Oxide Sol Research Articles

Fabrication of Functional Coating Layer for Emerging Transparent Electrodes using Antimony Tin Oxide Nano-colloid

This study fabricated a functional coating layer for transparent electrodes using antimony tin oxide nanopowder. The wet grinding method was employed to create a stable dispersion solution of antimony tin oxide nanopowder with aminopropyl tri-methoxysilane and acetyl acetone as primary dispersing agents. Various concentrations of these dispersing agents were used to determine optimal conditions, followed by a gel reaction to form a stable solution. The primary objective was to provide a viable alternative to indium-based transparent electrodes, specifically indium tin oxide, by incorporating antimony oxide. This approach not only addresses limitations associated with indium, but also enhances mechanical properties. The methodology involves the utilization of antimony tin oxide nanopowder and various solvents including ethanol and aforementioned dispersing agents to create a stable antimony tin oxide sol through wet grinding. Effects of dispersant concentration and milling time on the secondary particle size of the antimony tin oxide sol were thoroughly evaluated. Furthermore, this study examined sheet resistance of resulting coating layers by conducting a comparative analysis between antimony tin oxide and indium tin oxide under similar conditions. Findings of this study meticulously detailed in subsequent sections of the manuscript provide valuable insights into optimizing the entire process, encompassing synthesis, coating, heat treatment, and the production of high-quality transparent conductive coatings. These techniques and outcomes can significantly contribute to the development of more sustainable and cost-effective alternatives to traditional indium-based transparent electrodes.

Order–disorder–order mesophase transitions in self-assembled mesoporous alumina for enhanced CO2 adsorption

The addition of a hydrophobic micelle pore expander to self-assembling mesostructured hybrid materials enables access to new combinations with differently ordered mesophases and enhanced structural properties. Here we detail our investigations into the influence of 1,3,5-trimethylbenzene (TMB) on the self-assembly behaviors of an F127 Pluronic triblock copolymer with an aluminum oxide sol additive. By varying the chemical mixing sequence, the TMB-to-F127 mass ratio and the acid-to-metal molar ratio, we observe that TMB exhibits dual roles, functioning both as a hydrophobic swelling agent and as a low dielectric co-solvent. This induces a mesophase transition from an ordered p6mm lattice to a disordered state and subsequently back to the ordered p6mm phase. We propose a structure formation mechanism based on the DLVO theory to describe the thermodynamics and kinetic mobility of the hybrid micelles during the order-disorder and ensuing disorder-order mesophase transitions. The resulting ordered mesoporous alumina structures, with considerable pore sizes (up to 12 nm), high surface areas (up to 314 m2/g) and pore volumes (up to 0.74 cm3/g), organized pore geometry and variable inorganic wall thicknesses, have shown excellent CO2 adsorption capacities and are appealing for various applications, including stable high temperature catalyst supports, separation and sensing.

Preparation and patterning of HfO2 film via sol–gel method and resistive switching effect of Pt/HfO2/LaNiO3

Sol–gel method is a low-cost material preparation method; however, it is difficult to obtain a stable sol containing easily hydrolyzable metal ions via this method. In this study, a stable hafnium(IV) oxide (HfO2) sol was prepared by adding benzoyl acetone (BzAcH) modifier. Infrared absorption spectroscopy results showed that the BzAcH additive chelated with the Hf4+ ions in the sol, thus improving the hydrolysis resistance of the HfO2 sol, which in turn improved its stability. It was also found that the BzAcH-modified HfO2 gel film exhibited ultraviolet (UV) photosensitivity. After UV exposure, the film did not dissolve easily in organic solvents. Based on these properties, the micro processing of the HfO2 film was preliminarily explored, and HfO2 microstructures were successfully obtained. Additionally, the relative permittivity (εr) of HfO2 exhibited minimum (∼10.9) and maximum (∼20.6) values at heat-treatment (HT) temperatures of 350 and 450 °C, respectively. With the continuous increase in the HT temperature, εr first decreased and then increased slightly. Moreover, the current–voltage curves showed that the Pt/HfO2/LaNiO3 (LNO) structure exhibited a pronounced bipolar resistive switching (RS) effect, which was attributed to the fact that LNO could be used as an electrode and an oxygen vacancy (OV2+) storage layer for RS materials. Notably, the oxygen ions in HfO2 with a low degree of crystallinity are more likely to migrate within its body (which makes it easier to form OV2+s), therefore, the “Set” voltage of low-crystallinity HfO2 films is lower than that of high-crystallinity HfO2 films. The RS mechanism can be explained by the OV2+ conductive filament model. These results are of great practical significance for the low-cost preparation of HfO2 and the application of LNO as an oxide electrode.

Antimicrobial Activity of Citrate-Coated Cerium Oxide Nanoparticles.

The purpose of this study was to investigate the antimicrobial activity of citrate-stabilized sols of cerium oxide nanoparticles at different concentrations via different microbiological methods and to compare the effect with the peroxidase activity of nanoceria for the subsequent development of a regeneration-stimulating medical and/or veterinary wound-healing product providing new types of antimicrobial action. The object of this study was cerium oxide nanoparticles synthesized from aqueous solutions of cerium (III) nitrate hexahydrate and citric acid (the size of the nanoparticles was 3-5 nm, and their aggregates were 60-130 nm). Nanoceria oxide sols with a wide range of concentrations (10-1-10-6 M) as well as powder (the dry substance) were used. Both bacterial and fungal strains (Bacillus subtilis, Bacillus cereus, Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Proteus vulgaris, Candida albicans, Aspergillus brasielensis) were used for the microbiological studies. The antimicrobial activity of nanoceria was investigated across a wide range of concentrations using three methods sequentially; the antimicrobial activity was studied by examining diffusion into agar, the serial dilution method was used to detect the minimum inhibitory and bactericidal concentrations, and, finally, gas chromatography with mass-selective detection was performed to study the inhibition of E. coli's growth. To study the redox activity of different concentrations of nanocerium, we studied the intensity of chemiluminescence in the oxidation reaction of luminol in the presence of hydrogen peroxide. As a result of this study's use of the agar diffusion and serial dilution methods followed by sowing, no significant evidence of antimicrobial activity was found. At the same time, in the current study of antimicrobial activity against E. coli strains using gas chromatography with mass spectrometry, the ability of nanoceria to significantly inhibit the growth and reproduction of microorganisms after 24 h and, in particular, after 48 h of incubation at a wide range of concentrations, 10-2-10-5 M (48-95% reduction in the number of microbes with a significant dose-dependent effect) was determined as the optimum concentration. A reliable redox activity of nanoceria coated with citrate was established, increasing in proportion to the concentration, confirming the oxidative mechanism of the action of nanoceria. Thus, nanoceria have a dose-dependent bacteriostatic effect, which is most pronounced at concentrations of 10-2-10-3 M. Unlike the effects of classical antiseptics, the effect was manifested from 2 days and increased during the observation. To study the antimicrobial activity of nanomaterials, it is advisable not to use classical qualitative and semi-quantitative methods; rather, the employment of more accurate quantitative methods is advised, in particular, gas chromatography-mass spectrometry, during several days of incubation.

Way to a Library of Ti-Series Oxide Nanofiber Sponges that are Highly Stretchable, Compressible, and Bendable.

Ti-series oxide ceramics in the form of aerogels, such as TiO2, SrTiO3, BaTiO3, and CaCu3Ti4O12, hold tremendous potential as functional materials owing to their excellent optical, dielectric, and catalytic properties. Unfortunately, these inorganic aerogels are usually brittle and prone to pulverization owing to weak inter-particulate interactions, resulting in restricted application performance and serious health risks. Herein, a novel strategy is reported to synthesize an elastic form of an aerogel-like, highly porous structure, in which activity-switchable Ti-series oxide sols transform from the metastable state to the active state during electrospinning, resulting in condensation and solidification at the whipping stage to obtain curled nanofibers. These curled nanofibers are further entangled when flying in the air to form a physically interlocked, elastic network mimicking the microstructure of high-elasticity hydrogels. This strategy provides a library of Ti-series oxide nanofiber sponges with unprecedented stretchability, compressibility, and bendability, possessing extensive opportunities for greener, safer, and broader applications as integrated or wearable functional devices. As a proof-of-concept demonstration, a new, elastic form of TiO2, composed of both "white" and "black" TiO2 nanofiber sponges, is constructed as spontaneous air-conditioning textiles in smart clothing, buildings, and vehicles, with unique bidirectional regulation of radiative cooling in summer and solar heating in winter.

Rare earth metals ion intercalated hydrated vanadium oxides for high-performance aqueous zinc-ion batteries

Hydrated vanadium oxide (V2O5·nH2O) is promising cathode candidates for aqueous rechargeable Zn-ion batteries (ZIBs) owing to its high theoretical specific capacity, abundant resources and environmentally friendly. However, the higher charge density of Zn2+ lead to its structural instability, cyclic degradation and sluggish Zn2+ diffusion kinetics. Herein, rare earth metal ions intercalated into the interlayer of V2O5·nH2O materials (abbreviated as RE-VOH) are successfully synthesized to expand interlayer spacing and stabilize the layered structure via a simple sol-gel method, among, the yttrium ion intercalated V2O5·nH2O (Y–VOH) exhibits a honeycomb porous microstructure and a remarkably enlarged interlayer distance (13.6 Å), which can not only increase the contact area between the electrode material and the electrolyte but also offer rapid diffusion channel for Zn2+. Meanwhile, the problem of vanadium dissolution of cathode materials is inhibited by the electrolyte additive strategy through adding suitable vanadium oxide sol to aqueous electrolyte, furthermore, the zinc anode modification strategy in electroplating process inhibits the formation of zinc dendrites. Benefitting from the synergistic effect of modification design for the ZIBs systems of cathode, electrolyte and anode, the overall electrochemical performance of Y–VOH electrode is significantly improved, delivering a large specific capacity of 337 mAh g−1 at the current density of 500 mA g−1 and excellent rate capability of 170 mAh g−1 at 10 A g−1, along with an outstanding capacity retention of 90 % over 3000 cycles. Additionally, systematical ex situ characterizations prove the (de)intercalation reversibility of Zn2+ storage mechanism for the Y–VOH cathode. This research may provide a new way for exploiting high performance vanadium-based materials for aqueous ZIBs.

Photochromic properties of novel composites on the base of biopolymers and plasma‐modified Mo4O11 and W18O49 nanostructures

AbstractNovel photochromic composites based on biopolymers (polyvinyl alcohol, starch) and Mo4O11 and W18O49 as the fillers were obtained and characterized. To improve the photochromic properties, molybdenum and tungsten oxide sols were treated by an underwater diaphragm discharge to obtain binary structures of the MoOx/WOx and WOx/MoOx (2 < x < 3) types. The formation of such oxides was confirmed by TEM, EDX, XRD analysis, and Raman spectroscopy data. Plasma treatment is increased the color intensity and reversibility. The modified sols were incorporated into polymer matrices. Spectral studies have shown that the color of photo‐colored composites depends on the chemical structure of the polymer matrix. Mechanical tests have shown the possibility of obtaining hardened or plastic composites depending on the concentration and nature of the filler.Highlights Photochromic polymer composites with W18O49 and Mo4O11 as fillers were obtained. Diaphragm discharge used as a tool for sol modification. WOx/MoOx and MoOx/WOx structures have improved photochromic properties. Color of irradiated polymer composites depends on chemical structure of polymer. Mechanical properties are determined by the polymer filler concentration.

Effectively improving flame retardancy levels of finished cotton fabrics only by simple binary silicon-boron oxide sols

Effectively improving flame retardancy levels of finished cotton fabrics only by simple binary silicon-boron oxide sols

Cell Lysis, labeling efficacy and biodistribution of intravenously administered Technetium-99 m labeled multifunctional zirconia nanoparticles in animal model

Nanoparticles, to be used in biomedical applications, have been the subject of extensive investigation in recent years. Recently, zirconia and iron have gained significant relevance to the field due to their superior mechanical and structural qualities as well as their numerous biological applications. In this research, Fe3O4-stabilized zirconia nanopowders are fabricated using a low-cost sol–gel approach. Iron oxide sol is added in 1–10 wt% increments to a 0.1 M zirconia sol. The obtained crystallite size values match well with previously reported values for the tetragonally stable (t-zirconia) phase. Hardness values of approximately 1278 HV, along with fracture toughness values of ∼ 24.48 MPa.m-1/2 are observed for stable tetragonal zirconia. Results from cell lysis experiments indicate that the synthesized nanoparticles have the potential to combat cancerous cells. An encapsulation efficacy of up to ∼ 73% is observed after a 120-minute time period. Radio labeling techniques are employed to label the as-synthesized zirconia nanoparticles using Sodium Pertechnetate (Na99mTcO4) labeled radiopharmaceuticals, allowing for biodistribution assessment. Multiple CT scans of rabbits are performed to obtain accurate results and evaluate their survival. Studies show that radiolabeled nanoparticles are highly absorbed in the animals' bladders, making them a promising choice for tumor therapy. Various physical properties of the animals are periodically examined after administration of the nanoparticle-based injection for several months, and no abnormalities are found. The results obtained through these characterizations indicate that these nanoparticles can be used as future therapeutic agents as well as drug carriers.

Electrochemical, mechanical, and antibacterial properties of the AZ91 Mg alloy by hybrid and layered hydroxyapatite and tantalum oxide sol–gel coating

Abstract The corrosion and bacterial behavior of AZ91 magnesium alloy coated with sol–gel-deposited amorphous tantalum oxide and hydroxyapatite have been investigated. The objective was to assess the potential suitability of AZ91 for permanent prosthesis applications. The coatings were applied in layered and hybrid configurations and characterized using various techniques including X-ray diffractometry, Fourier transform infrared spectroscopy, scanning electron microscopy/energy dispersive spectrometry, and drop analyses. The antibacterial properties were evaluated through interactions with Staphylococcus aureus and Escherichia coli strains. Mechanical properties and adhesion were determined via linear scratch tests, and electrochemical corrosion tests were conducted in different media. The release of aluminum ions from the samples in Dulbecco’s Modified Eagle’s Medium was monitored over 28 days. The findings revealed that the amorphous tantalum oxide coating, particularly in combination with hydroxyapatite, improved antibacterial properties and positively influenced corrosion and scratch resistance. The layered and hybrid coatings demonstrated the highest corrosion resistance. The release of aluminum ions remained within acceptable levels in the tested medium. Overall, the study provides valuable insights into the potential of sol–gel coatings on AZ91 for prosthetic applications, considering antibacterial behavior, corrosion resistance, and aluminum release.

Sol–Gel Silica Coatings for Corrosion Protection of Aluminum Parts Manufactured by Selective Laser Melting (SLM) Technology

Metal additive manufacturing is a rapidly growing field based on the fabrication of complex parts with improved performance. The advantages of using this technology include the production of shapes that cannot be produced by traditional machining technologies, the possibility of using trabecular reinforcing structures, and the ability to make parts with topological optimization that allow for increased performance and decreased mass of the parts produced. Metal parts produced by selective laser melting technology exhibit high surface roughness, which limits their direct implementation. Corrosion protection of these surfaces is difficult, especially for galvanic processes. This paper analyzes the possibility of using sol–gel silica (silicon oxide) coatings to effectively protect various surfaces of aluminum alloys produced by selective laser melting technology. Silicon oxide sol–gel protective coatings have demonstrated excellent chemical stability and corrosion resistance, being able to be applied in very thin layers. These properties make them excellent candidates for protecting additive-manufactured metal parts, especially as-built surfaces with a high surface roughness. Nanostructured silica sol–gel protective coatings have demonstrated excellent corrosion resistance and have the potential to replace the highly toxic chromium-based galvanic treatments. Using nanostructured silica sol–gel coatings, aluminum parts can be seamlessly integrated into circular-economy cycles.

Molecular mechanisms of the metal oxide sol-gel process and their application in approaches to thermodynamically challenging complex oxide materials

This review presents a brief overview of recent insights into general reaction pathways in sol-gel synthesis of metal oxides. Metal-based sol-gel precursors display kinetically unhindered reactivity, combining high reaction speed with reversibility on a molecular level. The process producing metal oxide sols can thus be described as nucleation of an oxide phase with growth option efficiently precluded by extremely low solubility. The emerging nuclei are essentially Polyoxometalate (POM) species, with sizes in the colloid range starting from about 2 nm. They are stabilized in solution by colloid forces (charge interactions, hydrogen bonding, van der Waals forces), defined by the nature and arrangement of species on their surface, which permits them to be denoted as Micelles Templated by Self-Assembly of Ligands (MTSALs). The sol-gel transition occurs on aggregation of particles resulting in percolation. Exploiting this mechanism, it is possible to produce materials with controlled porosity, biocompatibility, and even to access thermodynamically challenging phases that cannot be produced by conventional synthetic techniques.Graphical Metal oxide Sol-Gel can be described as nucleation of an oxide phase resulting from one-step coordination equilibrium in solution, followed by aggregation without growth.

Functionalization of glass fiber woven fabrics by indium tin oxide (ITO) coatings for electromagnetic wave absorption

The effects of surface electrical conductivity and cascading order of ITO surface modified glass fiber woven fabrics (GFWF) on the electromagnetic (EM) behavior of hybrid type multilayered absorber structure were investigated. Additional objective was to create a design guideline for a multilayered absorbing structure according to the needs of specific EM wave absorber applications. For this purpose, indium tin oxide (ITO) sols were deposited on GFWFs by spray pyrolysis technique. The electrical conductivity of these conducting layers was controlled to incorporate EM wave absorbing characteristics to glass fabrics. Surface modified fabrics were then used as reinforcement in a hybrid type multilayered EM wave absorbing structure which is a combination of Jaumann and graded type absorbers effective in 8–12 GHz frequency range (X-band). The highest absorption performance design has been formed by cascading six ITO coated fabrics with gradually increasing electrical conductivity gradient from the front to back layer of the structure. The electromagnetic behavior of the multilayered absorber was tested both with and without metallic backing. The absorber design showed ∼−11 dB reflection loss and ∼−9 dB transmission loss corresponding to ∼80 % average absorption without metallic backing, while its reflection loss and average absorption values were ∼−10.5 dB and ∼93 %, respectively, with metallic backing. The front layer of the multilayered structure with the lowest surface electrical conductivity provided impedance matching between air and receiving surface of the structure minimizing reflection, where the gradual increase in surface conductivity of the layers towards the back provided balanced internal reflection and transmission leading to high overall EM wave absorption. Consequently, by controlling the grading of the surface conductivity of the layers through the thickness, responses of the absorbers can be adjusted to provide tailored characteristics for the required EM wave absorption levels.

Highly Transparent and Zirconia-Enhanced Sol-Gel Hybrid Coating on Polycarbonate Substrates for Self-Cleaning Applications.

To improve the efficacy of polymer-based substrate hybrid coatings, it is essential to simultaneously optimize mechanical strength and preserve the optical properties. In this study, a mixture of zirconium oxide (ZrO2) sol and methyltriethoxysilane modified silica (SiO2) sol-gel was dip-coated onto polycarbonate (PC) substrates to form zirconia-enhanced SiO2 hybrid coatings. Additionally, a solution containing 1H, 1H, 2H, and 2H-perfluorooctyl trichlorosilane (PFTS) was employed for surface modification. The results show that the ZrO2-SiO2 hybrid coating enhanced the mechanical strength and transmittance. The average transmittance of the coated PC reached up to 93.9% (400-800 nm), while the peak transmittance reached up to 95.1% at 700 nm. SEM images and AFM morphologies demonstrate that the ZrO2 and SiO2 nanoparticles were evenly distributed, and a flat coating was observed on the PC substrate. The PFTS-modified ZrO2-SiO2 hybrid coating also exhibited good hydrophobicity (WCA, 113°). As an antireflective coating on PC, with self-cleaning capability, the proposed coating has application prospects in optical lenses and automotive windows.

Fabrication of PbSe colloidal quantum dot solar cells using low-temperature Li-doped ZnO electron transport layer

The lead selenide quantum dots (PbSe QDs) have incredible features because of their tunable bandgap and synthesis process at low temperatures. Aside from the highly effective QDs active layer, the electron transport layer (ETL) also plays a significant part in obtaining high-efficiency colloidal quantum dots solar cells (CQDSCs). Here, we introduce undoped and 1–3% lithium-doped zinc oxide (LZO) sol–gel as an ETL and utilized it in CQDSCs to achieve high efficiency. ZnO and LZO thin films are obtained by low annealing temperature whereas the PbSe QDs-based absorber layer is deposited by layer-by-layer (LBL) technique in the presence of 1-ethyl-3-methylimidazolium iodide (EMII) which is acting as a ligand exchange material. Results show that 2 wt% Li-doping on one hand can maximumly increase the conduction band minimum, and transmittance, whereas on the other hand decreases the oxygen defects densities as well as the roughness of the thin film as compared to other ETLs. Subsequently, PbSe CQDSCs with 2 wt% Li-doped ZnO ETL display the highest power conversion efficiency (PCE) of 10.80% as compared to 10.12% PCE of ZnO-based PbSe CQDSCs (7.5% higher). Similarly, 2 wt% LZO-based PbSe CQDSCs devices show long-term stability of about 40 days. Furthermore, Li-doping in ZnO offers a viable approach for low-cost, high-performance CQDSCs.

Sol–Gel Photonic Glasses: From Material to Application

In this review, we present a short overview of the development of sol-gel glasses for application in the field of photonics, with a focus on some of the most interesting results obtained by our group and collaborators in that area. Our main attention is devoted to silicate glasses of different compositions, which are characterized by specific optical and spectroscopic properties for various applications, ranging from luminescent systems to light-confining structures and memristors. In particular, the roles of rare-earth doping, matrix composition, the densification process and the fabrication protocol on the structural, optical and spectroscopic properties of the developed photonic systems are discussed through appropriate examples. Some achievements in the fabrication of oxide sol-gel optical waveguides and of micro- and nanostructures for the confinement of light are also briefly discussed.

Preparation and antibacterial mechanism of cinnamaldehyde/tea polyphenol/polylactic acid coaxial nanofiber films with zinc oxide sol to Shewanella putrefaciens

In this study, the coaxial nanofiber films were prepared by coaxial electrospinning technique with cinnamaldehyde (CMA) and tea polyphenol (TP) as core material and polylactic acid (PLA) as shell material, and to obtain food packaging materials with great physicochemical and antibacterial properties, zinc oxide (ZnO) sol were added into PLA, and ZnO/CMA/TP-PLA coaxial nanofiber films were prepared. Meanwhile, the microstructure and physicochemical properties were determined, and the antibacterial properties and mechanism were investigated with Shewanella putrefaciens (S. putrefaciens) as target. The results show that the ZnO sol makes the physicochemical properties and antibacterial properties of the coaxial nanofiber films improve. Among them, the 1.0 % ZnO/CMA/TP-PLA coaxial nanofibers have smooth and continuous uniform surfaces, and their encapsulation effect on CMA/TP and antibacterial properties are the optimal. The synergistic action of CMA/TP and ZnO sol cause severe depression and folding of the cell membrane of S. putrefaciens, makes cell membrane permeability increase and of intracellular materials spillage, interference the bacteriophage protein expression, and makes macromolecular protein degraded. In this study, the introduction of oxide sols into polymeric shell materials by in-situ synthesis technique can provide theoretical support and methodological guidance for the application of electrospinning technology in the field of food packaging.

Effect of substrate surface on the wide bandgap SnO2 thin films grown by spin coating

Tin (IV) oxide (SnO2) sols have been synthesized from SnCl2·2H2O precursor solution by applying two different processing conditions. The prepared sols were then deposited on UV-Ozone-treated quartz and soda lime glass (SLG) substrates by spin coating. The as-synthesized film was soft baked at about 100 °C for 10 min. This process was repeated 5 times to get a compact film, followed by air annealing at 250 °C for 2 h. The pristine and annealed films were characterized by UV–Vis–NIR spectroscopy, Grazing Incident X-Ray Diffraction (GIXRD), and Field Emission Scanning Electron Microscope (FESEM). The effect of the substrate surface was investigated by measuring the contact angles with De-Ionized (DI) water. UV-Ozone treatment of substrate provides a cleaner surface to grow a homogeneous film. The electrical resistivity of annealed thin films was carried out by a four-point collinear probe employing the current reversal technique and found in the range of ~ 2 × 103 to 3 × 103 Ω·cm. Film thickness was found in the range of ~ 137–285 nm, measured by a stylus profilometer. UV–Vis–NIR transmission data revealed that all the thin-film samples showed maximum (82–89) % transmission in the visible range. The optical bandgap of the thin films was estimated to be ~ 3.75–4.00 eV and ~ 3.78–4.35 eV for the films grown on SLG and quartz substrates, respectively.

Industrial applications of sol-gel derived coatings.

Sol-gel derived coatings have many practical applications in different industries. In this paper, HI-GARD® hard coat, multi-layer antireflective coatings, and an anti-glare coating with organic particles are described. Optical and mechanical performances of these coatings are discussed in addition to adhesion properties. The HI-GARD® hard coat was dip or spin coated from a sol by hydrolyzing alkoxysilanes with water in an acidic condition. The hard coat acts as a protective coating for optical lenses with excellent optical properties with a Bayer ratio of 4.8 and an adhesion of 5B. The multi-layer antireflective coatings were prepared by incorporating titanium oxide sol into the HI-GARD® hard coat solution to obtain different layers by spin-coating with tunable refractive index. These two-layer or three-layer antireflective coatings increase transmittance by at least 3% compared to an uncoated glass substrate. Anti-glare coatings were spray-coated at room temperature on glass substrates by embedding cationic or anionic polystyrene particles in an acid-hydrolyzed silane sol. The anti-glare coating with organic particles can provide a significant glare reduction with a haze value of up to 13% for display surface without sparkling. In addition to these transparent coatings, non-transparent sol-gel derived coatings such as a sol-gel non-stick coating for cookware and bakeware, and two zinc-silicate protective coatings hydrolyzed from a silane with addition of zinc dusts for corrosion protection are also discussed briefly. The schematic structures of the hard coat on CR-39® substrate, three-layer AR coatings on glass substrate, and organic particle embedded anti-glare coatings on glass substrate, and their respective transmittance or reflective curves.

Metal oxide sol annealing on perovskite MAPbI3 film with thermal stability enhanced by caffeine additive and PMMA interlayer

Metal oxide sol annealing on perovskite MAPbI3 film with thermal stability enhanced by caffeine additive and PMMA interlayer