Nanotubular titanium oxide is widely known as a prospective semiconductor photocatalyst for the process of water splitting. Its photoelectrochemical (PEC) efficiency can be improved by doping with 3d metal. In this work, the synthesis of nanotubular titanium oxide (NTO) was carried out by anodizing titanium substrates using two doping techniques. First, Ni-doped TiO₂ was obtained by immersion in Ni salt solution; second, an ethylene glycol-based fluoride electrolyte containing Ni²⁺ ions solution was used. The obtained samples were analyzed using SEM, XRD, and photoelectrochemical methods. The produced Ni-doped NTO exhibited photocatalytic activity twice as high as that of nondoped NTO. Additionally, it was found that the immersion technique initiated a shift of the incident photon to converted electron (IPCE) spectra to the visible part of the spectrum.

This study investigates the synthesis and characterization of boron-modified nanotubular titania (NTO) arrays fabricated via a single-step anodizing process with varying concentrations of boric acid (BA). Following anodization, a reductive heat treatment was applied to facilitate the crystallization of the anatase phase in the boron-modified NTO. The effect of the BA concentration on the structural, morphological, and photoelectrochemical (PEC) properties of the NTOs was systematically explored through scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), luminescence, and UV-Vis spectrometry. The introduction of boron during anodization facilitated the formation of sub-bandgap states, thereby enhancing the light absorption and electron mobility. This study revealed the optimal BA concentration that yielded a 3.3-fold enhancement of the PEC performance, attributed to a reduction in the bandgap energy. Notably, the highest incident photon-to-current conversion efficiency (IPCE) was observed for NTO samples anodized at a 0.10 M BA concentration. These findings underscore the promise of boron-modified NTOs for advanced photocatalytic applications, particularly in solar-driven water-splitting processes.