Black TiO2-impregnated electrodes were prepared via a modified dip-coating method, using six deposition layers to investigate the influence of the TiO2 precursor phase (anatase, rutile, and P25) on their structural and optical properties, as well as their photoelectrooxidation performance toward acetaminophen degradation. A reductive thermal treatment under a H2/Ar atmosphere successfully modified the band gap energy and promoted the formation of oxygen vacancies (Vo) and Ti3+ species, as evidenced by UV–Vis diffuse reflectance spectroscopy and photoluminescence analysis. Among the precursor phases, anatase exhibited the most significant band gap reduction, whereas rutile and P25 showed greater structural stability after the reduction process. Photoelectrochemical experiments revealed that the supporting electrolyte plays a dominant role in the degradation process, with significantly higher removal efficiencies observed in chloride medium (0.1 M NaCl) compared with sulfate medium (0.1 M Na2SO4) due to the formation of active chlorine species. Among the tested materials, rutile- and P25-derived electrodes showed the highest degradation efficiencies, reaching concentrations (C/C0) of 0.631 and 0.650, respectively. The results highlight the combined influence of precursor phase, defect structure, and electrolyte composition on the photoelectrooxidation behavior of black TiO2 electrodes and provide insights for the design of electrochemical systems for pharmaceutical contaminants removal.
Solarte-Ferro et al. (2026) studied this question.