Magnetic recyclable α-Fe2O3-Fe3O4/Co3O4-CoO nanocomposite with a dual Z-scheme charge transfer pathway for quick photo-Fenton degradation of organic pollutants

Khaled Alkanad, Abdo Hezam, G. C. Sujay Shekar, Q. A. Drmosh, A. L. Amrutha Kala, Murad Q.A. Al-Gunaid, N. K. Lokanath*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

The integration of multiple degradation pathways in a single catalyst is a potential approach to advance the technologies of organic pollutant degradation. To integrate both the heterogeneous photo-Fenton reaction and Z-scheme configuration in a single catalyst, a novel magnetic separable α-Fe2O3-Fe3O4/Co3O4-CoO nanocomposite enriched with oxygen vacancies is fabricated via the solution combustion method by optimizing the fuel and nitrate ion concentration. The Z-scheme configuration along with oxygen vacancies contributes to in situ H2O2 generation and simultaneous reactivation with high H2O2 performance, which is required for the photo-Fenton process. Oxygen vacancies facilitate the charge carrier transfer in the Z-scheme system and promote interfacial electronic transmission involved in the redox cycle from CoIII/FeIII to CoII/FeII, inducing the generation of O2-, 1O2, SO4- and OH radicals. Consequently, the transcendental catalyst exhibits excellent photo-Fenton photocatalytic features facilitating highly improved pollutant degradation under sunlight irradiation and Fenton reaction promoting the degradation in the dark as well. The photodegradation rate is enhanced 5.33 times and 3.6 times in the presence of H2O2 and persulfate, respectively. This study opens the possibility of designing a single catalyst with different degradation mechanisms.

Original languageEnglish
Pages (from-to)3084-3097
Number of pages14
JournalCatalysis Science and Technology
Volume11
Issue number9
DOIs
StatePublished - 7 May 2021

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry.

ASJC Scopus subject areas

  • Catalysis

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