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Doped with high-quality neodymium ions, poly(methyl methacrylate) (PMMA) [(PMMA)-x wt% Nd3+] by using the traditional solution casting method, polymeric composite films with [x = 0, 0.025, 0.1, 0.25, 1.25, and 2.5 wt%] were formed. The XRD, SEM, UV–Vis–NIR, and electrical characteristics were used to characterize the films. According to XRD research, some interactions between PMMA and Nd2O3 result in a decrease in composite crystallinity. According to SEM, Nd2O3 particles were uniformly distributed throughout the host matrix. With Nd2O3 filler rose, the size of the particles also increased, leading to rising agglomeration. Incorporating Nd3+ ions into the polymer chains of (PMMA) significantly changed the optical energy gaps, causing the indirect optical gap to fall from 4.82 to 4.47 eV and the direct optical gap to drop from 4.98 to 4.85 eV. The behavior of the Urbach energy is the opposite of that of the bandgap energy. Additionally, the measured dielectric constant of the investigated composites showed a very alluring dielectric constant for the dielectric media. The examined films' dielectric constant and dielectric loss both decline exponentially as the incident frequency rises, while their AC electrical conductivity enhances as the Nd3+-ions content rises. The produced sheets were then used in the artificial UV-induced photodegradation of Methylene Blue. They demonstrated good potential for immobilizing Nd3+ for the photodegradation of contaminants typically present in water. [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]

The present study, La0.7Sr0.3MO3 (M = Mn-, Co-, and Fe-), perovskite, has successfully been synthesized via co-precipitation and sol–gel auto-combustion. XRD, SEM, and EDX characterized the prepared samples. XRD and SEM showed that the as-prepared La0.7Sr0.3MnO3 and La0.7Sr0.3CoO3 have multiphase. La0.7Sr0.3FeO3, in comparison, is nanosized, has a single-phase perovskite, and has a rather homogenous particle size distribution. Additionally, EDX mapping analysis shows that all pieces are distributed uniformly. According to X-ray diffractometer results, all calcined powders contain 100% LSF, more than 15% perovskite phase of LSC, 47% LSM, and other secondary phases, such as cobalt oxide. Aِt room temperature and magnetic field of ± 20 kG, La0.7Sr0.3MnO3 exhibited weak ferromagnetic behavior in a low magnetic field, whereas diamagnetic behavior was seen in a high magnetic field. La0.7Sr0.3FeO3 samples behave as strong ferromagnetic. On the contrary, the photodegradation of La0.7Sr0.3MnO3 is 99% compared to 75% and 91% for other samples under UVC lights of wavelength = 254 nm. The degradation rate for La0.7Sr0.3MnO3 is 0.179 higher, about 3.25 and 2.23, than the other samples. A La0.7Sr0.3MnO3 nanocomposite performs as a photocatalyst to enhance the efficiency of methylene blue photodegradation. This study boosts good UVC photocatalysts with high efficiency for different kinds of dyes. Hence, the catalyst possessed high stability and efficiency for continuous wastewater treatment. [ABSTRACT FROM AUTHOR]

An efficient and practical method for the synthesis of novel fused phosphorus heterocycles incorporating diethyl phosphonate by the one-pot in the presence of Fe3O4 nanoparticles as a reusable catalyst was achieved. The four-component reactions of ortho-substituted anilines, namely 2-aminophenol, 2-aminothiophenol and 1,2-phenylenediamine with salicylaldehyde, diethyl phosphite and hexaethylphosphorus triamide in the presence of Fe3O4 nanoparticles as a catalyst at 80–90 °C afforded the corresponding 1,3,2-benzo(oxaza/thiaza/diaza)phospholo[2,3-b][1,3,2]benzoxazaphosphinines 1–3 in good yields (80-84%). When the same reactions were repeated by substitution of salicylaldehyde with benzaldehyde, the 1,2-benzazaphospholo[2,1-b][1,3,2]benzo(oxaza/thiaza)phospholes 4 and 5 and 1,3,2-benzodiazaphosphole 6 derivatives were isolated in 78–83% yields. The structures of the synthesized compounds were established by elemental analysis and spectroscopic techniques (IR, MS and NMR). [ABSTRACT FROM AUTHOR]

A lanthanum oxide (La2O3)-ZnO nanostructured material was synthesized in the proposed study with different La2O3 concentrations, 0.001 g to 5 g (named So to S7), using the combustion method. X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transformation infrared spectroscopy (FT-IR) were utilized for investigating the structure, morphology, and spectral studies of the La2O3- ZnO nanomaterials, respectively. The results obtained from previous techniques support ZnO's growth from crystalline to nanoparticles' fine structure by changing the concentrations of lanthanum oxide (La2O3) dopants in the host matrix. The percentage of ZnO doped with La- influences the ZnO photocatalytic activity. SEM analysis confirmed the grain size ranged between 81 and 138 nm. Furthermore, UV-Vis diffuse reflectance spectroscopy was performed to verify the effects of La2O3 dopants on the linear optical properties of the nano-composite oxides. There was a variation in the energy bandgaps of La2O3-ZnO nanocomposites, increasing the weight concentrations of lanthanum dopants. The AC electrical conductivity, dielectric properties, and current–voltage properties support the enactment of the electrical characteristics of the ZnO nanoparticles by adding La2O3. All the samples under investigation were used for photodegradation with Rhodamine B (RhB) and Methylene Blue (MB). In less than 30 min of visible light irradiation, S4 (0.5 g) La2O3-ZnO reached 99% of RhB and MB degradation activity. This study showed the best photocatalytic effect for RhB and MB degradation of 0.13 and 0.11 min−1 by 0.5 g La2O3-ZnO. Recycling was performed five times for the nanocatalysts that displayed up to 98 percent catalytic efficiency for RhB and MB degradation in 30 min. The prepared La2O3-ZnO nanostructured composites are considered novel candidates for various applications in biomedical and photocatalytic studies. [ABSTRACT FROM AUTHOR]

An efficient and environmentally friendly combustion technique was employed to produce ZnO nanopowders with different Eu concentrations (from 0.001 g to 5 g). The structural morphology of the Eu2O3-ZnO nanocomposites was examined using XRD, SEM, and infrared spectroscopy (FT-IR). In addition, UV-Vis diffuse reflectance spectroscopy was also used to investigate the effects of europium (Eu) dopant on the optical behaviors and energy bandgaps of nano-complex oxides. The photocatalytic degradation efficiency of phenol and methylene blue was investigated using all the prepared Eu2O3-ZnO nanostructured samples. Photocatalytic effectiveness increased when europium (Eu) doping ratios increased. After adding moderate Eu, more hydroxyl radicals were generated over ZnO. The best photocatalyst for phenol degradation was 1 percent Eu2O3-ZnO, while it was 0.5 percent Eu2O3-ZnO for methylene blue solutions. The obtained Eu2O3-doped ZnO nanostructured materials are considered innovative, promising candidates for a wide range of nano-applications, including biomedical and photocatalytic degradation of organic dyes and phenol. [ABSTRACT FROM AUTHOR]

The incorporation of tungsten trioxide (WO3) by various concentrations of graphitic carbon nitride (g-C3N4) was successfully studied. X-ray diffraction (XRD), Scanning Electron Microscope (SEM), and Diffused Reflectance UV-Vis techniques were applied to investigate morphological and microstructure analysis, diffused reflectance optical properties, and photocatalysis measurements of WO3/g-C3N4 photocatalyst composite organic compounds. The photocatalytic activity of incorporating WO3 into g-C3N4 composite organic compounds was evaluated by the photodegradation of both Methylene Blue (MB) dye and phenol under visible-light irradiation. Due to the high purity of the studied heterojunction composite series, no observed diffraction peaks appeared when incorporating WO3 into g-C3N4 composite organic compounds. The particle size of the prepared composite organic compound photocatalysts revealed no evident influence through the increase in WO3 atoms from the SEM characteristic. The direct and indirect bandgap were recorded for different mole ratios of WO3/g-C3N4, and indicated no apparent impact on bandgap energy with increasing WO3 content in the composite photocatalyst. The composite photocatalysts' properties better understand their photocatalytic activity degradations. The pseudo-first-order reaction constants (K) can be calculated by examining the kinetic photocatalytic activity. [ABSTRACT FROM AUTHOR]

The growth of the textile industry results in a massive accumulation of dyes on water. This enormous rise in pigments is the primary source of water pollution, affecting the aquatic lives and our ecosystem balance. This study aims to notify the fabrication of neodymium incorporated copper oxide (Nd2O3 doped CuO) nanoparticles by combustion method for effective degradation of dye, methylene blue (MB). X-ray diffraction (XRD), Field emission Scanning electron microscopy (FESEM), Zeta potential have been applied for characterization. Photocatalyst validity has been evaluated for methylene blue degradation (MB). Test conditions such as time of contact, H2O2, pH, and photo-Fenton have been modified to identify optimal degradation conditions. Noticeably, 7.5% Nd2O3 doped CuO nanoparticle demonstrated the highest photocatalytic efficiency, up to 90.8% in 80 min, with a 0.0227 min−1 degradation rate. However, the photocatalytic efficiency at pH 10 becomes 99% with a rate constant of 0.082 min−1. Cyclic experiments showed the Nd2O3 doped CuO nanoparticle's stability over repeated use. Scavenge hydroxyl radical species responsible for degradation using 7.5% Nd2O3 doped CuO nanoparticles have been investigated under visible irradiation. [ABSTRACT FROM AUTHOR]

The cyclo condensation of some bi-functionally quinazolinones with some phosphorus dihalides in dry pyridine led to novel 1,3,4,2-oxadiazaphospholo[5,4-b]quinazolinones, 1,3,4,2-thiadiazaphospholo[5,4-b]quinazolinones and 1,2,4,3-triazaphospholo[5,1-b]quinazolinones. The structure of novel products was established by IR and NMR spectroscopy. [ABSTRACT FROM AUTHOR]

A series of La-doped (0.001-1 g) graphitic carbon nitride (g-C3N4) samples was prepared through the air atmospheric pyrolysis of melamine. Different analytical techniques were employed to characterize the structural, morphological, optical, and photocatalytic properties of both pure and doped g-C3N4 samples. The phase structures of pure and La-doped g-C3N4 samples were revealed by X-ray diffraction. The scanning electron microscopy analysis expressed that the well-defined particle shape became ambiguous, and the particle size gradually decreased with the increasing doping amount of La nitrate ions. Due to La doping on g-C3N4, the optical properties of the samples were improved. In comparison to pure g-C3N4, La-doped g-C3N4 manifested higher photocatalytic degradation efficiency toward methylene blue (MB) and phenol under visible light irradiation. [ABSTRACT FROM AUTHOR]

Designing heterostructure photocatalysts is a promising approach for developing highly efficient photocatalysts for hydrogen energy production. In this work, we synthesized a series of a covalent organic framework (COF)/g-C 3 N 4 (CN) heterojunction photocatalysts, denoted as x % COF/CN (in which x indicates the weight % of COF and x  = 5, 10, 20, 30, 40, 50, 90, 95, 100), for hydrogen production. The COF, which is a key component of the photocatalyst, was prepared by assembling benzothiadiazole (BT) and pyrene (Py) derivatives as building blocks. Integrating COF rods into the two-dimensional (2D) layered g-C 3 N 4 structure significantly improved photocatalytic H 2 production. The hybrid system (30 % COF/CN) displayed an outstanding hydrogen evolution rate (HER) of 27540 ± 805 μmol g -1 h -1 , outperforming most known COFs and g-C 3 N 4 -based photocatalysts, besides exhibiting stable photocatalytic performance. Moreover, the apparent quantum yield (AQY) was 15.5 ± 0.8 % at 420 nm. Experimental techniques and density functional theory (DFT) calculations demonstrated that the 30 % COF/CN heterostructure has broad visible-light absorption, adequate band energy levels, and the best chemical reactivity descriptors compared to the individual components, resulting in effective carrier separation and excellent performance. Our findings offer a valuable strategy for developing highly efficient and stable heterojunction photocatalysts for visible-light-driven H 2 evolution., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)