V2O5-Fe3O4/rGO Ternary Nanocomposite with Dual Applications as a Dye Degradation Photocatalyst and OER Electrocatalyst.
ACS Omega
; 8(38): 35427-35439, 2023 Sep 26.
Article
em En
| MEDLINE
| ID: mdl-37779947
The design and synthesis of structured nanomaterials with dual properties have always been highly attractive in various fields, especially in the reduction of environmental pollution as well as the generation of renewable energy. In this study, the synthesized ternary V2O5-Fe3O4/rGO nanocomposite was investigated to evaluate both the photocatalytic and electrocatalytic activities for the removal of methylene blue (MB) dye under UV/visible light radiation and oxygen evolution reaction (OER), respectively. The magnetized V2O5-Fe3O4/rGO nanocomposite is characterized by TEM, FE-SEM (with coupling by elemental mapping), EDS, XRD, FTIR, Raman, PL, DRS, and UV-vis analyses. The obtained results show that the graphene oxide substrate is decorated very well using Fe3O4 and V2O5 nanoparticles and converted to reduced graphene oxide (rGO). Furthermore, the V2O5-Fe3O4/rGO nanocomposite is considered as an active catalyst material to modify the commercial glassy carbon electrode for OER using linear sweep voltammetry (LSV). The photocatalytic activity of this novel nanocomposite revealed 89.2% (kobs = 1.7 × 10-2 min-1) and 76% (kobs = 8.3 × 10-3 min-1) degradation efficiencies of MB dye under UV and visible light irradiation at room temperature, respectively, and the surface area of the V2O5-Fe3O4/rGO nanocomposite was examined to be 705.8 cm2/g by N2 adsorption-desorption isotherms. In addition, electrochemical measurements determined the best OER performance of the ternary nanocomposite with the lowest overpotential (458 mV) and Tafel slope (132 mV dec-1) compared to the rGO substrate, Fe3O4, V2O5 nanoparticles, and binary nanocomposites. This work shows much enhancements in both photocatalytic and electrocatalytic activities due to the synergistic effect of the decorated GO support with V2O5 and Fe3O4 nanoparticles.
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MEDLINE
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En
Ano de publicação:
2023
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Article