Ca-induced changes in the crystal structure and magnetic properties of barium hexaferrite
Ca-doped barium hexaferrite (Ba 1− x Ca x Fe 12 O 19; x = 0.1–0.6) samples were synthesized successfully using solid-state reaction route. Further, the limit of the Ca solubility in BaFe 12 O 19 has been investigated in the 900–1200°C temperature range. X-ray analysis reveals maximum Ca solubility i...
Gespeichert in:
Veröffentlicht in: | Bulletin of materials science 2023-09, Vol.46 (4), p.196, Article 196 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Ca-doped barium hexaferrite (Ba
1−
x
Ca
x
Fe
12
O
19;
x
= 0.1–0.6) samples were synthesized successfully using solid-state reaction route. Further, the limit of the Ca solubility in BaFe
12
O
19
has been investigated in the 900–1200°C temperature range. X-ray analysis reveals maximum Ca solubility in BFO at 1200°C (≈50%). The emergence of a hematite secondary phase at Ca concentrations ≈50 and 60 at% was observed. The XRD analysis also confirmed a gradual reduction in the
c
-parameter from 23.195 Å (at
x
= 0.1) to 23.147 Å (at
x
= 0.5). The structural data further suggested an enhancement of sample density with Ca substitution. Field-emission transmission electron microscopy micrographs reveal (a) distinct grain morphology at lower Ca concentration (
x
= 0.1) and (b) enhanced secondary grain growth and grain amalgamation at higher Ca concentration (
x
= 0.5). The
M–H
studies reveal that
M
r
and
M
s
almost stay constant up to
x
= 0.2, beyond which they start rising rapidly.
M
r
≈ 42.65 emu g
−1
and
M
s
≈ 92.19 emu g
−1
, exhibit a maximum at
x
= 0.4. The coercivity first decreases rapidly from 4168 Oe (at
x
= 0.0) to 2326 Oe (at
x
= 0.1) followed by a marginal decrease to 2045 Oe (at
x
= 0.4). An
H
c
value ≥1200 Oe in a majority of our samples makes them potentially suitable for perpendicular recording media and permanent magnet applications. |
---|---|
ISSN: | 0973-7669 0250-4707 0973-7669 |
DOI: | 10.1007/s12034-023-03031-0 |