Oxide Growth Research Articles

The Immunomodulatory Effect of Silver Nanoparticles in a Retinal Inflammatory Environment.

Activation of immune response plays an important role in the development of retinal diseases. One of the main populations of immune cells contributing to the retinal homeostasis are microglia, which represent a population of residential macrophages. However, under pathological conditions, microglia become activated and rather support a harmful inflammatory reaction and retinal angiogenesis. Therefore, targeting these cells could provide protection against retinal neuroinflammation and neovascularization. In the recent study, we analyzed effects of silver nanoparticles (AgNPs) on microglia in vitro and in vivo. We showed that the AgNPs interact in vitro with stimulated mouse CD45/CD11b positive cells (microglia/macrophages), decrease their secretion of nitric oxide and vascular endothelial growth factor, and regulate the expression of genes for Iba-1 and interleukin-1β (IL-1β). In our in vivo experimental mouse model, the intravitreal application of a mixture of proinflammatory cytokines tumor necrosis factor-α, IL-1β and interferon-γ induced local inflammation and increased local expression of genes for inducible nitric oxide synthase, IL-α, IL-1β and galectin-3 in the retina. This stimulation of local inflammatory reaction was significantly inhibited by intravitreal administration of AgNPs. The application of AgNPs also decreased the presence of CD11b/Galectin-3 positive cells in neuroinflammatory retina, but did not influence viability of cells and expression of gene for rhodopsin in the retinal tissue. These data indicate that AgNPs regulate reactivity of activated microglia in the diseased retina and thus could provide a beneficial effect for the treatment of several retinal diseases.

Oxidation-Induced Oxide Shell Rupture and Phase Separation in Eutectic Gallium-Indium Nanoparticles.

Eutectic gallium-indium (EGaIn), a room-temperature liquid metal, has garnered significant attention for its applications in soft electronics, multifunctional materials, energy engineering and drug delivery. A key factor influencing these diverse applications is the spontaneous formation of a native passivating oxide shell that not only encapsulates the liquid metal but also alters the properties from the bulk counterpart. Using environmental scanning transmission electron microscopy, we report in situ observations of the oxidation of EGaIn nanoparticles by ambient air under high-energy electron beam irradiation. Our findings demonstrate that uneven oxide shell growth, driven by inward diffusion of adsorbed O species, creates unbalanced stresses. This compels the liquid metal to deform toward regions with slower oxide growth, resulting in shell rupture and allowing the liquid metal core to flow out. This process initiates top-down self-similar replication of the core-shell liquid metal nanoparticles, causing larger particles to break down into smaller particles. Additionally, internal oxidation triggers phase separation within the liquid core, ultimately leading to the pulverization of the liquid metal into finer solid particles rich in indium. These mechanistic insights into the oxidation behavior of the liquid metal hold practical implications for leveraging this process to reconfigure EGaIn nanoparticles for various applications.

Understanding of the irradiation response of Cr-based ATF coatings using in-situ TEM

Although CrNb coated zirconium alloy materials are considered as ATF candidates with excellent oxidation resistance and mechanical properties, the irradiation response behavior under harsh and complex service conditions is still unrevealed. Here, we report the evolution of the microstructure of pure Cr and CrNb coatings with different Nb contents under simultaneous irradiation with Cr+-He+-H2+ triple ion beams at 633 K by using an advanced in-situ transmission electron microscope (TEM). The results show that CrNb coatings with high Nb content have better irradiation stability. Under high-temperature irradiation conditions, irradiation-induced oxidation and grain growth or crystallization are observed for both Cr-8 Nb with a nanocrystalline structure and Cr-18 Nb coatings with an almost amorphous structure, whereas Cr-37 Nb coatings maintains relatively intact in the amorphous phase after irradiation at a dose of 10 dpa. Based on the in-situ tracking of the microstructural evolution, it is revealed that the mechanism of irradiation-accelerated oxidation and crystallization of coatings originates from displacement cascades enhancing local atomic diffusion and rearrangement.

H2O-based atomic layer deposition mechanism of aluminum oxide using trimethylaluminum

As a nanofabrication technology, atomic layer deposition (ALD) has been widely used in the fields of displays, microelectronics, nanotechnology, catalysis, energy and coatings. It demonstrates excellent conformality, large-area uniformity and precise control of the sub-monolayer film. Al2O3 ALD using trimethylaluminum (TMA) and water (H2O) as precursors is the most ideal ALD model system. In this work, the reactions of TMA and H2O with the surface have been investigated using density functional theory (DFT) calculations in order to obtain more information on the reaction mechanism of the complicated H2O-based ALD of Al2O3. In the TMA reaction, the methyl ligands can be eliminated and new Al-O bonds can be formed via ligand exchange reactions. In the H2O reaction, the methyl ligand on the surface can be further eliminated and new AlO bonds can be formed. Meanwhile, the coupling reactions between the surface methyl and hydroxyl groups can further form new AlO bonds and release CH4 or H2O to densify the Al2O3 film. These complicated reaction mechanisms of Al2O3 H2O-based ALD can provide theoretical guidance for the precursor design and ALD growth of other oxides and aluminum-based compounds.

Polyethylene glycol-assisted hydro-solvothermal growth of anisotropic magnetic iron oxides: The role of mixed environment conditions

In this study, an alternative mixed hydro-solvothermal route has been investigated for the synthesis of magnetic iron oxide nanoparticles with anisotropic shape. The synthesis was performed at mild conditions (150 °C) in a water/2-propanol environment, using poly(ethylene glycol) (PEG400) as structure directing agent, sodium thiosulfate as reducing agent, and NaOH as precipitating agent. The resulting systems were characterized by combining morphological, structural, and magnetic techniques. Experimental results clearly demonstrate that magnetite/maghemite nanorods are preferentially obtained in water/PEG400 environment, whereas 2-propanol/PEG400 environment promotes the growth of magnetite/maghemite polyhedral systems. Interestingly, synthesis performed in a mixed hydro-solvothermal (i.e., water/2-propanol) environment favors the preferential growth of hematite phase.

Unveiling the nucleation and growth of Zr oxide precipitates in internally oxidized Nb3Sn superconductors

We report on atomic-scale analyses of nucleation and growth of Zr oxide precipitates and the microstructural evolution of internally oxidized Nb3Sn wires for high-field superconducting magnet applications, utilizing atom probe tomography (APT), transmission electron microscopy (TEM), and first-principles calculations. APT analyses reveal that oxygen and zirconium are already segregated at grain boundaries (GBs) in the unreacted Nb-1Zr-4Ta (at%) alloy prior to forming Nb3Sn through reacting the Nb alloy with Sn and SnO2. After forming Nb3Sn, Zr oxide precipitates nucleate both at the Nb3Sn/Nb heterophase interfaces and in the Nb3Sn grains, driven by the small solubilities of Zr and O in Nb3Sn compared to their value in Nb. A high number density (Nv) of Zr oxide nanoprecipitates is observed in the Nb3Sn layers, ∼1023 m−3, with a mean diameter <10 nm for a heat treatment at 625 °C. Quantitative APT and TEM analyses of the Zr oxide precipitates in the reacted Nb3Sn layers elucidate details of the nucleation, growth, and coarsening processes of the Zr oxide precipitates in Nb3Sn. First-principles calculations and classical nucleation theory are employed to study the nucleation of Zr oxide precipitates in Nb3Sn and to estimate the maximum energy barrier and critical radius for nucleation. Our research unveils the kinetic pathways for nucleation and growth of Zr oxide precipitates and the microstructural evolution of Nb3Sn layers, which helps to understand and improve the superconducting properties of internally oxidized Nb3Sn wires for use in high-field superconducting magnets.

Role of magnesium ions in modifying oxide growth rate on Zircaloy under breakaway corrosion regimes

General corrosion of nuclear reactor in core material like Zircaloy-2 and breakaway corrosion in particular are of great importance in ensuring its smooth long term operation. Metal ions like Mg2+ added to the coolant, to mitigate corrosion of other structural materials like Carbon steel, can get incorporated in the corrosion product oxide on Zircaloy-2 and alter its corrosion behavior. Plasma Electrolytic Oxidation (PEO) method was employed to investigate the effect of Mg2+ ions during breakaway corrosion of Zircaloy-2. The main objective was to understand the morphology, protectiveness, semiconducting properties of the Mg modified oxide films on Zircaloy-2 surface. DC potentials 300, 400 and 500 V were used to accelerate corrosion kinetics and form oxide mimicking the breakaway corrosion regime. Borate buffer (pH 9.8) was used as the electrolyte, and Mg acetate was added as Mg source for probing the effect of Mg2+ ions. Oxide morphology depended largely on the formation potentials. The presence of magnesium resulted in thinner oxides with lower defect densities. GIXRD of the oxide showed stabilization of tetragonal phase in presence of Mg at 300 and 400 V. Oxide resistance and charge transfer resistances measured by EIS were observed to be higher due to Mg incorporation at these potentials. Mg addition facilitated formation of t-ZrO2. The electrochemical measurements suggested that the presence of Mg in ZrO2 could reduce the connected porosity in the oxide thereby stifling the diffusion paths. These factors lead to improved corrosion protectiveness of the oxide formed in the presence of Mg.

Oxide Growth Behaviour of 800H and HR-120 Series Ni-based Alloys on Isothermal Oxidation

Oxide Growth Behaviour of 800H and HR-120 Series Ni-based Alloys on Isothermal Oxidation

Deep-level transient spectroscopy of defect states at p-type oxide/β-Ga2O3 heterojunctions

Defects in p-type oxide/β-Ga2O3 heterojunction diodes were investigated using p-type Cu2O as a case study. Diodes with polycrystalline and epitaxial Cu2O films were analyzed using deep-level transient spectroscopy. For both diodes, two electron bulk defects were detected, including a minority defect at 0.23 eV below EC within Cu2O and a majority defect at 0.53 eV below EC within β-Ga2O3. Furthermore, a high-density interface state of 4.5 × 1012 cm−2/eV was observed in the polycrystalline Cu2O/β-Ga2O3 diode. The presence of a high density of interface states helped reduce the turn-on voltage owing to the interface recombination current. However, it also enabled electron carriers to tunnel through the interface to β-Ga2O3, followed by variable range hopping through the bulk defect in the β-Ga2O3 layer, ultimately causing undesirable premature breakdown. The results of this study underscore the critical role of optimizing the crystal structure during p-type oxide growth for desired defect characteristics, particularly concerning interface states, in β-Ga2O3 bipolar devices for different applications, offering insights for high-performance power rectifier development.

Monotonic Surface Charging at Polycrystalline Platinum-Electrolyte Interface in the Presence of Chemisorbed Species Using Streaming Current Method

Surface charging characteristics at a polycrystalline Pt-electrolyte interface were studied using electrokinetic streaming current method integrated with in-situ electrochemical cell, which was developed by our group [1-3]. Experimentally, surface charging relations are determined from the potential-dependent capacitance data. For catalytic surfaces (e.g., platinum), this method is challenging to apply due to the strong chemisorption properties of the metal [4]. We developed a method to measure surface charge of a metal in presence of strong chemisorption of ions by incorporating electrokinetic streaming current technique with traditional electrochemical 3-electrode setup (Figure 1a).Generally, the metal charge increases monotonically with applied potential. Based on theoretical models, it was suggested that the Pt-electrolyte interface might deviate from this trend and have negative charge above the potential of zero charge (PZC) due to the metal’s strong chemisorption properties [5,6]. We attempted to experimentally determine the validity of this claim using our method. In addition, we also observed the effect of anion adsorption (oxide, chloride, sulfate, etc.) on surface charging. The experimental method also allowed us to observe the slow time-dependent growth of oxides on Pt surface.Since our first publication in 2019 [1], we were able to develop the setup to be more efficient by reducing noise, electrolyte resistance, current fluctuations, etc. that enabled us to apply higher potential on the metal, observe stronger ion adsorption effects on surface charging, and obtain more reliable data. Our recent experimental study shows that Pt charging remains monotonic and does not reverse due to chemisorption of oxides in the potential window where the charge reversal was speculated to occur (Figure 1b). Figure 1c shows that metal charge (at 1.2 V vs SHE) grows slowly over time to settle down to an equilibrium value. We hypothesize that it was caused by the slow growth of oxides at the interface. The time-dependent growth of oxides has already been observed [7]. The electrolyte used in our experiments was HClO4 where the anion (ClO4 -) is less adsorbing than Cl-, SO4 2-, Br- etc. The only adsorbing anions in this electrolyte solution are OH- and O2-. In this work, we will present a brief description of the improvements of the electrokinetic-electrochemical method and our experimental results showing monotonic charging behavior for Pt in the presence of ion adsorption and oxide growth.

Recent Fundamental Advances in Quality of High-Performance and Highly-Scaled Carbon Nanotube Transistors

Recently a number of breakthroughs have been reported by our team in the component qualities of transistors built on Carbon Nanotube (CNT) channels. However, any emerging channel material which seeks to outperform established semiconductors for transistor logic applications has a substantial hill to climb, given the incredible capabilities of advanced Si-based logic technology platforms. This talk will first aim to frame our progress on Carbon Nanotube CMOS technology in the broader context of the value proposition and desired component qualities needed to realize practical impact in computing applications. Next, we will share advances in the fundamental building blocks for Carbon Nanotube transistors towards these targets including channel, contact, doping, and gate-stack modules. Finally we will describe new record CNT MOSFET performance milestones achieved by integrating best available device components for first time, which gives insight into the remaining performance limiters and future directions.[1] G. Pitner, et al., "Building High Performance Transistors on Carbon Nanotube Channel," VLSI 2023.[2] S. Li, et al., "High-Performance and Low Parasitic Capacitance CNT MOSFET: 1.2 mA/um at Vds of 0.75 V by self-aligned doping in sub-20 nm spacer," IEDM 2023.[3] N. Safron, et al., "Low N-type Contact Resistance to Carbon Nanotubes in Highly Scaled Contacts through Dielectric Doping," IEDM 2023.[4] H.-Y. Chiu, et al., "Self-Aligned Contact Doping for Performance Enhancement of Low-Leakage Self-Alignment Method for High-Density Aligned CNT Array," Advanced Materials Interfaces, 2023.[5] T.A. Chao, et al., "Small Molecule Additives to Suppress Bundling in Dimensional-Liminted Self-Alignment Method for High-Density Aligned CNT Array," Advanced Materials Interfaces, 2023.[6] Q. Lin, et al., " Band-to-Band Tunneling Leakage Current Characterization and Projection in Carbon Nanotube Transistors," ACS Nano 2023.[7] Z. Zhang, et al., "Complementary Carbon Nanotube Metal-Oxide-Semicondcutor Field-Effect Transistors with Localized Solid-State Extension DOping," Nature Electronics, 2023.[8] S.K. Su, et al., " Perspective on Low-Dimensional Channel Materials for Extremely Scaled CMOS," VLSI 2022.[9] Z. Zhang, et al., "Sub-Nanometer Interfacial Oxides on Highly Oriented Pyrolytic Graphite and Carbon Nanotubes Enabled by Lateral Oxide Growth," ACS Applied aterials & Interfaces, 2022.[10] G. Pitner, et al., "Sub-0.5 nm Interfacial Dielectrics Enables Superior Electrostatics: 65 mV/dec top-gated Carbon Nanotube FETs at 15 nm gate length," IEDM 2020.

Antioxidant and antimicrobial activities of Myrtus communis essential oils in cold-stored lactic butter.

The use of natural antioxidants and antimicrobials in dairy production can increase the variety of dairy-based products. In this study, the antioxidant and antimicrobial changes in lactic butter samples made from heat-treated creams and enriched with M. communis essential oils (EOs) were investigated. The best lactic butter properties were achieved by optimizing the process at 70 and 80 °C. M. communis EOs decreased lipid oxidation and spoilage microorganism growth in lactic butter during cold storage. M. communis EOs have antioxidant and antimicrobial activity in lactic butter equal to that of ascorbyl palmitate. α-Pinene, p-cymene, limonene, 3-carene, 1,8-cineol, β-linalool, α-terpineol and myretenol are the major contributors to the antioxidant and antimicrobial activities of M. communis EOs. They exhibit antioxidant activity by neutralizing free radicals by donating hydrogen or acting as termination enhancers, and antimicrobial activity by disruption of cell membranes, which may result in the leakage of macromolecules or the loss of essential metabolites, ultimately leading to cell death during the storage of lactic butter samples. The addition of M. communis EOs improves lactic butter stability equal to that of ascorbyl palmitate, and may be applied as a natural and effective preservative to maintain butter from lipid oxidation and microbial spoilage and enhance its safety. The growing recognition of the health benefits of natural antioxidants, as opposed to synthetic ones, has led to the development of new applications for natural antioxidants. In this regard, M. communis L. EOs can be used to enhance the shelf stability of cold-stored lactic butter. © 2024 The Author(s). Journal of the Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Glutathione hybrid poly (beta-amino ester)-plasmid nanoparticles for enhancing gene delivery and biosafety

IntroductionCRISPR/Cas9 gene editing technology has significantly advanced gene therapy, with gene vectors being one of the key factors for its success. Poly (beta-amino ester) (PBAE), a distinguished non-viral cationic gene vector, is known to elevate intracellular reactive oxygen species (ROS) levels, which may cause cytotoxicity and, consequently, impact gene transfection efficacy (T.E.). ObjectivesTo develop a simple but efficient strategy to improve the gene delivery ability and biosafety of PBAE both in vivo and in vitro. MethodsWe used glutathione (GSH), a clinically utilized drug with capability to modulating intracellular ROS level, to prepare a hybrid system with PBAE-plasmid nanoparticles (NPs). This system was characterized by flow cytometry, RNA-seq, Polymerase Chain Reaction (PCR) and Sanger sequencing in vitro, and its safety and efficacy in vivo was evaluated by imaging, PCR, Sanger sequencing and histology analysis. ResultsThe particle size of GSH-PBAE-plasmid NPs were 168.31 nm with a ζ-potential of 15.21 mV. An enhancement in T.E. and gene editing efficiency, ranging from 10 % to 100 %, was observed compared to GSH-free PBAE-plasmid NPs in various cell lines. In vitro results proved that GSH-PBAE-plasmid NPs reduced intracellular ROS levels by 25 %–40 %, decreased the total number of upregulated/downregulated genes from 4,952 to 789, and significantly avoided the disturbance in gene expression related to cellular oxidative stress-response and cell growth regulation signaling pathway compared to PBAE-plasmid NPs. They also demonstrated lower impact on the cell cycle, slighter hemolysis, and higher cell viability after gene transfection. Furthermore, GSH hybrid PBAE-plasmid NPs exhibited superior safety and improved tumor suppression ability in an Epstein–Barr virus (EBV)-infected murine tumor model, via targeting cleavage the EBV related oncogene by delivering CRISPR/Cas9 gene editing system and down-regulating the expression levels. This simple but effective strategy is expected to promote clinical applications of non-viral vector gene delivery.

Dynamic transition of internal oxides during high dew point heat treatment in Fe-2.4Mn-0.4Si-0.13C alloy

The origin of the dynamic transition of internal oxides was clarified in Fe‐2.4Mn‐0.4Si‐0.13C‐based steel during decarburization annealing at 1073 K. High dew point with H2 gas leads to the formation of deep decarburized ferrite layers containing grain boundary internal oxides. Microstructural characterization reveals the oxide transition from Mn2SiO4 to α-SiO2 at the tip of the internal oxidation layer and from α-SiO2 to Mn2SiO4 at the middle range of the internal oxidation layer. The dynamic transition between Mn2SiO4 and α-SiO2 is understood by the depletion in Mn contents and change of oxygen content, which change the normalized driving force of both oxides. The study gives a detailed mechanism of internal oxide formation and growth in multi-phase steel during high dew point annealing. Impact statementDuring high dew-point decarburization annealing, the fluctuation of Mn contents affects the driving force to form an internal oxide, resulting in the dynamic transition between Mn2SiO4 and α-SiO2.

Effects of Al and refractory alloying elements (W, Ta and Hf) on oxidation kinetics, oxygen dissolution and diffusion in titanium alloys

The effect of aluminium, tungsten, tantalum and hafnium on the oxidation behaviour of titanium was investigated. Model alloys were oxidized in air for 5000 h at 650 °C. All alloying elements decreased oxide growth and oxygen dissolution in the metal; tungsten was the most efficient. The oxygen diffusivity decreased with aluminium. Tungsten enhanced the formation of Ti2N at the oxide/metal interface which decreased oxygen dissolution in the alloys. Experiments in Ar-20%O2, where Ti2N could not form, confirmed the major role of nitrogen on the oxidation resistance of tungsten-containing alloys. The ternary model alloy Ti-10Al-2W outperformed the high-temperature alloy Ti6242S.

Effect of CO on the corrosion behavior of 304 stainless steel in wet CO2 gas at 710°C

AbstractThe corrosion behavior of 304 stainless steel in wet CO2 gas with or without CO and CO plus 400 ppmv SO2 was investigated in this study. Corrosion kinetics was studied by thermogravimetric analysis at 710°C for 100 h under three gas conditions. After isothermal exposure, the corroded coupons were characterized in detail by X‐ray diffraction, scanning electron microscopy, an electron probe microanalyzer, and transmission electron microscopy. CO addition to wet CO2 resulted in lower oxygen partial pressure and lower oxide growth kinetics. It also suppressed iron‐rich oxide nodule formation, as compared to the wet CO2 gas environment. A Cr‐depletion zone was observed underneath the oxide scale in the substrate, but no obvious internal carburization was observed in all three gas environments. A thin, protective oxide scale consisting of an outer layer of a Cr‐rich spinel and an inner Cr‐rich chromia layer was developed in CO‐containing gas conditions, with or without SO2. The effect of CO on oxidation and scale formation is discussed in comparison with that in wet CO2 conditions.

Very Long Transient Oxidation of a Nickel-based Single-Crystal Superalloy at 900 °C and 850 °C

AbstractThe isothermal oxidation of Ni-base single-crystal superalloy AM1 was investigated for up to 3600 h at 850 °C and 900 °C. The aim of the study was to test an existing model of oxidation kinetics that considers transitory oxide growth. The samples were characterized at various intervals to correlate the microstructure of the oxide scale with the oxidation kinetics. Transition alumina (θ) was observed among other transition oxides such as spinel, rutile, and chromia, which helped in understanding the nature and kinetics of the transitory stage. After a sufficiently long duration, all samples formed a continuous α-alumina layer at the metal/oxide interface. The previously published model, based on three kinetic parameters, was validated in the temperature range of 800–1200 °C. The duration of the transient regime characterized in this study at 850 °C and 900 °C was consistent with the kinetics model, with a slight increase in the value of the model parameter describing the lateral growth kinetics of α-alumina. This modification resulted in a slight reduction in the duration of the transient regime at low temperatures.

Insights into Oxide Growth: In Situ Atomic-Scale Visualization of Mass Transport during Copper Oxidation

Insights into Oxide Growth: In Situ Atomic-Scale Visualization of Mass Transport during Copper Oxidation

In situ oxidative growth to form compact TiO2–Ti3C2 heterojunctions for photocatalytic hydrogen evolution

Solar photocatalytic hydrogen production shows promise in addressing global energy and environmental concerns. The limited efficiency of photocatalysts is mainly due to ineffective separation and transfer of photogenerated charges. To improve this, we enhance the TiO2–Ti3C2 heterojunction by in-situ oxidation through interfacial engineering, resulting in a more compact composition. Subsequently, we anchor single-atom Pt at the TiO2–Ti3C2 interface through photo-Ti3C2 reduction. The in-situ growth of TiO2 on Ti3C2 introduces an interfacial driving force for carrier separation and provides a channel for electron transfer from TiO2 to Ti3C2. This further facilitates transfer onto Pt, shortening the migration distance and enhancing the photocatalytic efficiency. The best Pt/TiO2–Ti3C2 composite demonstrates an impressive hydrogen precipitation efficiency of 767 μmol g−1 h−1, surpassing TiO2 and Pt/TiO2 by factors of 12 times and 1.46 times, respectively. Furthermore, we developed a higher efficiency photocatalyst using the molten salt method to avoid the risks associated with conventional hydrofluoric acid etching. This research opens up new possibilities for the preparation of MXenes interface-modified catalysts, offering a valuable avenue for future exploration in the field.

Enhanced mechanical properties and tribological performance of anodic oxide coating by using thermal power plant waste material

Numerous researchers have dedicated their efforts to exploring the utilization of industrial waste, specifically fly ash (FA), as a reinforcement for developing economical composites and minimizing ecological pollution problems. FA consists of multiple phases, including quartz (SiO2) and mullite (3Al2O3·2SiO2), which can significantly enhance the mechanical properties of materials. In tribological applications, incorporating FA into surface coatings can offer a cost-effective alternative to enhance surface properties. Meanwhile, the usage of FA and its difference from other commercial ceramics (e.g., SiO2) is still unknown. Thus, the present study aims to clarify the role of FA and factors that contribute to improving mechanical properties and tribological performance with commercial SiO2 as a comparison using electrochemical anodization. The growth mechanism was investigated by varying the anodizing times while maintaining a constant (100 g/L FA) in the electrolyte for the first phase. Meanwhile, the mechanical and tribological properties of different reinforcement content (0, 10, 50, and 100 g/L) were determined for the second phase. Then, evaluations were conducted on the surface morphology, chemical composition, surface hardness, and tribological properties. The results revealed that growth of oxide coating was initiated within the first 5–10 min by forming the barrier layer. Pores began to appear visibly after 30 min of anodizing time, while the complete formation of porous anodic oxide coating was achieved at 60-min with pores dimension (width: 30.75 ± 14.45 μm and depth: 13.4 ± 6.43 μm). Interestingly, 100 g/L of FA-reinforced anodic oxide coating demonstrated lower surface roughness (4.08 ± 0.41 μm), higher surface hardness (444.4 ± 8.63 HV), lowest coefficient of friction (COF) (0.46), and low wear rate (reduction almost 31.8 %) compared to 100 g/L of commercial SiO2 reinforced anodic oxide coating. The electrophoretic deposition effect, combined with the quartz (SiO2) and mullite (3Al2O3·2SiO2) phase structure, enhances mechanical properties and tribological performance.