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Pure and Ni-doped (1%, 2%, and 3%) nanostructures were synthesized using a novel laser-assisted chemical bath synthesis (LACBS) technique. For the first time, LACBS was used to create a doping solution utilizing a 7 W blue laser with a 444.4 nm wavelength and a continuous beam. The Ni-doping concentration was varied by changing the amount of Ni precursor added. All samples were analyzed using XRD, SEM, EDX, FTIR, UV–Vis, and photocatalysis tests for photodegradation under blue laser illumination. XRD was used to confirm that the tested ZnO had a hexagonal wurtzite structure. The crystallite size decreased as the Ni-doping concentration rose. EDX experiments were conducted to analyze the elemental characteristics of the pure and Ni-doped (1%, 2%, and 3%) nanostructures. The existence of nanoscale hexagonal structures was confirmed through SEM studies. The band gap values of the pure and Ni-doped ZnO nanostructures decreased as the doping concentration increased. FTIR studies were conducted to examine the functional groups of the pure and doped samples. The produced materials exhibited excellent photocatalytic performance toward the degradation of MB organic dye, an example of a pollutant found in wastewater. [ABSTRACT FROM AUTHOR]

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. [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]

Pure and Molybdenum (Mo)-doped zinc oxide (ZnO) nanoparticles were prepared by a cost-effective combustion synthesis route. XRD results revealed the decrement in crystallite size of ZnO with an increase in Mo-doping concentration. Optical bandgap (Eg) values were determined using optical reflectance spectra of these films measured in the range of 190–800 nm. The Eg values decreased with increasing the Mo-doping concentration. The dielectric properties of these samples were studied to determine the dielectric constant values. Raman spectra of these samples were recorded to know the structure. These sample absorption spectra were recorded for electrocatalytic applications. All the prepared samples were subjected to electrocatalytic degradation of Rhodamine B. The 0.01 wt% Mo doped ZnO showed 100% in 7 min electrocatalytic degradation. [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 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]

In the present work we report the sol-gel synthesis of pure TiO2 and (TiO2)1−x(Fe2O3)x nanocomposites with different Fe2O3 contents (x = 0, 0.1, 0.5, and 1.0 for pure TiO2, Fe2O3 incorporated 0.1, 0.5, and pure Fe2O3 which are denoted as PT, 0.1F, 0.5F, and PF, respectively). The structural, morphological, optical, and surface texture of the prepared nanocomposites were characterized using various techniques. The structural studies confirm the strong influence of Fe2O3 contents on the crystallite sizes and dislocation values. The size of the crystallites was increased by the increase in Fe2O3 contents. The bandgap values elucidated from DRS analysis were decreased from 3.15 eV to 1.91 eV with increasing Fe2O3 contents. The N2-Physorption analysis has confirmed the mesoporous nature of the samples with a comparable specific surface area of 35 m2/g. The photoelectrochemical measurements (CV, CA and EIS) were performed to assess the photoelectric properties of the prepared materials. It was found that the PT samples have the highest catalytic activity and photocurrent response compared to other composites. The reduction in current density was as follows: 2.8, 1.65, 1.5 and 0.9 mA/cm2, while the photocurrent response was ca. 800, 450, 45, 35 µA/cm2 for PT, 0.1F, 0.5F and PF samples, respectively. The EIS results showed that the (TiO2)1−x(Fe2O3)x nanocomposites exhibit lower charge transfer resistance than pure titania and hematite samples. [ABSTRACT FROM AUTHOR]