Defect as the essential factor in engineering carbon-nitride-based visible-light-driven Z-scheme photocatalyst

In designing of carbon nitride-based Z-scheme systems, band structure engineering of graphitic carbon nitride (g-C 3 N 4 ) is unquestionably a crucial demand but paid rare attention to. Here, the broadened light absorption and charge transfer on sub gaps induced by thermal defects in defect-rich carbon nitride (d-C 3 N 4 ) are simultaneously utilized to engineer a novel and more efficient Z-scheme system. The as-prepared α-Fe 2 O 3 /d-C 3 N 4 -1 exhibits dramatically improved photocatalytic degradation rate for tetracycline compared withα-Fe 2 O 3 /g-C 3 N 4 -1 under visible light. Dye photosensitization effect on photocatalytic reaction was ruled out, and the tetracycline decomposition mechanism was proposed. The efficiently restrained charge recombination and broadened light absorption in this Z-scheme system are key parameters of the outstanding photocatalytic activity. This proposed mechanism has the potential to push the limit of traditional carbon-nitride-based Z-scheme photocatalysts and can also shed substantial light on the engineering strategies for other polymeric Z-scheme photocatalysts.