Constructing 0D/2D Z-scheme photocatalysts is a great promising path to improve photocatalytic activity by efficiently enhancing charge separation. Herein, we fabricated a visible-light-responsive Bi₃TaO₇ quantum dots (QDs)/g-C₃N₄ nanosheets (NSs) 0D/2D Z-scheme composite via a facile ultrasound method, and Bi₃TaO₇ QDs could be interspersed on the surface of g-C₃N₄ NSs uniformly. Furthermore, the strong interaction between Bi₃TaO₇ QDs and g-C₃N₄ NSs disturbed the CN heterocycles by forming C═O bonds between C atoms of the N-(C)₃ group and O atoms of the Ta-O bond. The optimum composite with 20 wt % g-C₃N₄ NSs showed the superior photocatalytic activity for degradation of ciprofloxacin (CIP) over the composites prepared by mechanical mixing and solid-state methods, the photocatalytic efficiency of which were 4 and 12.2 times higher than those of bare Bi₃TaO₇ and g-C₃N₄. Photoluminescence (PL), time-resolved transient PL decay spectra, and photocurrent together verify that the photogenerated hole-electron pairs in this 0D/2D Z-scheme composite have been effectively separated. The enhanced photocatalytic activity of as-synthesized photocatalysts could be attributed to the synergistic effect of efficient Z-scheme charge separation, highly dispersed 0D Bi₃TaO₇ nanocrystals, coordinating sites of 2D g-C₃N₄ NSs and the strong coupling between them. This study might pave the way toward designing novel visible-light-induced 0D/2D photocatalyst systems for highly efficient degradation of antibiotics.

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