Rational modification of hydroxy-functionalized covalent organic frameworks for enhanced photocatalytic hydrogen peroxide evolution.

Covalent organic frameworks (COFs), a class of flexibly tunable crystalline materials, have fascinating potential in photocatalytic hydrogen peroxide (HO) evolution under visible light irradiation. However, achieving efficient catalytic activity by tuning the composition of COFs and the linkages of building blocks is still a challenge. Herein, four imine-linked COFs with different numbers of hydroxy-functionalized are constructed to unveil the latent structure-activity relationship between the reversibility of bonding in supramolecular chemistry and the photocatalytic HO performance. As the optimized material, TAPT-HTA-COF (1H-COF) containing single hydroxy group in aldehyde node exhibits a highest ordered structure and conjugation degree along and across the plane in the extended frameworks originating from the flexibly reversible iminol-to-ketoenamine tautomerism than others, which broadens the visible light absorption and accelerates the dissociation of photogenerated carriers in 1H-COF. These merits ensure that 1H-COF has the highest HO yield (44.5 μmol L) and O two-electron reduction pathway among the four COFs under visible light irradiation (λ > 420 nm, 10 vol% isopropanol aqueous solution). At the same time, the long-range ordered framework of 1H-COF is well preserved during the photocatalytic HO evolution process assisted by the proton-induced tautomerization. This work facilitates the design and development of COF-based photocatalysts in the evolution of HO.