Structural properties and catalytic activity of a novel ternary CuO/gC3N4/Bi2O3 photocatalyst

Hanggara Sudrajat; Sri Hartuti

doi:10.1016/j.jcis.2018.04.020

Structural properties and catalytic activity of a novel ternary CuO/gC₃N₄/Bi₂O₃ photocatalyst

J Colloid Interface Sci. 2018 Aug 15:524:227-235. doi: 10.1016/j.jcis.2018.04.020. Epub 2018 Apr 6.

Authors

Hanggara Sudrajat¹, Sri Hartuti²

Affiliations

¹ Division of Computational Physics, Institute for Computational Science, Ton Duc Thang University, Ho Chi Minh City 70000, Viet Nam; Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City 70000, Viet Nam. Electronic address: hanggara.sudrajat@tdt.edu.vn.
² Department of Environmental and Renewable Energy Systems, Graduate School of Engineering, Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.

PMID: 29655141
DOI: 10.1016/j.jcis.2018.04.020

Abstract

In the present study, CuO/gC₃N₄/Bi₂O₃ composite is constructed as a ternary visible light active photocatalyst. Since CuO plays a critical role in enhancing the photocatalytic activity of the formed composite, its structural properties are particularly studied using synchrotron X-ray absorption spectroscopy (XAS), including X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS). XANES confirms the presence of Cu species with +2 oxidation state in the form of CuO. EXAFS furthermore confirms that each Cu cation is coordinated to four O anions in an approximately square planar configuration. The length of the Cu-O coordination is estimated to be 1.92 Å, slightly shorter than that of bulk CuO (1.95 Å). The CuO/gC₃N₄/Bi₂O₃ composite exhibits highly enhanced photocatalytic activity in the 2,4-dichlorophenol decomposition under visible light. The enhanced photocatalytic activity is due to the increased population of electrons and the successful consumption of the photoproduced electrons by the dissolved oxygen through the one-electron transfer reaction.

Keywords: Bi(2)O(3); CuO; EXAFS; Photocatalysis; XANES.