Photogeneration of reactive oxygen species over ultrafine TiO2 particles functionalized with rutin–ligand induced sensitization and crystallization effects

• Published in: Research on chemical intermediates 2019-12, Vol.45 (12), p.5781-5800
• Main Authors: Łabuz, Przemysław, Gryboś, Joanna, Pietrzyk, Piotr, Sobańska, Kamila, Macyk, Wojciech, Sojka, Zbigniew
• Format: Article
• Language: English
• Subjects: Aqueous solutions; Catalysis; Catechol; Charge efficiency; Charge transfer; Chemistry; Chemistry and Materials Science; Crystallization; Electron states; Hydrogen peroxide; Hydroxyl groups; Hydroxyl radicals; Inorganic Chemistry; Ligands; Light irradiation; Nanomaterials; Nanoparticles; Organic chemistry; Physical Chemistry; Raman spectra; Redox reactions; Stability; Terephthalic acid; Titanates; Titanium dioxide; Ultrafines
• ISSN: 0922-6168; 1568-5675
• DOI: 10.1007/s11164-019-04002-z

Interaction of amorphous and crystalline TiO 2 ultrafine particles (2–6 nm) with rutin results in the formation of colored nanomaterials of an excellent dispersity and enhanced colloidal stability in aqueous media. The FTIR and Raman spectra confirmed attachment of the rutin ligand via vicinal hydroxyl groups in a catechol-like fashion. The binding of rutin to amorphous TiO 2 gives rise to spontaneous crystallization of the parent nanoparticles into hydrogen titanates (H 2 Ti 3 O 7 and H 2 Ti 12 O 25 ). Such structural transformations result in photosensitization toward visible light with enhanced efficiency of the charge separation and interfacial charge transfer processes, confirmed by detailed photoelectrochemical studies of the examined nanomaterials. The effectiveness of the photocatalytic ROS generation reactions was also strongly influenced by hydrogen peroxide, which plays a double role of a reactant prone to reduction and generation of hydroxyl radicals or a redox agent destroying the intra-band gap electronic states, suppressing thereby charge recombination. The photoinduced charge transfer processes lead to generation of various reactive oxygen species, which were detected by EPR using DMPO spin trap (HOO · detection) and in the reaction with terephthalic acid acting as a chemical scavenger (HO · detection). Complexation of TiO 2 particles with rutin shifts the photogeneration of hydroperoxyl (HOO · ) and hydroxyl (HO · ) radicals toward visible light ( λ  > 400 nm). A triple effect of rutin attachment to titania was established. It consists in pronounced photosensitization, promotion of crystallization and enhancement of the colloidal stability of ultrafine titania particles. Environmental implications of these assets on the photoinduced redox reactions with hydrogen peroxide in aqueous solutions upon UV or visible light irradiation were also discussed.