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Constructing Bi(24)O(31)Cl(10)/BiOCl heterojunction via a simple thermal annealing route for achieving enhanced photocatalytic activity and selectivity

This work reports on the construction of a Bi(24)O(31)Cl(10)/BiOCl heterojunction via a simple thermal annealing method. The X-ray diffraction (XRD) results indicated that the phase transformation from BiOCl to Bi(24)O(31)Cl(10) could be realized during the thermal annealing process. The high-resolu...

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Detalles Bibliográficos
Autores principales: Liu, Xiaoyan, Su, Yiguo, Zhao, Qihang, Du, Chunfang, Liu, Zhiliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919631/
https://www.ncbi.nlm.nih.gov/pubmed/27340032
http://dx.doi.org/10.1038/srep28689
Descripción
Sumario:This work reports on the construction of a Bi(24)O(31)Cl(10)/BiOCl heterojunction via a simple thermal annealing method. The X-ray diffraction (XRD) results indicated that the phase transformation from BiOCl to Bi(24)O(31)Cl(10) could be realized during the thermal annealing process. The high-resolution transmission electron microscopy (HRTEM) images, X-ray photoelectron spectroscopy (XPS) binding energy shifts, Raman spectra and Fouier transform infrared spectroscopy (FT-IR) spectra confirmed the formation of the Bi(24)O(31)Cl(10)/BiOCl heterojunction. The obtained Bi(24)O(31)Cl(10)/BiOCl photocatalyst showed excellent conversion efficiency and selectivity toward photocatalytic conversion of benzyl alcohol to benzaldehyde under visible light irradiation. The radical scavengers and electron spin resonance (ESR) results suggested that the photogenerated holes were the dominant reactive species responsible for the photocatalytic oxidation of benzyl alcohol and superoxide radicals were not involved in the photocatalytic process. The in-situ generation of Bi(24)O(31)Cl(10)/BiOCl heterojunction may own superior interfacial contact than the two-step synthesized heterojunctions, which promotes the transfer of photogenerated charge carriers and is favorable for excellent photocatalytic activities.