Issue 9, 2022

Activation of Na2S2O8 by α-Fe2O3/CuS composite oxides for the degradation of Orange II under visible light irradiation

Abstract

Layered α-Fe2O3/CuS nanoflowers with abundant active sites were synthesized by a hydrothermal method. The heterogeneous composite catalyst of α-Fe2O3/CuS nanoflowers exhibited a remarkable degradation capacity of 97.8% within 25 min for the Orange II (OII) dye under visible light, which was attributed to the synergistic effect of Na2S2O8 to generate ˙SO4 and ˙OH radicals. The initial pH tests revealed that this system showed better adaptability for its application in a wider pH range (pH = 3–9). In addition, the degradation of different azo dyes such as methylene blue (MB), Orange G (OG) and malachite green (MG) was also studied under the same conditions. The catalyst was characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) to analyze its size, morphology, valence states of elements and chemical components. α-Fe2O3/CuS was further characterized using a vibrating sample magnetometer (VSM) and diffuse reflectance spectroscopy (DRS) to demonstrate its magnetic properties and light absorption capacity. Moreover, α-Fe2O3/CuS showed good recovery and reuse performance as a catalyst after four repeated cycles. A possible mechanism of degradation was proposed by quenching and ESR experiments, which revealed that the highly active species of ˙SO4, ˙OH and ˙O2 enhanced the photocatalytic performance of the photocatalytic system.

Graphical abstract: Activation of Na2S2O8 by α-Fe2O3/CuS composite oxides for the degradation of Orange II under visible light irradiation

Article information

Article type
Paper
Submitted
13 Nov 2021
Accepted
27 Jan 2022
First published
27 Jan 2022

New J. Chem., 2022,46, 4272-4282

Activation of Na2S2O8 by α-Fe2O3/CuS composite oxides for the degradation of Orange II under visible light irradiation

Y. Lei, H. Wu, J. Ma, H. Cheng and S. Komarneni, New J. Chem., 2022, 46, 4272 DOI: 10.1039/D1NJ05426K

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