Search Results (71)

To improve the rutting resistance and low-temperature cracking performance of polymer-modified asphalt under extreme conditions, hierarchically structured ZnO-loaded porous activated carbon (ZnO/PAC) nanosheets were introduced as a synergistic reinforcing agent for SBS-modified asphalt. The ZnO/PAC hybrids were synthesized via template-assisted carbonization followed by hydrothermal growth, and their effects were evaluated by microscopic characterization and rheological tests, including temperature sweeps, multiple stress creep and recovery (MSCR), and bending beam rheometer (BBR) analyses. ZnO was successfully anchored onto the PAC, forming a three-dimensional flower-like nanostructure. Among the investigated samples, ZPS3 with 3 wt.% ZnO/PAC showed the best overall performance. At 64 °C, the rutting factor increased from 4.2 kPa for the SBS-modified asphalt to 6.8 kPa for ZPS3, representing a ~62% enhancement and indicating markedly improved high-temperature deformation resistance. MSCR results further confirmed the superior rutting resistance of ZPS3, which exhibited the highest recovery and the lowest non-recoverable creep compliance. In addition, BBR results showed that the low-temperature performance grade improved from −12 °C for conventional the SBS-modified asphalt to −18 °C for the ZnO/PAC-modified system. These results demonstrate that ZnO/PAC nanosheets can effectively enhance both the high-temperature rutting resistance and low-temperature cracking resistance of SBS-modified asphalt. Full article

Given the increasing environmental degradation, this study investigates advanced zinc oxide (ZnO)-based materials for the mineralization of toxic compounds through the combined action of photo- and piezocatalysis. Two complementary strategies were employed to enhance catalytic efficiency. First, ZnO_1−xN_x thin films were deposited by reactive high-power impulse magnetron sputtering (R-HiPIMS) to reduce the band gap energy. Second, flower-like ZnO nanostructures were synthesized using the pulsed thermionic vacuum arc (p-TVA) technique to increase the specific surface area. Both systems were further modified by decoration with Ag₂O nanoparticles to improve charge separation. The R-HiPIMS technique offers significant advantages in terms of precise control over processing parameters, enabling accurate tuning of film properties, including microstructure, chemical composition, and electronic structure. However, films produced via R-HiPIMS generally exhibit lower photo-piezocatalytic activity compared to nanostructured counterparts, primarily due to their comparatively reduced effective surface area and limited charge separation efficiency. In contrast, the p-TVA technique enables the synthesis of nanostructured thin films with substantially enhanced photo-piezocatalytic performance. This improvement is attributed to the increased effective surface area and the promotion of more efficient electron–hole pair separation. The materials were comprehensively characterized in terms of optical properties (UV–Vis spectroscopy), chemical composition and bonding (XPS), crystalline structure (XRD), surface morphology (FE-SEM), and photo-piezocatalytic performance. Catalytic activity was evaluated via the degradation of methylene blue (MB) under visible light irradiation and mechanical vibrations. Nitrogen incorporation in ZnO_1−xN_x thin films led to an increase in photocatalytic efficiency from 20% to 28.7%, while the simultaneous application of light and mechanical stimulation increased efficiency to approximately 50%. Under identical irradiation conditions, Ag₂O-decorated ZnO and Ag₂O-decorated ZnO_1−xN_x exhibited photo-degradation reaction rate constants up to 65% higher than bare counterparts, attributed to reduced electron–hole recombination. ZnO nanostructures achieved degradation efficiencies of 59%, rising to 88.3% with Ag₂O decoration under solar illumination for 120 min. When combined with mechanical vibrations, after 60 min, the degradation efficiencies reached 93% for ZnO and 98% for Ag₂O/ZnO systems. A photodegradation mechanism of Ag₂O NPs-decorated ZnO heterostructures was proposed. Full article

Mechanical energy is a plentiful, environmentally friendly, and sustainable energy source in the natural world. In this work, we successfully use friction to transform mechanical energy into ZnO and ZnO/Nd₂O₃ (1, 2, 3, 4 and 5 mol%) tribocatalysts. Under magnetic stirring, the catalyst particles and the polytetrafluoroethylene (PTFE)-sealed magnetic bar rubbed against one another, transferring electrons across the contact interface. While the PTFE absorbed the electrons, holes were simultaneously left on the catalyst. Because of their potent oxidative power, the holes in the valence band of sol–gel catalysts can efficiently oxidize organic pollutants, much like photocatalysis. In the absence of light, the tribocatalytic tests showed that ZnO and ZnO/Nd₂O₃ flowers could remove antibiotics (Doxycycline) when magnetized. We could further improve the tribocatalytic performance by adjusting the quantity of rare earth elements (1, 2, 3, 4 and 5 mol%), stirring speed, and magnetic rod type. Besides creating a green tribocatalysis method for organic pollutants’ oxidative purification, this work provides a possible pathway for transforming environmental mechanical energy into chemical energy, which may be applied to environmental remediation and sustainable energy. Full article

Organic pollutants pose a significant threat to both the ecological environment and human health. In this study, BiVO₄@ZnO heterojunction composites were synthesized via a two-step hydrothermal method. The incorporation of polyhedral BiVO₄ onto the flower-like structure of ZnO effectively enhanced the photocatalytic performance of the composite. Compared with ZnO flower-like nanorods, the BiVO₄@ZnO heterojunction composite photocatalysts achieved degradation efficiencies of 93.18% (k = 0.09063) and 89.64% (k = 0.007661) for methylene blue (MB) within 30 min under ultraviolet and visible light irradiation, respectively. The photocatalytic activity of the BiVO₄@ZnO composites was also evaluated against various organic dyes, including rhodamine B (RhB), Congo red (CR), methyl orange (MO), and methylene blue (MB). Under ultraviolet light, the catalysts showed particularly high activity toward MB and CR. The enhanced photocatalytic performance can be attributed to two main factors: firstly, the heterojunction facilitates the separation of photogenerated electron-hole pairs, thereby improving photocatalytic efficiency; secondly, the composite exhibits a broadened and enhanced light absorption range. Furthermore, the BiVO₄@ZnO heterojunction composites demonstrate excellent cyclic catalytic stability and structural integrity. This study offers a clean and efficient strategy for the photocatalytic degradation of aqueous organic pollutants. Full article

Aqueous zinc-ion batteries (ZIBs) have emerged as a promising candidate for large-scale energy storage due to their inherent safety, low cost, and environmental friendliness. However, manganese dioxide (MnO₂)-based cathodes, which are widely studied for ZIBs owing to their high theoretical capacity and low cost, face severe capacity fading issues that hinder the commercialization of ZIBs. This performance degradation mainly stems from the weak van der Waals forces between MnO₂ layers leading to structural collapse during repeated Zn²⁺ insertion and extraction; it is also exacerbated by irreversible Mn dissolution via Mn³⁺ disproportionation that depletes active materials, and further aggravated by dynamic electrolyte pH fluctuations promoting insulating zinc hydroxide sulfate (ZHS) formation to block ion diffusion channels. To address these interconnected challenges, in this study, a synergistic strategy was developed combining crystal engineering and pH buffer regulation. We synthesized three MnO₂ polymorphs (α-, δ-, γ-MnO₂), identified δ-MnO₂ with flower-like microspheres as optimal, and introduced sodium dihydrogen phosphate (NaH₂PO₄) as a pH buffer (stabilizing pH at 2.8 ± 0.2). The modified electrolyte improved δ-MnO₂ wettability (contact angle of 17.8° in NaH₂PO₄-modified electrolyte vs. 26.1° in base electrolyte) and reduced charge transfer resistance (Rct = 78.17 Ω), enabling the optimized cathode to retain 117.25 mAh g⁻¹ (82.16% retention) after 2500 cycles at 1 A g⁻¹. This work provides an effective strategy for stable MnO₂-based ZIBs, promoting their application in renewable energy storage. Full article

Zinc oxide (ZnO) is a wide bandgap semiconductor with optoelectronic and photocatalytic properties, which depend on its optical, structural, and morphological characteristics. In this study, we synthesized ZnO thin films by chemical bath deposition (CBD) and then thermally annealed them at 400 °C and 600 °C to evaluate the effect of thermal treatments. We characterized their structural, optical, morphological, and chemical properties using X-ray diffraction (XRD), UV–Vis spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The optical bandgap values were 3.20 eV for the as-grown thin films, and 3.23 eV and 3.21 eV after annealing at 400 °C and 600 °C, respectively. SEM micrographs revealed a change from elongated agglomerates in the as-grown thin films to uniform flower-like structures after annealing at 600 °C. XPS analysis confirmed ZnO formation in all samples, and we detected residual precursor species only in the as-grown thin films, which were completely removed by annealing at 600 °C. These results demonstrate that the CBD synthesis of ZnO can tune its optical and morphological properties through thermal annealing, making it suitable for optoelectronic, sensing, and photocatalytic applications. Full article

In this work, ZnO nanorods were grown on vertically aligned and randomly aligned silica nanosprings using the hydrothermal method. The initial step was the deposition of a ZnO seed layer by atomic layer deposition to promote nucleation. For hydrothermal growth, equimolar (0.2 M) solutions of Zinc nitrate hexahydrate and hexamethylene tetraamine prepared in DI water were used. The ZnO NR grown on the VANS were flower-like clusters, while for the RANS, the ZnO NR grew radially outward from the individual nanosprings. The lengths and diameters of ZnO NR grown on VANS and RANS were 175 and 650 nm, and 35 and 250 nm, respectively. Scanning electron microscopy confirmed the formation of ZnO nanorods, while X-ray diffraction and Raman spectroscopy verified that they have a hexagonal wurtzite crystal structure with preferential growth along the c-axis. X-ray photoelectron spectroscopy, in conjunction with in vacuo annealing, was used to examine the surface electronic structure of ZnO nanorods and defect healing. Photoluminescence of the ZnO nanorods indicates high crystal quality, as inferred from the weak defect band relative to strong excitonic band edge emission. Full article

The study of the processes of low-temperature synthesis of one-dimensional particles, which are the basis for two- and three-dimensional structures, is relevant for materials science. The modified metal-stimulated electrochemical etching method made it possible to synthesize silicon nanowires with an average thickness of about 292.6 nm. Scanning electron microscopy has shown the formation of nanowires, flower-like structures, and clusters of matter after the deposition of zinc oxide on the porous surface. The hexagonal structure of ZnO crystallites was determined by X-ray diffraction spectroscopy. Studies of the initial sample by electron paramagnetic resonance (EPR) spectroscopy revealed a narrow signal in the center of the spectrum. The subtraction of the EPR spectra with a sequential increase in microwave power up to 8 mW shows the absence of saturation of the signal. This indicates an almost free flow of charges through the surface nanostructures under the influence of an external field. Heat treatment in an air atmosphere at 300 °C caused a significant increase in the intensity of the EPR spectrum. This led to an increase in the intensity of charge transfer through paramagnetic centers. Full article

Wearable tactile sensors with high sensitivity can be potentially used to continuously monitoring physiological signals that are closely related to disease diagnosis and health condition tracking. However, the development of such tactile sensors involves a number of challenges, including a series of expensive patterning processes for microstructure manufacturing and addressing the large thickness of the microstructured composite film. Herein, a mold-free approach is presented to develop an ultra-thin ZnO/PEDOT:PSS composite film with flower-like microstructures via a feasible solution process for highly sensitive tactile sensors. The fabricated tactile sensors exhibit a high sensitivity of 4 × 10³ kPa⁻¹ in the pressure range 0–10 kPa, a fast response to various pressures in merits of the hierarchical microstructures on top of the ultra-thin composite films. Thanks to the fascinating performance of the devices, the tactile sensors are demonstrated with the ability to monitor physiological signals, subtle human body motions, and spatial pressure distribution. Full article

Exploring advanced sulfur cathode materials is important for the development of lithium-sulfur batteries (LSBs), but they still present challenges. Herein, zinc oxide dots-modified vanadium nitride flower-like heterojunctions (Zn-QDs-VN) as sulfur hosts are prepared by a phase separation strategy. Characterizations confirm that the flower structure with high specific surface area and pores improves active site exposure and electron/mass transfer. In situ phase separation enriches the Zn-QDs-VN interface, addressing the issues of uneven distribution and interface reduction of Zn-QDs-VN. Further theoretical computations reveal that ZnO-QDs-VN with optimized intermediate spin states can constitute a stable LiS* bond sequence, which can conspicuously facilitate the adsorption and conversion of LiPSs and reduce the battery reaction energy barrier. Therefore, the ZnO-QDs-VN@S cathode shows a high initial specific capacity of 1109.6 mAh g⁻¹ at 1.0 C and long cycle stability (maintaining 984.2 mAh g⁻¹ after 500 cycles). Under high S loading (8.5 mg cm⁻²) and lean electrolyte conditions (E/S = 6.5 μL mg⁻¹), it also exhibits a high initial area capacity (10.26 mAh cm⁻²) at 0.2 C. The interfacial synergistic effect accelerates the adsorption and conversion of LiPSs and reduces the energy barriers in cell reactions. The study provides a new method for designing heterojunctions to achieve high-performance LSBs. Full article

The demand for high-performance supercapacitors has driven extensive research into novel electrode materials with superior electrochemical properties. This study explores the supercapacitive behavior of quaternary CuNiCoZnO (CNCZO) films engineered into a three-dimensional (3D) flower-like morphology and developed on versatile substrates, including carbon cloth, stainless steel mesh, and nickel foam. The unique structural design, comprising interconnected nanosheets, enhances the electroactive surface area, facilitates ion diffusion, and improves charge storage capability. The synergistic effect of the multi-metallic composition contributes to remarkable electrochemical characteristics, including high specific capacitance, excellent rate capability, and outstanding cycling stability. Furthermore, the influence of different substrates on the electrochemical performance is systematically investigated to optimize material–substrate interactions. Electrochemical evaluations reveal outstanding specific capacitance values of 2318.5 F/g, 1993.7 F/g, and 2741.3 F/g at 2 mA/cm² for CNCZO electrodes on stainless steel mesh, carbon cloth, and nickel foam, respectively, with capacitance retention of 77.3%, 95.7%, and 86.1% over 5000 cycles. Furthermore, a symmetric device of CNCZO@Ni exhibits a peak specific capacitance of 67.7 F/g at a current density of 4 mA/cm², a power density of 717.4 W/kg, and an energy density of 25.6 Wh/kg, maintaining 84.5% stability over 5000 cycles. The straightforward synthesis of CNCZO on multiple substrates presents a promising route for the development of flexible, high-performance energy storage devices. Full article

With the rapid growth of renewable energy, the need for efficient and stable energy storage systems has become increasingly urgent. Aqueous zinc-ion batteries (AZIBs) can offer high safety, abundant zinc supply, and promising electrochemical properties. However, their performance is limited by poor electronic conductivity, slow Zn²⁺ diffusion, and structural degradation of conventional cathode materials. To address these issues, an in situ polyaniline (PANI) intercalation strategy for vanadium oxide cathodes is introduced in this paper. The conductive PANI chains play three key roles: (1) expand and stabilize interlayer spacing, (2) enhance electronic conductivity, and (3) provide mechanical support to prevent structural collapse and zinc-dendrite formation. A flower-like PANI-V₂O₅ hybrid is synthesized via synchronous oxidative polymerization, forming a hierarchical architecture without inert intercalants. The resulting electrode achieves a high specific capacity of 450 mAh·g⁻¹ at 0.1 A·g⁻¹ and retains 96.7% of its capacity after 300 cycles at 1 A·g⁻¹, with excellent rate performance. These findings demonstrate that PANI intercalation enhances ion transport, electronic conductivity, and structural integrity, offering a promising design approach for next-generation AZIBs cathodes. Full article

Photocatalytic degradation has the advantages of high efficiency and stability compared with traditional antibiotic treatment. Therefore, the development of efficient and stable photocatalysts is essential for antibiotic degradation in water treatment. In this study, layered g-C₃N₄/flower-like ZnO heterojunction loaded with different amounts of CQDs (C_x%CNZO (x = 1, 2, 3, 4)) were precisely synthesized at room temperature. The as-prepared photocatalyst showed enhanced performance in degrading ciprofloxacin (CIP). The heterojunction with CQDs loaded at 3 wt% (C_3%CNZO) achieved a 91.0% removal rate of CIP at 120 min under a sunlight simulator illumination, and the photodegradation reaction data were consistent with the first-order kinetic model. In addition, cycling experiments confirmed that the C_3%CNZO heterojunction had good reusability and photocatalytic stability after four cycles. According to the experimental results, superoxide radical (•O₂⁻) was the main active species involved in CIP degradation. Furthermore, C_3%CNZO was found to conform to a type II electron transfer pathway. Finally, the possible degradation pathways of CIP were analyzed. This work may provide an effective strategy for the removal of various antibiotics in water treatment. Full article

Loss of implant function is a common complication in orthopaedic and dental surgery. Among the primary causes of implant failure are peri-implant infections which often result in implant removal. This study demonstrates the development of a new antimicrobial titanium coating with ZnO nanoparticles of various sizes and morphologies immobilised in poly(allylamine hydrochloride) and alginate multilayers, combined with epitaxially grown vaterite crystals. The coated samples were characterised with various methods (FTIR, XRD, SEM) and surface properties were evaluated via water contact angle and surface charge measurements. Zinc ion release was quantified using ICP-MS. The antimicrobial efficacy of the coatings was tested against Staphylococcus aureus, Staphylococcus epidermidis, and Candida albicans while the biocompatibility was tested with preosteoblast cells (MC3T3-E1). Results demonstrated the successful preparation of a calcium carbonate/ZnO composite coating with epitaxially grown vaterite on titanium surfaces. The Zn ions released from ZnO nanoparticles dramatically influenced the morphology of vaterite where a new flower-like morphology was observed. The coated titanium surfaces exhibited robust antimicrobial activity, achieving over 90% microbial viability reduction for Staphylococcus aureus, Staphylococcus epidermidis, and Candida albicans. Importantly, the released Zn²⁺ concentrations remained below the cytotoxicity limit for MC3T3-E1 cells, showing potential for safe and effective implant applications. Full article

This work focuses on the green synthesis of zinc oxide nanoparticles (ZnO NPs) to be used as a photocatalyst, preparing a blueberry (Vaccinium corymbosum) extract as a reducing agent, zinc chloride as a precursor, and NaOH as precipitating agent (1, 7 and 14 M). Characterization techniques included X-ray diffraction (XRD), transmission electron microscopy (TEM), ultraviolet-visible (UV-Vis), Fourier-transform infrared (FTIR), X-ray photoelectron (XPS), and Raman spectroscopy. The XRD analysis confirmed the hexagonal wurtzite crystalline structure of ZnO NPs, while the SEM and TEM revealed a flower-like morphology. Moreover, the ZnO NPs exhibited a band gap energy in the range of 3.17 to 3.27 eV, depending on the concentration of NaOH. Regarding the photocatalytic activity, the synthesized ZnO NPs showed a photocatalytic efficiency greater than 90%, degrading malachite green (MG) dye in 60 min under sunlight. The proposed photocatalytic mechanism includes reactive oxygen species (ROS) generation (hydroxyl radicals (OH^•) and superoxide radicals (O²⁻)). The XRD and Raman analysis also revealed that the ZnO NPs maintained structural integrity after repeated photocatalytic cycles, emphasizing their stability and suitability for practical applications. Full article