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Injection of interstitial atoms by specially prepared surfaces submerged in liquid water near room temperature offers an attractive approach for post-synthesis defect manipulation and isotopic purification in device structures. However, this approach can be limited by trapping reactions that form small defect clusters. The compositions and dissociation barriers of such clusters remain mostly unknown. This communication seeks to address this gap by measuring the dissociation energies of oxygen interstitial traps in rutile TiO2 and wurtzite ZnO exposed to liquid water. Isotopic self-diffusion measurements using 18O, combined with progressive annealing protocols, suggest the traps are small interstitial clusters with dissociation energies ranging from 1.3 to 1.9 eV. These clusters may comprise a family incorporating various numbers, compositions, and configurations of O and H atoms; however, in TiO2, native interstitial clusters left over from initial synthesis may also play a role. Families of small clusters are probably common in semiconducting oxides and have several consequences for post-synthesis defect manipulation and purification of semiconductors using submerged surfaces. [ABSTRACT FROM AUTHOR]

Despite rather extensive study of the random lasing effect in ZnO structures, the issue of the optical gain mechanisms in microstructured ZnO random lasers remains poorly understood. In this work, the radiative properties of an array of vertically aligned ZnO microrods, synthesized by a modified thermal evaporation method, were studied. The microrods exhibited lengths up to 60 μm and diameters ranging from 1 to 5 μm. Random lasing from a microrod array was observed in the near-UV range (with a laser emission peak wavelength of ∼391 nm) with a threshold down to 40 kW/cm2 under optical excitation. An analysis of the nature of optical gain in the grown structure was conducted at various temperatures. It was found that at room temperature, two-phonon-assisted exciton recombination is the main process leading to light amplification. [ABSTRACT FROM AUTHOR]

Artificial synapses based on memristors are used in emulating the synaptic plasticity behavior of a human brain. Here, we have proposed a transparent memristor based on aluminum zinc oxide (AZO) on a flexible substrate—polyethylene naphthalate. We have analyzed the elemental composition of the gadget subjected to the optimized flow rate of Ar/O2 = 2/1 by x-ray photoelectron spectroscopy. The prepared AZO/ZnO/indium-doped tin oxide memristor exhibits a bipolar switching behavior with Vset/Vreset of 1.4/−2.0 V. The results reflect an acceptable endurance of >500 cycles and retention of 104 s. The optimized device shows an improvement in the non-linearity of potentiation—2.31/depression—3.05 and has more than 25 cycles of stability. The transparency is checked using a UV-visible spectrophotometer showing 90% transparency in the visible region making the device suitable for applications in invisible electronics. Our results reflect that the proposed device can be used as a transparent electrode in making artificial synapses for neuromorphic applications. [ABSTRACT FROM AUTHOR]

Purpose: To develop the most compatible cementation protocol for ensuring minimal residual cement and optimal retention of cement-retained implant-supported fixed dental prostheses. Materials and Methods: A total of 30 custom implant abutments and zirconia crowns with bilateral wings were prepared. Three cement types were used for cementation: noneugenol resin cement (Premier Implant Cement; Group IC), dual-polymerizing self-adhesive resin cement (SmartCem2; Group SC), and zinc oxide eugenol cement (Temp-Bond; Group TB; n = 30 per group). Three cementation methods were applied for each cement type, and the samples were divided into subgroups: (1) cement was injected using a graduated syringe (ICN, SC-N, and TB-N); (2) a cementation jig made with a silicone impression material and temporary resin material was used (IC-CJ, SC-CJ, and TB-CJ); (3) 3D-printed abutments were used as replicas for cementation (IC-3DP, SC-3DP, and TB-3DP). The amount of cement injected, surface area of the residual cement, and retentive strength were measured. Kruskal-Wallis and post-hoc Mann-Whitney tests were used for statistical analyses. Results: Excess cement was not observed when cementation jig or 3D-printed replicas were used. For IC and SC subgroups, non-use of these auxiliary tools resulted in significantly higher amounts of injected cement. The retentive strength differed significantly among the IC subgroups but not among the SC subgroups. The retentive strength of subgroups TB-N and TB-CJ was significantly higher than that of subgroup TB-3DP. Conclusions: To prolong the main purpose of each cement type, a cementation jig or 3D-printed replica is highly recommended regardless of the cement type. [ABSTRACT FROM AUTHOR]

With the anticipated foliar application of nanoparticles (NPs) as a potential strategy to improve crop production and ameliorate heavy metal toxicity, it is crucial to evaluate the role of NPs in improving the nutrient content of plants under Lead (Pb) stress for achieving higher agriculture productivity to ensure food security. Herein, Brassica napus L. grown under Pb contaminated soil (300 mg/kg) was sprayed with different rates (0, 25, 50, and 100 mg/L) of TiO2 and ZnO-NPs. The plants were evaluated for growth attributes, photosynthetic pigments, leaf exchange attributes, oxidant and antioxidant enzyme activities. The results revealed that 100 mg/L NPs foliar application significantly augmented plant growth, photosynthetic pigments, and leaf gas exchange attributes. Furthermore, 100 mg/L TiO2 and ZnO-NPs application showed a maximum increase in SPAD values (79.1%, 68.9%). NPs foliar application (100 mg/L TiO2 and ZnO-NPs) also substantially reduced malondialdehyde (44.3%, 38.3%), hydrogen peroxide (59.9%, 53.1%), electrolyte leakage (74.8%, 68.3%), and increased peroxidase (93.8%, 89.1%), catalase (91.3%, 84.1%), superoxide dismutase (81.8%, 73.5%) and ascorbate peroxidase (78.5%, 73.7%) thereby reducing Pb accumulation. NPs foliar application (100 mg/L) significantly reduced root Pb (45.7%, 42.3%) and shoot Pb (84.1%, 76.7%) concentration in TiO2 and ZnO-NPs respectively, as compared to control. Importantly, macro and micronutrient analysis showed that foliar application 100 mg/L TiO2 and ZnO-NPs increased shoot zinc (58.4%, 78.7%) iron (79.3%, 89.9%), manganese (62.8%, 68.6%), magnesium (72.1%, 93.7%), calcium (58.2%, 69.9%) and potassium (81.5%, 68.6%) when compared to control without NPs. The same trend was observed for root nutrient concentration. In conclusion, we found that the TiO2 and ZnO-NPs have the greatest efficiency at 100 mg/L concentration to alleviate Pb induced toxicity on growth, photosynthesis, and nutrient content of Brassica napus L. NPs foliar application is a promising strategy to ensure sustainable agriculture and food safety under metal contamination.

Soil salinity is a major nutritional challenge with poor agriculture production characterized by high sodium (Na+) ions in the soil. Zinc oxide nanoparticles (ZnO NPs) and biochar have received attention as a sustainable strategy to reduce biotic and abiotic stress. However, there is a lack of information regarding the incorporation of ZnO NPs with biochar to ameliorate the salinity stress (0, 50,100 mM). Therefore, the current study aimed to investigate the potentials of ZnO NPs application (priming and foliar) alone and with a combination of biochar on the growth and nutrient availability of spinach plants under salinity stress. Results demonstrated that salinity stress at a higher rate (100 mM) showed maximum growth retardation by inducing oxidative stress, resulted in reduced photosynthetic rate and nutrient availability. ZnO NPs (priming and foliar) alone enhanced growth, chlorophyll contents and gas exchange parameters by improving the antioxidant enzymes activity of spinach under salinity stress. While, a significant and more pronounced effect was observed at combined treatments of ZnO NPs with biochar amendment. More importantly, ZnO NPs foliar application with biochar significantly reduced the Na+ contents in root 57.69%, and leaves 61.27% of spinach as compared to the respective control. Furthermore, higher nutrient contents were also found at the combined treatment of ZnO NPs foliar application with biochar. Overall, ZnO NPs combined application with biochar proved to be an efficient and sustainable strategy to alleviate salinity stress and improve crop nutritional quality under salinity stress. We inferred that ZnO NPs foliar application with a combination of biochar is more effectual in improving crop nutritional status and salinity mitigation than priming treatments with a combination of biochar.

Vacancies are generated in semiconductor devices while operating in the space radiation environment, impacting semiconductor carrier concentrations and dynamics. Positron annihilation lifetime spectroscopy (PALS) is used to probe these defect concentrations in bulk grown GaN, GaP, InAs, InP, Si, MgO, and ZnO both as-grown and as a function of 2–4 MeV proton irradiation. All samples were irradiated to yield a common initial damage production and characterized identically. In as-grown samples, PALS reveals vacancy concentrations above the saturation limit in the oxides, disabling further analysis. As a function of dose, of the materials in which defect accumulation could be probed, it is observed that GaN is the most resistant to the accumulation of defects (attributed to the Ga vacancies) and Si is the least. GaP (attributed to the Ga vacancy) and InAs exhibit slightly higher rates of vacancy accumulation than GaN. InP exhibits high defect accumulation rates approaching that of Si. This information is key to understanding the operation of a diverse set of semiconductors in the space radiation environment. [ABSTRACT FROM AUTHOR]

In this paper, we have investigated red light (∼ 660 nm) and magnetic field dependence of impedance across (100 − x)% ZnO(zinc oxide)– x % rGO(reduced graphene oxide)/La 0.7 Sr 0.3 MnO 3 (LSMO)/ITO (x =0,0.6,0.8,100) heterostructure devices. Field-induced scattering due to the spin filter effect and spin polarized tunneling (SPT) have been extracted from the zinc oxide–reduced graphene oxide nanocomposite/LSMO space charge region (ZnO–rGO/LSMO SCR) and the LSMO active region of the devices, respectively. Higher SPT leads to higher LSMO SCR scattering across the devices. Devices with higher rGO contents could not be fitted with two RC circuits as resistance values because the two phenomena are incomparable with each other. Light-induced scattering has been observed at the ZnO–rGO nanocomposite active region and ZnO–rGO/LSMO SCR of the devices. For composite devices with x =0.8 and 0.6, higher photocarrier generation at ZnO–rGO nanocomposite active layer leads to enhanced scattering at LSMO SCR with light illumination. Light-dependent scattering at both regions, however, follows almost same decreasing trend for bare devices with x =0, 100. The decreasing trend of light-dependent scattering for ZnO/LSMO/ITO and rGO/LSMO/ITO bare devices suddenly gets reversed and, eventually, follows an increasing trend at magnetic field ambiance of 0.5 and 1 kOe, respectively. The LSMO SCRs of the bare devices got enhanced with the field, leading to a light-dependent response similar to composite devices at the higher field. [ABSTRACT FROM AUTHOR]

In order to greatly improve the photocatalytic properties, corn-like ZnO/ZnS heterojunctions with a particle size of about 60–71 nm have been synthesized by the solvothermal method and the subsequent sulfuration process. A declining trend is found for the specific surface area with increasing sulfuration time. The corn-like ZnO/ZnS heterojunctions exhibit good photocatalytic properties. With increasing sulfuration time, the degradation rate increases first and then decreases. The best degradation rate is observed for the heterojunction sulfurated for 90 min. The strong broad luminescence band is extremely beneficial to the absorption of visible light by multiphoton process. In addition, the energy transfer from ZnS to ZnO contributes to charge separation, forming a type-II heterojunction mechanism. After one cycle of photocatalytic process, except that corns become more broken, variation of particle size and shape is very small. The degradation speed of RhB after a second cycle of photocatalytic process is slower than the first one except when using the sample sulfurated for 360 min. [ABSTRACT FROM AUTHOR]

Two-dimensional transition metal dichalcogenides and semiconductor metal oxides have shown great potential in photocatalysis. However, their stability and efficiency need to be further improved. In this paper, porous ZnO nanorods with high specific surface area were prepared from metal-organic framework ZIF-8 by a simple hydrothermal method. A MoS2/ZnO composite was constructed by loading MoS2 onto the surface of porous ZnO nanorods. Compared with ZnO materials prepared by other methods, MoS2/ZnO prepared in this paper exhibits superior photocatalytic performance. The enhanced photocatalytic activity of the MoS2/ZnO composite can be attributed to the formation of heterojunctions and strong interaction between them, which greatly facilitate the separation of electrons and holes at the contact interface. In addition, due to the wide absorption region of the visible spectrum, MoS2 can greatly broaden the light absorption range of the material after the formation of the composite material, increase the utilization rate of visible light, and reduce the combination of electrons and holes. This study provides a new way to prepare cheap and efficient photocatalysts. [ABSTRACT FROM AUTHOR]

Adsorption, desorption, and diffusion dynamics of hydrogen gas molecules over a hexagonal ZnO monolayer have been studied thoroughly in the van der Waals Density Functional Theory (vdW-DFT) framework in association with kinetic Monte Carlo (kMC) simulations. Hydrogen molecules can attach to a ZnO sheet via a weak physisorption process with a limitation of maximum attachment of three molecules per hexagonal ring. Pressure and temperature are the main deciding parameters for the overall storage capacity of hydrogen on a ZnO substrate. kMC simulations are performed to capture the stochastic behavior of surface dynamics of gas molecules. Adsorption energy and diffusion barrier are predicted to be around 50–60 meV and 4–12 meV, respectively, according to vdW-DFT calculations. kMC simulations with these energy parameters estimate the surface coverage of hydrogen to be pretty high below room temperature and high pressure. Furthermore, the hydrogen adsorption in the ZnO monolayer leads to the increase of the bandgap value, subsequently changing the conductivity of the material. The present research work sheds light on the usage of a ZnO monolayer for suitable hydrogen gas storage and sensing applications. [ABSTRACT FROM AUTHOR]

Optoelectronic synapses are inevitable for realizing neuromorphic vision systems, which require the integration of image recognition, memory and image processing into a single platform. In this work, we present a three terminal optoelectronic synapse created using zinc oxide (ZnO) thin film transistor. The persistent photoconductivity (PPC) of ZnO thin film is utilized to demonstrate the synaptic behavior. The change in conductance of the device under UV illumination has been interpreted as the weight change in the synapse. The basic synaptic functions such as sensory memory, short term memory, long term memory, duration-time-dependent plasticity and paired pulse facilitation (PPF) have been successfully demonstrated. The device shows a PPF index of 160%, comparable to other optoelectronic synapses reported in literature. Further, to corroborate the existing theory that PPC is caused by oxygen vacancies, additional characterizations are carried out and the presence of oxygen vacancies is detected in the fabricated ZnO device. Subsequently, pattern recognition of MNIST handwritten dataset has been performed using the conductance tuning curves of the proposed ZnO TFT based synapses in a neural network architecture, thereby demonstrating their feasibility to be used in neuromorphic applications. [ABSTRACT FROM AUTHOR]

The rapid and skillful detection of toxic gases is a crucial requirement for the advancement of gas sensors. In this study, we fabricated undoped and In-doped (1 %, 3 %, and 5 % by weight) ZnO films using a two-step modified SILAR deposition technique. The ethanol gas sensing properties of both undoped and In-doped ZnO films were examined across a range of operating temperatures (from room temperature, 27 °C–200 °C) and concentrations (1 ppm–50 ppm). Of all the films, those doped with 5 % Indium exhibited the most stable, reproducible, and highest response, achieving 86.27 % at 50 ppm ethanol at an operating temperature of 100 °C. Compared to the undoped ZnO films, all Indium-doped ZnO films demonstrated significantly shorter response times (17 s) and recovery times (19 s). The response of all the deposited films to various gases such as acetone, methanol, toluene, xylene, and formaldehyde was lower than their response to ethanol. The mechanism behind the enhanced sensing characteristics of the Indium-doped ZnO films is explored. Additionally, the impact of humidity on sensor performance was investigated. This study reveals that 5 % In-doped ZnO films hold great potential as materials for ethanol gas sensing applications. [ABSTRACT FROM AUTHOR]

Organic-inorganic hybrid nanocomposites are rapidly evolving as a new generation of materials with attractive properties for electrochemical energy storage. Unfortunately, their practical applications in sodium-ion batteries (SIBs) still require further research due to the unsatisfactory cycling stability and rate performance. This work explores using zinc antimony oxide/reduced graphene oxide (ZSO/rGO) hybrid nanocomposite as an anode material in SIBs. After 150 cycles at 0.05 A g−1, the ZSO/rGO electrode delivers a specific capacity of 357.21 mAh g−1 with a coulombic efficiency of 99.3 %, which is almost 2.5-fold higher than the specific capacity of the pristine ZSO electrode. An in-situ Raman spectroscopy study demonstrates that the sodiation/desodiation mechanism in the ZSO/rGO electrode involves the conversion and alloying reactions in the ZSO nanoparticles. Further electrochemistry analysis reveals that the nanocomposite anode shows synergistic effects by coupling diffusion and surface contribution, in which the latter plays an important role. [ABSTRACT FROM AUTHOR]

A series of 150-nm-thick Al-doped ZnO (AZO) thin films with various Al doping concentrations were deposited by atomic layer deposition technique to determine their applicability in transparent electronic devices. For incorporation into transparent electrodes, the electrical properties of AZO films must be modulated to minimize the parasitic effect. The results show that AZO thin films with various Al dopant concentrations had different work-functions and electrical contact properties, while the other physical characteristics were not significantly changed. Hence, AZO thin films can be used as transparent conducting oxide materials and are potential alternatives for the currently used indium-tin-oxide (ITO) thin films. [ABSTRACT FROM AUTHOR]

Augmentation of optical and magnetic properties of ZnO system via mono- and co-doping is an efficient approach to achieve enhanced ferromagnetism and photocatalytic activity. In this scenario, we made an endeavor to prepare the nanocrystalline ZnO, ZnO:Eu, and ZnO:(Eu, Er) samples through a co-precipitation technique. Structural analysis ruled out the effectual substitution of Eu and Er in the ZnO lattice without disturbing the original structure. Both ZnO:Eu and ZnO:(Eu, Er) NPs exhibited lower optical band gap values than pure ZnO. In M − H studies at room temperature, ferromagnetic behavior was observed in ZnO, ZnO:Eu, and ZnO:(Eu, Er) NPs. Expectedly, ZnO:(Eu, Er) NPs showed highest H 2 evolution than both ZnO and ZnO:Eu NPs beneath solar spectrum. The possible roots behind the extended H 2 production are discussed in detail. Hence, ZnO:(Eu, Er) NPs may find in applications is photocatalysis and spintronics. [ABSTRACT FROM AUTHOR]

In this work, we introduced ZnO through hydrothermal reaction to improve the breakdown strength and piezoelectric properties of potassium-sodium niobate (KNN) ceramics. The impact of ZnO synthesized at different reaction times on the structure, breakdown strength, dielectric performance, and piezoelectric performance of 0.9KNN-0.1ZnO ceramics was investigated. The findings reveal that the KNN ceramics incorporating ZnO exhibit a dense microstructure, reduced grain size, enhanced breakdown strength, and piezoelectric performance. Notably, the breakdown field strength of KNN-Z-3 ceramic significantly increased to 7.42 kV/mm, exhibiting an 80.98 % improvement compared to KNN ceramics (4.10 kV/mm). Furthermore, the d 33 value of the KNN-Z-3 ceramic also had a significant increase, reaching 104 pC/N, having a 30 % enhancement compared to KNN ceramics (80 pC/N). Such enhancement is ascribed to the increased piezoelectric response due to the stress bending between KNN and ZnO as well as adjacent domains. [ABSTRACT FROM AUTHOR]

ZnO linear resistors, due to its excellent performance, are widely used in numerous industries and gradually replacing traditional conductive resistors, presenting a broad prospect for application. To study the effects of lanthanide oxides on the microstructure and electrical properties of ZnO-based linear resistors, this paper prepared Dy 2 O 3 -doped ZnO-Al 2 O 3 -TiO 2 -NiO based linear resistors using a solid-state sintering method. The results showed that proper doping of Dy 2 O 3 could inhibit the growth of ZnO grains, leading to more uniform grain growth. Additionally, doped with appropriate amount of Dy 2 O 3 could enhance the linear performance of ZnO linear resistors, reduce the grain boundary barrier height (φ b), and decrease dielectric loss. Linear resistors with nonlinearity coefficient (α) of 1.07, grain boundary barrier height (φ b) of 0.0934 eV and resistance-temperature coefficient (α T) of −5.39 × 10−3/°C were obtained. The doping of Dy 2 O 3 could improve the comprehensive performance of ZnO linear resistors, making the fabricated ZnO linear resistors are more suitable for working in high frequency electric fields. The study and analysis of Dy 2 O 3 doped ZnO linear resistors are of significant importance for the preparation of high performance ZnO linear resistors. [ABSTRACT FROM AUTHOR]

This research paper investigates the impact of loading nano-oxides of zinc and copper metal particles into a polyethersulfone (PES) matrix to enhance its structural and mechanical responses. The co-precipitation method was adopted for the synthesis of metallic oxides consisting of zinc and copper. The presence of strain in metallic oxide NPs illustrated in metallic oxide-loaded PES films arises due to the interaction between NPs and PES. As a result of NPs and PES interactions, the particle size of PES has also been increased in PES blended films. Furthermore, we observed that the mechanical properties of PES-loaded films have been improved as the tensile strength was increased from 2.63 to 5.65 MPa, Young's modulus was enhanced from 8.92 to 10.02 MPa by adding ZnO NPs, whereas the more prominent increase in mechanical properties has been noticed in case of CuO NPs loaded PES blended films. The present work suggested that the loading of nano-oxides in PES enhances the mechanical strength of PES, which may significantly contribute to the field of mechanical engineering as oil level indicators, part for miking machines, and automatic beverage dispensers and pumps. Employing solution casting methodology synthesized metallic oxide NPs were loaded in PES to prepare their blended films. Three major functional groups such as sulfone, benzene, and ether are present in PES, and metal–oxygen vibrational groups have been identified in all prepared polymeric composites by FTIR spectroscopy. The electron microscopy (FESEM) reveals that the oxides of zinc appeared in rod-like structures, copper oxide adopted spherical and rhombus shapes, whereas the composite blended sheets appeared smooth. [ABSTRACT FROM AUTHOR]

In this study, modification of regular masks using composite nanofibers containing porous nanostructures has been considered in order to increase their efficiency in dealing with new threats. For this purpose, polystyrene was used as a low-cost polymer to prepare nanofibers and modify the surface of the respirator mask. ZIF-8 nanostructures with different sizes (14, 23, 65,144, and 265 nm) and zinc oxide nanoparticles, with an approximate size of 36 nm, were added to polymer nanofibers.2-methyl imidazole and Zn(NO3)2 were used to synthesize nanostructures. Two different methods (injection and stabilization) were used to incorporate nanostructures into fibers. The percentage of ZIF-8 and ZnO nanostructures were 0.5 and 2 wt% respects to polystyrene, respectively. Synthesis reactions and preparation of fibrous filters were carried out at ambient temperature. FESEM, FTIR, EDAX, TGA, and XRD techniques were used to identify the prepared nanoparticles and fibers. To evaluate the performance of the modified filters, their efficiency in removing suspended particles below 2.5 microns as well as CO2, SO2 and NO2 gases was surveyed. The results showed that ZIF nanoparticles with arbitrary sizes have been synthesized and successfully stabilized on the surface of nanofibers. Modifying the surface of the commercial mask by electrospinning method resulted in forming a fibrous layer with an approximate diameter of 700 nm and the presence of stabilized nanostructures in both methods was confirmed using FESEM images. Adding the nanofibers to the surface of the filter significantly increased their efficiency in removing suspended particles and toxic gases. The optimized modified filter contained ZIF-8 with14nm dimension and could remove sub-micron particles, CO2, NO2, and SO2 gases by 99, 91, 87, and 86%, respectively, making it as effective as commercially available N-95 masks. Moreover, it was observed that the incorporation of nanostructures by the stabilization method was more effective in improving the filtering efficiency of the fibrous mask. [ABSTRACT FROM AUTHOR]

Research on high dielectric constant materials, such as zinc oxide (ZnO), has received significant attention due to their potential for modern microelectronics and high-density energy storage applications. However, the use of ZnO has been limited by its high dielectric loss. This study aims to reduce the dielectric loss of ZnO by investigating the effects of adding niobium oxide (Nb 2 O 5) on its electrical properties. Four compositions with varying amounts of Nb 2 O 5 (0, 0.5, 1, and 2wt%) were prepared. The disk samples were made via the pressing method and sintered at 1250 °C. In the sample with a high additive content, a secondary phase of ZnNb 2 O 6 was identified. The addition of Nb 2 O 5 resulted in substantial grain growth in the ZnO ceramic. The samples containing Nb 2 O 5 showed reduced electrical conductivity and increased electrical resistance. The sample with 2 wt% Nb 2 O 5 exhibited the lowest dielectric constant, dielectric loss, and electrical conductivity, along with the highest electrical resistance and ferromagnetic behavior. Particularly, this sample achieved an impressive dielectric constant of 52730 and a low dielectric loss of 0.32 at 1 kHz. This makes it a promising candidate for energy storage applications. [ABSTRACT FROM AUTHOR]

Magnesium-doped zinc oxide thin films were dip-coated onto porous ceramic and glass substrates under identical conditions (50 layers, same doping ratio). Structural, morphological, and photocatalytic properties were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), UV–visible spectrophotometry, and confocal microscopy. XRD analysis indicated a shift in peak positions towards higher angles, increased grain size, and lattice distortion on both substrates. Unique flower-shaped crystalline granulates were observed exclusively on the ceramic substrate (DD3Z). The energy gap decreased on the ceramic and increased on the glass substrate. The photocatalytic activity was evaluated using an aqueous orange II solution, showing significantly higher decomposition (80 ± 0.53 % after 6 h) on the ceramic compared to the glass substrate (30 %). The enhanced performance on ceramic substrates, particularly with DD3+ZrO 2 , was attributed to increased microporosity, surface roughness, and active material incorporation, facilitating greater photocatalytic efficiency. The findings suggest promising applications of these materials for efficient and cost-effective photocatalysis, with potential for reuse after thermal treatment at 500 °C. [ABSTRACT FROM AUTHOR]

This study aims to enhance the piezocatalytic activity of ZnO by modifying it with a thin carbon layer (TCL). The composite catalysts were synthesized using a simple hydrothermal method. The tightly adhered TCL served as an effective electron transfer medium, enabling the rapid migration of piezoinduced charge carriers from the ZnO to the catalyst surface, thereby facilitating the catalytic degradation of Rhodamine B (RhB). The optimized TCL/ZnO sample exhibits an RhB degradation rate 13.4 times higher than that of pure ZnO. This work demonstrates that TCL/ZnO has significant potential in piezocatalytic water purification and offers new insights into the design of efficient piezocatalytic materials. [ABSTRACT FROM AUTHOR]

ZnO nanorods (NRs) were synthesized hydrothermally on a pre‐seeded graphene/nickel foam (NF) substrate. The effects of concentration on the photoelectrochemical (PEC) cell performance and hydrothermal reaction were studied. The field emission scanning electron microscopy images revealed that the precursor concentrations influenced the shape of the ZnO NRs on graphene/NF (ZGN). The X‐ray diffraction pattern for hexagonal wurtzite demonstrated strong orientation along the (002) direction. Notably, compared with the other concentrations, 0.04 M ZGN exhibited the highest photocurrent density, which was attributed to the optimal diameter and length of the rods for efficient light absorption. This research showed enhanced PEC performance, compared with existing literature, emphasizing the exceptional quality of the produced ZGN. [ABSTRACT FROM AUTHOR]

The role of oxygen vacancies in enhancing photocatalytic activity has attracted increasing attention. In this work, ZnO nanorods with enriched surface oxygen vacancies were successfully synthesized via a facile hydrothermal process combined with calcination in the presence of urea, and the content of the oxygen vacancies could be tuned by adjusting the calcination temperature and time. The characterization results proved that the content of oxygen vacancies reached 45.47% with a calcination temperature and time of 500 °C and 4 h, respectively. Additionally, the increased oxygen vacancy content was conducive to not only narrowing the ZnO bandgap, but also accelerating the separation and transfer of photoproduced electron–hole pairs, thus enhancing the methylene blue (MB) removal. The maximum removal efficiency of MB reached 97.65% within 120 min under simulated sunlight irradiation, and the catalyst exhibited stable performance after five consecutive cycles. The degradation intermediates of MB determined by liquid chromatograph–mass spectrometer (LC–MS) were the aromatic and ring-opening products of demethylation, desulfurization and hydroxylation. The toxicities of these compounds decreased significantly based on the germination and growth of Vigna radiata. This study provides a controllable and simple strategy for the design of ZnO with abundant oxygen vacancies and high activity in a photocatalytic system under simulated sunlight. [ABSTRACT FROM AUTHOR]

The use of metal oxide nanoparticles (NPs) in skincare products has significantly increased human skin exposure, raising safety concerns. Whilst NP's ability to penetrate healthy skin is minimal, studies have demonstrated that metal oxide NPs can induce toxicity in keratinocytes through direct contact. Moreover, NP's effect on common skin disorders like psoriasis, where barrier impairments and underlying inflammation could potentially increase NP penetration and worsen nanotoxicity is largely unstudied. In this paper, we investigated whether psoriasis-like human keratinocytes (Pso HKs) would exhibit heightened toxic responses to titanium dioxide (TiO2), zinc oxide (ZnO), and/or silica (SiO2) NPs compared to healthy HKs. Cells were exposed to each NP at concentrations ranging between 0.5 and 500 µg/ml for 6, 24, and 48 h. Amongst the metal oxide NPs, ZnO NPs produced the most pronounced toxic effects in both cell types, affecting cell viability, inducing oxidative stress, and activating the inflammasome pathway. Notably, only in ZnO NPs-treated Pso HKs, trappin-2/pre-elafin was cleaved intracellularly through a non-canonical process. In addition, tissue remodelling-related cytokines were upregulated in ZnO NP-treated Pso HKs. The full impact of the observed outcomes on psoriatic symptoms will need further evaluation. Nonetheless, our findings indicate the importance of understanding the sub-lethal impacts of NP exposures on keratinocytes, even though direct exposure may be low, particularly in the context of skin disorders where repeated and long-term exposures are anticipated. [ABSTRACT FROM AUTHOR]

BACKGROUND: Nanotechnology has been widely applied in agricultural science. During the process of reducing metal toxicity and accumulation in rice, nanomaterials exhibit size effects. However, there is limited knowledge regarding these size effects. We aim to explore the impact of fertilizer with various sizes of ZnO nanoparticles (ZnO‐NPs) on rice growth and cadmium (Cd) accumulation and to elucidate the potential mechanism of Cd reduction in rice. Foliar applications of different concentrations (0.5 and 2 mmol L−1) and different sizes (30 and 300 nm ZnO‐NPs) of zinc (Zn) fertilizer (Zn(NO3)2) were performed to investigate the effects on rice growth, Cd accumulation and subcellular distribution, and the expression of Zn–Cd transport genes. RESULTS: The results suggested that all the foliar sprayings can significantly reduce the Cd concentrations in rice grains by 41–61% with the highest reduction in the application of ZnO‐NPs with large size and low concentration. This is related to the enhancement of Cd fixation in leaf cell walls and downregulation of Cd transport genes (OsZIP7, OsHMA2, OsHMA3) in stem nodes. Foliar ZnO‐NPs applications can increase the Zn concentration in grains by 9–21%. Foliar applications of Zn(NO3)2 and small‐sized ZnO‐NPs promoted plant growth and rice yield, while the application of large‐sized ZnO‐NPs significantly reduced rice growth and yield. CONCLUSION: The study suggests that the rice yield and Cd reduction are dependent on the size and concentration of foliar spraying and the use of large‐sized ZnO‐NPs is the most effective strategy when considering both yield and Cd reduction comprehensively. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Adsorption is a highly effective method for wastewater quality adjustment, offering advantages such as low cost and availability of adsorbents. This study investigates the efficient removal of Anionic Actas Pink dye (AAPD), a major contributor to environmental pollution. Green adsorbents including lead oxide (PbO), zinc oxide (ZnO), cadmium oxide (CdO), and copper oxide (CuO) were synthesized via eco-friendly routes for AAPD removal. Maximum adsorption capacities (qe) were observed at pH 7 (PbO, ZnO, CdO) and pH 2 (CuO and native) with values of 83.83 mg/g at 100 ppm, 75.65 mg/g at 100 ppm, 70.50 mg/g 75 ppm, 61.21 mg/g at 150 ppm, and 52.69 mg/g at 150 ppm, respectively, using an adsorbent dose of 0.05 g/50 mL at temperature of 37°C, and 90 min contact time. Adsorption followed Langmuir isotherm for all adsorbents except native, with PbO also fitting Freundlich and Dubinin–Radushkevich isotherms. Kinetics adsorption data supported pseudo-second-order, while thermodynamic analysis indicated spontaneous and exothermic nature. Effects of electrolytes, surfactants, and desorption were also evaluated. Characterization through FTIR, SEM, and XRD confirmed the morphology and functional groups of these nano-quantum dots. Citrus limon peel-based biosynthesis offers sustainable, eco-friendly, and cost-effective alternatives, highlighting their potential for dye adsorption. Highlights: Explore cost-effective and efficient adsorption methods for wastewater treatment Discover effective adsorbents capable of efficiently removing Anionic Actas Pink Sustainable synthesis of green quantum dot was made using agricultural waste Gain insights into adsorption mechanisms through robust modeling techniques [ABSTRACT FROM AUTHOR]

In this study, by combining the polymers of polyvinylidene fluoride (PVDF) and 10,12-pentacosadinoic acid and adding the zinc oxide (ZnO) nanoparticles to their solution, three component composite nanofibers were electrospun and their thermo-chromic reversibility were investigated. Different amounts of ZnO nanoparticles based on the weight of PVDF were added to the mixture of PVDF/PDA (polydiacetylene) polymers and composite nanofibers were produced by electrospinning method. Adding ZnO to the electrospinning solvent affects nanofibers structural morphology and helps formation of beads in the electrospun nanofibers in comparison with that of PVDF/PDA sample. The crystal structure of the samples and the chemical changes in the structure of the polymers indicate that the addition of ZnO nanoparticles increases the stability of the nanofiber structure against heat and chromic change. Samples containing more than 2% ZnO with different UV irradiation times were reversible up to 140 °C. The best thermo-chromic reversibility of the PVDF/PDA/ZnO composite nanofibers could be obtained by sample containing 3% ZnO nanoparticles where the minimum irreversible temperature with an UV irradiation time of 5 min for this sample is 170 °C. [ABSTRACT FROM AUTHOR]

In conventional white light-emitting diodes (WLEDs), the combination of blue-LED chips with a yellow-phosphor type is the commonly employed method of production. However, this approach often results in low angular correlated color temperature (CCT) homogeneity. To address this issue, this research proposes the incorporation of ZnO nanostructures into WLED packages to enhance color homogeneity. The impacts of varying concentrations of ZnO nanoparticles on the morphologies, scattered energy, and CCT deviations in WLED packages are studied utilizing the Mie-scattering theory and MATLAB measurement techniques to analyze the scattering effects of ZnO nanoparticles. The scattering analysis reveals that the presence of ZnO nanoparticles significantly increases the scattered strength of WLEDs, especially with larger particles' radii, due to their strong scattering influence. Then, 1 µm is the selected size of the ZnO used in further tests. With different ZnO concentrations (2-50 wt.%) in the phosphor layer, the CCT deviation holds an inverse proportion to the luminous efficiency. Particularly, higher concentrations of ZnO nanoparticles reduce the CCT deviation, leading to improved color homogeneity, but a decline in lumen efficiency. The findings provide the basis of ZnO scattering performance, which can be utilized to explore potential ways for enhancing WLED's color uniformity and overall performance. [ABSTRACT FROM AUTHOR]

Silver nanoparticles (AgNPs) and Zinc oxide nanoparticles (ZnONPs) have been widely used and are eventually been discharged into the natural aquatic ecosystem. The current study examined and correlated the toxicity of AgNPs and ZnONPs on the Mozambique tilapia, Oreochromis mossambicus. Lethal concentration (LC50) was determined with four different concentrations (0.05, 0.10, 0.15, and 0.20 mg/L) of AgNPs and ZnONPs; subsequently, the fishes were exposed to sublethal concentrations for a period of 21 days, and the oxidative stress and antioxidant and nonantioxidant parameters were studied. Results revealed oxidative stress evinced by increased lipid peroxidation (LPO) protein carbonyl activity (PCA), glutathione‐S‐transferase (GST), glutathione peroxidase (GPx), superoxide dismutase (SOD), catalase (CAT) activity, metallothionein (MT) activity, and reduced glutathione in chronic exposure compared with acute exposure. Nonspecific immunological characteristics such as lysozyme (LYZ), myeloperoxidase (MPO), and respiratory burst activity (RBA) were also noticed in the serum. Furthermore, severe histological damages including damages in telangiectasia and epithelial cell hyperplasia were found in the combined treated group with Ag and ZnONPs than in individual treatments. When Ag and ZnONPs were combined, a reduction in the accumulation of Ag was observed in the liver, which increased drastically in individual exposure. The current findings highlight the importance of taking into account the combined exposure and correlation of NPs, their bioavailability, and toxicity in the aquatic ecosystem. [ABSTRACT FROM AUTHOR]

The present work aimed to reduce the COD of petroleum refinery wastewater using individual and combined processes based on the electrocoagulation and photocatalytic process with immobilized nano-zinc oxide. Also, energy savings alongside performance improvements were evaluated within this conglomerated system. Results showed that the removal efficiency of COD was 72% after 120 min when using electrocoagulation process under the given conditions (15 mA/cm2, pH of 7, and flow rate of 0.5 L/min). Regarding the process involving photocatalysis, the removal efficiency of COD was 76% after 120 min under the analyzed conditions (ZnO concentration of 80 g/m2, pH of 7, power of irradiation equal to 65 W, and flow rate of 0.5 L/min). Several combined sequential and simultaneous systems were tested. Results confirmed that the simultaneous photo-EC system operated at 30 min is the best one and has the ability to achieve COD removal of 82% under the studied conditions (15 mA/cm2, pH of 7, and flow rate of 0.5 L/min, ZnO concentration of 80 g/m2, and 65 W). Furthermore, the further notable features of the combined simultaneous photo-EC system were operating at shorter operation time and lowering dissolution rate of anode electrode (0.2 gram) that makes the system to be the most economic process with an energy consumption of 28.44 kWh/kg COD. [ABSTRACT FROM AUTHOR]

Objective: Given the significant role of retention in the long‐term success of implant‐supported prostheses, this study aimed to compare the retentive strength of three‐unit implant‐supported frameworks manufactured using the conventional, subtractive milling, and 3D printing methods. Materials and Methods: In this in vitro study, two fixture analogs were placed in the mandibular right first premolar and first molar region of a Dentiform model, and two prefabricated abutments were secured in the fixture analogs. A total of 27 three‐unit frameworks were fabricated utilizing wax patterns prepared through conventional, milling, and 3D printing techniques (n = 9 per group). The frameworks were cemented with zinc oxide eugenol and subjected to thermocycling. The retentive strength of each specimen was evaluated through a pull‐out test conducted with a universal testing machine. The data were analysed using one‐way ANOVA and Tukey's post hoc test (p < 0.05). Results: The three groups were found to be significantly different (p = 0.01). While the 3D printing and milling groups were not significantly different (p = 0.99), they yielded significantly higher retentive strength compare to the conventional group (p = 0.02 for 3D printing and p = 0.03 for milling group). Conclusion: The utilization of 3D printing and milling technique for wax pattern preparation significantly increased the retention of the implant‐supported framework, with no statistically significant difference between the two methods. [ABSTRACT FROM AUTHOR]

Copyright of Baghdad Science Journal is the property of Republic of Iraq Ministry of Higher Education & Scientific Research (MOHESR) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Baghdad Science Journal is the property of Republic of Iraq Ministry of Higher Education & Scientific Research (MOHESR) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

This work is devoted to studying and manufacturing a highly sensitive nonenzymatic glucose biosensing system of metal oxides via the sol–gel technique. The X‐ray diffraction patterns of all the prepared samples confirm that the samples present hexagonal crystal lattice structures of ZnO and Ag–ZnO nanoparticles. Ultraviolet (UV) analysis of all the samples is carried out to evaluate the absorption of silver in the UV region for electrical and chronoamperometric analysis. The transmittance of all the samples is observed, and the maximum transmittance is 11% for 4% AgZnO. Fourier transform infrared spectroscopy reveal the functional group stretching and vibration of the particles at different wavelength ranges. Scanning electron microsocpy analysis reveals the grain size and morphology of the samples, which decrease with increasing doping agent. Chronoamperometric analysis of all the samples reveals that the value increases with time for the 4% doped sample. The sensing response is also observed and is enhanced with increasing temperature for the 4% doped sample. The sensing response of the samples coated with carbon fiber electrodes is assessed from −0.2 to +0.5 V at a scan rate of 50 mV s−1. [ABSTRACT FROM AUTHOR]

In this work, the ZnO microsphere is prepared by hydrothermal method and modified with different concentrations of Eu. The morphology of ZnO:Eu sample shows flower-like microspheres with many nanosheets. The gas performance of ZnO:Eu microsphere is investigated for detecting NO 2. Compared with pure ZnO, the response of ZnO:2 % Eu sensor is increased by 8 times, and the optimal operating temperature of that is decreased to 130 °C. Especially, the gas sensing properties of ZnO:2 % Eu sensor is enhanced under UV excitation. The recovery time of ZnO:Eu sensor is reduced by 1200 s, and the response is increased by 3.6 times under UV excitation. The above results show an increase in sensor response due to doping Eu and UV excitation. At last, the possible gas mechanism of ZnO:Eu is discussed with and without UV excitation. This finding provides important guidance for UV-assisted sensors to enhance NO 2 response. [ABSTRACT FROM AUTHOR]

Zinc aluminate (ZnAl 2 O 4 , ZA) ceramic plays an important role in the development of industry and technology because of its many excellent characteristics. ZA ceramic was prepared by solid-state reaction sintering at 1550 °C from bauxite and zinc oxide (ZnO). The effects of different mass ratios of bauxite to ZnO and milling time on the densification, linear shrinkage, porosity, strength and microstructure of ZA ceramic were investigated. It is found that as the relative content of bauxite decreases, the strength of ZA ceramic first increases and then decreases. In addition, suitable milling time is beneficial to improve the performance of ZA ceramic, but too long milling time will be detrimental to its performance. As the mixture with 1:1 of mass ratio of bauxite to ZnO is milled for 5 h, the prepared ZA ceramic has the best performance, 4.79 g/cm3 of bulk density, 3.53 % of apparent porosity, 177.38 MPa of flexural strength and 523.62 MPa of compressive strength. [ABSTRACT FROM AUTHOR]

The green method provides stable, rapid, and eco-friendly methods for synthesis nanoparticles with plant extract as capping and reducing agents. This method renders biocompatibility, scalability, and potential medical applications of nanoparticles. This study green synthesized CuO/TiO 2 and ZnO/TiO 2 nanocomposites using Parkia timoriana bark extract. The synthesized nanocomposites were determined utilizing UV–vis DRS FTIR, XRD, TGA, AFM, FE-SEM, E -DAX, HR-TEM, and XPS. Antioxidant assay and antidiabetic studies revealed the biological activity of nanocomposites. The antioxidant property in ZnO/TiO 2 (84.07 %) was higher than in CuO/TiO 2 nanocomposites (72.76 %). The IC 50 value of CuO/TiO 2 and ZnO/TiO 2 in α-amylase inhibition assay was 72.12 μg/mL and 75.95 μg/mL, respectively and IC 50 value of CuO/TiO 2 and ZnO/TiO 2 in α-glucosidase inhibition assay was 30.80 μg/ml and 25.69 μg/ml. Thus, it concludes ZnO/TiO 2 nanocomposites exhibited higher antioxidant and antidiabetic activity than CuO/TiO 2 nanocomposites. These results show that biosynthesized nanocomposites can be used for treating diseases. [ABSTRACT FROM AUTHOR]

The TiO 2 substrate coatings containing varied ZnO or ZrO 2 nanoparticles were made using the polymeric and microwave combustion methods and then thermally treated at various temperatures. Furthermore, before coating on the substrate, the produced nanoparticles undergo characterization and calcination to optimize the conditions for developing ZnO and ZrO 2 phases and track their composition. The X-ray diffraction method (XRD), transmission electron microscopy (TEM), and infrared analysis (IR) are used to characterize the calcined produced nanoparticles. After heat treatment at 1000 °C, the TiO 2 substrate is prepared. The produced coated substrate is studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), infrared (IR), apparent porosity, bulk density, chemical corrosive properties and electrochemical measurement in 3.5 % NaCl and 1 M HCl solutions. The corrosion resistance of ZnO or ZrO 2 -covered TiO 2 substrate is ascertained by anticorrosive behaviors, which include weight loss, apparent porosity, corrosion rate, and SEM. The findings showed that 800 °C is the ideal temperature for preparing ZrO 2 -coated substrate, whereas 1000 °C is the perfect temperature for preparing ZnO-coated substrate. The microstructure reveals surface micro-cracks on the ZrO 2 -coated TiO 2 substrate. Good dispersion, homogeneity, and compaction were noted for the ZnO-coated substrate. Between 14 and 17 % of the ZnO-coated substrate and 20–21 % of the ZrO 2 -coated substrate, made via polymeric and microwave combustion techniques, had visible porosity when ZnO-coated samples exhibited greater corrosion resistance against NaCl media. In contrast, ZrO 2 -coated samples had much stronger anticorrosive qualities in HCl media than uncoated and Zn-coated samples. According to the electrochemical results, the ZnO-coated TiO 2 synthesized by polymeric technique at 1000 °C showed 99.86 % inhibitory efficiency against NaCl. An inhibitory efficiency of 94.4 % was observed in a ZrO 2 -coated TiO 2 substrate that was produced at 800 °C using a polymeric technique. [ABSTRACT FROM AUTHOR]

Electrolyte plays crucial roles in electrochemical CO2 reduction reaction (e‐CO2RR), yet how it affects the e‐CO2RR performance still being unclarified. In this work, it is reported that Sn‐Zn hybrid oxide enables excellent CO2‐to‐HCOO− conversion in KHCO3 with a HCOO− Faraday efficiency ≈89%, a yield rate ≈0.58 mmol cm−2 h−1 and a stability up to ≈60 h at −0.93 V, which are higher than those in NaHCO3 and K2SO4. Systematical characterizations unveil that the surface reconstruction on Sn‐Zn greatly depends on the electrolyte using: the Sn‐SnO2/ZnO, the ZnO encapsulated Sn‐SnO2/ZnO and the Sn‐SnO2/Zn‐ZnO are reconstructed on the surface by KHCO3, NaHCO3 and K2SO4, respectively. The improved CO2‐to‐HCOO− performance in KHCO3 is highly attributed to the reconstructed Sn‐SnO2/ZnO, which can enhance the charge transportation, promote the CO2 adsorption and optimize the adsorption configuration, accumulate the protons by enhancing water adsorption/cleavage and limit the hydrogen evolution. The findings may provide insightful understanding on the relationship between electrolyte and surface reconstruction in e‐CO2RR and guide the design of novel electrocatalyst for effective CO2 reduction. [ABSTRACT FROM AUTHOR]

AbstractZinc oxide quantum dots, also known as ZnO QDs, are highly desirable due to their numerous favorable characteristics, such as their beneficial photoluminescence, solubility in water, along with sunlight absorption. They are well-suited for use in biomedical applications, drugs, and bioimaging. However, study on the in-vivo toxicology of these QDs is needed before they can be used in humans. Zebrafish (Danio rerio) are cheap, fast-growing, and similar to humans, which makes them ideal as in vivo model for studying the toxicity of nanomaterials. The toxicity investigations involving zinc oxide QDs (ZnO QDs) and zinc oxide bionanocomposite (ZnO BC) in zebrafish that were concentration-dependent are evaluated, and the Box-Behnken design (BBD) was utilized to optimize the results. To determine the proper dosage, a study on cell line as well as hemocompatibility was carried out prior to testing the toxic effects of ZnO QDs along with ZnO BC upon zebrafish. When administered at 2.5 μg/l of ZnO BC and 2 μg/l of ZnO QDs, neither ZnO BC nor ZnO QDs appeared to be toxic to embryos during hatching and development. The testing of larval behavior in visible light revealed a dose-dependent decrease in both the total diving distance as well as speed. Nevertheless, at ZnO BC and ZnO QDs levels >250 μg/l and >200 μg/l, respectively, notable effects were seen in zebrafish embryos. Hence, ZnO QDs and BC at low concentrations were notably nontoxic. In order to guarantee the safety of nanomaterials in bio applications, this research supports upcoming in-vivo imaging investigations on their harmful effects. [ABSTRACT FROM AUTHOR]

Electronic and magnetic properties of transition metal (TM) ion-doped monolayer zinc oxide (ML-ZnO) have been analyzed using ab-initio calculations in the frame work of density functional theory. Spin–spin interaction study reveals that Cr, Mn, Fe and Cu doped at Zn site of ML-ZnO show stable ferromagnetic ordering along with the half-metallic behavior for most of the cases. The electronic and magnetic properties of the pristine system can also be modified by using co-doping. 3d orbital electrons of the dopants are primarily responsible for the origin of magnetic moment and the remaining part comes from the 3d and 2p orbital electrons of Zn and O atoms, respectively. Moreover, the magnetic ordering in Fe-doped ML-ZnO can change with the doping distance between the dopants. [ABSTRACT FROM AUTHOR]

Zinc oxide nanoparticles (ZnO NPs) have recently been applied in various veterinary and medical fields, however, the toxicological evaluations of these NPs in dogs are lacking. Therefore, the current study is designed to assess the impact of exposure to daily subcutaneous (SC) injections of ZnO NPs at different concentrations on various organs of mongrel dogs. Nine dogs were randomly divided into three groups (n = 3 for each) as follows: group (1) served as the control group, whereas groups (2&3) received SC injections of 50 and 100 ppm ZnO NPs (8 and 16 μg/kg bwt), respectively, once/day for 7 days. Our results revealed that ZnO NPs disrupted the oxidant/antioxidant balance in the lungs, liver, and kidneys of dogs in a dose-dependent manner. ZnO NPs induced dose-dependent radiological, ultrasonographical, and histopathological alterations in various organs especially lungs, spleen, liver, and kidneys along with disturbance in both liver and kidney biomarkers levels. Most organs of both ZnO NPs receiving groups displayed strong caspase-3 protein expression. Additionally, it upregulates the transcriptase levels of TNF-α and VEGF, as well as downregulates the antiapoptotic gene IL-10 in lung, kidney, and liver tissue homogenates. It was concluded that the daily SC injections of dogs with ZnO NPs at concentrations of 50 and 100 ppm caused extensive oxidative stress damage in various organs which provoked serious pathological processes such as apoptosis and inflammation. [ABSTRACT FROM AUTHOR]

Duckweeds (Spirodela polyrrhiza) are free-floating macrophytes that grow profusely in nutrient-rich waters. Under ideal conditions, they exhibit a rapid growth rate and can absorb a substantial amount of nutrients, macromolecules, and pollutants from bodies of water. Zinc oxide nanoparticles (ZnO NPs) synthesized from plant extracts, particularly under stress conditions, have opened new research avenues in the field of nanotechnology. Under salinity stress, the accumulation of flavonoids in duckweeds can affect the structure of ZnO NPs, helping researchers ascertain their antimicrobial role. In our study, we exposed mid-log phase duckweed monocultures to 75 mM NaCl in a full-strength Murashige and Skoog medium for 7 days, followed by a 15-day recovery period. We observed significant overexpression of superoxide and hydrogen peroxide as reactive oxygen species. As a result, chlorophyll and certain metabolites were produced in lesser amounts, while flavonoid and phenol content increased by 12% and 8%, respectively. This overproduction persisted up to 10 days into the recovery treatment period but dropped by 8% and 5%, respectively, by the 15th day. The flavonoid coating transformed the NPs into rosette clusters, which exhibited reduced antimicrobial activity against Aeromonas hydrophila, a Gram-negative, fish-pathogenic bacterium. Herein, we discuss potential mechanisms for the conformational transformation of ZnO NPs into finer dimensions in response to NaCl-induced oxidative stress in duckweed. In this study, the azo dye degradation capacity of salinity-treated plants increased as the flavonoid profile became enriched. Zinc oxide nanoparticles, both prior to and after salinity treatment, were found to be efficient in scavenging azo dye and mitigating its toxicity, as evidenced by improved germination, growth, and overall plant morphometry. [ABSTRACT FROM AUTHOR]