Loading…
Structural, spectral, magnetic, and electrical properties of Gd–Co-co-substituted M-type Ca–Sr hexaferrites synthesized by the ceramic method
Gd–Co-co-substituted M-type Ca–Sr hexaferrites with nominal compositions Ca 0.40 Sr 0.60− x Gd x Fe 12.00− x Co x O 19 (0.00 ≤ x ≤ 0.32) were prepared using the standard ceramic method. The particle size of obtained hexaferrite powders is between 2 and 5 µm. These hexaferrites were characterized b...
Saved in:
Published in: | Applied physics. A, Materials science & processing Materials science & processing, 2019, Vol.125 (1), p.1-13, Article 37 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Gd–Co-co-substituted M-type Ca–Sr hexaferrites with nominal compositions Ca
0.40
Sr
0.60−
x
Gd
x
Fe
12.00−
x
Co
x
O
19
(0.00 ≤
x
≤ 0.32) were prepared using the standard ceramic method. The particle size of obtained hexaferrite powders is between 2 and 5 µm. These hexaferrites were characterized by thermal analyzer (TG-DSC), X-ray diffractometer (XRD), Fourier transformer infrared (FT-IR) spectroscopy, field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), vibrating sample magnetometer (VSM), and resistivity testing system. XRD patterns showed that the single M-type hexaferrite phase was obtained only if Gd–Co content (
x
) ≤ 0.16. FE-SEM micrographs indicated that the grains were platelet-like shapes. The saturation magnetization (
M
s
) and remanent magnetization (
M
r
) decreased with increasing Gd–Co content (
x
) from 0.00 to 0.32. The coercivity (
H
c
) first increased with Gd–Co content (
x
) from 0.00 to 0.24, and then decreased when Gd–Co content (
x
) ≥ 0.24. The DC electrical resistivity decreased with increasing Gd–Co content (
x
) from 0.00 to 0.32. |
---|---|
ISSN: | 0947-8396 1432-0630 |
DOI: | 10.1007/s00339-018-2339-1 |