This review aims to comprehensively and systematically analyze the anodic oxidation process to form nanostructured oxide films on the surface of the most technologically relevant Fe-based alloys and steels. A special emphasis is put on detailed analysis of the mechanisms of the anodic formation of Fe-based nanostructured materials. The effect of anodizing parameters including the type of Fe-alloy, electrolyte composition, potential/current regimes, as well as various post-treatment procedures (including annealing treatment) on the growth, morphology, composition, and properties of the resulting oxide films is discussed in detail. Examples of possible applications of the anodic films grown on Fe-alloys in various fields including photocatalysis, energy storage, sensors, biomedicine, and others are also provided. Finally, current trends, challenges, and perspectives in the anodizing of Fe-alloys are addressed.

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.

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.

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.