Morphological and semiconductive properties of the anodic oxide layers made on Fe3Al alloy by anodizing in tartaric-sulfuric acid mixture.

It has recently been found that the anodizing of FeAl alloys allows the formation of iron-aluminum oxide layers with interesting semiconducting properties. However, the lack of systematic research on different anodizing regimes is hampering their full exploitation in numerous photoelectrochemical-related applications. This study address, for the first time, the systematic effect of the electrolyte composition on the formation of self-ordered oxide films by anodizing on cast Fe3Al alloy. The Fe3Al alloy was anodized in 3 electrolytes with different water-ethylene glycol (EG) ratios (pure water, 25 vol.%-EG, and 50 vol.%-EG solutions) at a constant tartaric-sulfuric acids concentration, different voltages (10-20 V) and treatment times (2-60 min). After anodizing, all anodic oxide layers were annealed at 900 °C to form semiconductive iron-aluminum crystalline phases. Conventional techniques were used to systematically ascertain the morphological (SEM/EDS, XRD, eddy-current measurements) and semiconductive (UV-VIS reflectance spectroscopy) properties of these oxide layers. The results confirmed the formation of homogeneous and self-ordered anodic oxide layers at 10 and 15 V, regardless of the electrolyte composition. Namely, anodic films formed in electrolytes containing EG showed lower pore sizes, growth rates, and film thicknesses than those anodic films formed in the aqueous-based electrolyte. The annealing post-treatment results in different Fe-Al oxides (FexOy, FeAl2O4, etc.) with superior band gap values than those for non-annealed films.

Estimation of spectroscopic parameters and TL glow curve analysis of Eu3+-activated CaY2O4 phosphor.

The solid-state reaction method was utilised to create a down-conversion phosphor in an air environment in CaY2O4:Eu3+ nanocrystalline material. The calcination temperature was set at 1000 °C, and the sintering temperature was set at 1300 °C. Following annealing, confirmation of the crystallinity quality of the phosphor was accomplished by the use of X-ray diffraction analysis. The particle size was predicted to be 43.113 nm using Scherrer's formula. To produce down-conversion luminescence spectra, an excitation wavelength of 247 nm was applied with a fluorescence spectrophotometer. The PL got increasingly intense as the concentration of the dopant increased. The maximum intensity was measured at 2.0 mol% of Eu3+ ion, which gradually decreased as the concentration increased because of concentration quenching. To analyse spectrophotometric peak determinations, the approach developed by the Commission Internationale de l'Éclairage (CIE) was used. Thermoluminescence (TL) glow curve analysis of the CaY2O4:Eu3+-doped phosphor manufactured here revealed a wide TL centred at 225 °C, which comprised of so many peaks that may be extracted by the computerised glow curve deconvolution (CGCD) approach using glow-fit software. The associated kinetic parameters were then determined. The prepared phosphor may be useful for application in various display devices upon excitation by 247 nm; the prominent 613 nm peak of the Eu3+ ion (5D0 → 7F2) electric dipole transition features a red component. CaY2O4:Eu3+ phosphors show promise as materials for potential use in phosphor-converted white LEDs in the field of solid-state lighting technology. The linear connection that the TL glow curve has with UV dose provides evidence for its possible use in dosimetry.

Application of Anodic Titanium Oxide Modified with Silver Nanoparticles as a Substrate for Surface-Enhanced Raman Spectroscopy.

The formation of nanostructured anodic titanium oxide (ATO) layers was explored on pure titanium by conventional anodizing under two different operating conditions to form nanotube and nanopore morphologies. The ATO layers were successfully developed and showed optimal structural integrity after the annealing process conducted in the air atmosphere at 450 °C. The ATO nanopore film was thinner (1.2 +/- 0.3 µm) than the ATO nanotube layer (3.3 +/- 0.6 µm). Differences in internal pore diameter were also noticeable, i.e., 88 +/- 9 nm and 64 +/- 7 nm for ATO nanopore and nanotube morphology, respectively. The silver deposition on ATO was successfully carried out on both ATO morphologies by silver electrodeposition and Ag colloid deposition. The most homogeneous silver deposit was prepared by Ag electrodeposition on the ATO nanopores. Therefore, these samples were selected as potential surface-enhanced Raman spectroscopy (SERS) substrate, and evaluation using pyridine (aq.) as a testing analyte was conducted. The results revealed that the most intense SERS signal was registered for nanopore ATO/Ag substrate obtained by electrodeposition of silver on ATO by 2.5 min at 1 V from 0.05M AgNO3 (aq.) (analytical enhancement factor, AEF ~5.3 × 104) and 0.025 M AgNO3 (aq.) (AEF ~2.7 × 102). The current findings reveal a low-complexity and inexpensive synthesis of efficient SERS substrates, which allows modification of the substrate morphology by selecting the parameters of the synthesis process.

Optimizing the luminescence efficiency of an europium (Eu3+) doped SrY2O4 phosphor for flexible display and lighting applications.

This research paper reports the synthesis and luminescence study of an Eu3+ activated SrY2O4 phosphor prepared by a modified solid-state reaction method with varying concentrations of Eu3+ ions (0.1-2.5 mol%). X-ray diffraction (XRD) revealed the orthorhombic structure and Fourier transform infrared spectroscopy (FTIR) methods were used to analyse the produced phosphors. Photoluminescence emission and excitation spectra were recorded for varying concentrations of Eu3+ ions, and an optimum concentration of 2.0 mol% was found to produce the highest intensity. Under 254 nm excitation the emission peaks were found to be at 580 nm, 590 nm, 611 nm and 619 nm, corresponding to transitions at 5D0 → 7F0, 5D0 → 7F1, and 5D0 → 7F2 respectively. Because of Eu3+ inherent luminosity, these emission peaks indicate radiative transitions between excited states of ions, making them useful for developing white light-emitting phosphors for optoelectronic and flexible display applications. The 1931 CIE (x, y) chromaticity coordinates were calculated from the photoluminescence emission spectra and found to be near white light emission, indicating the potential application of the prepared phosphor for light emitting diodes (white component). TL glow curve analysis was also performed for various concentrations of doping ions and UV exposure times, and a single broad peak was observed at 187 °C. Using the computerised glow curve deconvolution (CGCD) method, kinetic parameters were computed.

Modification of Anodic Titanium Oxide Bandgap Energy by Incorporation of Tungsten, Molybdenum, and Manganese In Situ during Anodization.

In this research, we attempted to modify the bandgap of anodic titanium oxide by in situ incorporation of selected elements into the anodic titanium oxide during the titanium anodization process. The main aim of this research was to obtain photoactivity of anodic titanium oxide over a broader sunlight wavelength. The incorporation of the selected elements into the anodic titanium oxide was proved. It was shown that the bandgap values of anodic titanium oxides made at 60 V are in the visible region of sunlight. The smallest bandgap value was obtained for anodic titanium oxide modified by manganese, at 2.55 eV, which corresponds to a wavelength of 486.89 nm and blue color. Moreover, it was found that the pH of the electrolyte significantly affects the thickness of the anodic titanium oxide layer. The production of barrier oxides during the anodizing process with properties similar to coatings made by nitriding processes is reported for the first time.

Understanding the influence of electrolyte aging in electrochemical anodization of titanium.

Titania nanotubes or nanopores self-ordered on electrochemically anodized (EA) titanium have been widely applied towards photocatalysis, solar cells, purification and biomedical implants. As a result, significant research has been focused towards optimizing anodization to fabricate controlled, stable and reproducible nanostructures. Among these, the use of organic-based electrolyte, like ethylene glycol (with NH4F and water), to anodize Ti has been widely applied and researched. Interestingly, among the various influencing EA factors, electrolyte aging (repeated EA using non-target Ti, prior to EA of target Ti substrate) has been underexplored, with only few studies aiming to optimize electrolyte aging and its influence on the nanostructures fabricated. Moreover, many research laboratories utilize electrolyte aging in Ti anodization, but this practice is seldom reported. In this extensive and pioneering review, we discuss and detail electrolyte aging in Ti anodization to fabricate controlled nanostructures, and its influence on nanostructure characteristics including morphology, chemistry, stability and application-specific performance. This review will inform future research aimed at optimizing electrolyte aging and Ti anodization to fabricate controlled nanostructures catering to specific application needs.

Morphological and Optical Characterization of Colored Nanotubular Anodic Titanium Oxide Made in an Ethanol-Based Electrolyte.

In this paper, the possibility of color controlling anodic titanium oxide by changing anodizing conditions of titanium in an ethanol-based electrolyte is demonstrated. Colored anodic titanium oxide was fabricated in an ethanol-based electrolyte containing 0.3 M ammonium fluoride and various amounts of deionized water (2, 3.5, 5, or 10 vol%), at voltages that varied from 30 to 60 V and at a constant anodization temperature of 20 °C. Morphological characterization of oxide layers was established with the use of a scanning electron microscope. Optical characterization was determined by measuring diffusion reflectance and calculating theoretical colors. The resulting anodic oxides in all tested conditions had nanotubular morphology and a thickness of up to hundreds of nanometers. For electrolytes with 3.5, 5, and 10 vol% water content, the anodic oxide layer thickness increased with the applied potential increase. The anodic titanium oxide nanotube diameters and the oxide thickness of samples produced in an electrolyte with 2 vol% water content were independent of applied voltage and remained constant within the error range of all tested potentials. Moreover, the color of anodic titanium oxide produced in an electrolyte with 2 vol% of water was blue and was independent from applied voltage, while the color of samples from other electrolyte compositions changed with applied voltage. For samples produced in selected conditions, iridescence was observed. It was proposed that the observed structural color of anodic titanium oxide results from the synergy effect of nanotube diameter and oxide thickness.

Green Synthesis of Nanomaterials Using Plant Extract: A Review.

For the last two decades, extensive research is conducted on metal and metal oxide nanoparticles and their application in the field of medical, cosmetics, catalysts, packaging, photonics, agriculture and electronics. However, these nanoparticles show toxicity to the environmental, human and animal health. The toxicity effects of nanoparticles are mainly due to their size, which can easily pass through physiological barriers and also due to the synthesis procedure. The toxicity due to their size cannot be avoided, but toxicity due to the synthesis process can be nullified by adopting the biosynthesis process. Bacteria, fungus, fish scales, plant extracts and algae are used to synthesize metal and metal- oxide nanoparticles such as silver, gold, iron-oxide, zinc-oxide, zirconia, etc. For the last few years, researchers have been working on synthesis methods of plant extracts to produce stable, cost-effective and economical nanoparticles. In this review, we focus on the biosynthesis of nanoparticles using different parts of plant extracts. The review contains a summary of selected papers from 2018-20 with a detailed description of the process of synthesis, mechanism, characterization and their application in various fields of biosynthesized metal and metal oxide nanoparticles.

Self-Organized Anodic Oxides on Titanium Alloys Prepared from Glycol- and Glycerol-Based Electrolytes.

The anodization of commercially pure Ti alloy (99.5 wt %) and two biomedical titanium alloys, Ti6Al7Nb and Ti6Al4V, was performed, and the resulting anodic oxides were studied. The biomedical alloys were made by Laser Engineered Net Shaping. The glycol-based and glycerol-based electrolytes with 0.3 M ammonium fluoride and 2 wt % of deionized water content were tested. It was found that electrolyte type as well as the chemical composition of the base substrate affected the final morphology and chemical composition of the anodic oxide formed. A higher current density, ionic mobility, and oxide growth rate were obtained in glycol-based electrolyte as compared to those obtained in glycerol-based electrolyte for all tested alloys. A self-organized nanotubular and nanoporous morphology of the anodic oxide in both types of electrolyte was obtained. In each electrolyte, the alloy susceptibility to oxidation increased in the following order: Ti6Al4V < Ti 99.5% < Ti6Al7Nb, which can be correlated to the oxidation susceptibility of the base titanium alloy. It was observed that the more impurities/alloying elements in the substrate, the lower the pore diameters of anodic oxide. There was a higher observed incorporation of electrolyte species into the anodic oxide matrix in the glycerol-based electrolyte compared with that in glycol-based electrolyte.

Fabrication of Ag-modified hollow titania spheres via controlled silver diffusion in Ag-TiO2 core-shell nanostructures.

Inorganic hollow spheres find a growing number of applications in many fields, including catalysis and solar cells. Hence, a simple fabrication method with a low number of simple steps is desired, which would allow for good control over the structural features and physicochemical properties of titania hollow spheres modified with noble metal nanoparticles. A simple method employing sol-gel coating of nanoparticles with titania followed by controlled silver diffusion was developed and applied for the synthesis of Ag-modified hollow TiO2 spheres. The morphology of the synthesized structures and their chemical composition was investigated using SEM and X-ray photoelectron spectroscopy, respectively. The optical properties of the synthesized structures were characterized using UV-vis spectroscopy. Ag-TiO2 hollow nanostructures with different optical properties were prepared simply by a change of the annealing time in the last fabrication step. The synthesized nanostructures exhibit a broadband optical absorption in the UV-vis range.

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.

Synthesis and characterization of noble metal-titania core-shell nanostructures with tunable shell thickness.

Core-shell nanostructures have found applications in many fields, including surface enhanced spectroscopy, catalysis and solar cells. Titania-coated noble metal nanoparticles, which combine the surface plasmon resonance properties of the core and the photoactivity of the shell, have great potential for these applications. However, the controllable synthesis of such nanostructures remains a challenge due to the high reactivity of titania precursors. Hence, a simple titania coating method that would allow better control over the shell formation is desired. A sol-gel based titania coating method, which allows control over the shell thickness, was developed and applied to the synthesis of Ag@TiO2 and Au@TiO2 with various shell thicknesses. The morphology of the synthesized structures was investigated using scanning electron microscopy (SEM). Their sizes and shell thicknesses were determined using tunable resistive pulse sensing (TRPS) technique. The optical properties of the synthesized structures were characterized using UV-vis spectroscopy. Ag@TiO2 and Au@TiO2 structures with shell thickness in the range of ≈40-70 nm and 90 nm, for the Ag and Au nanostructures respectively, were prepared using a method we developed and adapted, consisting of a change in the titania precursor concentration. The synthesized nanostructures exhibited significant absorption in the UV-vis range. The TRPS technique was shown to be a very useful tool for the characterization of metal-metal oxide core-shell nanostructures.