ENHANCED PHOTOCATALYTIC PROPERTIES OF MnOx CO-CATALYTIC MODIFIED ZnO NANOSTRUCTURED FILMS FOR ORGANIC DYE DEGRADATION

Authors

  • Dobrina Ivanova Laboratory of Nanoparticle Science and Technology Department of General and Inorganic Chemistry Faculty of Chemistry and Pharmacy, University of Sofia
  • Silviya Simeonova Laboratory of Atomic Force Microscopy Department of Physical Chemistry, Faculty of Chemistry and Pharmacy University of Sofia
  • Nina Kaneva Laboratory of Nanoparticle Science and Technology Department of General and Inorganic Chemistry Faculty of Chemistry and Pharmacy, University of Sofia

DOI:

https://doi.org/10.59957/jctm.v59.i2.2024.13

Keywords:

co-catalytic modification, UV, sol-gel films, Reactive Black 5.

Abstract

This work aims to enhance the photocatalytic activity of ZnO films for persistent organic pollutants. The photocatalysis method has gained significant interest as a sustainable and environmentally friendly approach to enhance the safety of clean water by eliminating persistent organic pollutants. Zinc oxide as a transition metal oxide is recognized as a highly effective material for photocatalysis. Even so, ZnO can be modified to increase its action and result in a more significant degradation of organic pollutants. In the photocatalytic process, an electron from the valence band is excited and moves to a higher energy level, the conduction band. Thus, an electron-hole
pair is formed. Unstoichiometry transition metal oxides, such as MnOx are hole-trapping co-catalysts that promote oxidation processes.
This research reported the sol-gel synthesis of ZnO nanostructured films co-catalytic modified with MnOx for organic dye degradation. The confirmed features of ZnO/MnOx films are characterized by different analytical tools such as atomic force microscopy (AFM), X-ray diffraction analysis (XRD) and UV-Vis spectroscopy. The surface of the zinc oxide revealed a hexagonal wurtzite structure and a visible ganglia-like pattern. MnOx co-catalytic modification plays a vital role in the percent degradation of the organic dye under UV-irradiation conditions. 

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Published

2024-01-03

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Section

Articles