Photodepositing CdS on the Active Cyano Groups Decorated g-C₃ N₄ in Z-Scheme Manner Promotes Visible-Light-Driven...

g-C₃ N₄ /CdS heterojunctions are potential photocatalysts for hydrogen production but their traditional type-II configuration generally leads to weak oxidative and reductive activity. How to construct the novel Z-scheme g-C₃ N₄ /CdS counterparts to address this issue remains a great challenge in this field. In this work, a new direct Z-scheme heterojunction of defective g-C₃ N₄ /CdS is designed by introducing cyano groups (NC-) as the active bridge sites. Experimental observations in combination with density functional theory (DFT) calculations reveal that the unique electron-withdrawing feature of cyano groups in the defective g-C₃ N₄ /CdS heterostructure can endow this photocatalyst with numerous advantageous properties including high light absorption ability, strong redox performance, satisfactory charge separation efficiency, and long lifetime of charge carriers. Consequently, the resultant photocatalytic system exhibits more active performance than CdS and g-C₃ N₄ under visible light and reaches an excellent hydrogen evolution rate of 1809.07 µmol h^-1 g^-1 , which is 6.09 times higher than pristine g-C₃ N₄ . Moreover, the defective g-C₃ N₄ /CdS photocatalyst maintains good stability after 40 h continuous test. This work provides new insights into design and construction of Z-scheme heterojunctions for regulating the visible-light-induced photocatalytic activity for H₂ evolution.