TY - JOUR
T1 - Tri-layer Co@CoxFe1− x @Fe@Fe3O4thorny core–shell composite particles and their electromagnetic absorption properties
AU - Li, Hong
AU - Li, Hongyang
AU - Wang, Ran
AU - Zeng, Shentao
AU - Xie, Ruiling
AU - Luo, Cui
AU - Liu, Ying
N1 - Publisher Copyright:
This journal is © the Partner Organisations, 2026
PY - 2026/1/5
Y1 - 2026/1/5
N2 - By the combination of chemical liquid-phase reduction, in situ self-oxidation and thermal treatment, tri-layer Co@CoxFe1−x@Fe@Fe3O4 thorny core–shell composite magnetic particles were synthesized, and their microstructure, static magnetic properties, and electromagnetic wave absorption performance were investigated. Results show that the tri-layer Co@CoxF1−x@Fe@Fe3O4 thorny particles largely retained the morphology of thorny Co@Fe@Fe3O4 particles, but some particles are aggregated, resulting in an increase in the particle size. The tri-layer Co@CoxF1−x@Fe@Fe3O4 thorny particles exhibit a typical core–shell structure with an internal core and 200–300 nm thick external coating. The center of the particle contains Co, while the outer layer comprises Fe and O. With heat treatment, a discernible transition phase of CoFe and Co7Fe3 was formed at the Co/Fe interface. With the increase in self-oxidation temperature, the specific saturation magnetization of the Co@CoxF1−x@Fe@Fe3O4 particles exhibits a slight increase before a downward trend, while the coercivity decreases slightly and then increases. At an oxidation temperature of 70 °C, the tri-layer Co@CoxFe1−x@Fe@Fe3O4 thorny particle samples exhibit optimal absorption performance, with a minimum reflection loss of −24.42 dB at a coating thickness of 1.6 mm and a maximum effective absorption bandwidth of 4.80 GHz.
AB - By the combination of chemical liquid-phase reduction, in situ self-oxidation and thermal treatment, tri-layer Co@CoxFe1−x@Fe@Fe3O4 thorny core–shell composite magnetic particles were synthesized, and their microstructure, static magnetic properties, and electromagnetic wave absorption performance were investigated. Results show that the tri-layer Co@CoxF1−x@Fe@Fe3O4 thorny particles largely retained the morphology of thorny Co@Fe@Fe3O4 particles, but some particles are aggregated, resulting in an increase in the particle size. The tri-layer Co@CoxF1−x@Fe@Fe3O4 thorny particles exhibit a typical core–shell structure with an internal core and 200–300 nm thick external coating. The center of the particle contains Co, while the outer layer comprises Fe and O. With heat treatment, a discernible transition phase of CoFe and Co7Fe3 was formed at the Co/Fe interface. With the increase in self-oxidation temperature, the specific saturation magnetization of the Co@CoxF1−x@Fe@Fe3O4 particles exhibits a slight increase before a downward trend, while the coercivity decreases slightly and then increases. At an oxidation temperature of 70 °C, the tri-layer Co@CoxFe1−x@Fe@Fe3O4 thorny particle samples exhibit optimal absorption performance, with a minimum reflection loss of −24.42 dB at a coating thickness of 1.6 mm and a maximum effective absorption bandwidth of 4.80 GHz.
UR - https://www.scopus.com/pages/publications/105022688344
U2 - 10.1039/d5qm00489f
DO - 10.1039/d5qm00489f
M3 - Article
AN - SCOPUS:105022688344
SN - 2052-1537
VL - 10
SP - 100
EP - 111
JO - Materials Chemistry Frontiers
JF - Materials Chemistry Frontiers
IS - 1
ER -