摘要
The efficient exploitation of visible light while optimizing the charge migration of the photocatalysts is a critical strategy to achieve a significant enhancement of solar energy conversion efficiency. Herein, a g-C 3 N 4 /WO 3 (P/W-x%) Z-scheme heterojunction photocatalyst was successfully engineered by incorporating unique WO 3 nanocubes into g-C 3 N 4 nanosheets with n-π* electronic transition (PCN). Under visible light irradiation, the optimized P/W-2 % presents excellent photocatalytic activity with the H 2 production rate of 3.82 mmol h −1 g −1 , which is 13.2 and 3.9 times higher than that of BCN and PCN, respectively. The excellent photocatalytic H 2 production performance is attributed to the n-π* electronic transition of the lone electron of the N atoms in g-C 3 N 4 , which enhances the visible light trapping ability. More importantly, In-situ X-ray photoelectron spectroscopy (ISI-XPS) measurement confirms the transport of photo-generated electrons from WO 3 nanocubes to PCN nanosheets. Consequently, a Z-scheme P/W-2 % heterojunction is proposed based on the flow direction of photogenerated electrons in combination with the energy band structure. It not only promotes the rapid separation and migration of photogenerated carriers, but also enhances the reduction capability. This study provides a valuable design idea to enhance the performance of photocatalytic H 2 production via light absorption and charge dynamics.
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