Abstract
Interaction of amorphous and crystalline TiO2 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 TiO2 gives rise to spontaneous crystallization of the parent nanoparticles into hydrogen titanates (H2Ti3O7 and H2Ti12O25). 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 TiO2 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.
Highlights
Transition metal oxide semiconductors, such as titania [1, 2], are promising materials for wide ranging applications as photo-electro-catalysts [3,4,5], energy conversion materials [6], environmental clean-up agents [7, 8], food additives [9] components of biomaterials [10] and advanced products of pharmaceutical [11], cosmetic [12] or medical relevance [13, 14]
The effectiveness of the photocatalytic reactive oxygen species (ROS) generation reactions was 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 dimethyl-1-pyrroline N-oxide (DMPO) spin trap (HOO· detection) and in the reaction with terephthalic acid acting as a chemical scavenger (HO· detection)
Summary
Transition metal oxide semiconductors, such as titania [1, 2], are promising materials for wide ranging applications as photo-electro-catalysts [3,4,5], energy conversion materials [6], environmental clean-up agents [7, 8], food additives [9] components of biomaterials [10] and advanced products of pharmaceutical [11], cosmetic [12] or medical relevance [13, 14]. We present the results of sensitization and spontaneous crystallization of ultra-small T iO2 particles (2–6 nm) upon ligation of molecules of natural origin, such as rutin [34], for visible light activity and ROS generation efficiency in aquatic media.
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