Zirconium-based metal–organic cages (Zr-MOCs) have garnered significant interest for their exceptional stability, tunable functionality, processability, and ease of synthesis. Herein, an imine-based zirconium-organic cage (designated ZrC-IM) was precisely synthesized via Schiff-base condensation between presynthesized aldehyde-functionalized zirconium-oxo clusters and p -phenylenediamine (PPD) linkers. To enhance light absorption capacity, protonation of the imine bonds in ZrC-IM was achieved via acetic acid treatment. Consequently, the protonated sample (ZrC-IM-AC) exhibits significant absorption red-shifts and improved charge separation efficiency, further demonstrating superior catalytic activity for H 2 O 2 photogeneration, with a yield rate of 507.1 μmol g –1 h –1 . Radical trapping experiments combined with electron spin resonance (ESR) spectroscopy demonstrated that both ZrC-IM and ZrC-IM-AC catalysts promote photocatalytic H 2 O 2 generation through an indirect two-electron oxygen reduction pathway involving the sequential reactions: O 2 + e – → • O 2 –, followed by • O 2 – + e – + 2H + → H 2 O 2 . This work not only expands the structural diversity of imine-based Zr-MOCs, but also offers new insights for the regulation of MOC-based photocatalysts with enhanced performance.
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Sun et al. (2025) studied this question.
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