Issue 53, 2015

Synthesis and properties of visible light responsive g-C3N4/Bi2O2CO3 layered heterojunction nanocomposites

Abstract

Visible light responsive g-C3N4/Bi2O2CO3 layered heterojunction nanocomposites were prepared by two methods, self-assembly and chemical precipitation. X-ray diffraction (XRD), UV-Vis spectroscopy, N2 adsorption, Scanning electron microscopy (SEM), electrochemical impedance spectra (EIS) and X-ray photoelectron spectroscopy (XPS) were used to characterize the prepared catalysts. The results indicated that the preparation method does not influence the crystal phase, morphology and optical property of the obtained nanocomposites, but affects the interaction strength between g-C3N4 and Bi2O2CO3, leading to an obvious difference in the separation rate of photogenerated electrons and holes. The activities were tested in photocatalytic rhodamine B (RhB) and phenol degradation under visible light. The g-C3N4/Bi2O2CO3 nanocomposite with a stronger interaction showed the better activity. The ˙O2 radicals are responsible for the degradation of RhB. No obvious decrease in activity was observed for g-C3N4/Bi2O2CO3 nanocomposites prepared by the self-assembly method after three cycles. The significant enhancement of the photocatalytic activity was attributed to the high charge-separation efficiency due to the hybrid effect of RhB, Bi2O2CO3 and g-C3N4. The self assembly method assisted by CTAB leads to tight decoration of Bi2O2CO3 nanoparticles on g-C3N4 sheets facilitating intimate contact and formation of a stable heterojunction.

Graphical abstract: Synthesis and properties of visible light responsive g-C3N4/Bi2O2CO3 layered heterojunction nanocomposites

Supplementary files

Article information

Article type
Paper
Submitted
10 Mar 2015
Accepted
07 May 2015
First published
08 May 2015

RSC Adv., 2015,5, 42736-42743

Synthesis and properties of visible light responsive g-C3N4/Bi2O2CO3 layered heterojunction nanocomposites

Q. Zhang, H. Wang, S. Hu, G. Lu, J. Bai, X. Kang, D. Liu and J. Gui, RSC Adv., 2015, 5, 42736 DOI: 10.1039/C5RA04189A

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