Preparation of hexagonal nanoporous Al2O3/TiO2/TiN as a novel photodetector with high efficiency

The unique optical properties of metal nitrides enhance many photoelectrical applications. In this work, a novel photodetector based on TiO2/TiN nanotubes was deposited on a porous aluminum oxide template (PAOT) for light power intensity and wavelength detection. The PAOT was fabricated by the Ni-imprinting technique through a two-step anodization method. The TiO2/TiN layers were deposited by using atomic layer deposition and magnetron sputtering, respectively. The PAOT and PAOT/TiO2/TiN were characterized by several techniques such as X-ray diffraction (XRD), scanning electron microscope (SEM), and energy dispersive X-ray (EDX). The PAOT has high-ordered hexagonal nanopores with dimensions ~ 320 nm pore diameter and ~ 61 nm interpore distance. The bandgap of PAOT/TiO2 decreased from 3.1 to 2.2 eV with enhancing absorption of visible light after deposition of TiN on the PAOT/TiO2. The PAOT/TiO2/TiN as photodetector has a responsivity (R) and detectivity (D) of 450 mAW-1 and 8.0 × 1012 Jones, respectively. Moreover, the external quantum efficiency (EQE) was 9.64% at 62.5 mW.cm−2 and 400 nm. Hence, the fabricated photodetector (PD) has a very high photoelectrical response due to hot electrons from the TiN layer, which makes it very hopeful as a broadband photodetector.

Fabrication and characterization of highly ordered nanotubes of anodic aluminum oxide

Investigated the electrochemical synthesis and characterized of a nanometer scale porous anodic aluminum oxide (AAO) membrane with a mean pore diameter about of 80-100 nm. The anodizing process done by varying the anodizing temperature from 20 °C to 25 °C. The membranes exhibit interesting properties such as controllable pore diameters, periodicity and density distribution. These properties can preselect by adjusting the controlling parameters of a temperature-controlled two-step anodization process. The surface features of the nanometer scale membrane such as pore density, pore diameter and interpore distance were quantified using scanning electron microscopy (SEM) and atomic force microscopy (AFM). SEM and AFM investigations revealed the presence of focal adhesion sites over the surface of the porous membranes. The positive outcomes of the study, indicates that AAO membranes can used for applications in the future.

Self-ordered nanospike porous alumina fabricated under a new regime by an anodizing process in alkaline media

High-aspect ratio ordered nanomaterial arrays exhibit several unique physicochemical and optical properties. Porous anodic aluminum oxide (AAO) is one of the most typical ordered porous structures and can be easily fabricated by applying an electrochemical anodizing process to Al. However, the dimensional and structural controllability of conventional porous AAOs is limited to a narrow range because there are only a few electrolytes that work in this process. Here, we provide a novel anodizing method using an alkaline electrolyte, sodium tetraborate (Na2B4O7), for the fabrication of a high-aspect ratio, self-ordered nanospike porous AAO structure. This self-ordered porous AAO structure possesses a wide range of the interpore distance under a new anodizing regime, and highly ordered porous AAO structures can be fabricated using pre-nanotexturing of Al. The vertical pore walls of porous AAOs have unique nanospikes measuring several tens of nanometers in periodicity, and we demonstrate that AAO can be used as a template for the fabrication of nanomaterials with a large surface area. We also reveal that stable anodizing without the occurrence of oxide burning and the subsequent formation of uniform self-ordered AAO structures can be achieved on complicated three-dimensional substrates.

Low-Cost Nanostructured Coating of Anodic Aluminium Oxide Synthesized in Sulphuric Acid as Electrolyte

The anodic oxidation of aluminium is an electrochemical technique that allows obtaining nanostructures with easily adjustable morphology depending on the synthesis variables, for its application in medicine, engineering, biotechnology, electronics, etc. In this work, low-cost aluminium oxide nanostructured films were synthesized and morphologically characterized using two anodization steps in sulphuric acid, varying the concentration and temperature of the electrolyte and anodization voltage. The order of the porous matrix, pore diameter, interpore distance, pore density, thickness, and porosity were measured and statistically analyzed. The results showed that under the proposed conditions it is possible to synthesize low-cost nanoporous aluminium oxide films, with a short-range ordering, being the best ordering conditions 10 °C and 0.3 M sulphuric acid at 20 V and 5 °C and 2 M sulphuric acid at 15 V. Furthermore, it was determined that the pore diameter and the interpore distance vary proportionally with the voltage, that the pore density decreases with the voltage and increases with the concentration of the electrolyte, and that the thickness of the oxide film increases with electrolyte concentration, temperature, and anodization voltage.

FORMATION OF ANODIC POROUS ALUMINA IN OXALIC ACID AND ELECTRODEPOSITION OF NI.

Nanoporous anodic aluminum oxide (AAO) tubular membranes were fabricated from aluminum alloy tubes in sulfuric and oxalic acid electrolytes using a two-step anodization process. The membranes were investigated for characteristics such as pore size, interpore distance and thickness by varying applied voltage and electrolyte concentration. Morphology of the membranes was examined using light optical and scanning electron microscopy and characterized using Image software. Results showed that membranes having narrow pore size and uniform pore distribution with parallel channel arrays were obtained. The pore sizes were ranging from 10 to 100 nm and the wall thicknesses 60 μm. The catalysts are obtained by impregnation of 3d metals into nanosized pores of aluminum oxide. The obtained catalysts based on nickel and porous Al2O3 are studied by scanning microscopy (SEM-EDX). The results of SEM-EDX analysis shows that a spongy structure with filament sizes of 100 nanometers containing particles of 3d metals formed on the surface of the aluminum oxide matrix.

Development of Nanoporous AAO Membrane for Nano Filtration Using the Acoustophoresis Method

A concept of a nanoporous anodic aluminum oxide (AAO) membrane as a vibro-active micro/nano-filter in a micro hydro mechanical system for the filtration, separation, and manipulation of bioparticles is reported in this paper. For the fabrication of a nanoporous AAO, a two-step mild anodization (MA) and hard anodization (HA) technique was used. Atomic force microscopy (AFM) and scanning electron microscopy (SEM) were used to analyze the surface morphology of nanoporous AAO. A nanoporous structure with a pore diameter in the range of 50–90 nm, an interpore distance of 110 nm, and an oxide layer thickness of 0.12 mm with 60.72% porosity was obtained. Fourier-transform infrared spectroscopy (FTIR) and energy-dispersive X-ray spectroscopy (EDS) were employed to evaluate AAO chemical properties. The obtained results showed that the AAO structure is of hexagonal symmetry and showed where Al2O3 is dominant. The hydrophobic properties of the nanoporous surface were characterized by water contact angle measurement. It was observed that the surface of the nanoporous AAO membrane is hydrophilic. Furthermore, to determine whether a nanomembrane could function as a vibro-active nano filter, a numerical simulation was performed using COMSOL Multiphysics 5.4 (COMSOL Inc, Stockholm, Sweden). Here, a membrane was excited at a frequency range of 0–100 kHz for surface acoustics wave (SAW) distribution on the surface of the nanoporous AAO using a PZT 5H cylinder (Piezo Hannas, Wuhan, China). The SAW, standing acoustic waves, and travelling acoustic waves of different wavelengths were excited to the fabricated AAO membrane and the results were compared with experimental ones, obtained from non-destructive testing method 3D scanning vibrometer (PSV-500-3D-HV, Polytec GmbH, Waldbronn, Germany) and holographic interferometry system (PRISM, Hy-Tech Forming Systems (USA), Phoenix, AZ, USA). Finally, a simulation of a single nanotube was performed to analyze the acoustic pressure distribution and time, needed to center nanoparticles in the nanotube.

Formation and tribological properties of MoS2 self-lubricating porous anodic alumina thin flims

MoS2 self-lubricating films were prepared on long-range ordered porous anodic alumina (PAA) by an electrophoretic deposition (EPD) method. The PAA was prepared by two-step anodization of aluminum plates. Oxalic-acid-based electrolytes were used in the first step and phosphoric-acid-based electrolytes were used in the second step. This process offers a new approach to preparing PAA with wide adjustable boundary distances (43.5–21 nm) by increasing the voltage from 80 V to 100 V. The boundary distances were decreased from 78 nm to 42.2 nm by increasing the solution concentration, which increased the interpore distance. The coefficient of friction and hard-wearing of the MoS2 lubrication film on the PAA were studied by a ball-on-disk friction and wear tester. The results showed that the nanotubes stored MoS2 particles, which provided continuous lubrication.

Formation of Nanoporous Mixed Aluminum-Iron Oxides by Self-Organized Anodizing of FeAl3 Intermetallic Alloy

Nanostructured anodic oxide layers on an FeAl3 intermetallic alloy were prepared by two-step anodization in 20 wt% H2SO4 at 0 °C. The voltage range was 10.0–22.5 V with a step of 2.5 V. The structural and morphological characterizations of the received anodic oxide layers were performed by field emission scanning electron microscopy (FE-SEM). Therefore, the formed anodic oxide was found to be highly porous with a high surface area, as indicated by the FE-SEM studies. It has been shown that the morphology of fabricated nanoporous oxide layers is strongly affected by the anodization potential. The oxide growth rate first increased slowly (from 0.010 μm/s for 10 V to 0.02 μm/s for 15 V) and then very rapidly (from 0.04 μm/s for 17.5 V up to 0.13 μm/s for 22.5 V). The same trend was observed for the change in the oxide thickness. Moreover, for all investigated anodizing voltages, the structural features of the anodic oxide layers, such as the pore diameter and interpore distance, increased with increasing anodizing potential. The obtained anodic oxide layer was identified as a crystalline FeAl2O4, Fe2O3 and Al2O3 oxide mixture.

Formation of Nanoporous Mixed Aluminum-Iron Oxides by Self-Organized Anodizing of FeAl3 Intermetallic Alloy

Nanostructured anodic oxide layers on an FeAl3 intermetallic alloy were prepared by two-step anodization in 20 wt.% H2SO4 at 0°C. The voltage range was 10.0 – 22.5 V with a step of 2.5 V. The structural and morphological characterizations of the received anodic oxide layers were performed by FE-SEM. Therefore, the formed anodic oxide was found to be highly porous with a high surface area, as indicated by the FE-SEM studies. It has been shown that the morphology of fabricated nanoporous oxide layers is strongly affected by the anodization potential. The oxide growth rate first increased slowly (from 0.010 μm/s for 10 V to 0.02 μm/s for 15 V) and then very rapidly (from 0.04 μm/s for 17.5 V up to 0.13 μm/s for 22.5 V). The same trend was observed for the change in the oxide thickness. Moreover, for all investigated anodizing voltages, the structural features of the anodic oxide layers, such as the pore diameter and interpore distance, increase with increasing anodizing potential. The obtained anodic oxide layer was identified as a crystalline FeAl2O4, Fe2O3 and Al2O3 oxide mixture.

Synthesis and Morphological Characterization of Nanoporous Aluminum Oxide Films by Using a Single Anodization Step

Nanoporous anodic aluminum oxide (AAO) films play an important role in nanotechnology due to their easily adjustable morphological properties and wide range of applications. Thus, a deep and systematic characterization of the morphological properties of these coatings is essential. The most important variables in the synthesis of nanoporous AAO films include the anodization voltage, nature, concentration and temperature of the electrolyte, which, combined, result in pores of different sizes and geometries. In the present work, AA 1050 alloy was used to synthesize AAO films, using 0.3 and 0.9 M oxalic acid as the electrolyte and combining different electrolyte temperatures (20, 30 and 40 °C) and anodizing voltages (30, 40 and 60 V), with the aim to correlate the morphological properties of the coatings with the synthesis parameters of a single anodization step. The coatings obtained were characterized by optical microscopy and scanning electron microscopy, determining pore diameter, interpore distance, pore density and coating thickness. The results showed that, by varying the anodic synthesis conditions, it is possible to obtain coatings with a pore diameter between 21 and 97 nm, an interpore distance between 59 and 138 nm, pore density between 2.8 × 1010 and 5.4 × 109 pores/cm2 and thicknesses between 15 and 145 µm. In this way, the right combination of synthesis variables allows synthesizing AAO coatings with morphological characteristics best suited to each particular application.