Structural characterization of cuboidal α-Fe2O3 nanoparticles synthesized by a facile approach

α-Fe 2 O 3 nanoparticles were synthesized using Tabebuia aurea leaf extract by a facile approach. The signature peaks for Fe and O in the EDX spectrum verified the formation of Fe 2 O 3 nanoparticles. Cuboidal-shaped nanoparticles were observed in the FE-SEM image. In the XRD pattern, it was observe...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied nanoscience 2023-08, Vol.13 (8), p.5605-5613
Hauptverfasser: Sridevi, H., Bhat, M. Ramananda, Kumar, P. Senthil, Kumar, N. Manoj, Selvaraj, Raja
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:α-Fe 2 O 3 nanoparticles were synthesized using Tabebuia aurea leaf extract by a facile approach. The signature peaks for Fe and O in the EDX spectrum verified the formation of Fe 2 O 3 nanoparticles. Cuboidal-shaped nanoparticles were observed in the FE-SEM image. In the XRD pattern, it was observed that the peaks belong to α-Fe 2 O 3 nanoparticles. These particles were pure and crystalline with an average particle size of 25.69 nm. The signals at 538 and 494 cm −1 in the FTIR image confirmed the formation of hematite nanoparticles. BET analysis showed a comparatively greater surface area (31.03 m 2 /g) than the commercial α-Fe 2 O 3 nanoparticles, and the pores were mesoporous. XPS analysis confirmed the existence of α-Fe 2 O 3 by showing the specific oxidation states for iron and oxygen at 710.34 and 529.67 eV, respectively. The saturation magnetization value of 13.97 emu/g confirmed the superparamagnetic nature. The TGA, which determined the thermal stability of the nanoparticles, reported a total weight loss of 12.75%. Hence, the highly crystalline, pure, mesoporous, superparamagnetic α-Fe 2 O 3 nanoparticles with high surface area synthesized using T. aurea leaf extract can be potentially applied in diverse fields.
ISSN:2190-5509
2190-5517
DOI:10.1007/s13204-023-02780-y