摘要
Semiconductor photocatalytic organic reactions have garnered extensive interest owing to their environmentally friendly and sustainable advantages. Herein, the preparation of Ag 2 S@CdS p-n heterojunction through in-situ ion exchange reaction for photocatalytic benzylamine coupling is reported. Compared with pure CdS, Ag 2 S@CdS exhibited significantly enhanced photocatalytic activity for the oxidative coupling reaction of benzylamine. In particular, Ag 2 S@CdS showed high photocatalytic benzylamine conversion (>99 %) after 90 min under sunlight irradiation. The photocatalytic performance test at different wavelengths shows that the broadening of the light absorption range of Ag 2 S@CdS effectively improves the utilization of visible light. The photoelectric performance test demonstrates that the internal electric field of the p-n heterojunction effectively enhances the efficiency of separating photogenerated carriers. Moreover, Ag 2 S@CdS exhibited excellent compatibility with various benzylamine derivatives. The mechanism of photocatalytic benzylamine oxidation by Ag 2 S@CdS was investigated. This work provides some insights into the design of visible-light photocatalysts for selective organic synthesis.
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