Metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) have been proved as e cient catalysts for photocatalytic H 2 evolution, thanks to their tunable functionalities, permanent porosity, excellent visible light response, as well as physicochemical stability. Herein, a series of photocatalysts (termed NUBC) were fabricated by loading different amounts of Zr-UiO-66-NH 2 (NU) onto a benzoic acid modi ed covalent triazine-based framework (BC) based on post-synthetic covalent modi cation. The resulting NUBC catalysts exhibited a type-II Z-scheme heterojunction structure formed via the amide covalent bonds between the amine groups on NU and carboxyl groups on BC. The optimal loading of NU on BC is 30 wt.% (30NUBC) and the corresponding photocatalytic H 2 evolution rate was 378 μmol h −1 g −1 , almost 445 and 2 times than that of NU and BC, respectively. The synergistic effect between the type-II Z-scheme heterojunctions and amide bonds was conducive to boosting visible light harvesting and facilitating charge transportation and separation. Furthermore, the prepared NUBC catalysts show great reusability and stability. Overall, this work sheds light on the design of novel MOFs/COFs hybrid materials and provides a systematic exploration of their photocatalytic H 2 evolution properties.