Structure, magnetic, and photocatalysis of La0.7Sr0.3MO3 (M = Mn, Co, and Fe) perovskite nanoparticles: Novel photocatalytic materials.

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.

Electrocatalytic Degradation of Rhodamine B Using Li-Doped ZnO Nanoparticles: Novel Approach.

In this paper, we discuss the preparation of Li-doped ZnO nanostructures through combustion and report on their structural, morphological, optical, and electrocatalysis properties. X-ray diffraction analyses show that the samples have a structure crystallized into the usual hexagonal wurtzite ZnO structure according to the P63mc space group. The scanning electron microscope images conceal all samples' nanosphere bundles and aggregates. The reflectance spectra analysis showed that the direct bandgap values varied from 3.273 eV (for pure ZnO, i.e., ZnL1) to 3.256 eV (for high Li-doped ZnO). The measured capacitance concerning frequency has estimated the variation of dielectric constant, dielectric loss, and AC conductivity against AC electric field frequency. The dielectric constant variations and AC conductivity are analyzed and discussed by well-known models such as Koop's phenomenological theory and Jonscher's law. The Raman spectra have been recorded and examined for the prepared samples. Rhodamine B was electro-catalytically degraded in all prepared samples, with the fastest time for ZnL5 being 3 min.

The Auto-Combustion Method Synthesized Eu2O3- ZnO Nanostructured Composites for Electronic and Photocatalytic Applications.

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.

The Photocatalytic Performance of Nd2O3 Doped CuO Nanoparticles with Enhanced Methylene Blue Degradation: Synthesis, Characterization and Comparative Study.

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.

Fabrication and Characterization of Highly Efficient As-Synthesized WO3/Graphitic-C3N4 Nanocomposite for Photocatalytic Degradation of Organic Compounds.

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.

Hybrid multifunctional core/shell g-C3N4@TiO2 heterojunction nano-catalytic for photodegradation of organic dye and pharmaceutical compounds.

The pyrolysis of melamine was an effective one-pot method for preparing a nanostructured multifunctional photocatalytic based on core/shell g-C3N4@TiO2 heterojunction. Various techniques entirely characterized these materials: X-ray diffraction (XRD) proved to enhance the as-prepared materials' crystallinity through the variation of dislocation, strain, and crystallite size with TiO2 loading. The stacked layered/sheet-like with a smooth surface of the as-prepared samples have been shown via scanning electron microscopy (SEM). Diffuse reflectance spectroscopy (DRS) showed an apparent decrease in the energy bandgap for these nanocomposites with TiO2 loading. All the prepared materials were subjected to visible photocatalytic applications under the same conditions. The dye model (Methylene Blue, MB), and antibiotic model (Amoxicillin, AMO), was photodegraded using the as-prepared nanocomposites under visible light irradiation. In the recombination reduction among TiO2 and g-C3N4 interfaces, g-C3N4 has been effectively utilized as a matrix. Our findings proved that g-C3N4@TiO2 photocatalysts exhibited superior photocatalytic performance. CNT-5 of 2.58 eV bandgap had a higher activity of 99.7 in 50 min for MB and 100% in 20 min for AMO than the other represented photocatalysts in this work. The migration of photogenerated electrons from a g-C3N4 to TiO2 via heterojunction among them as g-C3N4 (1 0 1) removes the electrons accumulated on (1 0 1) of TiO2, improve the photodegradation efficiency. Therefore, the increase in photocatalytic reaction rates, recycling, and the sample's photostability can be considered the result of successful interactions among the TiO2 and g-C3N4 systems. The suggested photodegradation mechanism of MB and AMO was discussed in detail and compared with previously reported work. Therefore, the photodegradation rate of MB and AMO via CNT-5 composite is 6 and 3 times, respectively, higher than that of g-C3N4 under simulated solar irradiation. This research creates a new perspective on the production of nanocomposite materials in the area of treatment of pharmaceutical and dye contaminants.

Flexible photocatalytic membrane based on CdS/PMMA polymeric nanocomposite films: multifunctional materials.

In this study, poly(methyl methacrylate) with different doping nano-cadmium sulfide (CdS/PMMA) is prepared and characterized. CdS/PMMA polymeric nanocomposite films were synthesized using solution casting methodology. SEM and XRD are used for structure analysis for the studied nanocomposite films. XRD revealed the amorphous domains of PMMA polymer, which increased with increasing CdS nanoparticle contents. SEM revealed the CdS dispersion within the PMMA matrix. CdS nanoparticles in the PMMA matrix are expected to be aggregated due to the casting technique. The optical energy gap is found to be decreased after the CdS addition. ε' and ε″ have the same behavior with the applied frequency. Maxwell-Wagner interfacial polarization is the responsible factor for higher values of ε'-ε″ at the higher frequencies. Electrical conductivity behavior σAC tends to obtain a constant value at lower frequencies that approach from its DC conductivity values. After doping PMMA with nano-CdS, an exponential increase after a critical frequency value and the values of σAC was also increased. Besides, a significant reduction in laser energy power is identified by the reduction of the output power. CdS/PMMA can attenuate the laser power due to its nonlinear effect. CdS/PMMA nanocomposite can act as a photocatalyst to improve the performance of the photodegradation of Rhodamine B (RhB). Among the different CdS/PMMA nanocomposite films, 3.33 wt% CdS/PMMA demonstrates the highest efficiency in visible photocatalysis of Rhodamine B. CdS/PMMA can be utilized as multifunctional materials use like laser optical limiting to reduce the power of laser sources and as a photocatalyst membranes.