Confining Metal‐Organic Framework in the Pore of Covalent Organic Framework: A Microscale Z‐Scheme System for Boosting Photocatalytic Performance

The search for building hierarchical porous materials with accelerated photo-induced electrons and charge-carrier separation is important because they hold great promise for applications in various fields. Here, a facile strategy of confining metal-organic framework (MOF) in the 1D channel of the 2D covalent organic framework (COF) to construct a novel COF@MOF micro/nanopore network is proposed. Specifically, a nitrogen-riched COF (TTA-BPDA-COF) is chosen as the platform for in-situ growth of a Co-based MOF (ZIF-L-Co) to form a TTA-BPDA-COF@ZIF-L-Co hybrid material. The hierarchical porous structure endows TTA-BPDA-COF@ZIF-L-Co with superior adsorption capacity. In addition, the integration of TTA-BPDA-COF and ZIF-L-Co forms a Z-scheme photocatalytic system, which significantly improved the redox properties and accelerated the separation of photogenerated charges and holes, achieving great improvement in photocatalytic activity. This confinement engineering strategy provides a new idea to construct a versatile molecular-material photocatalytic platform.