Constructing Donor‐Acceptor Covalent Organic Frameworks for Highly Efficient H₂O₂ Photosynthesis Coupled with Oxidative Organic Transformations

Abstract The development of photocatalytic systems that enable the simultaneous production of H 2 O 2 and value‐added organic chemicals presents a dual advantage: generating valuable products while maximizing the utilization of solar energy. Despite the potential, there are relatively few reports on photocatalysts capable of such dual functions. In this study, we synthesized a series of donor‐acceptor covalent organic frameworks (COFs), designated as JUC‐675 to JUC‐677, to explore their photocatalytic efficiency in the co‐production of H 2 O 2 and N‐benzylbenzaldimine (BBAD). Among them, JUC‐675 exhibited exceptional performance, achieving a H 2 O 2 production rate of 22.8 mmol g −1 h −1 with an apparent quantum yield of 15.7 %, and its solar‐to‐chemical conversion efficiency was calculated to be 1.09 %, marking it as the most effective COF‐based photocatalyst reported to date. Additionally, JUC‐675 demonstrated a high selectivity (99.9 %) and yield (96 %) for BBAD in the oxidative coupling of benzylamine. The underlying reaction mechanism was thoroughly investigated through validation experiments and density functional theory (DFT) calculations. This work represents a significant advancement in the design of COF‐based photocatalysts and the development of efficient dual‐function photocatalytic platforms, offering new insights and methodologies for enhanced solar energy utilization and the synthesis of value‐added products.