The energy band gap of commercial TiO 2 (P25, ~ 3.04 eV) is slightly narrower than that of pure TiO 2 (~ 3.2 eV), yet remains inactive under visible light. In contrast, ligand-to-metal charge transfer (LMCT) introduced by surface complexation with organic ligands can significantly enhance light absorption and effectively narrow the band gap. Here, electron-rich ethylenediaminetetraacetic acid (EDTA) serves as an electron donor and coordinates with TiO 2 via carboxylate linkers. As a result, the EDTA–TiO 2 complex exhibits efficient visible-light-driven photoreduction of toxic Cr(VI) to non-toxic Cr(III). Individually, the optimal loading of EDTA was 200 ppm, which further decreased to 100 ppm upon the introduction of methanol (MeOH, 20 vol%) as a hole scavenger and/or electron donor. Upon visible light illumination, electrons from the HOMO of EDTA move towards the conduction band (CB) of TiO 2 through the LMCT process, enabling visible-light absorption and driving the efficient reduction of Cr(VI) to Cr(III). The characteristic FT-IR bands at 1410 and 1677 cm − 1 confirm EDTA−TiO 2 complex formation, which is further supported by the calculated adsorption energy ( E ads = −18.83 kcal/mol). This study provides mechanistic insight into the adsorption mode of EDTA through carboxylate coordination and elucidates the role of LMCT in enhancing light-harvesting efficiency.
Afrin et al. (Thu,) studied this question.