Vertically oriented, self-organized TiO₂–MnO₂ nanotube arrays were successfully obtained by one-step anodic oxidation of Ti–Mn alloys in an ethylene glycol-based electrolyte. The as-prepared samples were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), UV-Vis absorption, photoluminescence spectroscopy, X-ray diffraction (XRD), and micro-Raman spectroscopy. The effect of the applied potential (30–50 V), manganese content in the alloy (5–15 wt. %) and water content in the electrolyte (2–10 vol. %) on the morphology and photocatalytic properties was investigated for the first time. The photoactivity was assessed in the toluene removal reaction under visible light, using low-powered LEDs as an irradiation source (λ_max = 465 nm). Morphology analysis showed that samples consisted of auto-aligned nanotubes over the surface of the alloy, their dimensions were: diameter = 76–118 nm, length = 1.0–3.4 μm and wall thickness = 8–11 nm. It was found that the increase in the applied potential led to increase the dimensions while the increase in the content of manganese in the alloy brought to shorter nanotubes. Notably, all samples were photoactive under the influence of visible light and the highest degradation achieved after 60 min of irradiation was 43%. The excitation mechanism of TiO₂–MnO₂ NTs under visible light was presented, pointing out the importance of MnO₂ species for the generation of e⁻ and h⁺.

V₂O₅-TiO₂ mixed oxide nanotube (NT) layers were successfully prepared via the one-step anodization of Ti-V alloys. The obtained samples were characterized by scanning electron microscopy (SEM), UV-Vis absorption, photoluminescence spectroscopy, energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (DRX), and micro-Raman spectroscopy. The effect of the applied voltage (30–50 V), vanadium content (5–15 wt %) in the alloy, and water content (2–10 vol %) in an ethylene glycol-based electrolyte was studied systematically to determine their influence on the morphology, and for the first-time, on the photocatalytic properties of these nanomaterials. The morphology of the samples varied from sponge-like to highly-organized nanotubular structures. The vanadium content in the alloy was found to have the highest influence on the morphology and the sample with the lowest vanadium content (5 wt %) exhibited the best auto-alignment and self-organization (length = 1 μm, diameter = 86 nm and wall thickness = 11 nm). Additionally, a probable growth mechanism of V₂O₅-TiO₂ nanotubes (NTs) over the Ti-V alloys was presented. Toluene, in the gas phase, was effectively removed through photodegradation under visible light (LEDs, λ_max = 465 nm) in the presence of the modified TiO₂ nanostructures. The highest degradation value was 35% after 60 min of irradiation. V₂O₅ species were ascribed as the main structures responsible for the generation of photoactive e⁻ and h⁺ under Vis light and a possible excitation mechanism was proposed.

TiO₂/Cu_xO_y nanotube (NT) arrays were synthesized using the anodization method in the presence of ethylene glycol and different parameters applied. The presence, morphology, and chemical character of the obtained structures was characterized using a variety of methods—SEM (scanning electron microscopy), XPS (X-ray photoelectron spectroscopy), XRD (X-ray crystallography), PL (photoluminescence), and EDX (energy-dispersive X-ray spectroscopy). A p-n mixed oxide heterojunction of Ti-Cu was created with a proved response to the visible light range and the stable form that were in contact with Ti. TiO₂/Cu_xO_y NTs presented the appearance of both Cu₂O (mainly) and CuO components influencing the dimensions of the NTs (1.1–1.3 µm). Additionally, changes in voltage have been proven to affect the NTs’ length, which reached a value of 3.5 µm for Ti₉₀Cu₁₀_50V. Degradation of phenol in the aqueous phase was observed in 16% of Ti₈₅Cu₁₅_30V after 1 h of visible light irradiation (λ > 420 nm). Scavenger tests for phenol degradation process in presence of NT samples exposed the responsibility of superoxide radicals for degradation of organic compounds in Vis light region. Inactivation of bacteria strains Escherichia coli (E. coli), Bacillus subtilis (B. subtilis), and Clostridium sp. in presence of obtained TiO₂/Cu_xO_y NT photocatalysts, and Vis light has been studied showing a great improvement in inactivation efficiency with a response rate of 97% inactivation for E. coli and 98% for Clostridium sp. in 60 min. Evidently, TEM (transmission electron microscopy) images confirmed the bacteria cells’ damage.

The use of heterogeneous photocatalysis in biologically contaminated water purification processes still requires the development of materials active in visible light, preferably in the form of thin films. Herein, we report nanotube structures made of TiO₂/Ag₂O/Au⁰, TiO₂/Ag₂O/PtO_x, TiO₂/Cu₂O/Au⁰, and TiO₂/Cu₂O/PtO_x obtained via one-step anodic oxidation of the titanium-based alloys (Ti₉₄Ag₅Au₁, Ti₉₄Cu₅Pt₁, Ti₉₄Cu₅Au₁, and Ti₉₄Ag₅Pt₁) possessing high visible light activity in the inactivation process of methicillin-susceptible S. aureus and other pathogenic bacteria—E. coli, Clostridium sp., and K. oxytoca. In the samples made from Ti-based alloys, metal/metal oxide nanoparticles were formed, which were located on the surface and inside the walls of the NTs. The obtained results showed that oxygen species produced at the surface of irradiated photocatalysts and the presence of copper and silver species in the photoactive layers both contributed to the inactivation of bacteria. Photocatalytic inactivation of E. coli, S. aureus, and Clostridium sp. was confirmed via TEM imaging of bacterium cell destruction and the detection of CO₂ as a result of bacteria cell mineralization for the most active sample. These results suggest that the membrane ruptures as a result of the attack of active oxygen species, and then, both the membrane and the contents are mineralized to CO₂.

Heterogeneous photocatalysis in the presence of semiconductor materials, especially TiO2, is increasingly studied due to its potential application in hydrogen generation, carbon dioxide conversion, and pollutant degradation. TiO2, known for its cost-effectiveness, stability, and safety, is particularly effective in its nanometric form, with nanotubes standing out for their structure that improves light absorption and charge carrier mobility. One approach to improve the properties of TiO2 for its application in photocatalytic processes involves its modification. Modifications of TiO2 nanotubes aim to reduce the rate of recombination of photogenerated charge carriers, increase photocatalytic activity in the UV range, extend its activity to the visible radiation range, and enhance reaction selectivity. Enhancing TiO2 photocatalytic efficiency involves modifications such as doping, creating heterojunctions, and introducing structural defects. The objective of this mini-review is to present selected methods of modifying TiO2 nanotubes obtained through anodic oxidation, leading to the enhancement of their photocatalytic properties.