Abstract

It is vital for environment purification to design and prepare an artificial photocatalyst that can effectively separate photogenerated carriers and maintain the redox ability of system. In this paper, a g-C3N4/BiOI/Bi2O2CO3 photocatalyst was rationally designed and successfully prepared via two-step in-situ transforming process. The results of X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, energy dispersive X-ray analysis, and transmission electron microscopy confirm the successful synthesis of ternary g-C3N4/BiOI/Bi2O2CO3 catalysts. The photocatalytic activities of all catalysts were assessed by the degradation of Rhodamine B (RhB) under simulated sunlight illumination. The g-C3N4/BiOI/Bi2O2CO3 catalysts showed much higher photocatalytic activities than single g-C3N4, or BiOI and dual g-C3N4/BiOI. The results of electron spin resonance and active species trapping experiments revealed that h+ and •O2− were responsible for the photodegradation of RhB, and a possible photogenerated carrier transport mechanism was proposed.

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