A partially fluorinated, metal-free, imine-linked two-dimensional triazine covalent organic framework (TF₅₀ -COF) photocatalyst was developed. Fluorine (F)-substituted and nonsubstituted units were integrated in equimolar amounts on the edge aromatic units, where they mediated two-electron O₂ photoreduction. F-substitution created an abundance of Lewis acid sites, which regulated the electronic distribution of adjacent carbon atoms and provided highly active sites for O₂ adsorption, and widened the visible-light-responsive range of the catalyst, while enhancing charge separation. Varying the proportion of F maximized the interlayer interactions of TF₅₀ -COF, resulting in improved crystallinity with faster carrier transfer and robust photostability. The TF₅₀ -COF catalyst demonstrates high selectivity and stability in O₂ photoreduction into H₂ O₂ , with a high H₂ O₂ yield rate of 1739 μmol h⁻¹ g⁻¹ and a remarkable apparent quantum efficiency of 5.1 % at 400 nm, exceeding the performance of previously reported nonmetal COF-based photocatalysts.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2022) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: