Multiferroic properties of NiFe2O4-Ba0.7Ca0.3TiO3 nanocomposites

In this report, we present results on the multiferroic properties of four nanocomposite samples of NiFe2O4-Ba0.7Ca0.3TiO3 (NFO/BCTO), which were fabricated through combinations of high-energy ball milling, heat treatment, and spark plasma sintering techniques. Structural analyses revealed that these...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Advances in natural sciences. Nanoscience and nanotechnology 2024-09, Vol.15 (3), p.035003
Hauptverfasser: Giang, Tran Thi Ha, Thi Viet Chinh, Nguyen, Lam, Dao Son, Linh, Dinh Chi, Nam, Pham Hong, Bach, Ta Ngoc, Long, Nguyen The, Manh, Do Hung, Dung, Dang Duc, Toan, Huynh Ngoc, Poddubnaya, N N, Thanh, Tran Dang
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:In this report, we present results on the multiferroic properties of four nanocomposite samples of NiFe2O4-Ba0.7Ca0.3TiO3 (NFO/BCTO), which were fabricated through combinations of high-energy ball milling, heat treatment, and spark plasma sintering techniques. Structural analyses revealed that these samples simultaneously contain two phases of nano-sized NiFe2O4 (NFO) and Ba0.7Ca0.3TiO3 (BCTO) crystals. The addition of NFO into the BCTO-host did not alter the crystal structure but significantly improved the multiferroic characteristics compared to pure BCTO. Furthermore, variations in saturation magnetization (Ms) and coercivity (Hc) were investigated as a function of temperature. The results showed that Ms increased gradually with the concentration of NFO. In terms of temperature dependence, Ms(T) data deviated from the Bloch’s law with an exponent coefficient α changing in the range of 1.8–1.9, decreasing gradually as the NFO concentration increased. Meanwhile, Hc decreased gradually as the NFO concentration increased and followed the Kneller’s law in terms of temperature dependence.
ISSN:2043-6254
2043-6262
DOI:10.1088/2043-6262/ad6b7c