ABSTRACT
The photocatalytic reduction of Cr6+ to Cr3+ in an aqueous solution, using 3 wt% Ag/g-C3N4 in the presence of ethylenediaminetetraacetic acid (EDTA), has been investigated here. The photocatalytic reduction of Cr6+ with pure g-C3N4 was very low. The addition of Ag and EDTA can significantly improve the photocatalytic reduction of Cr6+ using g-C3N4. In the presence of EDTA, the efficiency with Ag/g-C3N4 was better than those with Au/g-C3N4 and Cu/g-C3N4. With EDTA, the reduction rate constant increased from 0.0005 for pure g-C3N4 to 0.12 min−1 for 3 wt% Ag/g-C3N4. By increasing the concentration of EDTA from 0 to 500 mg L−1, the reduction efficiency of Cr6+ increased extremely, and the rate constant raised from 0.008 to 0.12 min−1. The optimal EDTA concentration was 500 mg L−1 for the photocatalyst Ag/g-C3N4. The Ag-EDTA complex may be reduced to metallic silver by the conduction band electrons of g-C3N4. The electron–hole recombination was significantly suppressed by the electron trapping of Ag. EDTA may act in by the formation of Cr3+-complex and the separation of Cr3+ from the g-C3N4 surface and by the valence band hole scavenger of g-C3N4. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), UV–Vis diffuse reflectance spectroscopy (DRS) and photoluminescence spectra (PL) were used to characterize g-C3N4 and Ag/g-C3N4 nanoparticles. A possible mechanism for photocatalytic Cr6+ reduction has also been demonstrated.
GRAPHICAL ABSTRACT
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No potential conflict of interest was reported by the author(s).
Data availability statement
The authors confirm that the data supporting the findings of this study are available within the article and its supplementary material. Raw data that supports the findings of this study are available from the corresponding author, upon reasonable request.