Photocatalytic degradation of brilliant green and 4-nitrophenol using Ni-doped Gd(OH)3 nanorods.

Gadolinium hydroxide (Gd(OH)3) was synthesized via a microwave-assisted synthesis method. Nickel ion (Ni2+) was doped into Gd(OH)3, in which 4-12% Ni-Gd(OH)3 was synthesized, to study the effect of doping. The structural, optical, and morphological properties of the synthesized materials were analyzed. The crystallite sizes of the hexagonal structure of Gd(OH)3 and Ni-Gd(OH)3, which were 17-30 nm, were obtained from x-ray diffraction analysis. The vibrational modes of Gd(OH)3 and Ni-Gd(OH)3 were confirmed using Raman and Fourier-transform infrared spectroscopies. The band gap energy was greatly influenced by Ni-doping, in which a reduction of the band gap energy from 5.00 to 3.03 eV was observed. Transmission electron microscopy images showed nanorods of Gd(OH)3 and Ni-Gd(OH)3 and the particle size increased upon doping with Ni2+. Photocatalytic degradations of brilliant green (BG) and 4-nitrophenol (4-NP) under UV light irradiation were carried out. In both experiments, 12% Ni-Gd(OH)3 showed the highest photocatalytic response in degrading BG and 4-NP, which is about 92% and 69%, respectively. Therefore, this study shows that Ni-Gd(OH)3 has the potential to degrade organic pollutants.

Impact of Co-Doping on the Visible Light-Driven Photocatalytic and Photoelectrochemical Activities of Eu(OH)3.

The microwave-assisted synthesis approach was used to synthesize Eu(OH)3 and Co-Eu(OH)3 nanorods. Various techniques were used to investigate the structural, optical, and morphological features of the Eu(OH)3 and Co-Eu(OH)3 NRs. Both Eu(OH)3 and Co-Eu(OH)3 NRs were found to be hexagonal with crystallite sizes ranging from 21 to 35 nm. FT-IR and Raman spectra confirmed the formation of Eu(OH)3 and Co-Eu(OH)3. Rod-shaped Eu(OH)3 and Co-Eu(OH)3 with average lengths and diameters ranging from 27 to 50 nm and 8 to 12 nm, respectively, were confirmed by TEM. The addition of Co was found to increase the particle size. Furthermore, with increased Co doping, the band gap energies of Co-Eu(OH)3 NRs were lowered (3.80-2.49 eV) in comparison to Eu(OH)3, and the PL intensities with Co doping were quenched, suggesting the lessening of electron/hole recombination. The effect of these altered properties of Eu(OH)3 and Co-Eu(OH)3 was observed through the photocatalytic degradation of brilliant green dye (BG) and photoelectrochemical activity. In the photocatalytic degradation of BG, 5% Co-Eu(OH)3 had the highest response. However, photoelectrochemical experiments suggested that 10% Co-Eu(OH)3 NRs showed improved activity when exposed to visible light. As a result, Co-Eu(OH)3 NRs have the potential to be a promising visible-light active material for photocatalysis.

α-Glucosidase Inhibitory Activity and Cytotoxicity of CeO2 Nanoparticles Fabricated Using a Mixture of Different Cerium Precursors.

A mixture of three distinct cerium precursors (Ce(NO3)3·6H2O, CeCl3·7H2O, and Ce(CH3COO)3·H2O) was used to prepare cerium oxide nanoparticles (CeO2 NPs) in a polyol-mediated synthesis. Different ratios of diethylene glycol (DEG) and H2O were utilized in the synthesis. The properties of the synthesized CeO2 NPs, such as structural and morphological properties, were investigated to observe the effect of the mixed cerium precursors. Crystallite sizes of 7-8 nm were obtained for all samples, and all synthesized samples were confirmed to be in the cubic phase. The average particle sizes of the spherical CeO2 were between 9 and 13 nm. The successful synthesis of CeO2 can also be confirmed via the vibrational band of Ce-O from the FTIR. Antidiabetic properties of the synthesized CeO2 NPs were investigated using α-glucosidase enzyme inhibition assay, and the concentration of the synthesized CeO2 NPs was varied in the study. The biocompatibility properties of the synthesized CeO2 NPs were investigated via cytotoxicity tests, and it was found that all synthesized materials showed no cytotoxic properties at lower concentrations (62.5-125 µg/mL).

Effects of NO3-, Cl-, and CH3COO- anions and diethylene glycol on the morphological, structural, antidiabetic, and cell viability properties of CeO2 nanoparticles.

Cerium oxide (CeO2) nanoparticles (NPs) were synthesized using a modified conventional polyol method. The ratio of diethylene glycol (DEG) and water in the synthesis was varied, and three different cerium precursor salts (Ce(NO3)3, CeCl3, and Ce(CH3COO)3) were used. The structure, size, and morphology of the synthesized CeO2 NPs were studied. An average crystallite size of 13 to 33 nm was obtained from the XRD analysis. Spherical and elongated morphologies of the synthesized CeO2 NPs were acquired. Average particle sizes in the range of 16-36 nm were obtained by varying different ratios of DEG and water. The presence of DEG molecules on the surface of CeO2 NPs was confirmed using FTIR. Synthesized CeO2 NPs were used to study the antidiabetic and cell viability (cell cytotoxicity) properties. Antidiabetic studies were carried out using α-glucosidase enzymes inhibition activity. CeO2 synthesized using Ce(NO3)3 and CeCl3 precursors showed approximately 40.0% α-glucosidase enzyme inhibition activity, while CeO2 synthesized using Ce(CH3COO)3 showed the lowest α-glucosidase enzyme inhibition activity. Cell viability properties of CeO2 NPs were investigated using an in vitro cytotoxicity test. CeO2 NPs prepared using Ce(NO3)3 and CeCl3 were non-toxic at lower concentrations, while CeO2 NPs prepared using Ce(CH3COO)3 were non-toxic at all concentrations. Therefore, polyol-mediated synthesized CeO2 NPs showed quite good α-glucosidase inhibition activity and biocompatibility.

Recent development of metal oxides and chalcogenides as antimicrobial agents.

Pathogenic microbes are a major concern in hospitals and other healthcare facilities because they affect the proper performance of medical devices, surgical devices, etc. Due to the antimicrobial resistance or multidrug resistance, combatting these microbial infections has grown to be a significant research area in science and medicine as well as a critical health concern. Antibiotic resistance is where microbes acquire and innately exhibit resistance to antimicrobial agents. Therefore, the development of materials with promising antimicrobial strategy is a necessity. Amongst other available antimicrobial agents, metal oxide and chalcogenide-based materials have shown to be promising antimicrobial agents due to their inherent antimicrobial activity as well as their ability to kill and inhibit the growth of microbes effectively. Moreover, other features including the superior efficacy, low toxicity, tunable structure, and band gap energy has makes metal oxides (i.e. TiO2, ZnO, SnO2 and CeO2 in particular) and chalcogenides (Ag2S, MoS2, and CuS) promising candidates for antimicrobial applications as illustrated by examples discussed in this review.

Visible-Light-Induced Photocatalytic and Photoantibacterial Activities of Co-Doped CeO2.

As one of the most significant rare earth oxides, the redox ability of cerium oxide (CeO2) has become the primary factor that has attracted considerable interest over the past decades. In the present study, irregular pentagonal CeO2 (S-CeO2) and different amounts of (1, 4, 8, and 12% Co) cobalt-doped CeO2 nanoparticles (Co-CeO2 NPs) with particle sizes between 4 and 13 nm were synthesized via the microwave-assisted synthesis method. The structural, optical, and morphological studies of S-CeO2 and Co-CeO2 were carried out using various techniques. The shifts in the conduction band and valence band were found to cause the reduction of the band gap energies of S-CeO2 and Co-CeO2 NPs. Moreover, the quenching of photoluminescence intensity with more Co doping showed the enhanced separation of charge carriers. The photocatalytic activities of S-CeO2 and Co-CeO2 NPs for methylene blue dye degradation, 4-nitrophenol reduction, and their photoantibacterial properties under visible-light irradiation were investigated. Findings showed that, due to the lower band gap energy (2.28 eV), more than 40% of both photocatalytic activities were observed for 12% Co-CeO2 NPs. On the other hand, higher antibacterial impact in the presence of light shows that the Co doping has a considerable influence on the photoantibacterial response of Co-CeO2. Therefore, microwave-assisted synthesized CeO2 and Co-CeO2 NPs have shown potential in photocatalytic dye degradation, chemical reduction, and photoantibacterial activities.

Recent Progress of Metal-Organic Frameworks and Metal-Organic Frameworks-Based Heterostructures as Photocatalysts.

In the field of photocatalysis, metal-organic frameworks (MOFs) have drawn a lot of attention. MOFs have a number of advantages over conventional semiconductors, including high specific surface area, large number of active sites, and an easily tunable porous structure. In this perspective review, different synthesis methods used to prepare MOFs and MOFs-based heterostructures have been discussed. Apart from this, the application of MOFs and MOFs-based heterostructures as photocatalysts for photocatalytic degradation of different types of pollutants have been compiled. This paper also highlights the different strategies that have been developed to modify and regulate pristine MOFs for improved photocatalytic performance. The MOFs modifications may result in better visible light absorption, effective photo-generated charge carriers (e-/h+), separation and transfer as well as improved recyclability. Despite that, there are still many obstacles and challenges that need to be addressed. In order to meet the requirements of using MOFs and MOFs-based heterostructures in photocatalysis for low-cost practical applications, future development and prospects have also been discussed.

Role of Anions in the Synthesis and Crystal Growth of Selected Semiconductors.

The ideal methods for the preparation of semiconductors should be reproducible and possess the ability to control the morphology of the particles with monodispersity yields. Apart from that, it is also crucial to synthesize a large quantity of desired materials with good control of size, shape, morphology, crystallinity, composition, and surface chemistry at a reasonably low production cost. Metal oxides and chalcogenides with various morphologies and crystal structures have been obtained using different anion metal precursors (and/or different sulfur sources for chalcogenides in particular) through typical synthesis methods. Generally, spherical particles are obtained as it is thermodynamically favorable. However, by changing the anion precursor salts, the morphology of a semiconductor is influenced. Therefore, precursors having different anions show some effects on the final forms of a semiconductor. This review compiled and discussed the effects of anions (NO3 -, Cl-, SO4 2-, CH3COO-, CH(CH3)O-, etc.) and different sources of S2- on the morphology and crystal structure of selected metal oxides and chalcogenides respectively.

Recent progress of phytogenic synthesis of ZnO, SnO2, and CeO2 nanomaterials.

A critical investigation on the fabrication of metal oxide nanoparticles (NPs) such as ZnO, SnO2, and CeO2 NPs synthesized from green and phytogenic method using plants and various plant parts have been compiled. In this review, different plant extraction methods, synthesis methods, characterization techniques, effects of plant extract on the physical, chemical, and optical properties of green synthesized ZnO, SnO2, and CeO2 NPs also have been compiled and discussed. Effect of several parameters on the size, morphology, and optical band gap energy of metal oxide have been explored. Moreover, the role of solvents has been found important and discussed. Extract composition i.e. phytochemicals also found to affect the morphology and size of the synthesized ZnO, SnO2, and CeO2 NPs. It was found that, there is no universal extraction method that is ideal and extraction techniques is unique to the plant type, plant parts, and solvent used.