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Spontaneous Production of Ultrastable Reactive Oxygen Species on Titanium Oxide Surfaces Modified with Organic Ligands
Author(s) -
Ritacco Ida,
Imparato Claudio,
Falivene Laura,
Cavallo Luigi,
Magistrato Alessandra,
Caporaso Lucia,
Farnesi Camellone Matteo,
Aronne Antonio
Publication year - 2021
Publication title -
advanced materials interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.671
H-Index - 65
ISSN - 2196-7350
DOI - 10.1002/admi.202100629
Subject(s) - dibenzoylmethane , anatase , radical , materials science , acetylacetone , ligand (biochemistry) , density functional theory , photochemistry , titanium , superoxide , catechol , titanium oxide , oxygen , molecule , oxide , inorganic chemistry , chemistry , organic chemistry , computational chemistry , catalysis , photocatalysis , biochemistry , receptor , metallurgy , enzyme
The spontaneous formation and long‐term surface stabilization of superoxide radicals are observed on specific TiO 2 hybrid materials in which titanium is coordinated to an organic ligand. Here the rationale for this uncommon phenomenon is investigated by a synergistic theoretical and experimental approach involving density functional theory (DFT) calculations and spectroscopic techniques. Stoichiometric and reduced anatase (101) surfaces modified with acetylacetone, dibenzoylmethane, and catechol are comparatively examined. These results reveal that the interaction between organic ligands and adsorbed O 2 molecules improves when O vacancies are present on the external layer of the surface, promoting O 2 reduction. The electronic features of the ligand play a pivotal role for both an effective electronic interaction with the surface and the stabilization of the generated reactive oxygen species. These results agree with experimental data showing that sol–gel‐derived Ti‐diketonate hybrid oxides spontaneously produce very persistent superoxide radicals under ambient conditions, thus holding a high intrinsic oxidative activity.