Properties Of Oxide Research Articles

Neutrophil-Mimicking Nanozyme with Cascade Catalytic Releasing Nitric Oxide and Signet Oxygen Property for Synergistic Bimodal Therapy of Methicillin-Resistant Staphylococcus Aureus Infections.

Recently, chloroperoxidase (CPO)-mediated enzyme dynamic therapy (EDT) by mimicking the antipathogen function of neutrophils via generating highly active signet oxygen (1O2) has attracted great interest in biomedical applications. However, the therapeutic efficiency of EDT is largely restricted by the low CPO delivery efficiency and insufficient hydrogen peroxide (H2O2) supply. In the present work, a neutrophil-mimicking nanozyme of MGBC with high CPO delivery efficiency, H2O2 self-supply, and enzyme-cascade catalytic properties is designed for high-efficient treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections. In the infection microenvironment, MGBC can effectively catalyze glucose to self-supply substantial H2O2, which enables long-lasting 1O2 generation via the CPO-mediated catalytic reaction. At the meantime, MGBC can also catalyze H2O2 to sustainably release NO for gas therapy (GT), which synergistically strengthens the therapeutic effect of EDT. As a result, MGBC displayed effective MRSA-killing and MSRA biofilms-eradicating properties, and high efficiency in treating both MRSA infected full-thickness excision wounds and subcutaneous MRSA infection by exerting the synergistic bimodal EDT/GT therapeutic effects. In-depth mechanism study revealed that the synergistic EDT/GT antibacterial effects of MGBC can attenuate the drug resistance and toxicity of MRSA by significantly downregulating quorum sensing, multidrug efflux, virulence, and biofilm formation-related genes.

The Hydroxylated Carbon Nanotubes as the Hole Oxidation System in Electrocatalysis.

The hydroxylated carbon nanotubes (CNTs-OH), due to their propensity to trap electrons, are considered in many applications. Despite many case studies, the effect of the electronic structure of the CNT-OH electrode on its oxidation properties has not received in-depth analysis. In the present study, we used Fe(CN)63-/4- and Ru(NH3)63+/2+ as redox probes, which differ in charge. The CNT-OH and CNT electrodes used in the cyclic voltammetry were in the form of freestanding films. The concentration of holes in the CNTs-OH, estimated from the upshift of the Raman G-feature, was 2.9×1013 cm-2. The standard rate constant of the heterogeneous electron transfer (HET) between Fe(CN)63-/4- and the CNTs-OH electrode was 25.9×10-4 cm·s-1. The value was more than four times higher than the HET rate on the CNT electrode (ks=6.3×10-4 cm·s-1), which proves excellent boosting of the redox reaction by the holes. The opposite effect was observed for the Ru(NH3)63+/2+ redox couple. While the redox reaction rate constant at the CNT electrode was 1.4×10-4 cm·s-1, there was a significant suppression of the redox reaction at the CNT-OH electrode (ks<0.1×10-4 cm·s-1). Based on the DFT calculations and the Gerischer model, we find that the boosting of the HET from the reduced form of the redox couple to CNT-OH occurs when the reduced forms of the redox couples are negatively charged and the occupied reduced states are aligned with acceptor states of the nanotube electrode.

Interfacial Engineering of Fluorescent Carbon Dots with Metal Oxides for Real-Time Visualization of Oxygen Vacancy Dynamics.

Oxygen vacancy (Vo), as one of the most common surface defects, significantly influence the physiochemical properties of metal oxides. However, it remains a challenge for existing techniques to visualize the evolution of Vo during redox process due to its heterogeneous distribution, small size, and dynamic nature. Herein, the real-time monitoring of such microscopic interfacial events is reported by advantage of the high-contrast fluorescence response of carbon dots (H-CDs) to Vo. The green emissive H-CDs possess a unique disc-shaped structure and exceptional hydrophilicity, allowing their tight adhesion to the surfaces of Vo-rich MgO by simple mixing. Subsequently, a water involved interfacial reaction occurred between H-CDs and Vo, resulting in gradual quenching of the original green emission and simultaneously emergence of bright red fluorescence. Moreover, the spatiotemporal diffusion dynamics and reaction kinetics are investigated by confocal laser scanning microscopy, revealing the time-dependent reorganization and structural heterogeneity at the interface. The finding provides a new toolbox for in situ imaging of Vo-triggered phenomena at a microscopic level, which will be helpful in promoting the rational design of oxide materials.

Green-assisted synthesis of highly defective nanostructured Fe-doped SnO2: Magnetic and photocatalytic properties evaluation

Here we present a comprehensive characterization of the properties of undoped and Fe-doped SnO2 nanoparticles prepared with Syzygium cumini leaves extract. The phytochemicals present in the leaves extract act as cation chelating and capping of the nanoparticles. It is observed a relative high concentration of tin (up to 10 %) and oxygen (up to 5%) vacancies promoted by surface adsorbed OH− and by Fe-doping, respectively. The magnetic characterization reveals a ferromagnetic with a saturation monetization up to 20×10−3 emu/g for the higher defective and Fe-doped sample. This behavior associated mainly to tin vacancies for the undoped samples, and to the formation of bound magnetic polarons between the incorporated Fe and the oxygen vacancies for the doped samples. Oxygen vacancies and incorporated Fe improve the SnO2 photocatalytic efficiency in the visible range of the electromagnetic spectrum by decreasing the SnO2 effective bandgap from 3.6 eV for the undoped SnO2 sample to only 1.9 eV for the Fe-doped SnO2 sample, and by acting as electron-trapping centers increasing the system quantum efficiency. Due to the ferromagnetic behavior of the studied samples, it was also considered the effect of spin-dependent processes in the observed photocatalytic improvement. Our results highlight the key role of defect engineering strategies to optimize the physical and chemical properties of semiconductor oxides for application in the development of spintronic and quantum information devices, and in systems devoted to wastewater purification through advanced oxidation processes.

Influence of Oxygen Vacancies Introduced via Acceptor (Gadolinium) Doping to the Pseudocapacitive Properties of Nano-Sized Cerium Oxide.

The voluntary introduction of defects can be considered an effective strategy for enhancing the electrochemical properties of metal oxide electrodes. In this study, the enhanced pseudocapacitive properties of an acceptor (Gd) doped cerium oxide nanoparticle-a sustainable metal oxide with low environmental and human toxicity-are investigated in depth using ex situ X-ray photoemission spectroscopy (XPS) and electrochemical impedance spectroscopy (EIS). Interestingly, with 15at% Gd doping (15GDC), the specific capacitance of the nanoparticles measured at 1Ag-1 enhanced to 547.8Fg-1, which is fivefold higher than undoped CeO2 (98.7Fg-1 at 1Ag-1). The rate-dependent capacitance is also improved for 15GDC, which showed a 31.0% decrease in the specific capacitance upon a tenfold increase in the current density, while CeO2 showed a 49.9% decrease. The enhanced electrochemical properties are studied in depth via ex situ XPS and EIS analysis, which revealed that the oxygen vacancies at the surface of the nanoparticles played important roles in enhancing both the specific capacitance and the high-rate performance of 15GDC by acting as the active site for pseudocapacitive redox reaction and allowing fast diffusion of oxygen ions at the surface of 15GDC nanoparticles.

A Study of Characteristics and Properties of Nano-metal Oxides (Zinc Oxide, Cadmium Oxide, Titanium Dioxide, Iron Oxide)

Nanotechnology is a rapidly developing scientific discipline with promise for enhancing human well-being via its applications in nanomedicine. It describes the technology used to accurately manipulate atoms and molecules to create new materials with dimensions that are on the nanoscale. The usual size range of nanoparticles (NPs) is 1-100 nm. Since nanoparticles are important in preventing infections, they can be used as therapeutic nanocarriers having antibacterial properties. This paper reviews the literature on the various production techniques, characteristics, and biological uses of several nano-metal oxides (iron oxide, titanium dioxide, zinc oxide, and cadmium oxide). The utilization of nanoparticles and their applications will grow due to the cost-effective ways available for biomodification. Because of their special qualities, nanoparticles are helpful in several scientific domains, including biology, materials science, engineering, electronics, and food science. Researchers have become interested in nanotechnology because of its benefits, particularly its potential uses in the healthcare system for improved diagnosis and treatment.

Sulfur-Promoted Access to 3-Arylquinoxalin-2-ones by Oxidative Coupling of o-Phenylenediamines with Arylacetates.

We disclose the synthesis of 3-arylquinoxalin-2-ones from o-phenylenediamines and readily available arylacetates. The method harnesses the selective oxidative property of elemental sulfur in the presence of amine base catalyst and DMSO. The reactions are operationally simple and tolerate a wide range of functional groups.

Study the structural and optical properties of Zinc Oxide prepared by pulse laser deposition

Study the structural and optical properties of Zinc Oxide prepared by pulse laser deposition

Contribution of Sc doping to the growth and adhesion of alumina scale on AlCoCrFeNi high-entropy alloy

Equimolar AlCoCrFeNi high-entropy alloy (HEA) often experiences serious oxidation degradation despite its superior mechanical properties at elevated temperatures. Herein, we reveal that minor Sc addition can enhance the oxidation resistance of AlCoCrFeNi HEA at 1100 °C, and the microstructure and oxidation properties for (AlCoCrFeNi)100−xScx HEAs (Sc-0, Sc-0.1, Sc-0.5 and Sc-1) are evaluated. Except for the original A2 + B2 phases, the Laves phase is found with increasing Sc addition. Moderate Sc addition is beneficial for interface adhesion by lowering the driving force for scale spallation and enhancing the interface toughness, and excessive Sc addition, however, results in serious internal oxidation due to the generation of Sc2O3 stringers as the high diffusivity paths for inward O ions. It is also proved that enhancing the interface toughness is more beneficial to improve the oxidation resistance compared to reducing scale growth rate. Our results can offer guidance for designing advanced alloys with excellent oxidation resistance.

Microstructural and antibacterial properties of copper oxide deposited on polypropylene fabric by magnetron sputtering

In this study, antibacterial coatings composed of copper and its oxides were deposited on polypropylene (PP) fabrics using magnetron sputtering. The coatings were deposited under varying oxygen partial pressures to facilitate the formation of cupric and cuprous oxides in different quantities. The formation of these oxides was confirmed by the surface morphology (Scanning Electron Microscopy [SEM]) and X-Ray Diffraction (XRD) analysis. Additionally, the antibacterial properties of the coated fabrics were evaluated. The results show that both copper and copper oxides achieved a 4-log reduction in gram-positive bacteria. Inductively Coupled Plasma Mass Spectroscopy (ICPMS) results indicated that the release of copper atoms into water from the coated fabrics was minimal, even after 30 days of immersion.

Shelf Life Enhancement of Structured Lipids Rich in Omega-3 Fatty Acids Using Rosemary Extract: A Sustainable Approach.

This study investigates the efficacy of rosemary extract (RE) in stabilizing structured lipids (SL) developed using perilla seed oil (PSO) and palmolein (PO) under accelerated storage conditions. The oil samples, comprising PSO, Blend, and SL formulations with and without RE (1500 ppm) and BHT (200 ppm), were studied for their storage stability during a 30 day storage period at 65 °C, with the analysis carried out at 6 day intervals. Oxidative properties were comprehensively assessed, including both physical attributes (color, viscosity, and refractive index) and chemical parameters (peroxide value, free fatty acid (FFA), p-anisidine value, TOTOX value, conjugated dienes, and trienes). The results demonstrated that RE-enriched oil samples exhibited significantly higher oxidative stability (p < 0.05) compared to the control group. SL added with 1500 ppm of RE exhibited notable enhancements in quality parameters, showcasing reductions in FFA, TOTOX value, conjugated diene, and triene value by 44.01%, 35.42, 39.03, and 47.36, respectively, when compared to SL without any antioxidant. The RE at 1500 ppm concentration showed a similar effect as the synthetic antioxidant BHT at 200 ppm. Also, the RE demonstrated potent inhibition of the oxidation of polyunsaturated fatty acids, thereby contributing to the improved oxidative stability of the SLs. Furthermore, SL with RE also exhibited reduced degradation of the tocopherol content and total phenolic content during the storage period. Principal component analysis demonstrated that SL and blend followed similar oxidative characteristics as they fell within the same quadrant. These findings underscore RE as a potent source of antioxidants capable of scavenging free radicals and enhancing the oxidative stability of omega-3 fatty acid-rich SLs.

Optimizing luminous efficiency in polymer light-emitting diodes through anode oxygen-plasma treatment under diverse pressure conditions

This study investigates the impact of oxygen-plasma (O2-plasma) treatment on the microscale electrical properties of indium tin oxide (ITO) surfaces for enhancement of the luminous efficiency of polymer light-emitting diodes (PLEDs). Significant effects on conductivity distribution were observed when treatment was performed at pressures exceeding 0.4 Torr. ITO-6, the ITO treated with O2-plasma at 0.6 Torr, emerged as the preferred anode substrate for PLEDs, displaying a 72.5 % coverage of stable-conductive regions. When utilized as the anode in PLED, it exhibited a remarkable 209 % increase in average current efficiency and a 184 % enhancement in electroluminescent intensity compared to the reference PLED. These findings provide valuable insights for optimizing PLEDs through surface modification of ITO.

Catalytic properties of trivalent rare-earth oxides with intrinsic surface oxygen vacancy

Oxygen vacancy (Ov) is an anionic defect widely existed in metal oxide lattice, as exemplified by CeO2, TiO2, and ZnO. As Ov can modify the band structure of solid, it improves the physicochemical properties such as the semiconducting performance and catalytic behaviours. We report here a new type of Ov as an intrinsic part of a perfect crystalline surface. Such non-defect Ov stems from the irregular hexagonal sawtooth-shaped structure in the (111) plane of trivalent rare earth oxides (RE2O3). The materials with such intrinsic Ov structure exhibit excellent performance in ammonia decomposition reaction with surface Ru active sites. Extremely high H2 formation rate has been achieved at ~1 wt% of Ru loading over Sm2O3, Y2O3 and Gd2O3 surface, which is 1.5–20 times higher than reported values in the literature. The discovery of intrinsic Ov suggests great potentials of applying RE oxides in heterogeneous catalysis and surface chemistry.

Efficient Sb(Ⅲ) removal from printing and dyeing wastewater using TiCl4 as a potential coagulant instead of polyferric sulfate

With increasing health concerns and the tightening of discharge standards, there is growing demand for more efficient Sb(Ⅲ) removal from printing and dyeing wastewater (PDW). Currently, the most common coagulant used in Sb removal in industry is polyferric sulfate (PFS). However, the residual Fe ions in the effluent cause colorimetric problems and irreversibly damage the membrane components during the subsequent reverse osmosis treatment process. Therefore, identifying novel coagulants to replace PFS in the removal of Sb(Ⅲ) is necessary. In this study, TiCl4 was employed for in-situ hydrolysis to produce flocs for Sb(Ⅲ) removal in simulated and real PDW. TiCl4 exhibited an excellent performance compared to PFS in terms of dosage, turbidity, application pH, and anti-interference properties. Sb(Ⅲ) removal of 97.3 % was realized at a dosage of 30 mg/L and a final pH of 5.0 in slightly contaminated PDW, whereas PFS required a higher dosage, resulting in higher disposal costs. Furthermore, the application of TiCl4 led to lower turbidity and reduced secondary contamination. An investigation of the co-existing ions revealed that TiCl4 was considerably more tolerant than PFS toward PO43–, humic acid, and silicate at a lower concentration. Simultaneously, Sb(Ⅲ) was partially oxidised to Sb(Ⅴ) during removal, but TiCl4 exhibited lower oxidative properties. The results of PDW treatment indicated that TiCl4 could realize 85.6 % Sb(Ⅲ) removal at a dosage of 30 mg/L, and the pre-reduction of Sb(Ⅴ) to Sb(Ⅲ) was a safe, effective treatment. The results of zeta potential measurements and X-ray photoelectron spectroscopy revealed that Sb(Ⅲ) removal was mainly realised via chemical adsorption. Overall, this study provides a promising alternative material for use in practical Sb(Ⅲ) removal from PDW, particularly for reducing coagulation sludge, operational costs, and damage during the possible subsequent reverse osmosis process.

The effect of particles size of Gd2O3 on the radiation protection mechanisms of ZnO

There are two mechanisms established for increasing the radiation resistance of optical properties of micron-sized zinc oxide (mZnO) powder modified by gadolinium oxide (nGd2O3) nanoparticles by means of relaxation of the primary radiation defects (electrons and holes): — in atoms of rare-earth element gadolinium; — on Gd2O3 nanoparticles. During modification with gadolinium oxide micron-sized particles, only one (first) mechanism for radiation resistance increasing is enabled. These results are obtained by recording diffuse reflectance spectra in high vacuum in the range of 0.2–2.5 μm under radiation exposure by accelerated electrons (in situ). The established mechanisms for increasing radiation resistance refer not only to the types of powders under the study, but also to other types of oxide semiconductor powders and rare-earth elements. These mechanisms can also be extended to the photo résistance of oxide powders modified by nanoparticles and solid solutions based on them.

Synthesis and characterization of bagasse cellulose-based quaternary ammonium peroxyphosphotungstate and their catalytic properties for cyclohexene oxidation in the absence of any solvent

Bagasse cellulose, an industrial waste byproduct of sugar production, was demonstrated to be a viable solid support for a solid-phase ionic oxidation catalyst enabling organic solvent-free aqueous reaction conditions and facile catalyst recovery. Bagasse cellulose-supported quaternary ammonium peroxyphosphotungstate was synthesized from bagasse cellulose-supported quaternary ammonium chloride, phosphotungstic acid, and hydrogen peroxide. The chemical structure of this material was characterized by SEM, XRD, FT-IR, XPS, and 13C NMR, revealing stability of the cellulose matrix to the catalyst loading conditions and effective dispersion of the acicular catalyst crystals throughout the matrix. High catalytic activity of this synthetic complex was demonstrated in the oxidation of cyclohexene to 1,2-cyclohexanediol with hydrogen peroxide in the absence of solvent. Optimized conditions providing trans-1,2-cyclohexanediol with 86.2 % selectivity were 12 wt% catalyst and 4 mL/g 30 % H2O2 (vs. cyclohexene) at 50 °C for 10 h.

High pressure coupled with Cu deficiency boosts thermoelectric performance in BiCuSeO oxides

Low carrier concentration and mobility have been the primary obstructions to improving the electrical transport properties of BiCuSeO thermoelectric oxides, particularly for excessively low carrier mobility, heavily impeding the development of its thermoelectric performance. Herein, high-pressure technology is adopted to tune the electronic structure motivating carrier mobility, incorporated with the contribution of Cu deficiency to carrier concentration, achieving high carrier mobility of 25 cm2V−1s−1 and outstanding electrical conductivity of 2834.57 Sm−1. Moreover, high densities of grain boundaries and dislocations are introduced by high pressure, accompanied by the effect of Cu vacancies, suppressing phonon transport and depressing lattice thermal conductivity, finally realizing an acceptable zT of 0.56 at 823 K in BiCu0.97SeO. This work demonstrates that high pressure can be compatible with other methods, realizing synergetic optimizations in coupled parameters and thus improving thermoelectric performance in BiCuSeO oxides.

Groups IV, V and VI metal oxide-containing hydrotalcite catalysts: state of the art on their catalytic applications

The present contribution is a review paper that summarizes the structure, properties and catalytic applications of hydrotalcite based materials when they are modified by the incorporation of oxide metals from groups 4, 5 and 6. The unique properties of hydrotalcites, with a double layer structure able to host ions in the interlayer space and its basicity, together with the properties of transitions metal oxides from groups 4, 5 and 6, leads to materials highly promising as catalysts. The incorporation can form dispersed species of those oxides on the hydrotalcite-like structure, which acts as support, or by the incorporation of those elements into the hydrotalcite structure. The structure and properties of these materials have been reviewed and analyzed, in order to give a detailed description of the main factors that affect the catalytic properties of these interesting materials.

Natural Rubber/Styrene-Butadiene Rubber Blend Composites Potentially Applied in Damping Bearings.

Natural rubber (NR) composites have been widely applied in damping products to reduce harmful vibrations, while rubber with only a single composition barely meets performance requirements. In this study, rubber blend composites including various ratios of NR and styrene butadiene rubber (SBR) were prepared via the conventional mechanical blending method. The effects of the rubber components on the compression set, compression fatigue temperature rising and the thermal oxidative aging properties of the NR/SBR blend composites were investigated. Meanwhile, the dynamic mechanical thermal analyzer and rubber processing analyzer were used to characterize the dynamic viscoelasticity of the NR/SBR blend composites. It was shown that, with the increase in the SBR ratio, the vulcanization rate of the composites increased significantly, while the compression fatigue temperature rising of the composites decreased gradually from 47 °C (0% SBR ratio) to 31 °C (50% SBR ratio). The compression set of the composites remained at ~33% when the SBR ratio was no more than 20%, and increased gradually when the SBR ratio was more than 20%.

In Vitro Evaluation of DNA Damage Induction by Silver (Ag), Gold (Au), Silica (SiO2), and Aluminum Oxide (Al2O3) Nanoparticles in Human Peripheral Blood Mononuclear Cells.

Nanoparticles (NPs) are increasingly applied in a wide range of technological and medical applications. While their use offers numerous benefits, it also raises concerns regarding their safety. Therefore, understanding their cytotoxic effects and DNA-damaging properties is crucial for ensuring the safe application of NPs. In this study, DNA-damaging properties of PVP-coated silver, silica, aluminum oxide (13 nm and 50 nm), and gold (5 nm and 40 nm) NPs in human peripheral blood mononuclear cells (PBMCs) were investigated. NPs' internalization and induction of reactive oxygen species were evaluated using flow cytometry. Cytotoxic properties were determined using a dual acridine orange/ethidium bromide staining technique while DNA-damaging properties were assessed using an alkaline comet assay. We observed that Ag, SiO2, and both sizes of Al2O3 NPs were efficiently internalized by human PBMCs, but only PVP-AgNPs (at 10-30 µg/mL) and SiO2 NPs (at concentrations > 100 µg/mL) induced significant DNA damage after a 24 h exposure. In contrast, the uptake of both sizes of gold nanoparticles was limited, though they were able to cause significant DNA damage after a 3 h exposure. These findings highlight the different responses of human PBMCs to various NPs, emphasizing the importance of their size, composition, and internalization rates in nanotoxicology testing.