Effect of Zr doping on photoantioxidant and antibiofilm properties of CeO2 NPs fabricated using aqueous leaf extract of Pometia pinnata.

Synthesized cerium oxide nanoparticles (S-CeO2 NPs) and 1%, 5% and 10% zirconium doped CeO2 (Zr-doped CeO2) NPs were fabricated using aqueous leaf extract of Pometia pinnata. The synthesized NPs were characterized using standard techniques which confirmed successful synthesis of NPs with particle size ranging from 12 to 23 nm and band gap energy of 2.54-2.66 eV. Photoantioxidant activities showed enhanced activities under visible light irradiation in comparison to the dark condition in the dose-dependent study. Biofilm inhibition studies showed ~ 73% biofilm inhibition of Staphylococcus aureus at 512 µg/mL for S-CeO2, whereas 10% Zr-doped CeO2 NPs showed biofilm inhibition of 52.7%. The bactericidal tests showed killing properties at 1024 µg/mL of S-CeO2 NPs and at 512 µg/mL of 1% Zr-doped CeO2. Reduced bactericidal activities were observed for 5% and 10% Zr-doped CeO2. These studies showed that the fabricated NPs have both good photoantioxidant and antibacterial properties.

Zinc oxide and zinc oxide-based nanostructures: biogenic and phytogenic synthesis, properties and applications.

Zinc oxide nanoparticles (ZnO NPs) are considered as very significant and essential material due to its multifunctional properties, stability, low cost and wide usage. Many green and biogenic approaches for ZnO NPs synthesis have been reported using various sources such as plants and microorganisms. Plants contain biomolecules that can act as capping, oxidizing and reducing agents that increase the rate of reaction and stabilizes the NPs. This review emphasizes and compiles different types of plants and parts of plant used for the synthesis of ZnO and its potential applications at one place. The influence of biogenic and phytogenic synthesized ZnO on its properties and possible mechanisms for its fabrication has been discussed. This review also highlights the potential applications and future prospects of phytogenic synthesized ZnO in the field of energy production and storage, sun light harvesting, environmental remediation, and biological applications.

Effect of Mg doping on ZnO fabricated using aqueous leaf extract of Ziziphus mauritiana Lam. for antioxidant and antibacterial studies.

Aqueous leaf extract of Ziziphus mauritiana Lam. was successfully used to synthesize zinc oxide (ZnO) and magnesium-doped ZnO (Mg-doped ZnO) particles and acted as capping and stabilizing agent. UV-Vis diffuse reflectance spectra showed that optical band gap energy of ZnO has narrowed from 3.11 to 3.08 eV and 3.03 eV when doped with 1% Mg and 5% Mg, respectively. Powder X-ray diffraction and X-ray photoelectron spectroscopy studies confirmed the purity and crystalline nature of the synthesized materials. FT-IR spectroscopy revealed the presence of phytochemicals coated on the surface of synthesized materials. The synthesized materials were found to effectively scavenge DPPH radicals in the presence of visible light in comparison to the dark. The antibacterial properties of the synthesized materials were evaluated against Staphylococcus aureus and Escherichia coli. The obtained results revealed that Staphylococcus aureus seemed to be more sensitive to the green synthesized ZnO and Mg-doped ZnO than Escherichia coli.

Antibacterial activities of zinc oxide and Mn-doped zinc oxide synthesized using Melastoma malabathricum (L.) leaf extract.

Zinc oxide (ZnO) is considered as a potential antimicrobial agent. This work aims to investigate the properties of ZnO and Mn-doped ZnO (1% and 5%) fabricated using aqueous leaf extract of Melastoma malabathricum via green synthesis and its antibacterial activities. The synthesized ZnO and Mn-doped ZnO were characterized using different techniques such as powder X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis diffuse reflectance spectroscopy. The synthesized ZnO and Mn-doped ZnO were tested for its antibacterial properties on two Gram-negative bacteria: Escherichia coli and Pseudomonas aeruginosa, and two Gram-positive bacteria: Bacillus subtilis and Staphylococcus aureus. The results showed positive antibacterial effects for B. subtilis and S. aureus only. Among the three materials tested, 1% Mn-doped ZnO exhibited the highest antibacterial activity for B. subtilis with the minimum inhibitory concentration being 50 mg/mL.

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.

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.

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).

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.

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.

Sn-doped BiOCl for photoelectrochemical activities and photocatalytic dye degradation under visible light.

In this work, bismuth oxychloride (BiOCl) and Sn-doped BiOCl (SBCl) with improved visible light photocatalytic activity were synthesized via the co-precipitation method. The XRD analysis determined the tetragonal phase of BiOCl, 1 %, 5 %, and 10 % SBCl. The crystallite sizes were in the range of 20-34 nm. These results confirmed that the Sn ion was successfully incorporated into the BiOCl lattice. This was further confirmed by FT-IR and Raman analysis. The optical properties, such as the band gap energy, were studied using UV-vis DRS. It was found that doping BiOCl with Sn has a minor effect on the band gap tuning. BET shows that the SBCl samples have acquired a larger specific surface area (14.66-42.20 m2/g) than BiOCl (13.49 m2/g). The photocatalytic performance showed that SBCl samples have higher photocatalytic activity than BiOCl in degrading Rhodamine B (RhB) dye under visible light irradiation. Among the SBCl samples, 5 % SBCl exhibited the highest photocatalytic efficiency which degraded 91.2 % of the RhB dye in 60 min. Moreover, the photoelectrochemical activities of the as-synthesized BiOCl and SBCl were investigated using linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS) in the dark and under visible light irradiation. Both studies showed that SBCl exhibits enhanced photoelectrochemical activities than BiOCl. Hence, it can be suggested that SBCl possesses visible light active properties and can be potentially used as a photocatalyst and photoelectrode material.

Zr, La-dual doped silver niobate for photocatalytic degradation of dyes under visible light irradiation.

Sol-gel-assisted synthesis of silver niobate, 1%, 5%, and 10% Zr, La-dual doped silver niobates were carried out. Analysis done using XRD showed that increasing Zr and La dual doping caused the synthesized materials to adopt an AgNbO3-like structure. This is also supported by FT-IR results. FESEM revealed that the silver niobate has a prism-like morphology while Zr, La-dual doped samples are irregular in shape. EDX mapping of the 10% Zr, La dual silver niobate confirmed the presence of Nb, Ag, Zr, and La metals. When compared with the silver niobate, the band gap energy of Zr, La-dual doped silver niobates are narrower, as shown by UV-Vis DRS measurements. It was revealed that dual doping of silver niobates with Zr and La has significantly improved the photocatalytic degradation of methylene blue (MB) and Rhodamine B (RhB) dyes. The 1% Zr, La-dual doped silver niobate showed the best photocatalytic results in terms of degrading MB while 10% Zr, La-dual doped silver niobate achieved the best performance when degrading RhB.

Green-synthesized CeO2 nanoparticles for photocatalytic, antimicrobial, antioxidant and cytotoxicity activities.

Cerium oxide nanoparticles (CeO2 NPs) are a sought-after material in numerous fields due to their potential applications such as in catalysis, cancer therapy, photocatalytic degradation of pollutants, sensors, polishing agents. Green synthesis usually involves the production of CeO2 assisted by organic extracts obtained from plants, leaves, flowers, bacteria, algae, food, fruits, etc. The phytochemicals present in the organic extracts adhere to the NPs and act as reducing and/or oxidizing agents and capping agents to stabilize the NPs, modify the particle size, morphology and band gap energy of the as-synthesized materials, which would be advantageous for numerous applications. This review focuses on the green extract-mediated synthesis of CeO2 NPs and discusses the effects on CeO2 NPs of various synthesis methods that have been reported. Several photocatalytic, antimicrobial, antioxidant and cytotoxicity applications have been evaluated, compared and discussed. Future prospects are also suggested.

Green synthesis of CeO2 and Zr/Sn-dual doped CeO2 nanoparticles with photoantioxidant and antibiofilm activities.

Cerium oxide (CeO2) and 1%, 5% and 10% zirconium/tin-dual doped CeO2 nanoparticles (Zr/Sn-dual doped CeO2 NPs) were synthesized using an aqueous leaf extract of Pometia pinnata. By using UV-visible diffuse reflectance spectroscopy, the band gap energies of these materials were found to be in the range of ∼2.49 to 2.66 eV. The average crystallite sizes of the fluorite phase obtained from X-ray diffraction were between 7 and 16 nm. X-ray photoelectron spectroscopy (XPS) analysis further confirmed the synthesis of CeO2 and Sn-doped CeO2 NPs. Almost spherical shapes of the nanomaterials with an average particle size of 12-17 nm were determined using scanning electron microscopy and transmission electron microscopy studies. Photoantioxidant activities of the synthesized materials showed enhanced photoantioxidant response under visible light irradiation in comparison with those under dark conditions in both dose- and time-dependent manner. The CeO2 NPs exhibited a significant concentration-dependent antibiofilm activity against the Gram-positive bacteria Staphylococcus aureus (S. aureus) and Listeria monocytogenes (L. monocytogenes). Only the 10% Zr/Sn-dual doped-CeO2 NPs were found to inhibit S. aureus biofilm formation at higher concentrations. All Zr/Sn-dual doped CeO2 NPs exhibited a concentration-dependent biofilm inhibition of L. monocytogenes and also bactericidal activity towards S. aureus. These nanomaterials exhibited enhanced photoantioxidant activities and antibacterial properties, which make them suitable for various biological applications.