Sonophotocatalytic degradation of methylene blue with magnetically separable Zn-Doped-CoFe2O4/α-Fe2O3 heterostructures

This work reports an approach of highly active sonophotocatalysts through the combined Zn-doping and heterojunction of CoFe 2 O 4 /α-Fe 2 O 3 heterostructures. The novelty lies in the combined Zn-doping and α-Fe 2 O 3 coupling strategy to tune the electronic structure and enhance charge separation o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of materials science. Materials in electronics 2024-03, Vol.35 (7), p.520, Article 520
Hauptverfasser: Shuaibov, Abdulatip O., Abdurakhmanov, Magomed G., Magomedova, Asiyat G., Omelyanchik, Alexander, Salnikov, Vitalii, Aga-Tagieva, Sayara, Rodionova, Valeria, Rabadanov, Murtazali Kh, Orudzhev, Farid F.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:This work reports an approach of highly active sonophotocatalysts through the combined Zn-doping and heterojunction of CoFe 2 O 4 /α-Fe 2 O 3 heterostructures. The novelty lies in the combined Zn-doping and α-Fe 2 O 3 coupling strategy to tune the electronic structure and enhance charge separation of spinel-based magnetic nanocatalyst. A sol–gel auto-combustion method was used to synthesize Zn 0.3 Co 0.7 Fe 2 O 4 nanoparticles with ~12% α-Fe 2 O 3 content. The Zn-doping increased the magnetization saturation from ~65 to 86 emu/g and narrowed the optical bandgap from ~1.48 to 1.62 eV compared to undoped CoFe 2 O 4 , indicating a modified electronic structure. Under sonophotocatalysis, near complete methylene blue decomposition was achieved in 45 min for both catalysts, with a 30% synergistic effect observed. The Zn-doping also activated the semiconductor photocatalysis mechanism. The combined Zn-doping and heterojunction approach enables highly active sonophotocatalysts to effectively degrade dye pollutants and mitigate water pollution.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-024-12252-w