Abstract
Structure design of photocatalysts is highly desirable for taking full advantage of their abilities for H2 evolution. Herein, the highly-efficient TiO2{001}/g-C3N4 (TCN) heterostructures have been fabricated successfully via an in situ ethanol-thermal method. And the structure of g-C3N4 in the TCN heterostructures could be exfoliated from bulk g-C3N4 to nanosheets, nanocrystals and quantum dots with the increase of the synthetic temperature. Through detailed characterization, the structural evolution of g-C3N4 could be attributed to the enhanced temperature of the ethanol-thermal treatment with the shear effects of HF acid. As expected, the optimal TCN-2 heterostructure shows excellent photocatalytic H2 evolution efficiency (1.78 mmol h−1 g−1) under visible-light irradiation. Except for the formed built-in electric field, the significantly enhanced photocatalytic activity of TCN-2 could be ascribed to the enhanced crystallinity of TiO2{001} nanosheets and the formed g-C3N4 nanocrystals with large surface area, which could extend the visible light absorption, and expedite the transfer of photo-generated charge carriers further. Our work could provide guidance on designing TCN heterostructures with the desired structure for highly-efficient photocatalytic water splitting.
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