摘要
Z -scheme g-C 3 N 4 /Au/BiVO 4 photocatalyst has been prepared successfully by assembling gold nanoparticles on the interface of super-thin porous g-C 3 N 4 and BiVO 4 , which exhibits outstanding photocatalytic performance toward hydrogen evolution and durable stability in the absence of cocatalyst. The highest photocatalytic hydrogen production rate of g-C 3 N 4 /Au/BiVO 4 was about 410.0 μmol g −1 h −1 , which largely beyond that obtained of g-C 3 N 4 /BiVO 4 (23.3 μmol g −1 h −1 ), Au/g-C 3 N 4 (244.6 μmol g −1 h −1 ) and pristine g-C 3 N 4 (2.2 μmol g −1 h −1 ). The optimal apparent quantum efficiency was counted to be 6.8% at λ = 420 nm and 1.1% at λ = 600 nm. Moreover, the photocatalytic property of g-C 3 N 4 /Au/BiVO 4 could remain unchanged almost with 50 h in 5 cycles. The improvement of photocatalytic H 2 yield is attributed to the result of rapid separation of photogenic carriers in space and surface plasmon resonance effect of Au nanoparticles. In combination of photoelectrochemical measurement, active species capture experiment and electron paramagnetic resonance spectra, the underlying mechanism was illuminated. The pathway of charge carrier migration between semiconductor photocatalysts could be changed to Z-system through Au as an electron intermediate, which could not only benefit to maintain outstanding redox capability but also help to accelerate photo-generated carrier separation, and thus improve the photocatalytic activity .
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