Anodic Technique Research Articles

Isoelectric Point of Metal Oxide Films Formed by Anodization.

The surface charge of metal oxides is an important property that significantly contributes to a wide range of phenomena, including adsorption, catalysis, and material science. The surface charge can be predicted by determining the isoelectric point (IEP) of a material and the pH of a solution. Although there have been several studies of the IEP of metal oxide (nano)particles, only a few have reported the IEP of metal oxide films. The IEP of various compact metal oxide films such as TiO2, Nb2O5, WO3, ZrO2, NiO, and Al2O3 formed via electrochemical anodization was determined using the streaming potential technique. Nanostructured TiO2 and NiO were additionally produced using a single-step anodization technique, and their IEP was compared with the compact ones. The surface morphology and wettability of the oxides were studied by scanning electron microscopy and contact angle measurements, respectively. X-ray powder diffraction and X-ray photoelectron spectroscopy measurements were carried out to assess the phase and elemental composition, respectively. The IEP of compact anodic oxides deviates from that of their nanoparticle and atomic layer-deposited counterparts. The comparative results indicate that the IEP of metal oxides is influenced by factors such as the chemical composition, degree of hydroxylation, and crystallographic phases of the oxide.

Nanoscale Titanium Oxide Memristive Structures for Neuromorphic Applications: Atomic Force Anodization Techniques, Modeling, Chemical Composition, and Resistive Switching Properties.

This paper presents the results of a study on the formation of nanostructures of electrochemical titanium oxide for neuromorphic applications. Three anodization synthesis techniques were considered to allow the formation of structures with different sizes and productivity: nanodot, lateral, and imprint. The mathematical model allowed us to calculate the processes of oxygen ion transfer to the reaction zone; the growth of the nanostructure due to the oxidation of the titanium film; and the formation of TiO, Ti2O3, and TiO2 oxides in the volume of the growing nanostructure and the redistribution of oxygen vacancies and conduction channel. Modeling of the nanodot structure synthesis process showed that at the initial stages of growth, a conductivity channel was formed, connecting the top and bottom of the nanostructure, which became thinner over time; at approximately 640 ms, this channel broke into upper and lower nuclei, after which the upper part disappeared. Modeling of the lateral nanostructure synthesis process showed that at the initial stages of growth, a conductivity channel was also formed, which quickly disappeared and left a nucleus that moved after the moving AFM tip. The simulation of the imprint nanostructure synthesis process showed the formation of two conductivity channels at a distance corresponding to the dimensions of the template tip. After about 460 ms, both channels broke, leaving behind embryos. The nanodot, lateral, and imprint nanostructure XPS spectra confirmed the theoretical calculations presented earlier: in the near-surface layers, the TiO2 oxide was observed, with the subsequent titanium oxide nanostructure surface etching proportion of TiO2 decreasing, and proportions of Ti2O3 and TiO oxides increasing. All nanodot, lateral, and imprint nanostructures showed reproducible resistive switching over 1000 switching cycles and holding their state for 10,000 s at read operation.

N, P co-doped graphite felt cathode for efficient removal of ciprofloxacin in an ascorbic acid-coupled electro-Fenton process: Simultaneously enhancing H2O2 generation and Fe3+/Fe2+ cycling.

To enhance the contaminant removal efficiency of the electro-Fenton (E-Fenton) process, a nitrogen and phosphorus co-doped graphite felt (NPGF) cathode was synthesized using an anodic oxidation technique. An ascorbic acid-coupled NPGF E-Fenton system was then established for the degradation of ciprofloxacin (CIP). The NPGF cathode featured abundant oxygen-containing functional groups (such as -COOH and -OH), which enhanced the selectivity of oxygen reduction and facilitated the formation of H2O2. The introduction of N and P doping disrupted the charge balance within the carbon framework, accelerating electron transfer. Together, the NPGF electrode and ascorbic acid enhanced the cycling of Fe3+/Fe2+ while preventing the formation of iron sludge. Under optimal conditions (ascorbic acid concentration of 0.3mM, current density of 2.0mAcm-2, pH of 3.0, aeration rate of 0.6Lmin-1, and Fe2+ concentration of 0.2mM), CIP was completely removed within 20min. The NPGF electrode exhibited excellent stability, maintaining 95.35% CIP removal even after 8 cycles. Analysis revealed that singlet oxygen primarily mediated the degradation of CIP, with its concentration measured at 1.23×10-7M. Density functional theory was used to analyze the characteristics and potential attack sites of CIP, enabling the proposal of plausible degradation pathways. Toxicity simulations and Escherichia coli growth inhibition experiments demonstrated a reduction in the toxicity of CIP and its intermediate products. This study offers a valuable reference for improving the efficiency of E-Fenton technology in antibiotic wastewater treatment.

Photoelectrochemical properties of Single walled and Double walled TiO2 nanotubes

Titanium dioxide (TiO2) is one of the most studied materials to be applied in various filed due to its high environmental compatibility and corrosion resistance [1-2]. Among the nanostructures of TiO2 is including nanoparticles, nanorods, nanoplates, and nanotubes, nanotubular TiO2 acquires not only a high surface area but also rapid charge carrier transfer, providing higher efficiency for photocatalytic application such as, the degradation of organic contaminants and hydrogen production. Although various methods have been investigated to fabricate TiO2 nanotubes, the anodization technique is favored with its straightforward control over structure and direct growth on Ti substrates[3]. However, conventional anodic TiO2 nanotubes exhibit surface irregularities and double-walled structure consisting of carbon-rich inner and TiO2 out layer[4]. The inner layer of TiO2 nanotubes diminishes the photoelectrochemical efficiency owing to the carbon contamination.In this study, double walled TiO2 nanotubes were synthesized by anodization with an applied voltage of 60 V for various periods. A piranha solution was utilized to eliminate the inner layer for double walled TiO2 nanotubes, achieving a single-walled TiO2 nanotube configuration. The morphological properties, crystallinity, and surface resistance of both single and double-walled TiO2 nanotubes were evaluated using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Electrochemical Impedance Spectroscopy (EIS). In addition, the photoelectrochemical efficiencies of all TiO2 nanotubes were evaluated employing linear sweep voltammetry (LSV) and Incident photon-to-current efficiency (IPCE) measurements. As a result, the single-walled TiO2 nanotubes, produced under the specific conditions of 60 V for 7 min, showed the highest photoelectrochemical efficiencies at LSV and IPCE. The higher photoelectrochemical properties of the single walled nanotube are attributed to the enhancenment of surfave chage dynamics and environmental reactions as eliminating the inner layer.[1] Fujishima A, Honda K, Electrochemical photolysis of water at semiconductor electrode. Nature 238 (1972) 37-38[2]Lee K, Mazare A, Schmuki P, One-dimensional titanium dioxide nanomaterials: nanotubes, Chem. Rev, 114 (2014) 9385–9454,[3] Yoo JE, Lee K, Altomare M, Selli E, Schmuki P, Self-organized arrays of single-metal catalyst particles in TiO2 cavities: a highly efficient photocatalytic system, Angew. Chem., Int. Ed, 52 (2013) 1002[4] Liu N, Mirabolghasemia H, Lee K, Albua SP, Tighineanua A, Altomareab M, Schmuki P, Anodic TiO2 nanotubes: double walled vs. single walled. Faraday Discuss, 164 (2013) 107-116.

High Quality-Factor All-Dielectric Metacavity for Label-Free Biosensing.

High sensitivity and high quality-factor are crucial for achieving outstanding sensing performance in photonic biosensors. However, strong optical field confinement and high light-biomolecule interactions on photonic surfaces are usually contradictory and challenging to satisfy simultaneously. Here, a distinctive configuration for addressing this issue is reported: embedding a nanophotonic metasurface inside a micro vertical cavity as a meta-channel (metacavity) biosensor. The analyte solution serves as the cavity medium, thereby maximizing the light-analyte interaction. Simulation validation is conducted to optimize the metacavity with high structural robustness and remarkable optical and sensing properties. Large-scale low-cost metacavity biosensors are realized by combining anodic aluminum oxide template technique and wafer bonding. Experimentally, the metacavity biosensor demonstrates a notable quality-factor (maximum 4140) and high bulk refractometric sensitivity (450nmRIU-1), resulting in an unprecedented figure-of-merit (1670 RIU-1). Moreover, the metacavity biosensor achieves high surface sensitivity, together with a detection-limit of 119 viral copies mL-1 for label-free severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pseudovirus sensing, revealing remarkable performance in both bulk and surface sensing.

Carboxymethyl chitosan/alendronate sodium/Sr2+ modified TiO2 nanotube arrays enhancing osteogenic activity and antibacterial property

Titanium and its alloys are widely used as orthopedic implants owing to their good mechanical properties and excellent corrosion resistance. However, the insufficient osteogenic activity and antibacterial properties hinder their clinical applications. To address these issues, TiO2 nanotube arrays (TNT) were first fabricated on the TA2 alloy surface via an anodizing technique, and strontium ions (Sr2+) were then loaded by hydrothermal reaction (TNT + Sr) and annealing treatment (TNT + A). Subsequently, the polydopamine layer (TNT + PDA) was constructed to immobilize the carboxymethyl chitosan and alendronate sodium (TNT + CA) mixture. The prepared coatings were thoroughly characterized by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), X-ray photoelectron spectrometer (XPS), attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray diffractometer (XRD), and water contact angle measurement. The results confirmed that Sr2+ ions, polydopamine, and carboxymethyl chitosan/alendronate sodium were successfully immobilized on the nanotubes. The coating of TNT + CA significantly enhanced the hydrophilicity, and effectively delayed the release of Sr2+ and alendronate. The TNT + CA coating significantly promoted osteoblast adhesion and proliferation, and up-regulated the expressions of alkaline phosphatase (ALP), osteocalcin (OCN), and osteoblast-specific transcription factor (RUNX2). TNT + CA was able to rapidly induce in situ hydroxyapatite deposition from the simulated body fluid (SBF). Moreover, TNT + CA coating showed inhibition against Escherichia coli and Staphylococcus aureus (especially against Escherichia coli). The prepared TNT + CA coating provides a novel strategy for enhancing bone affinity, improving osteoblast behaviors, and antibacterial properties of titanium-based biomaterials.

Producing Activated Biochar from the Reuse of Discarded Coffee Grounds with Enhanced Adsorptive Features Explored Towards the Stripping Voltammetric Sensing of Copper (II)

AbstractThis work aims to allocate coffee grounds waste to the production of biochar from pyrolysis under different temperatures (350 °C and 500 °C), to add value to it. The resulting materials were characterized by immediate, elemental, thermogravimetric analysis, SEM, FT‐IR, XRD and Raman spectroscopy. Additionally, the need to activate the biochar produced for the desired use was evaluated. The obtained biochars were applied in electroanalysis in the manufacture of modified carbon paste electrodes. This choice was made due to the possibility of reaching a high sensitivity towards the determination of Cu2+ ions. The differential pulse adsorptive anodic stripping voltammetry technique was applied to perform the Cu2+ determination and, in this case, several parameters were optimized, including biochar’ percentage, pH of pre‐accumulation step and reduction/stripping step, pre‐accumulation time, potential and time of reduction of adsorbed‐Cu2+. From this, the proposed modified electrode showed a linear voltammetric response towards Cu2+ in the range of 66.1 to 3997.3 ppb, with a limit of detection of 31.8 ppb, in addition to having been satisfactorily applied in the analysis of water samples (recoveries close to 100 %). Thus, demonstrating the potential for reuse of discarded coffee grounds for the preparation of activated biochar with outstanding electrochemical performance.

Comparative Analysis of Anodized TiO2 Nanotubes and Hydrothermally Synthesized TiO2 Nanotubes: Morphological, Structural, and Photoelectrochemical Properties.

This study presents a comparative analysis of anodization and hydrothermal techniques for synthesizing TiO2 nanotubes directly on titanium foil. It emphasizes its advantages as a substrate due to its superior conductivity and efficient charge transfer. Optimized synthesis conditions enable a thorough evaluation of the resulting nanotubes' morphology, structure, and optical properties, ultimately assessing their photoelectrochemical and photocatalytic performances. Scanning electron microscopy (SEM) reveals differences in tube diameter and organization. An X-ray diffraction (XRD) analysis shows a dominant anatase (101) crystal phase in both methods, with the hydrothermally synthesized nanotubes exhibiting a biphase structure after annealing at 500 °C. UV-Vis and photoluminescence analyses indicate slight variations in band gaps (around 0.02 eV) and recombination rates. The anodized TiO2 nanotubes, exhibiting superior hydrophilicity and order, demonstrate significantly enhanced photocatalytic degradation of a model pollutant, amido black (80 vs. 78%), and achieve a 0.1% higher photoconversion efficiency compared to the hydrothermally synthesized tubes. This study underscores the potential advantages of the anodization method for photocatalytic applications, particularly by demonstrating the efficacy of direct TiO2 nanotube growth on titanium foil for efficient photocatalysis.

Enhancing the corrosion resistance of oxide-ceramic composites by the cyclic anodic polarization technique

Enhancing the corrosion resistance of oxide-ceramic composites by the cyclic anodic polarization technique

Dynamic behaviors of bridge with corroded RC piers under barge collisions

Reinforced concrete (RC) bridge piers located in navigable waterways are susceptible to chloride-induced corrosion, which may cause severe damage or even entire collapse of bridge under potential barge collisions. The present study aims to examine the failure patterns and dynamic responses of typical simply supported girder bridge with corroded RC piers under barge collisions. Firstly, nine RC column specimens with three designed corrosion degrees and two corrosion strategies were prepared using the impressed anodic current technique. Secondly, the drop hammer impact and axial compression tests were successively performed to examine the residual axial load bearing capacities of both unimpacted and impacted specimens. Furthermore, by comprehensively considering the effects of corrosion-induced deteriorations on the effective cross-sectional area and yield strength of reinforcements, concrete strength, as well as the rebar-concrete bond-slip relationship, the refined finite element (FE) models of specimens were established and validated. Finally, the dynamic behaviors of a prototype simply supported girder bridge with corroded RC piers under barge collisions at different service lives, i.e., 0–60 years, were numerically assessed. It indicates that: (i) under drop hammer impact, six specimens all exhibit global flexure failure, and relatively severe concrete cracking and spalling occur in the specimens with 15 % designed corrosion degree; (ii) the axial load bearing capacities of specimens with 5 % and 15 % designed corrosion degrees are reduced by 15.46 % and 34.86 % compared to the unimpacted non-corroded specimen, and 11.29 % and 43.30 % compared to the impacted non-corroded specimen; (iii) the transverse impact resulted in 25.93 %, 22.27 % and 35.53 % reductions in axial load bearing capacities for 0 %, 5 % and 15 % designed corrosion degree, respectively; (iv) for the prototype barge-bridge collision scenario, the failure patterns vary from minor bending cracks to remarkable flexural failure as the service live increases from 0 to 60 years. The corrosion-induced degradations of bridge performance should be concerned for the vessel collision-resistant design of bridge.

Preparation, optical properties, room temperature ferromagnetism, and mechanism of ordered nanotube-like tantalum oxide films

Physical property changes caused by defects have recently attracted significant attention due to their potential applications in sensors, spintronic devices, and multifunctional memory. Due to their numerous surface defects, this study fabricated ordered Ta2O5 nanotube (NT) thin films on Ta foil through an anodization technique. Then, the oxygen bubble model was applied to explain the formation of NTs from the perspective of lattice orientation. Furthermore, this study investigated influence of anodization duration and annealing treatment on the crystal structure, optical properties, and magnetic behavior. Notably, room-temperature ferromagnetism was observed in the as-prepared Ta2O5 NTs for the first time. After annealing in an argon atmosphere, the band gap of the sample decreased, accompanied by an increase in ferromagnetism. The underlying mechanism for this phenomenon was elucidated using a hydrogen-like impurity model. Consequently, this study on the magnetism of Ta2O5 NTs holds excellent potential for expanding their application in spin electronic devices.

Submerged nanoporous anodized alumina structure for solar-powered desalination.

Development of nanoporous structures utilizing a single step of anodization technique is well recognized as a cost-effective and straightforward approach for several applications. In the current work, anodized alumina was developed with nanoporous structure by utilizing oxalic acid as an electrolyte with a continuous voltage of 40 V. The formed nanoporous structure was subjected to desalination application because of its high absorbance of broadband solar spectrum energy. The desalination setup consists of two solar stills namely conventional and modified. The developed structure is placed in the modified still to examine its performance. It was observed that the structure distributing heat to surrounding water by absorbing photon energy from the sun through the nanopores and giving an efficient pathway to the water vapours for developing effective desalination. The nanoporous structure having ~ 45 nm average diameter. Furthermore, the band gap energy of nanoporous structure was found to be ~ 2.5 eV (absorption spectrum fitting) and ~ 2.8 eV (Tauc plot). The nanoporous structure possess the visible light spectra in solar region which helps the band gaps of nanoporous structure to provide an additional supply of energy for generating more water to evaporate. Moreover, the Urbach energy of the structure is 0.5 eV which reveals less defects in the modified still. The overall distillate yield of modified still was increased to 21% in contrast to conventional. Water quality analysis was also carried out before and after the desalination experiments, and the results were within acceptable limits set by World Health Organization (WHO).

Plasmonic Bound States in the Continuum Metasurface-Semiconductor-Metal Architecture Enables Efficient Hot-Electron-Based Photodetector.

Plasmonic hot-electron-based photodetectors (HEB-PDs) have received widespread attention for their ability to realize effective carrier collection under sub-bandgap illumination. However, due to the low hot electron emission probability, most of the existing HEB-PDs exhibit poor responsivity, which significantly restricts their practical applications. Here, by employing the binary-pore anodic alumina oxide template technique, we proposed a compact plasmonic bound state in continuum metasurface-semiconductor-metal-based (BIC M-S-M) HEB-PD. The symmetry-protected BIC can manipulate a strong gap surface plasmon in the stacked M-S-M structure, which effectively enhances light-matter interactions and improves the photoresponse of the integrated device. Notably, the optimal M-S-M HEB-PD with near-unit absorption (∼90%) around 800 nm delivers a responsivity of 5.18 A/W and an IPCE of 824.23% under 780 nm normal incidence (1 V external bias). Moreover, the ultrathin feature of BIC M-S-M (∼150 nm) on the flexible substrate demonstrates excellent stability under a wide range of illumination angles from -40° to 40° and at the curvature surface from 0.05 to 0.13 mm-1. The proposed plasmonic BIC strategy is very promising for many other hot-electron-related fields, such as photocatalysis, biosensing, imaging, and so on.

Solar Light-Induced Photoelectrochemical H2 Generation Over Hierarchical TiO2 Nanotube Arrays Decorated with CdS Nanoparticles

The process of converting solar energy into chemical energy through photoelectrochemical (PEC) water splitting holds significant promise for hydrogen and oxygen gas production. In the current study, we have demonstrated the feasibility of designing a high-performance heterojunction photoanode in a scalable manner. This photoanode sensitizes visible light active CdS onto hierarchical TiO2 nanotubes (TNTs), thereby enhancing H2 generation. To achieve this, we initially employed an electrochemical anodization technique to fabricate vertically aligned self-organized TNT on a titanium (Ti) substrate. Subsequently, we designed a hierarchical structure for TNT by uniformly decorating them with TiO2 nanoparticles (NPs), thus amplifying the available surface area. By employing the sequential ionic layer adsorption and reaction (SILAR) technique, we establish visible light sensitization. The resulting decorated hierarchical TNT photoanode demonstrates an enhanced photocurrent of 2.60 mA cm−2 under AM 1.5 G simulated solar light, surpassing the performance of hierarchical TNT, and most importantly classic CdS/TNT structures by 17-fold, and 1.6-fold, respectively. Moreover, the developed photoanodes achieved photoconversion efficiency with an applied bias (ABPE) of 2.48%. Thus, this work shows that a hierarchical scaffold can be exploited to achieve enhanced activity in photoelectrochemical H2 generation.

Photoelectrode FTO/ Anodized TiO2 Production and Characterization for Methylene Blue Affected Photoelectrochemical Decomposition

Background: The production of thin film TiO2 nanostructured systems for electrocatalytic, photocatalytic, and photoelectrocatalytic applications has been an essential topic in recent years. Due to the light-sensitive effect of TiO2, it can be produced by various methods and used as a photoelectrode to remove dye. Using magnetron sputtering, Ti thin films can be deposited on different substrates and converted into transparent TiO2 structures by electrochemical anodization. Methods: In this study, the thin Ti film was produced using a magnetic spraying technique on the FTO substrate, and then an anodic TiO2 structure was obtained by the anodization technique. TiO2 films produced by the anodizing technique were used as a photoelectrode for the degradation of MB. The reactor contained 400 mL of 20 mg/L MB solution at 20 °C. The produced photoelectrode was characterized by the SEM/EDS, FTIR, XRD, and UV-Vis Spectrophotometer analyses. Results: The EDS analysis confirmed the presence of titanium and oxygen in the FTO/ Anodized TiO2 photoelectrode. The XRD results showed that all the peaks of the produced FTO/ Anodic TiO2 were associated with the anatase phase of TiO2. According to the FTIR spectroscopy, the functional groups of the anodized TiO2 were obtained for the FTO/ Anodized TiO2. The electrocatalytic, photocatalytic, and photoelectrocatalytic degradation experiments were performed with the degradation of the dye solution of MB on the FTO/ Anodic TiO2 photoelectrode, and the rates of dye degradation were determined as 17.12%, 64.67%, and 82.12%, respectively. Conclusion: This study showed that the methylene blue dye of FTO/ Anodic TiO2 is a suitable photoelectrode for electrocatalytic, photocatalytic, and photoelectrocatalytic degradation.

Improved Fog Collection on a Hybrid Surface with Acylated Cellulose Coating.

Fog collection serves as an efficient method to alleviate water scarcity in foggy, water-stressed regions. Recent research has focused on constructing a hybrid surface to enhance fog collection efficiency, with one approach being the prevention of liquid film formation at hydrophilic sites. Inspired by the desert beetle, a coating (10-MCC) made by partially acylating microcrystalline cellulose (MCC) exhibits hydrophilic sites alongside a hydrophobic skeleton enabling rapid droplet capture despite its overall hydrophobicity. The captured droplets quickly coalesce into a large droplet driven by the wetting gradient created by the hydrophobic backbone and hydrophilic sites. To achieve greater fog collection efficiency, a hydrophobic-superhydrophobic hybrid surface is formed by combining a coating of 10-MCC with a superhydrophobic surface. The construction of superhydrophobic surfaces typically involves creating a rough surface with a distinctive structure produced by the anodization technique and modifying it with stearic acid. The superhydrophobic surface exhibits excellent corrosion resistance and mechanical stability. Moreover, the hybrid surface shows high efficiency in fog collection, with a tested maximum efficiency of approximately 1.5092 g/cm2/h, 1.77 times that of the original Al sheets. The results demonstrate a remarkable enhancement in fog collection capacity. Furthermore, this work serves as an inspiration for the low-cost and innovative design of engineered surfaces for efficient fog collection.

Electroosmotic flow in soft clay and measures to promote movement under direct current electric field.

Electroosmosis has been proposed as a technique to reduce moisture and thus increase the stability of soft clay. However, its high energy consumption and uneven reinforcement effect has limited its popularization and application in practical engineering. This paper presents the results of some electrokinetic tests performed on clayey specimens with different electrification time and anode boundary conditions. The results indicate that the timing of the formation of electroosmotic flow (EF) by the water originally contained in different soil cross sections, from the anode to the cathode, varies. The measuring soil cross section nearest the anode first reached the limiting water content of 22%±3% and electroosmosis had to be stopped. Water injection into the anode during electroosmosis enhanced further drainage of other four measuring soil cross sections until the second soil cross section from the anode reached the limiting water content of 30%±2%. Electroosmosis with water injection into the anode technique provides more uniform reinforcement, increasing EF, and environmental protection. The experimental results highlighted the relevant and expected contribution of water injection into the anode on the effectiveness of the electroosmotic treatment as a soft clay improvement technique.

Enhanced bonding of polyphenylene sulfide-aluminum alloy composites using combined mild and hard anodizing techniques

High-strength direct joining between polymers and Al has attracted considerable attention, particularly for reducing the weight device. In this study, porous anodic alumina (PAA) films were fabricated on a commercial 6063 Al alloy using with mild and hard anodizing with varying durations, followed by etching. Subsequently, polyphenylene sulfide (PPS) was directly joined with Al through injection molding. The correlations between the interface bond strength of PPS-Al joints and the Al oxidation duration were systematically investigated. The porosity, diameter of nanopore, and wettability of anodic aluminum oxide (AAO) film surface significantly influenced the bonding strength of PPS-Al composite structure. The porosity increased with an etching duration, increasing the bonding strength. However, excessive porosity (>54 %) weaken the films and reduced their bonding strengths. When the durations of mild anodizing (MA), hard anodizing (HA), and etching treatment were set to 30, 30, and 60 min, respectively, the maximum bonding strength reached 25.2 MPa, approximately 77 % of the base-material shear strength. Scanning electron microscopy revealed nanopillars with two different top sizes (approximately 80 and 110–130 nm) on the surface of injection-molded PPS, which were attributed to the different anodizing preparation voltage. These findings are generally significant for the realization for high-strength direct-bonded polymer-Al joints.

Cathodic luminol electrochemiluminescence on TiO2 nanotube array

This study introduces a novel fabrication of screen-printed electrode of hierarchical thin layers of TiO2 nanotube arrays (TNA) and its preliminary investigation for cathodic electrochemiluminescence (ECL) of luminol. The TNA growth on titanium foil by anodization technique was studied under various anodization times and counter electrodes (Pt wire and stainless-steel plate). Characterization using FTIR, UV-VIS DRS, and XRD revealed the increase of TiO2 formation at longer anodization times. The TNA synthesized with a stainless-steel counter electrode (TNA-SS) for 2000 s exhibited better nanotube growth and a higher electrochemical active surface area compared to the one using Pt counter electrode (TNA-Pt). The SEM characterization verified the nanotube morphology of TNA-SS with an average pore diameter of 50.46 nm and a tube length of ∼1100 nm. Notably, when TNA applied as the working electrode for the ECL of luminol, a reduction peak at −0.8 V accompanied by a clear ECL signal were observed, reaching an optimum intensity at 15 μM luminol. A comparative analysis between TNA-SS and TNA-Pt revealed the same trend of ECL signals with a significantly higher ECL intensity of TNA-SS than that of TNA-Pt. The ECL intensity of TNA-SS 2000s was also higher than TNA-SS 300s, confirming the importance of TNA surface area to the ECL activity. Nevertheless, the synthesized SPE-TNA shows great prospect to be applied in electroanalytical and sensing fields, offering opportunities for the development of electrochemiluminescence technologies.

1‐2: High Performance of InSnO Thin‐Film Transistors Enabled by Anodization Techniques

1‐2: High Performance of InSnO Thin‐Film Transistors Enabled by Anodization Techniques