exhibit intense blue-light absorption but weak fluorescence. An electron-donating alkylamino group at position C4 is responsible for the solvatochromic behavior of the dyes since the lone electron pair of the nitrogen atom is variably delocalized toward the barbituric ring, which exhibits electron-withdrawing properties. This was elucidated, taking into account the different geometry of the amino group. The intramolecular charge transfer in the molecules is responsible for the relatively high redshift in absorption and fluorescence spectra. Additionally, an increase in solvent polarity moves the absorption and fluorescence to lower energy regions. The observed solvatochromism is discussed in terms of the four-parameter Catalán solvent polarity scale. The differences in the behavior of the dyes were quantified with the aid of time-dependent density functional theory calculations. The obtained results made it possible to find regularities linking the basic spectroscopic properties of the compounds with their chemical structure. This is important in the targeted search for new, practically important dyes. [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]

To achieve the actual application of MoO x in absorption removal of organic dye from water, eco-friendly, facilely-scalable, high-yield, and cost-efficient synthesis of MoO x with desirable structures and superior adsorption capacities remains a great challenge. Herein, for the first time, a novel synthetic route to MoO 3 micro-/nanocrystals with different microstructures was based on mechanochemical reactions and subsequent annealing, and their inherent formation mechanisms were also discussed. Moreover, the adsorption kinetics, thermodynamics, and mechanism of Rhodamine B (RhB) on α h -MoO 3 hybrid were systematically investigated. The results show that the microstructures of MoO 3 can be controlled by facile adjusting the dosage of H 2 C 2 O 4 ·2H 2 O, which leads to the different milling precursors. The bicrystalline hybrid of α-MoO 3 nanosheets and h -MoO 3 microrods (α h -MoO 3 hybrid) exhibits an ultrahigh maximum adsorptive capacity (751.88 mg g−1) for RhB at the high initial concentration (80 mg L−1), more than 3 times enhancement compared to that of α-MoO 3 particles (210.16 mg g−1), which can be attributed to the larger specific surface area (28.77 m2 g−1) and more negative surface potential (−72.00 mV). This work provides a scalable and controllable route to synthesize MoO 3 micro-/nanocrystals with desired microstructures, contributing a promising and excellent adsorbent for the practical removal of organic dyes from water. [ABSTRACT FROM AUTHOR]

A series of new granular carbonaceous adsorbents was prepared via single-stage physical and chemical activation of walnut shells. Their suitability for removing various types of organic pollutants (represented by dyes, surfactants and water-soluble polymers) from the liquid phase was assessed. The activation of the precursor was carried out with CO2 and H3PO4 using conventional heating. Activated biocarbons were characterized in terms of chemical composition, acidic–basic nature of the surface, textural and electrokinetic properties as well as thermal stability. Depending on the type of activating agent used during the activation procedure, the obtained biocarbons differed in terms of specific surface area (from 401 to 1361 m2/g) and the type of porous structure produced (microporosity contribution in the range of 45–75%). Adsorption tests proved that the effectiveness of removing organic pollutants from the liquid phase depended to a large extent on the type of prepared adsorbent as well as the chemical nature and the molecular size of the adsorbate used. The chemically activated sample showed greater removal efficiency in relation to all tested pollutants. Its maximum adsorption capacity for methylene blue, poly(acrylic acid), poly(ethylene glycol) and Triton X-100 reached the levels of 247.1, 680.9, 38.5 and 61.8 mg/g, respectively. [ABSTRACT FROM AUTHOR]

Organic dyes are widely used in many important areas, but they also bring many issues for water pollution. To address the above issues, a reconstructed kaolinite hybrid compound (γ-AlOOH@A-Kaol) was obtained from raw kaolinite (Kaol) in this work. The product was then characterized by X-ray diffraction (XRD), Fourier-transform infrared (ATR-FTIR), Brunauer-Emmett-Teller (BET), and scanning electron microscopy (SEM), and the absorption properties of γ-AlOOH@A-Kaol for congo red were further studied. The results demonstrated that flower-like γ-AlOOH with nanolamellae were uniformly loaded on the surface of acid-treated Kaol with a porous structure (A-Kaol). In addition, the surface area (36.5 m2/g), pore volume (0.146 cm3/g), and pore size (13.0 nm) of γ-AlOOH@A-Kaol were different from those of A-Kaol (127.4 m2/g, 0.127 cm3/g, and 4.28 nm, respectively) and γ-AlOOH (34.1 m2/g, 0.315 cm3/g, and 21.5 nm, respectively). The unique structure could significantly enhance the sorption capacity for congo red, which could exceed 1000 mg/g. The reasons may be ascribed to the abundant groups of -OH, large specific surface area, and porous structure of γ-AlOOH@A-Kaol. This work provides an efficient route for comprehensive utilization and production of Kaol-based compound materials that could be used in the field of environmental conservation. [ABSTRACT FROM AUTHOR]

The qualitative impact of pollutants on water quality is mainly related to their nature and their concentration, but in any case, they determine a strong impact on the involved ecosystems. In particular, refractory organic compounds represent a critical challenge, and several degradation processes have been studied and developed for their removal. Among them, heterogeneous Fenton treatment is a promising technology for wastewater and liquid waste remediation. Here, we have developed mono- and bimetallic formulations based on Co, Cu, Fe, and Mn, which were investigated for the degradation of three model organic dyes (methylene blue, rhodamine B, and malachite green). The treated samples were then analyzed by means of UV-vis spectrophotometry techniques. Bimetallic iron-based materials achieved almost complete degradation of all three model molecules in very short time. The Mn-Fe catalyst resulted in the best formulation with an almost complete degradation of methylene blue and malachite green at pH 5 in 5 min and of rhodamine B at pH 3 in 30 min. The results suggest that these formulations can be applied for the treatment of a broad range of liquid wastes comprising complex and variable organic pollutants. The investigated catalysts are extremely promising when compared to other systems reported in the literature. [ABSTRACT FROM AUTHOR]

The results of evaluating the adsorption and fluorescent properties of azolotriazine compounds and phases based on cadmium sulfide quantum dots in vapors of volatile organic compounds (biomarkers of living systems) are considered. The adsorption properties of phases based on organic dyes and encapsulated semiconductors towards vapors of alcohols, ketones, amines, acids, ammonia, and aldehydes are investigated using direct high-sensitivity piezoelectric quartz microweighing. The spectral properties and their variations in analyte vapors are investigated using various spectroscopy methods (absorption, photoluminescence). The research results are compared, and the potential for optimizing this stage is assessed. It is proposed to evaluate the consistency of methods for predicting changes in fluorescent properties in test systems for volatile organic compounds using the Kendall coefficient of concordance, W. The highest level of agreement (W = 0.89) was observed between the methods of spectrofluorimetry and direct vapor microweighing upon adsorption on phases being potential fillers of test systems. A correlation between the results obtained by different fluorescence methods (visual plate test systems and fluorimetry of phases on paper substrates) is 0.80, which confirms a high degree of consistency in assessments using them in the degree of interaction between the analytes and organic, combined fluorochromes. The methods closely related in the nature of the analytical response do not exhibit better agreement than the method of direct vapor microweighing on microphases of fluorimetric reagents of different nature (cadmium sulfide quantum dots/chitosan, organic azolotriazine compounds, mixed phases). This, in turn, enables the selection of simpler, more available, and more rapid methods and means of analysis in routine experiments. [ABSTRACT FROM AUTHOR]

This work demonstrated enhanced adsorption capabilities of lignin nanoparticles (LNPs) synthesized via a straightforward hydrotropic method compared to pristine lignin (PL) powder for removing methylene blue dye from aqueous solutions. Kraft lignin was used as a precursor and p-toluenesulfonic acid as the hydrotrope to produce spherical LNPs with ~ 200 nm diameter. Extensive characterization by SEM, AFM, DLS, zeta potential, and BET verified successful fabrication of microporous LNPs with fourfold higher specific surface area (14.9 m2/g) compared to PL (3.4 m2/g). Significantly reduced particle agglomeration and rearranged surface chemistry (zeta potential of −13.3 mV) arising from the self-assembly of lignin fractions under hydrotropic conditions enabled the application of LNPs and superior adsorbents compared to PL. Batch adsorption experiments exhibited up to 14 times higher methylene blue removal capacity, from 20.74 for PL to 127.91 mg/g for LNPs, and ultrafast equilibrium uptake within 3 min for LNPs compared to 10 min for PL. Kinetic modeling based on pseudo-first-order and pseudo-second-order equations revealed chemisorption as the predominant mechanism, with a rate constant of 0.032825 g/mg·h for LNPs—over an order of magnitude higher than PL (0.07125 g/mg·h). Isotherm modeling indicated Langmuir monolayer adsorption behavior on relatively uniform lignin surface functional groups. The substantially augmented adsorption performance of LNPs arose from the increased surface area and abundance of surface functional groups, providing greater accessibility of chemically active binding sites for rapid dye uptake. Overall, this work demonstrates that tailoring lignin nanoparticle structure and surface chemistry via scalable hydrotropic synthesis is a simple and sustainable approach for producing highly efficient lignin-based nano-adsorbents for organic dye removal from industrial wastewater. [ABSTRACT FROM AUTHOR]

STED nanoscopy allows for the direct observation of dynamic processes in living cells and tissues with diffraction-unlimited resolution. Although fluorescent proteins can be used for STED imaging, these labels are often outperformed in photostability by organic fluorescent dyes. This feature is especially crucial for time-lapse imaging. Unlike fluorescent proteins, organic fluorophores cannot be genetically fused to a target protein but require different labeling strategies. To achieve simultaneous imaging of more than one protein in the interior of the cell with organic fluorophores, bioorthogonal labeling techniques and cell-permeable dyes are needed. In addition, the fluorophores should preferentially emit in the red spectral range to reduce the potential phototoxic effects that can be induced by the STED light, which further restricts the choice of suitable markers. In this work, we selected five different cell-permeable organic dyes that fulfill all of the above requirements and applied them for SPIEDAC click labeling inside living cells. By combining click-chemistry-based protein labeling with other orthogonal and highly specific labeling methods, we demonstrate two-color STED imaging of different target structures in living specimens using different dye pairs. The excellent photostability of the dyes enables STED imaging for up to 60 frames, allowing the observation of dynamic processes in living cells over extended time periods at super-resolution. [ABSTRACT FROM AUTHOR]

The preparation of metallic nanoparticles using green synthetic approaches and its application toward the efficient degradation of environmentally hazardous dyes constitutes an attractive alternative to currently employed methods. In the current report, the green synthesis of silver nanoparticles (AgNPs) was successfully achieved using Actinidia deliciosa (kiwifruit) peel aqueous extract as a bioreducing agent under optimized synthesis conditions. The experimental parameters were optimized in terms of reactant ratio, reaction temperature, and reaction time. The biogenic nanoparticles exhibited SPR absorption band at λmax 480 nm. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images revealed quasispherical monodisperse nanoparticles which were 36 nm in diameter. The hydrodynamic diameter of the nanoparticles was 106 nm as determined by dynamic light scattering, and the highly negative ζ-potential (−34 mV) supported its superior colloidal stability. Energy dispersive X-ray confirmed that silver is a major constituent of the nanoparticles. X-ray diffraction (XRD) diffractograms confirmed the crystallinity of the nanoparticles and its face-centered cubic (fcc) lattice structure. The functional groups in the plant's phytochemicals facilitating the reduction of Ag+ ions and stabilization of the formed AgNPs were identified by fourier transform infrared (FTIR) spectroscopy. In specific, the bands in the FTIR spectra at 3,412, 1,618, 1,419, and 1,237 cm−1 suggested the presence of phenolic compounds. Phytochemical analysis by colorimetric assays revealed that the kiwifruit peel extract was rich in phenolic compounds. When evaluated in the catalytic degradation of organic dyes, the biosynthesized AgNPs induced instant and complete discoloration of the methylene blue dye when 1.6 mg of nanoparticles was used. At a lower dose of AgNPs (0.4 mg), 80% degradation of the dye occurred after 3 hr of treatment. The degradation reaction followed second-order kinetics with a rate constant of 0.01083 mM−1s−1. The current study highlights the immense potential of the prepared nanoparticles as efficient catalysts for the degradation of hazardous organic dyes such as methylene blue and presents an intriguing argument for investigating the catalytic efficiency of the biogenic AgNPs for the degradation of other structurally different dye pollutants. [ABSTRACT FROM AUTHOR]

This article reviews the research recently undertaken to characterise and identify early synthetic dyes (ESDs) and synthetic organic pigments (SOPs) as well as study their degradation pathways with a focus on cultural heritage applications. Since the invention of the first fully synthetic dye in 1856, these materials have been used in a variety of historic objects and artworks, such as textiles, furniture, prints, paintings, drawings, etc. The synthesis of new dyes and their implementation into pigment formulations were rapid phenomena, so that by the beginning of the 20th century, thousands of new molecules were patented and commercialised. This review will focus on these early formulations synthesised up to approximately 1914 and the outbreak of World War I. ESDs and SOPs represent a challenge from an analytical point of view. Molecular databases are fundamental for the unequivocal identification of these compounds, but reference materials are not always readily available. A combination of analytical techniques is often needed for characterisation, especially in the case of SOPs, which have both organic and inorganic components. Furthermore, the degradation of these molecules can jeopardise their detection in historic objects that have been exposed to light, humidity and temperature fluctuations. Nevertheless, ESDs and SOPs are important research tools. As the dates of their first synthesis are often known with precision, based on patent information, their detection can be used to refine the production date of objects. Additionally, their trade from Europe to the world and their adoption in artistic practices around the globe is an active area of research. [ABSTRACT FROM AUTHOR]

Tribocatalysis is one of the emerging processes for organic dye degradation application. The process uses mechanical energy as a source for breaking down organic pollutants present in water. The synergistic effect of two catalysis processes for eliminating organic pollutants, here in the present study photocatalysis an advanced oxidation process is integrated with the tribocatalysis process for enhancing the degradation efficiency of the tribocatalysis process by using BaTiO3 ceramic powder as a catalyst. The responsible factors for dye degradation via the tribocatalysis process such as surface roughness of the materials utilized, force applied, and energy band gap of the catalyst are also studied. The Methylene Blue dye's degradation was ~39%, ~60%, and ~76% through tribocatalysis, photocatalysis, and photo-tribocatalysis respectively by using 400 mg BaTiO3 ceramic powder in 8 h. The synergistic effect of photocatalysis and tribocatalysis process showed enhanced degradation compared to individual processes. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are emerging as pivotal porous crystalline materials with diverse applications. Typically, MOFs are synthesized using solvothermal techniques at high temperatures and pressures. In this study, a novel approach was employed to synthesize zinc-based MOFs, specifically MOF-5, at low temperatures (up to 50 °C) via chemical mixing at standard pressures. Varying the temperature and solvents, N-methyl-2-pyrrolidone (NMP) and N,N-dimethylformamide (DMF), in the chemical mixing process, the highest yield of the material was observed with DMF at 50 °C (M1). Two additional samples, M2 and M3, are synthesized at room temperature using DMF and NMP, respectively. Despite similarities in XRD, Raman, and FTIR analyses confirming successful MOF-5 formation, noticeable differences in sample morphology arise due to distinct synthesis conditions, particularly solvent and temperature variations. The MOF-5 samples exhibit UV absorption with varying band gaps. Notably, when employed as photocatalysts for organic dye (methylene blue) degradation, M2 outperforms others, achieving an impressive 85% degradation under simulated solar light irradiation. This work underscores the significance of tuning MOF photocatalyst properties through tailored synthesis routes, recognizing the profound impact of morphology and elemental composition on enhancing photocatalytic dye degradation performance. [ABSTRACT FROM AUTHOR]

Metal-oxide nanomaterials represent a promising and inexpensive alternative to plasmonic metallic nanostructures currently used for surface-enhanced Raman scattering (SERS) spectroscopy. They profit from a chemical enhancing mechanism, i.e., charge transfer between the adsorbed molecule and the substrate. In this study, SERS-active nanostructured films based on vanadium pentoxide (V 2 O 5) are produced by the combination of gas-phase synthesis of nanoparticles followed by their thermal annealing, i.e., using a fully solvent- and linker-free procedure. The SERS performance of V 2 O 5 nanoparticle films was found to be strongly linked with porosity and the appropriate crystalline structure adjusted by annealing. A Raman spectroscopy and X-ray diffraction revealed that V 2 O 5 crystalline nanoparticles are formed only after the annealing at temperatures equal to or higher than 300 °C. Such produced V 2 O 5 nanoparticle films allow for sensitive and reproducible detection of organic dyes (methylene blue, rhodamine 6G and crystal violet), while their SERS enhancement (analytical enhancement factor close to 103) is significantly higher as compared with magnetron sputtered and annealed V 2 O 5 thin films. Our study represents an important step in designing novel plasmon-free SERS-active platforms with the aim of improving their stability and spectral reproducibility compared to other non-plasmonic and plasmonic ones. [ABSTRACT FROM AUTHOR]

[Display omitted] • A stable organic radical dye has been synthesized which showed high fluorescence intensity in the NIR-II region; • Polypeptide nanoparticles encapsulating the dye shows high bright in NIR-II region with high photothermal efficiency; • Mild photothermal therapy (m-PTT) has been achieved using the nanoparticle; • M−PTT led to the creation of immunostimulatory tumor vaccines. Stable organic radicals have emerged as a promising option to enhance fluorescence quantum yield (QY), gaining traction in medical treatment due to their unique electronic transitions from the ground state (D 0) to the doublet excited state (D 1). We synthesized a stable dicyanomethyl radical with a NIR-II fluorescence QY of 0.86 %, surpassing many NIR-II organic dyes. Subsequently, amphiphilic polymer-encapsulated nanoparticles (NPs) containing the radical were created, achieving a NIR-II fluorescence QY of 0.32 %, facilitating high-contrast bio-imaging. These CNPPs exhibit self-enhanced photothermal properties, elevating photothermal conversion efficiency (PCE) from 43.5 % to 57.5 % under 915 nm laser irradiation. This advancement enables more efficient photothermal therapy (PTT) with lower dye concentrations and reduced laser power, enhancing both feasibility and safety. Through regular fractionated mild photothermal therapy, we observed the release of damage-associated molecular patterns (DAMPs) and an increase in cytokine expression, culminating in combined mild phototherapy (m-PTT)-mediated immunogenic cell death (ICD). Consequently, we developed an immunostimulatory tumor vaccine, showcasing a novel approach for refining photothermal agents (PTA) and optimizing the PTT process. [ABSTRACT FROM AUTHOR]

Small CoTiO 3 nanoparticles were embedded in TiO 2 nanoshells to boost peroxymonosulfate (PMS) activation and enhance 4-chlorophenol (4-CP) degradation due to the enhanced mass transfer in the confined space, and efficient electron transfer between PMS and TiO 2 /CoTiO 3. [Display omitted] Creating a microenvironment for enhanced peroxymonosulfate (PMS) activation is vital in advanced oxidation processes. The objective of this study was to fabricate nanoshells composed of titanium dioxide embedded with cobalt titanate nanoparticles of perovskite to act as nanoreactors for effectively initiating PMS and degrading contaminants. The unique porous structure and confined space of the nanoreactor facilitated reactant absorption and mass transfer to the active sites, resulting in exceptional catalytic performance for pollutant elimination. Experimental findings revealed close to 100% decomposition efficiency of 4-chlorophenol (4-CP) within an hour utilizing the nanoreactors over a wide pH range. The TiO 2 /CoTiO 3 hollow nanoshells catalysts also displayed adaptability in disintegrating organic dyes and antibiotics. The radicals SO 4 •-, •OH, and non-radicals 1O 2 were determined to be accountable for eliminating pollutants, as supported by trapping experiments and electron paramagnetic resonance spectra. The catalyst was confirmed as an electron donor and PMS as an electron acceptor through electrochemical tests and density functional theory calculations. This study underscores the potential of incorporating stable perovskite catalysts in hollow nanoreactors to enhance wastewater treatment. [ABSTRACT FROM AUTHOR]

[Display omitted] • Nanosized ZnGa 2 O 4 :Cu was designed for continuously degrading pollutants. • The doping of Cu(II) highly increased the persistent production and availability of active species. • •H radicals were identified as the main active species. • A possible mechanism for the persistent degradation of dyes was proposed. Photocatalysis is considered as an environmentally friendly and sustainable method as it can produce active species to degrade pollutants. However, its applications are hindered by the turbidity of pollutants and the requirements for continuous or repeated in situ irradiation. To avoid the need for continuous in situ irradiation in the photocatalytic process, herein we report the doping of Cu(II) ions into zinc gallate (ZnGa 2 O 4) as traps to capture photo-generated electrons. In this way, long lifetime charge release and separation were effectively achieved for the persistent degradation of organic dyes in wastewater. The Cu(II) doped ZnGa 2 O 4 (ZGC) nanoparticles with a small size about 7.7 nm synthesized via a hydrothermal method exhibited a persistent photocatalytic activity with continuous production of reactive oxygen species for at least 96 h without in situ irradiation due to its unique electronic structure and carrier transport path, and enabled to degrade 82.2 % of rhodamine B in 1 h. Further investigation revealed that the doped Cu(II) ions occupied the octahedral sites of ZGC and highly increased the persistent production and availability of active species for the persistent degradation of organic dyes under pre-illuminated conditions. [ABSTRACT FROM AUTHOR]

The presence of organic dyes in wastewater raises significant environmental and human health concerns, owing to their high toxicity. In light of this, a novel adsorbent material with porous cryogel architecture was developed and employed for the effective removal of organic dyes from an aqueous solution. Initially, a titanium dioxide nanowire doped with zirconium HZTO was synthesized by the hydrothermal process. Subsequently, the beads (SA/HZTO) of sodium alginate and HZTO were successfully prepared through a cross-linking process, employing Ca2+ ions as the crosslinking agent. Structural analysis of SA/ HZTO beads was performed using FTIR, SEM, and EDX techniques. We systematically examined the impact of different conditions, including the initial dye concentration, pH, contact time, and adsorbent dosage, on the adsorption process. Batch experiments, both in signal and binary systems, were conducted to rigorously assess the dye adsorption capabilities. Kinetic modeling revealed that the adsorption process adhered to the pseudo-second-order kinetic model. Remarkably, the prepared beads exhibited impressive adsorption capacities of 26 and 29 mg/g toward methylene blue (MB) and safranin (SF), respectively. SA/ HZTO beads have demonstrated excellent adsorption properties, offering a promising avenue for the development of low-cost, efficient, and reusable adsorbent to remove dyes from wastewater. [ABSTRACT FROM AUTHOR]

The transient electron donor–acceptor (EDA) complex has been an emerging area in the photoinduced organic synthesis field, generating radicals without exogenous transition‐metal or organic dye‐based photoredox catalysts. The catalytic platform to form suitable photoactive EDA complexes for photochemical reduction reactions remains underdeveloped. Herein, a general photoinduced reductive alkylation via the EDA complex strategy is described. A simple yet multifunctional system, triphenylphosphine and iodide salt, promotes the photoinduced decarboxylative hydroalkylation, and reductive defluorinative decarboxylative alkylation of trifluoromethyl alkenes, to access trifluoromethyl alkanes and gem‐difluoroalkenes. Moreover, decarboxylative hydroalkylation can be applied to more kinds of electron‐deficient alkenes as a general Giese addition reaction. [ABSTRACT FROM AUTHOR]

Today, nanoscience explores the potential of nanoparticles due to their extraordinary properties compared to bulk materials. The synthesis of metal nanoparticles using plant extracts is a very promising method for environmental remediation, which gets global attention due to pollution-led global warming. In the present study, iron nanoparticles (FeNPs) were successfully synthesized by the green method using Vernonia amygdalina plant leaf extract as a natural reducing and capping agent. Biosynthesized FeNPs were characterized with different analytical techniques such as UV–visible, FT-IR, XRD, and SEM. The analysis revealed the formation of amorphous FeNPs with an irregular morphology and non-uniform distribution in size and shape. The average particle size was approximately 2.31 µm. According to the catalytic degradation investigation, the FeNPs produced via the green approach are highly effective in breaking down both CV and MB into non-toxic products, with a maximum degradation efficiency of 97.47% and 94.22%, respectively, when the right conditions are met. The kinetics study exhibited a high correlation coefficient close to unity (0.999) and (0.995) for the degradation of MB and CV, respectively, for the zero-order pseudo-kinetics model, which describes the model as highly suitable for the degradation of both dyes by FeNPs compared to other models. The reusability and stability of biosynthesized nano-catalysts were studied and successfully used as efficient catalysts with a slight decrease in the degradation rate more than four times. The results from this study illustrate that green synthesized FeNPs offer a cost-effective, environmentally friendly, and efficient means for the catalytic degradation of organic dyes. [ABSTRACT FROM AUTHOR]

In this study, a series of AgCl/ZnO-loaded nanofibrous membranes were prepared using coaxial electrospinning. Their physical and chemical characteristics were evaluated by SEM, TEM, XRD, XPS, IR, PL, and UV–visible spectrometer, and the photocatalytic experiments using methylene blue (MB) as a model pollutant. The formation of AgCl/ZnO heterojunction and the structure of core–shell nanofibers with porous shell layer were confirmed. AgCl/ZnO photocatalysts were also effectively loaded onto the surfaces of the porous core–shell nanofibers. The results of photocatalytic experiments revealed that the AgCl/ZnO (MAgCl:MZnO = 5:5)-loaded nanofibrous membrane achieved a degradation efficiency of 98% in just 70 min and maintained a photocatalytic efficiency exceeding 95% over the first five experimental cycles, which successfully addressed the issues of photocatalytic efficiency loss during the photodegradation of MB with AgCl/ZnO nanoparticles as photocatalyst. The photodegradation mechanism was also researched and proposed. [ABSTRACT FROM AUTHOR]

In this work, a novel adsorbent called magnetite/MXene (Fe3O4/Ti3C2) nanocomposite was prepared, characterized, and applied for the removal of organic dye, malachite green dye (MG), from both real water and model solutions. Numerous techniques were used to characterize the prepared Fe3O4/Ti3C2 nanocomposite: XRD, SEM, TEM, FTIR, and surface area analysis. The outcomes showed that the Al layer had been selectively etched, that the MAX phase (Ti3AlC2) had been transformed into layered Ti3C2 MXene, that the cubic Fe3O4 phase had been prepared, and that the prepared Fe3O4 NPs had been evenly distributed on the MXene surface. Also, SEM pictures showed the successful etching of the MAX phase and the formation of the ultrathin multi-layered MXene, which the Fe3O4 NPs covered upon forming the Fe3O4/Ti3C2 nanocomposite at the surface and inside the ultrathin multi-layered MXene. The effect of different operational parameters affecting the removal process was explored and optimized. The MG dye was removed mostly within 60 min, with a 4.68 mg/g removal capacity using 5 mg of the Fe3O4/Ti3C2 nanocomposite. The removal was examined from both kinetic and thermodynamic perspectives, and the findings demonstrated the spontaneity of the removal process as well as the applicability of fractal-like pseudo-first-order and fractal-like pseudo-second-order kinetics when compared to other kinetics models. The Fe3O4/Ti3C2 nanocomposite was used to remove MG dye from real spiked environmental water samples, and the results revealed the successful remediation of the real samples from the organic dye by the Fe3O4/Ti3C2 nanocomposite. Accordingly, Fe3O4/Ti3C2 nanocomposite could be considered a potential adsorbent for the environmental remediation of polluted water. [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]

Herein, core–shell magnetic nanoparticles are modified with imidazolium-tagged phosphine and propylene glycol moieties and used for the stabilization of bimetallic AuCu nanoparticles. The structure and morphology of the prepared material are identified with SEM, TEM, XRD, XPS, atomic absorption spectroscopy, Fourier translation infrared spectroscopy, and a vibrating sample magnetometer. This hydrophilic magnetic bimetallic catalyst is applied in the reduction of toxic nitroarenes and reductive degradation of hazardous organic dyes such as methyl orange (MO), methyl red (MR), and rhodamine B (RhB), as well as in the degradation of tetracycline (TC). This magnetic AuCu catalyst indicated superior activity in all three mentioned reactions in comparison with its single metal Au and Cu analogs. This catalyst is recycled for 17 consecutive runs in the reduction of 4-nitrophenol to 4-aminophenol without a significant decrease in catalytic activity and recycled catalyst is characterized. [ABSTRACT FROM AUTHOR]

Recent progress in the development of MnO2-based micromotors has shown the immense potential of these motile devices to remediate environmental contamination. However, the production of such micromotors on an industrial scale through a facile, efficient and reproducible process remains challenging. The present work aimed to address this issue using naturally occurring and abundant pine pollen (PP) grains. The immersion of PP in potassium permanganate (KMnO4) solutions was found to generate MnO2 nanoparticles (NPs) on the PP surfaces, the amount and distribution of which was readily adjusted by varying the coating time. Because of the asymmetrical shape of the PP grains, the MnO2/PP composites exhibited rapid self-propulsion at a maximum speed of 360.686 μm/s (approximately eight body lengths/s) in low-concentration hydrogen peroxide (H2O2) solutions. The ability of these materials to remediate heavy metal pollutants was also examined and was evidently increased by a factor of 1.5 compared with static counterparts. These composites could also be recovered and reused over three consecutive cycles. The competitive cost, continuous motion and superior decontamination capacity of these materials suggests potential applications in the rapid removal or degradation of heavy metal ions, toxic organic dyes, pathogenic bacteria and other pollutants in wastewater. These micromotors represent a new approach to the utilization of natural materials in environmental remediation. [ABSTRACT FROM AUTHOR]

The effect of plasmonic nanoparticles (NPs) on the fluorescence and phosphorescence intensity of organic dye molecules was studied theoretically and experimentally. A theoretical model that takes into account nonradiative transfer of excitation energy from a molecule to an NP and the changes in the rates of spontaneous emission and light absorption by a molecule near an NP was proposed to calculate the luminescence intensity of a molecule in the presence of a plasmonic NP. Numerical estimates for an erythrosine molecule and a silver NP showed that the greatest increase in luminescence was observed at distances of 4–8 nm between the molecule and the NP surface. Experimentally observed changes in luminescence spectra and shortening of the erythrosine triplet state lifetime in poly(vinyl alcohol) films doped with silver NPs were explained using the proposed model. [ABSTRACT FROM AUTHOR]

Context: A series of five organic dyes (Mi, i = 1–5) of the D-A'-π-A structure were designed based on reference dye (Ref), and the influence of different auxiliary acceptors (A') on their efficiency in dye-sensitized solar cells (DSSC). Methods: Was studied theoretically using density functional theory (DFT) and time-dependent DFT (TD-DFT) methods. In this context, the electronic structures, optical properties, and the parameters influencing the power conversion efficiency (PCE), such as light harvesting efficiency (LHE), electron injection driving force (∆Ginject.), and open circuit photo-voltage (VOC), have been evaluated and discussed. The modification of the auxiliary acceptor (A') in the D-A'-π-A structure of the designed organic dyes has the advantage of significantly decreasing the band gap, which leads to the broadening of the absorption band that is red-shifted and improves the photovoltaic characteristics compared to Ref. Theoretical results reveal that M1, and M5 can be used as excellent sensitizer candidates for DSSC applications. [ABSTRACT FROM AUTHOR]

The release of organic contaminants has grown to be a major environmental concern and a threat to the ecology of water bodies. Persulfate-based Advanced Oxidation Technology (PAOT) is effective at eliminating hazardous pollutants and has an extensive spectrum of applications. Iron-based metal–organic frameworks (Fe-MOFs) and their derivatives have exhibited great advantages in activating persulfate for wastewater treatment. In this article, we provide a comprehensive review of recent research progress on the significant potential of Fe-MOFs for removing antibiotics, organic dyes, phenols, and other contaminants from aqueous environments. Firstly, multiple approaches for preparing Fe-MOFs, including the MIL and ZIF series were introduced. Subsequently, removal performance of pollutants such as antibiotics of sulfonamides and tetracyclines (TC), organic dyes of rhodamine B (RhB) and acid orange 7 (AO7), phenols of phenol and bisphenol A (BPA) by various Fe-MOFs was compared. Finally, different degradation mechanisms, encompassing free radical degradation pathways and non-free radical degradation pathways were elucidated. This review explores the synthesis methods of Fe-MOFs and their application in removing organic pollutants from water bodies, providing insights for further refining the preparation of Fe-MOFs. [ABSTRACT FROM AUTHOR]

Functionalized conjugated microporous polymers (CMPs) containing amino, imino, and hydrazine groups are synthesized by the Sonogashira–Hagihara coupling reaction. Notably, the porosities, thermal stabilities, and morphologies of the CMPs can be controlled by the introduction of functional groups. Here, the relationships between the functional groups and photocatalytic performance are discussed for the first time. The CMP nanowires exhibit excellent photocatalytic performance in organic pollutant degradation: the degradation rate obtained by CMP-I3 bearing naphthalene groups via an imine bond is > 99.99%, and ~ 99.71% of the degradation activity is maintained after five cycles. Notably, the excellent photocatalytic properties of CMP-I3 are imparted by the introduction of the naphthalene groups, which reduced the band gap. The improved charge-transfer activity accounts for the highest and lowest photocurrent intensity and resistance achieved, respectively. Furthermore, the photocatalytic mechanism of CMPs reveals that the superoxide anion is the main active substance in the photocatalytic degradation of dyes. [ABSTRACT FROM AUTHOR]

This work aims to enhance the photocatalytic activity of ZnO films for persistent organic pollutants. The photocatalysis method has gained significant interest as a sustainable and environmentally friendly approach to enhance the safety of clean water by eliminating persistent organic pollutants. Zinc oxide as a transition metal oxide is recognized as a highly effective material for photocatalysis. Even so, ZnO can be modified to increase its action and result in a more significant degradation of organic pollutants. In the photocatalytic process, an electron from the valence band is excited and moves to a higher energy level, the conduction band. Thus, an electron-hole pair is formed. Unstoichiometry transition metal oxides, such as MnOx are hole-trapping co-catalysts that promote oxidation processes. This research reported the sol-gel synthesis of ZnO nanostructured films co-catalytic modified with MnOx for organic dye degradation. The confirmed features of ZnO/MnOx films are characterized by different analytical tools such as atomic force microscopy (AFM), X-ray diffraction analysis (XRD) and UV-Vis spectroscopy. The surface of the zinc oxide revealed a hexagonal wurtzite structure and a visible ganglia-like pattern. MnOx co-catalytic modification plays a vital role in the percent degradation of the organic dye under UV-irradiation conditions. [ABSTRACT FROM AUTHOR]

Combination of affordable organic dyes of high quantum yield with silicon can be an interesting way for development of highly efficient thin film photovoltaic cells utilizing silicon sensitisation. This work is focused on investigating the energy transfer processes including photon tunnelling from photosensitive molecules of BASF R305 high quantum yield dye to silicon substrate. Energy transfer from dye molecules to silicon substrate is evaluated by measuring the quenching of molecular photoluminescence lifetime using time-correlated single photon counting (TCSPC) technique. Energy transfer is further studied in dependence on dye layer thickness. The results can be useful for further studies leading to design of ultrathin silicon solar cells. [ABSTRACT FROM AUTHOR]

Piezoelectric materials can convert mechanical energy into electrical energy, and further piezocatalysis can be designed based on the product between piezoelectric effect and electrochemical redox effect, which is hopeful for the actual dye decomposition. Tourmaline is a natural mineral with spontaneous polarization, which is an ideal piezocatalytic material and is rarely reported in dye decomposition. In this work, after 100 mg tourmaline powder is vibrated for 120 min, the piezocatalytic dye decomposition ratios of rhodamine B (RhB), methylene blue, and methyl orange are ∼95%, ∼46%, and ∼23%, respectively. The corresponding first‐order reaction kinetic values for these three dyes are 0.02681, 0.00639, and 0.00246 min−1, respectively. By adjusting the pH value of the initial RhB solution to 5, the decomposition ratio can reach ∼99% after only 60 min of vibration. In the process of dye decomposition, it is determined that the main active substances are hydroxyl radicals and superoxide radicals via electron spin–resonance spectra test. The spontaneous polarization performance of tourmaline can effectively adsorb dye molecules to promote the catalytic reaction. Natural tourmaline minerals are abundant, low cost, and environmentally friendly making them suitable for large‐scale piezocatalysis of mineral materials. [ABSTRACT FROM AUTHOR]

Environmental contamination is a major global concern. Organic dyes pose a significant threat as water pollutants, leading to the depletion of natural resources. Molybdenum disulfide (MoS2), a type of two-dimensional transition metal dichalcogenide, has gained considerable attention due to its impressive properties, such as stability, surface area, and tunable interlayer spacing. It has emerged as a promising material for both photocatalytic degradation and adsorption of harmful organic dyes. This article provides an overview of recent advancements in MoS2-based nanomaterials for the removal of organic dyes from solutions through adsorption and photocatalytic processes. The review delves into the fundamental properties of MoS2, explores various synthesis methods, and various modifications of the material to enhance its dye removal efficiency, and addresses potential challenges associated with its application in this field. Furthermore, the article discusses the prospects for improving MoS2-based materials for enhanced adsorption and photocatalytic degradation of organic dyes. [ABSTRACT FROM AUTHOR]

The use of residual microbial biomass from various industries in emerging pollutant removal strategies represents a new area of research in the field. In this case, we examined how to remove reactive dyes from an aqueous solution utilizing a biosorbent made of residual biomass from immobilized Saccharomyces pastorianus (S. pastorianus) in a polymer matrix using a dynamic system. Fluidized bed column biosorption investigations were carried out on a laboratory scale. Brilliant Red HE-3B was chosen as the target molecule. The main parameters considered for this purpose were the flow rate (4.0 mL/min; 6.1 mL/min), initial pollutant concentration (51.2 mg/L; 77.84 mg/L), and biosorbent mass (16 g; 20 g). The experimental data of the fluidized bed study were evaluated by mathematical modeling. The Yoon–Nelson, Bohart–Adams, Clark, and Yan models were investigated for an appropriate correlation with the experimental data. An acceptable fit was obtained for a flow rate of 4 mL/min, an initial pollutant concentration of 51.2 mg/L, and a biosorbent amount of 20 g. The obtained results indicate that the biosorbent can be used efficiently in a dynamic system both for the removal of the studied dye and in extended operations with a continuous flow of wastewater. As a conclusion, the investigated biocomposite material can be considered a viable biosorbent for testing in the removal of reactive dyes from aqueous environments and creates the necessary conditions for the extension of studies toward the application of these types of biosorbents in the treatment of industrial effluents loaded with organic dyes. [ABSTRACT FROM AUTHOR]

Organic dyes in natural waters jeopardize human health. Whether semiconductor materials can effectively degrade dyes has become a challenge for scientific research. Based on this, this study rationally prepared different nanocomposites to remove organic dyes effectively. Pure SnO2 quantum dots, ZnO nanosheets, and SnO2/ZnO (ZS) binary nanocomposites are prepared using the hydrothermal method. Subsequently, SnO2/ZnO@GO (ZSG) ternary composites containing different amounts of GO, i.e., ZSG-5, ZSG-15, and ZSG-25, are synthesized by an ultrasonic water bath method, in which ZS was coupled with GO to form Z-type heterojunctions. The ZSG-15 ternary composites exhibited excellent photocatalytic activity for the degradation of rhodamine B by simulating sunlight. The test results show that the degradation rate of ZSG-15 is about 7.6 times higher than ZnO. The increase in photocatalytic activity is attributed to the synergistic effect of SnO2 and GO to improve the separation efficiency of photogenerated carriers in ZnO. Notably, the large specific surface area of GO increases the reactive sites. Compared with binary nanocomposites, ZSG-15 broadens the response range to light while further accelerating the electron transport rate and improving the photoelectric stability. [ABSTRACT FROM AUTHOR]

Synthetic organic dyes are coloring agents used in various industries. Despite the fact that they offer exciting colors and long-lasting effects, certain organic dyes can have harmful impacts on human health and aquatic ecosystems. This study investigates the photocatalytic degradation of malachite green dye using Ni–TiO2 nanoparticles (NPs) and Ni–TiO2/PANI nanocomposites (NCs) in various reaction conditions. The surface and compositional change of synthesized photocatalysts were characterized by XRD, FTIR, AAS, and UV–vis spectrophotometer. Accordingly, the XRD results signify the crystal structure of photocatalysts found to be tetragonal anatase phase while the FT-IR spectra indicate the titanium has predominantly form a coordination compound upon reaction with nitrogen atom through weakening the bond strength between C═N, C═C, and C─N in the PANI. The UV–vis measurement shows that the energy bandgaps were decreased from 3.20 to 2.77 eV and 2.59 eV for Ni–TiO2 NPs and Ni–TiO2/PANI NCs, respectively. From AAS data, the authors confirmed that Ni metal has significantly existed in the aforementioned photocatalysts after the calcination process. The photocatalytic degradation of Ni–TiO2 NPs and Ni–TiO2/PANI NCs on the model dye has studied and their efficiency was 94.22% and 99.09%, respectively. The photocatalytic degradation follows pseudo-first order with 2.23 × 10−2 min−1 reaction rate at optimum conditions of pH 8.5, initial dye concentration of 0.2 g/L, catalyst load of 0.2 g/L, and irradiation time of 90 min. With this, the outstanding result recorded using Ni–TiO2/PANI NCs is ascribed to the smaller particle size as compared to Ni–TiO2 NPs, and it is found to be the promising photocatalyst for the removal of wastewater containing organic dyes. [ABSTRACT FROM AUTHOR]

The accelerating use of organic dyes in various industries has led to a surge in water pollution, especially from non-biodegradable dye effluents discharged into water resources. This study addresses the critical issue of catalyzing the reduction of two prevalent dyes, methylene blue (MB) and rhodamine-B (RhB), using a multiwalled carbon nanotube-cobalt ferrite (MWCNT-CF) nanocomposite. The synthesized nanocomposite demonstrates exceptional catalytic activity, stability, and recyclability. Conventional methods for treating dye-containing wastewater often prove expensive. This study explores the efficacy of catalytic reduction, a relatively fast process facilitated by semiconductor nanoparticles. Structural analyses using X-ray diffraction and high-resolution transmission electron microscopy (HRTEM) confirm the formation of the nanocomposite, revealing unsaturated surface bonds and chains conducive to adsorption. The nanocomposite exhibits a remarkable reduction in both dyes, with easy recyclability for multiple cycles. Magnetization studies confirm the ferrimagnetic nature of the nanocomposite, facilitating its efficient separation from the reaction mixture using a magnet. The study delves into the kinetics of the catalytic reduction following pseudo-first-order kinetics. The surface modifications of the nanocomposite, as revealed by TEM, contribute to enhanced adsorption and catalytic efficiency. Notably, the MWCNT-CF nanocomposite demonstrates negligible loss of catalytic activity during recycling, highlighting its potential for cost-effective and sustainable applications in dye reduction across various industries. [ABSTRACT FROM AUTHOR]

Water contamination with synthetic dyes is an escalating problem worldwide. Herein, Co3O4-decorated reduced graphene oxide (Co3O4-rGO) is reported as an effective heterogeneous photocatalyst for the decomposition of organic dyes. The synthesis of Co3O4-rGO was confirmed via spectroscopic techniques including XRD, XPS, TEM, and FTIR. After characterization, the prepared Co3O4-rGO composite was tested as a photocatalyst for the degradation of methylene blue and methyl orange. The photocatalytic efficiency of Co3O4-rGO was >95% after 60 min, corresponding to 200 mg/L as the initial concentration of each dye. The photodegradation of MB and MO was confirmed by BOD and COD measurements. Experimental parameters like the re-usability of Co3O4-rGO, the effect of catalyst dosage, and the effect of dye concentration on photocatalytic activity were also investigated. The photocatalytic activity of Co3O4-rGO for the degradation of MB was 2.13 and 3.43 times higher than that of Co3O4 and rGO, respectively. Similarly, the photocatalytic activity of Co3O4-rGO for the degradation of MO was 2.36 and 3.56 times higher than that of Co3O4 and rGO, respectively. Hence, Co3O4-rGO was found to be an efficient and reusable photocatalyst for the decomposition of selected dyes in the aqueous medium. [ABSTRACT FROM AUTHOR]

Context: This research aims to investigate the potential of pyrazine-based small donor moieties as donor–acceptor switches for optical and photovoltaic applications. The designed organic dyes have a high light harvesting efficiency (LHE) and can potentially generate significant electrical energy. Methods: The study focuses on understanding the structural and electronic properties of these dyes through the analysis of dihedral angles, bond lengths, and energies of frontier molecular orbitals The UV–Vis spectroscopy parameters of the designed organic dyes revealed their absorption characteristics, including transition energies, wavelengths (λmax), and oscillator strengths (f). The photovoltaic properties of the developed organic dyes show a range of values: a range of 0.95–0.99 for LHE and a range of 1.77–33.02 W for maximum power output (Pmax) with the highest value for dye DDP5. For their stabilization energies, their natural bond orbitals had values ranging from 0.56 to 128.48 kcal/mol, their E(j)E(i) values from 0.22 to 1.29 a.u, and their Fi,j values from 0.024 to 0.213 kcal/mol. Out of all dyes, the DDP5 produced highest push–pull effect and can be good choice for further studies. The design of these novel organic materials for effective and economical solar energy conversion will be aided by evaluating the potential of 5,10-diphenyl-5,10-dihydrophenazine as a donor moiety and determining the structure–property correlations controlling the photovoltaic performance of the compounds. [ABSTRACT FROM AUTHOR]

Surface-enhanced Raman spectroscopy (SERS) is a highly sensitive and reliable fingerprinting technique. However, its analytical capability is closely related to the quality of a SERS substrate used for the analysis. In particular, conventional colloidal substrates possess disadvantages in terms of controllability, stability, and reproducibility, which limit their application. In order to address these issues, a simple, cost-effective, and efficient SERS substrate based on silver nanoparticle arrays (Ag NPAs) and sandpaper-molded polydimethylsiloxane (SMP) was proposed in this work. Successfully prepared via template lithography and liquid–liquid interface self-assembly (LLISA), the substrate can be applied to the specific detection of organic dyes in the environment. The substrate exhibited good SERS performance, and the limit of detection (LOD) of rhodamine 6G (R6G) was shown to be 10−7 M under the optimal conditions (1000 grit sandpaper) with a relative standard deviation (RSD) of 7.76%. Moreover, the SERS signal intensity was maintained at 60% of the initial intensity after the substrate was stored for 30 days. In addition, the Ag NPAs/SMP SERS substrate was also employed to detect crystal violet (CV) and methylene blue (MB) with the LODs of 10−6 M and 10−7 M, respectively. In summary, the Ag NPAs/SMP SERS substrate prepared in this study has great potential for the detection of organic dyes in ecological environments. [ABSTRACT FROM AUTHOR]

Herein, zinc oxide nanoparticles (ZnO NPs) were synthesized using Parthenium hysterophorus whole plant aqueous extract as reducing and capping agents. The synthesized ZnO NPs were characterized via UV-Vis spectroscopy, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and dynamic light scattering (DLS). An intrinsic optical absorbance of ZnO NPs occurred at 337 nm in the UV-Vis spectrum. The FTIR analysis revealed the presence of secondary metabolites responsible for reducing and stabilizing the nanoparticles. Furthermore, SEM and TEM images revealed that ZnO NPs were spherical with an average particle size of 38 nm. The XRD analysis revealed that ZnO NPs had a hexagonal wurtzite crystal structure with a crystallite size of 42.6 nm. The synthesized nanoparticles were investigated for degradation ability against methylene blue dye at varying conditions of ZnO NPs' dosage, methylene blue concentrations, pH, temperature, and interaction time. Degradation efficiency of 55.69% was obtained at optimal conditions using 50 mg of ZnO NPs, 5 mg/L of MB dye concentration, and pH 12 and at 65°C within 32 minutes. Due to their novel green synthesis route, Parthenium hysterophorus-mediated ZnO NPs are promising candidates for removing persistent organic dyes from aquatic environments. [ABSTRACT FROM AUTHOR]

In this study, the Fe3O4/rGO/Ag magnetic nanocomposite was synthesized and employed as an adsorbent for the removal of tetracycline (TC), crystal violet (CV), and methylene blue (MB) from water samples. The influential parameters in the removal process were identified and optimized using response surface methodology (RSM). Characterization of the product was performed through field emission scanning electron microscopy (FE-SEM), Fourier-transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), vibrating-sample magnetometer (VSM), and X-ray diffraction (XRD) analysis. XRD and SEM analysis revealed the successful synthesis of the Fe3O4/rGO/Ag nanocomposite. EDX analysis elucidated the accuracy and clarity of the chemical composition of the magnetic nanocomposite structure. Additionally, the separation of the nano-adsorbent from the solution can be achieved using a magnetic field. Maximum removal of analytes was obtained at pH of 6, amount of nanocomposite 0.014 g, ultrasonic time of 8 min and concentration of 21 mg L−1. Under optimal conditions, the removal efficiencies for TC, CV, and MB were 91.33, 95.82, and 98.19%, respectively. Also, it was observed that after each adsorption–desorption cycle, Fe3O4/rGO/Ag magnetic nanocomposite had good stability to remove TC, CV, and MB. Achieving nearly 98% removal efficiency in optimal conditions showed that Fe3O4/rGO/Ag magnetic nanocomposite is an effective adsorbent for removing TC, CV, and MB from wastewater samples. [ABSTRACT FROM AUTHOR]

The traditional pigments of Chinese painting are taken from the mountains and used naturally, and have been accompanied by the artistic belief of the Chinese nation in the unity of nature and man for thousands of years. These crystal brilliant, stable nature of inorganic ores and organic plants, in the hands of ancient Chinese painters fine grinding, dense glue, layer by layer dye, transformed into the Chinese people's imitation and expression of all things color. From the initial direct selection of color substances from nature as pigments to the peak of heavy color painting in Tang and Song dynasties, the traditional pigments of Chinese painting embodied too much time value and human wisdom. The material of these mountains contains the painting stories of human beings, which is ancient and new and unchanged, and is an important and irreplaceable carrier of ancient information. At the end of the Ming Dynasty and the beginning of the Qing Dynasty, modern organic synthetic pigments were brought from the West by Western missionaries. These bright colors and simple colors quickly captured the hearts of people and had the meaning of competing for national colors. However, the nature of organic synthetic pigments is very unstable, and structural changes will occur in many cases such as high temperature, direct exposure, climate, acid and base changes, resulting in a large degree of discoloration and decolorization. At present, raw materials of traditional Chinese painting are scarce and techniques are lost, so it is urgent to get extensive attention and rescue from the painting circle. [ABSTRACT FROM AUTHOR]

In this study, pure CdO nanoparticles, magnetic Fe3O4 nanoparticles, and Fe3O4-CdO nanocomposites were prepared via a solution combustion method using cetyltrimethylammonium bromide (CTAB) as a template. These prepared nanomaterial samples were characterized by X-ray diffraction (XRD), ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoelectron microscopy (XPS), transmittance electron microscopy (TEM), and scanning electron microscopy (SEM) analysis. XRD patterns confirmed the purity and the crystalline nature of the prepared samples. FTIR and Raman spectra observed the metal-oxygen (M-O) bond formation. UV-vis DRS studies were performed to investigate the optical properties and the bandgap energy determination. The surface morphology and the size of the pure CdO nanoparticles, magnetic Fe3O4, and nanocomposites of Fe3O4-CdO were determined via TEM and SEM analysis. Under optimum experimental conditions, the Fe3O4-CdO nanocomposites were applied for photocatalytic activity against Methylene blue dye. Under visible light irradiation, Fe3O4-CdO nanostructures showed an efficient photocatalytic degradation of 92% against Methylene blue organic dye and showed excellent stability for multiple cycles of reuse. [ABSTRACT FROM AUTHOR]

Historically, the photocatalytic efficacy of graphitic carbon nitride (g-C3N4) has been constrained by a rapid charge recombination rate and restricted sensitivity to visible light. To overcome these limitations and enhance the performance of g-C3N4, the strategic formation of heterojunctions with semiconductor materials is deemed the optimal approach. The present study employed a facile sonication-assisted pyrolysis method to synthesize a g-C3N4@ZrO2 nanocomposite photocatalyst. This hybrid material was characterized extensively using a comprehensive suite of analytical techniques, including XRD, SEM, EDX, FTIR, and UV-Vis DRS. A comparative analysis of photocatalytic applications under identical conditions was conducted for all synthesized materials, wherein they were subjected to UVc light irradiation. The photocatalytic degradation of various dye models, such as MB, EY, and a combination of dyes, was assessed using the prepared nanocomposites. The g-C3N4@ZrO2 photocatalysts showcased superior photocatalytic performance, with a particular variant, g-CNZ6, exhibiting remarkable activity. With a bandgap energy of 2.57 eV, g-CNZ6 achieved impressive degradation efficiencies of 96.5% for MB and 95.6% for EY within 40 min. Following previous studies, the superoxide radical anions (O2−. and h+) were largely accountable for the degradation of MB. Therefore, the observed efficacy of the g-C3N4@ZrO2 nanocomposite photocatalyst can be attributed to the increased generation of these reactive species. [ABSTRACT FROM AUTHOR]

This paper studies the composition and properties of shells of bivalve mollusks (Crenomytilus grayanus, Callista brevisiphonata, and Mizuhopecten yessoensis) from coastal discharges with a view to the possibility of their use in photocatalytic water treatment systems. The clam shells are considered in terms of application in the form of a powder material as a precursor for creating photocatalysts, and also as a carrier of photocatalytic coatings. It was shown that the main phase composing the shell material was calcium carbonate in two crystallographic modifications—calcite and aragonite. The presence of inorganic impurities in all studied clam shells did not exceed one mass percent. The main share was made up of elements included in the composition of calcium carbonate, which confirmed the high bio-indifference of the materials under study. Depending on the physiological and environmental features of the structure of clam shells, different contents of the organic component in their composition were observed. The granulometric characteristics of crushed clam shells (average diameter, specific surface area, and distribution modality) were studied. It was shown that the maximum values of bending strength of 5 MPa and compressive strength of 2 MPa are characterized by Mizuhopecten yessoensis shells with the lowest porosity of 2.91%. The features of sorption and photosorption processes of both whole and crushed shells in relation to four organic dyes at different temperatures and degrees of illumination were studied. Based on crushed shells of Mizuhopecten Yessoensis and titanium dioxide, functional materials (CaxTiyOz) were obtained, and their morphology and photocatalytic properties were studied. An example of the practical use of clam shells as a carrier of a photocatalytic coating is given. [ABSTRACT FROM AUTHOR]

Context: In this work, we designed ten new organic phenothiazine dyes bridged by different πi-spacers (PTZ1-PTZ10) of D-π-A type based on the synthesized dye CC202-III for their efficacy in dye-sensitized solar cells (DSSC) applications. To learn how various π-spacers affect their performance in DSSCs, these isolated dyes and dye-cluster systems have had their geometries, electronic structures, absorption spectra, dipole moments, and molecular electrostatic potential examined and talked about. Additionally, a number of quantization parameters that affect power conversion efficiency (PCE), including light collection efficiency (LHE), reorganization energy (λtotal), vertical dipole moment (μnormal), strength electron injection driving force (ΔGinject), regeneration driving force (ΔGreg), excited state lifetime (τ), and open circuit voltage (VOC), were calculated in order to identify the organic dyes that would be best suited for DSSC applications. Calculated results revealed that the designed dyes PTZ3, PTZ4, PTZ5, and PTZ10 exhibit a lower energy gap among all dyes compared to the corresponding CC202-III. Additionally, PTZ3, PTZ4, PTZ5, PTZ7, PTZ8, PTZ9, and PTZ10 exhibit significant red-shifted absorption spectra compared to the other dyes with a larger oscillator strength, which improves the photocurrent density of the devices. The findings thus imply that bridge modification is a workable tactic to raise DSSC effectiveness. Method: We used density functional theory (DFT) and time-dependent DFT (TD-DFT) methods to study the electronic and photovoltaic properties of the dyes designed (PTZ1–PTZ10) to assess their effectiveness in DSSCs. DFT and TD-DFT simulations are theoretically used to deeply analyze key characteristics of all organic dyes that affect open-circuit voltage (VOC) and short-circuit current (JSC) to identify structure–property relationships. [ABSTRACT FROM AUTHOR]

This review aimed to summarize the current knowledge regarding dibenzofulvene derivatives (DBF) investigated for photovoltaics and organic electronics applications. The work begins with a detailed analysis of the synthesis and modification methods for dibenzofulvene derivatives' structure. Then, the physicochemical properties (thermal, electrochemical, and optical) of the selected compounds are discussed in detail. Moreover, this article also presents the DFT calculations performed so far. Finally, the review presents the latest research on the applications of dibenzofulvene derivatives as dyes for DSSC cells, hole transport materials (HTMs) for perovskite solar cells (PSCs), organic light-emitting diodes (OLEDs), and luminescent and electrochromic materials. Considering the above, this review may be helpful when designing new organic compounds for photovoltaic and organic electronic applications. [ABSTRACT FROM AUTHOR]