Interfacial coupling induced direct Z-scheme water splitting in metal-free photocatalyst: C₃N/g-C₃N₄ heterojunctions

Abstract

Mimicking the natural photosynthesis in green plants, artificial Z-scheme photocatalysis enables more efficient utilization of solar energy for photocatalytic water splitting. Most currently designed g-C₃N₄-based Z-scheme heterojunctions are usually based on metal-containing semiconductor photocatalysts, thus exploiting metal-free photocatalysts for Z-scheme water splitting is of huge interest. Herein, we propose two metal-free C₃N/g-C₃N₄ heterojunctions with the C₃N monolayer covering g-C₃N₄ sheet (monolayer or bilayer) and systematically explore their electronic structures, charge distributions and photocatalytic properties by performing extensive hybrid density functional calculations. We clearly reveal that the relative strong built-in electric fields around their respective interface regions, caused by the charge transfer from C₃N monolayer to g-C₃N₄ monolayer or bilayer, result in the bands bending, renders the transfer of photogenerated carriers in these two heterojunctions following the Z-scheme instead of the type-II pathway. Moreover, the photogenerated electrons and holes in these two C₃N/g-C₃N₄ heterojunctions can not only be efficiently separated, but also have strong redox abilities for water oxidation and reduction. Compared with the isolated g-C₃N₄ sheets, the light absorption in visible to near-infrared region are significantly enhanced in these proposed heterojunctions. These theoretical findings suggest that these proposed metal-free C₃N/g-C₃N₄ heterojunctions are promising direct Z-scheme photocatalysts for solar water splitting.