Explore the vast range of titles available.

Significant research accomplishments have been made so far for the development and application of ZnO nanomaterials in enhanced optical biodetection. The unparalleled optical properties of ZnO nanomaterials and their reduced dimensionality have been successfully exploited to push the limits of conventional optical biosensors and optical biodetection platforms for a wide range of bioanalytes. ZnO nanomaterial-enabled advancements in optical biosensors have been demonstrated to improve key sensor performance characteristics such as the limit of detection and dynamic range. In addition, all nanomaterial forms of ZnO, ranging from 0-dimensional (0D) and 1D to 2D nanostructures, have been proven to be useful, ensuring their versatile fabrication into functional biosensors. The employment of ZnO as an essential biosensing element has been assessed not only for ensembles but also for individual nanomaterials, which is advantageous for the realization of high miniaturization and minimal invasiveness in biosensors and biodevices. Moreover, the nanomaterials’ incorporations into biosensors have been shown to be useful and functional for a variety of optical detection modes, such as absorption, colorimetry, fluorescence, near-band-edge emission, deep-level emission, chemiluminescence, surface evanescent wave, whispering gallery mode, lossy-mode resonance, surface plasmon resonance, and surface-enhanced Raman scattering. The detection capabilities of these ZnO nanomaterial-based optical biosensors demonstrated so far are highly encouraging and, in some cases, permit quantitative analyses of ultra-trace level bioanalytes that cannot be measured by other means. Hence, steady research endeavors are expected in this burgeoning field, whose scientific and technological impacts will grow immensely in the future. This review provides a timely and much needed review of the research efforts made in the field of ZnO nanomaterial-based optical biosensors in a comprehensive and systematic manner. The topical discussions in this review are organized by the different modes of optical detection listed above and further grouped by the dimensionality of the ZnO nanostructures used in biosensors. Following an overview of a given optical detection mode, the unique properties of ZnO nanomaterials critical to enhanced biodetection are presented in detail. Subsequently, specific biosensing applications of ZnO nanomaterials are discussed for ~40 different bioanalytes, and the important roles that the ZnO nanomaterials play in bioanalyte detection are also identified.

Undoped ZnO and group III (B, Al, Ga, and In)-doped ZnO thin films at 3% doping concentration level are dip-coated on glass substrates using a sol-gel technique. The optical properties of the as-prepared thin films are investigated using UV–Vis spectrophotometer measurements. Transmittance of all investigated thin films is found to attain high values of ≥80% in the visible region. We found that the index of refraction of undoped ZnO films exhibits values ranging between 1.6 and 2.2 and approximately match that of bulk ZnO. Furthermore, we measure and interpret nonlinear optical parameters and the electrical and optical conductivities of the investigated thin films to obtain a deeper insight from fundamental and practical points of view. In addition, the structural properties of all studied thin film samples are investigated using the XRD technique. In particular, undoped ZnO thin film is found to exhibit a hexagonal structure. Due to the large difference in size of boron and indium compared with that of zinc, doping ZnO thin films with these two elements is expected to cause a phase transition. However, Al-doped ZnO and Ga-doped ZnO thin films preserve the hexagonal phase. Moreover, as boron and indium are introduced in ZnO thin films, the grain size increases. On the other hand, grain size is found to decrease upon doping ZnO with aluminum and gallium. The drastic enhancement of optical properties of annealed dip-synthesized undoped ZnO thin films upon doping with group III metals paves the way to tune these properties in a skillful manner, in order to be used as key candidate materials in the fabrication of modern optoelectronic devices.

This work aims to explore how ZnO nanoparticles enhance the mechanical, photoaging, and self cleaning properties of water borne acrylic coating. Micro/nano ZnO particles (at 2 wt.% of total solid resin) were dispersed into the acrylic polymer matrices using ultrasonication to understand the effect of the size of the coating properties. The effect of ZnO particles on the properties of composite coatings (25 µm of thick) have been evaluated through various tests, such as abrasion measurement, ultraviolet/condensation (UV/CON) weathering aging, and methylene blue self cleaning. Experimental data indicated that the incorporation of ZnO particles enhanced both abrasion resistance and methylene blue removal efficiency of the water borne acrylic coatings, with nano ZnO particles being the best. However, the weathering degradation of nanocomposite coatings was more severe as compared to the coating with micro ZnO (at the same ZnO content).

In this paper, we propose a simple two-step method for the synthesis of Ag, Au, and Pt-doped ZnO nanoparticles. The method is based on the fabrication of targets using the pulsed laser deposition (PLD) technique where thin layers of metals (Ag, Pt, Au) have been deposited on a metal-oxide bulk substrate (ZnO). Such formed structures were used as a target for the production of doped nanoparticles (ZnO: Ag, ZnO: Au, and ZnO: Pt) by laser ablation in water. The influence of Ag, Au, and Pt doping on the optical properties, structure and composition, sizing, and morphology was studied using UV-Visible (UV-Vis) and photoluminescence (PL) spectroscopies, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), respectively. The band-gap energy decreased to 3.06, 3.08, and 3.15 for silver, gold, and platinum-doped ZnO compared to the pure ZnO (3.2 eV). PL spectra showed a decrease in the recombination rate of the electrons and holes in the case of doped ZnO. SEM, TEM, and AFM images showed spherical-shaped nanoparticles with a relatively smooth surface. The XRD patterns confirm that Ag, Au, and Pt were well incorporated inside the ZnO lattice and maintained a hexagonal wurtzite structure. This work could provide a new way for synthesizing various doped materials.

This work presents a facile sol–gel method for the deposition of ZnO and ZnO:Mg films. The films are spin coated on silicon and quartz substrates. The impact of magnesium concentrations (0, 0.5, 1, 2 and 3 wt%) and post-annealing treatments (300–600 °C) on the film’s structural, vibrational and optical properties is investigated. Undoped ZnO films crystallize in the wurtzite phase, with crystallite sizes ranging from 9.1 nm (300 °C) to 29.7 nm (600 °C). Mg doping deteriorates the film crystallization and shifting of 002 peak towards higher diffraction angles is observed, indicating the successful incorporation of Mg into the ZnO matrix. ZnO:Mg films (2 wt%) possess the smallest crystallite size, ranging from 6.2 nm (300 °C) to 25.2 nm (600 °C). The highest Mg concentration (3 wt%) results into a segregation of the MgO phase. Lattice constants, texture coefficients and Zn–O bond lengths are discussed. The diminution of the c lattice parameter is related to the replacement of Zn2+ by Mg2+ in the ZnO host lattice. The vibrational properties are studied by Fourier transform infrared (FTIR) spectroscopy. IR lines related to Mg–O bonds are found for ZnO:Mg films with dopant concentrations of 2 and 3 wt%. The optical characterization showed that the transmittance of ZnO:Mg thin films increased from 74.5% (undoped ZnO) to about 89.1% and the optical band gap energy from 3.24 to 3.56 eV. Mg doping leads to a higher refractive index compared to undoped ZnO films. The FESEM (field emission scanning electron microscopy) technique is used for observation of the surface morphology modification of ZnO:Mg films. The doped ZnO films possess a smoother grained surface structure, opposite to the wrinkle-type morphology of undoped sol–gel ZnO films. The smoother surface leads to improved transparency of ZnO:Mg films.

Composite metal oxide semiconductors are promising candidates for photoelectrochemical water splitting (PEC WS) toward environmentally friendly hydrogen production. Among them, ZnO and α‐Fe2O3 hold great potential thanks to a series of benefits, including fast charge transport in single‐crystalline structures, large surface area and tunable shapes (ZnO), and energy bandgap falling in the visible spectral range (α‐Fe2O3). However, both materials present significant drawbacks, which hinder their successful application in high‐efficiency PEC WS: the wide bandgap of ZnO limits its absorption in the UV range, while the low charge carrier mobility results in heavy recombination losses in α‐Fe2O3 during charge collection. The synthesis of ZnO/hematite composites has recently proven to be an effective approach to improve the overall WS performances. In this review, the recent developments on the application of different morphologies (0D, 1D, 2D, and 3D structures) for PEC WS are illustrated, analyzing the role of the shape and morphology in boosting the functional properties, both in single systems and in composite nanostructures. Complex networks show higher photocatalytic efficiency than the single building blocks and, consequently, composite materials exhibit higher performances. Possible paths for the development of an effective lab‐to‐fab transition based on application of ZnO/α‐Fe2O3 composite structures are also suggested. ZnO/hematite composite nanostructures are promising candidates for photoelectrochemical water splitting. Recent advancements demonstrate that the combination of single building blocks and the designing of complex morphologies may enhance the performances of both single and composite systems. The shape of a material can be a key parameter in producing new catalysts for energy and environmental applications.

Background: Therapeutic selectivity and drug resistance are critical issues in cancer therapy. Currently, zinc oxide nanoparticles (ZnO NPs) hold considerable promise to tackle this problem due to their tunable physicochemical properties. This work was designed to prepare SnO2-doped ZnO NPs/reduced graphene oxide nanocomposites (SnO2-ZnO/rGO NCs) with enhanced anticancer activity and better biocompatibility than those of pure ZnO NPs. Materials and Methods: Pure ZnO NPs, SnO2-doped ZnO (SnO2-ZnO) NPs, and SnO2-ZnO/rGO NCs were prepared via a facile hydrothermal method. Prepared samples were characterized by field emission transmission electron microscopy (FETEM), energy dispersive spectroscopy (EDS), field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), ultraviolet-visible (UV-VIS) spectrometer, and dynamic light scattering (DLS) techniques. Selectivity and anticancer activity of prepared samples were assessed in human breast cancer (MCF-7) and human normal breast epithelial (MCF10A) cells. Possible mechanisms of anticancer activity of prepared samples were explored through oxidative stress pathway. Results: XRD spectra of SnO2-ZnO/rGO NCs confirmed the formation of single-phase of hexagonal wurtzite ZnO. High resolution TEM and SEM mapping showed homogenous distribution of SnO2 and rGO in ZnO NPs with high quality lattice fringes without any distortion. Band gap energy of SnO2-ZnO/rGO NCs was lower compared to SnO2-ZnO NPs and pure ZnO NPs. The SnO2-ZnO/rGO NCs exhibited significantly higher anticancer activity against MCF-7 cancer cells than those of SnO2-ZnO NPs and ZnO NPs. The SnO2-ZnO/rGO NCs induced apoptotic response through the upregulation of caspase-3 gene and depletion of mitochondrial membrane potential. Mechanistic study indicated that SnO2-ZnO/rGO NCs kill cancer cells through oxidative stress pathway. Moreover, biocompatibility of SnO2-ZnO/rGO NCs was also higher against normal breast epithelial (MCF10A cells) in comparison to SnO2-ZnO NPs and ZnO NPs. Conclusion: SnO2-ZnO/rGO NCs showed enhanced anticancer activity and better biocompatibility than SnO2-ZnO NPs and pure ZnO NPs. This work suggested a new approach to improve the selectivity and anticancer activity of ZnO NPs. Studies on antitumor activity of SnO2-ZnO/rGO NCs in animal models are further warranted.

In the natural environment, mechanical energy is widely available as a sustainable and green energy source. In this paper, we successfully convert mechanical energy on ZnO and ZnO/Eu2O3 tribocatalysts via a friction route. Electrons were transferred across the contact interface when the catalyst particles and the polytetrafluoroethylene (PTFE)-sealed magnetic bar rubbed against each other under magnetic stirring. At the same time, holes were left on the catalyst while the PTFE absorbed the electrons. Similar to photocatalysis, organic pollutants can be effectively oxidized by the holes in the valence band of sol-gel catalysts due to their strong oxidative ability. The tribocatalytic tests demonstrated that ZnO and ZnO/Eu2O3 could eliminate organic analgesics (paracetamol) under magnetic stirring in the dark. By controlling the quantity of rare earth elements (1, 2, and 3 mol%), stirring speed, and the number of magnetic rods, we could further enhance the tribocatalytic performance. In addition to developing a green tribocatalysis approach for the oxidative purification of organic pollutants, this work offers a potential route for converting environmental mechanical energy into chemical energy, which could be used in sustainable energy and environmental remediation.

Thin films of zinc oxide (ZnO) doped with transition metals have recently gained significant attention due to their potential applications in a wide range of optoelectronic devices. This study focuses on ZnO thin films doped with the transition metals Co, Fe, and Zr, exploring various aspects of their structural, morphological, optical, electrical, and photoluminescence properties. The thin films were produced using RF and DC co-sputtering techniques. The X-ray diffraction (XRD) analysis revealed that all the doped ZnO thin films exhibited a stable wurtzite crystal structure, showcasing a higher structural stability compared to the undoped ZnO, while the atomic force microscopy (AFM) imaging highlighted a distinctive granular arrangement. Energy-dispersive X-ray spectroscopy was employed to confirm the presence of transition metals in the thin films, and Fourier-transform infrared spectroscopy (FTIR) was utilized to investigate the presence of chemical bonding. The optical characterizations indicated that doping induced changes in the optical properties of the thin films. Specifically, the doped ZnO thin film’s bandgap experienced a significant reduction, decreasing from 3.34 to 3.30 eV. The photoluminescence (PL) analysis revealed distinguishable emission peaks within the optical spectrum, attributed to electronic transitions occurring between different bands or between a band and an impurity. Furthermore, the introduction of these transition metals resulted in decreased resistivity and increased conductivity, indicating their positive influence on the electrical conductivity of the thin films. This suggests potential applications in solar cells and light-emitting devices.

In this research, Zinc Oxide-Ethylene @ glycol distilled water based nanofluid was synthesized using the sonochemical method. The convective heat transfer properties of as synthesized nanofluid were observed for a closed single circular tube pipe in turbulent flow regimes. The prepared nanofluids were characterized by ultra violet spectroscopy (UV–VIS), UV–VIS absorbance, X-Ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Transmission electron microscopy (TEM) and stability analysis. Five calibrated k-type thermocouples were mounted on the surface of the test section. Analytical data related to heat transfer properties of the synthesized nanofluid for the heat exchanger, incorporated with the closed circular tube test section were collected. The addition of ZnO solid nanoparticles in the EG@DW mixture enhanced the value of thermal conductivity and other thermophysical characteristics of the nanofluids. Maximum thermal conductivity was observed at 45 °C for using 0.1 wt.% of ZnO nanoparticles EG@DW nanofluid. Increasing the wt.% of ZnO solid nanoparticles in the EG@DW mixture had increased the thermal conductivity subsequently with change in temperature from 20 to 45 °C. Furthermore, Nusselt numbers of ZnO-EG@DW-based nanofluid was estimated for the various concentration of ZnO present in EG@DW-based fluid. The presence of ZnO solid nanoparticles into the EG@DW base fluid escalate the Nusselt (Nu) number by 49.5%, 40.79%, 37% and 23.06% for 0.1, 0.075, 0.05 and 0.025 wt.% concentrations, respectively, at room temperature. Varying wt.% of ZnO (0.1, 0.075, 0.05 and 0.025) nanoparticles had shown improved heat transfer (h) properties compared to the base fluid alone. The absolute average heat transfer of ZnO-EG@DW nanofluid using the highest concentration of 0.1 wt.% was improved compared to the EG@DW mixture. The magnitude of absolute average heat transfer was increased from 600 W/m2k for the EG@DW mixture to 1200 W/m2k for ZnO-EG@DW nanofluid. Similarly, the heat transfer improvement for the other three wt.% (0.075, 0.05 and 0.025) was noticed as 600–1160, 600–950 and 600–900 W/m2k, respectively, which is greater than base fluid.