A covalent organic framework constructed from a donor-acceptor-donor motif monomer for photocatalytic hydrogen evolution from water

Covalent organic frameworks (COFs), featuring semiconductor-like behavior, have recently garnered widespread interest for applications in photocatalysis by virtue of their well-defined and tailorable porous structures, high surface areas and excellent chemical stability. A facile strategy for designing COFs exerting efficient charge transfer and separation as well as suppressing charge carrier recombination is the precise integration of electron-donating and electron-withdrawing moieties to form long-range ordered donor-acceptor (D-A) type structures. In this work, we rationally designed and synthesized a novel imine-linked COF ( DABT-Py-COF ) by the condensation of a newly designed D-A-D type monomer of 4,4′,4′′,4′′′-(benzo[ c ][1,2,5]thiadiazole-4,7-diylbis(9,9-dimethyl-9,10-dihydroacridine-10,2,7-triyl))tetrabenzaldehyde and 1,3,6,8-tetrakis(4-aminophenyl)pyrene under solvothermal conditions. Remarkably, the obtained DABT-Py-COF exhibited outstanding and steady hydrogen production with a maximum hydrogen evolution rate (HER) of 5458 μmol g −1 h −1 under visible-light irradiation (AM 1.5). This work has paved the way for the rational design and preparation of more efficient D-A type COFs for photocatalysis. Derived from a D-A-D motif monomer, a novel COF was designed and synthesized, which exhibited excellent efficiency for hydrogen evolution from water under visible-light irradiation as a photocatalyst.