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Chinese Journal of Materials Research  2026, Vol. 40 Issue (4): 254-262    DOI: 10.11901/1005.3093.2025.269
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Preparation and Microwave Absorption Properties of Core/Shell Structured FeSiBCuNbZr@SiO2 Amorphous Composites
HUANG Shiha1, DONG Xinglong1(), PEI Leizhen1, ZHANG Xingguo1,2
1.School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024, China
2.Ningbo Institute of Dalian University of Technology, Ningbo 315016, China
Cite this article: 

HUANG Shiha, DONG Xinglong, PEI Leizhen, ZHANG Xingguo. Preparation and Microwave Absorption Properties of Core/Shell Structured FeSiBCuNbZr@SiO2 Amorphous Composites. Chinese Journal of Materials Research, 2026, 40(4): 254-262.

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Abstract  

FeSiBCuNbZr@SiO2 amorphous composite was prepared by single roller melt-spinning, mechanical ball milling and sol-gel method. The microstructure, phase composition, morphology, and electromagnetic properties of the composite were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, and vector network analysis. The influence of the matching thickness of SiO2 dielectric layer on the wave absorption performance of FeSiBCuNbZr amorphous composite powder was studied. The results indicate that the optimal reflection loss of the amorphous composite powder, obtained from FeSiBCuNbZr amorphous powder and the SiO2 dielectric layer generated by the hydrolysis and polycondensation of 5 mL tetraethyl orthosilicate is -58.19 dB at 11.2 GHz with a matching thickness of 2.18 mm. When the matching thickness is reduced to 1.85 mm, the maximum effective absorption bandwidth reaches 7.7 GHz. The excellent microwave absorption properties may be attributed to the synergistic effect between the magnetic loss from the Fe-based amorphous core and the dielectric loss from the SiO2 shell, which collectively optimize the impedance matching.

Key words:  composites      microwave absorbing materials      sol-gel method      core-shell structure      amorphous powder      SiO2 shell layer     
Received:  04 September 2025     
ZTFLH:  TB332  
Fund: National Nature Science Foundation of China(51331006)
Corresponding Authors:  DONG Xinglong, Tel: (0411)84706130, E-mail: dongxl@dlut.edu.cn

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https://www.cjmr.org/EN/10.11901/1005.3093.2025.269     OR     https://www.cjmr.org/EN/Y2026/V40/I4/254

Fig.1  XRD patterns of FeSiBCuNbZr amorphous powder before and after chemical coating
Fig.2  FTIR spectra of FeSiBCuNbZr amorphous powder before and after chemical coating
Fig.3  XPS spectra of FeSiBCuNbZr@SiO2 composite powders prepared by hydrolysis of TEOS at different concentrations (a) survey, (b) C 1s, (c) Si 2p, (d) O 1s
Fig.4  SEM and TEM images of FeSiBCuNbZr@SiO2 composite powders prepared by hydrolysis of TEOS at different concentrations (a) S0, (b) S1, (c) S2, (d) S3, (e) EDS mappings of S1, (f) TEM image of S2, (g) HRTEM, (h) SEAD
Fig.5  Two-dimensional and three-dimensional reflection loss curves of S0 (a, e), S1 (b, f), S2 (c, g) and S3 (d, h)
SampleRLmin / dBMatching thickness / mmMatching frequency / GHzEAB / GHzRef.
FeSiCr@SiO2-65.33.344.46[4]
FeNi@SiO2-36.252.696[5]
Co particle@SiO2-15.022.8914.042.89[17]
Carbonyl iron powder@SiO2-15.32.213.765.72[18]
FeSiAl@Al2O3@SiO2-46.29216.937.33[19]
Fe3O4@SiO2-38.7284[20]
Bead-like Co@SiO2-23.44184.3[21]
CoNi@SiO2-23.82.19.6-[22]
FeN@SiO2-23.15.517.22.4[23]
FeSiBCuNbZr amorphous@SiO2-58.192.1811.27.7This work
Table 1  Electromagnetic wave absorption performance of magnetic metal@SiO2 composites reported in the literature
Fig.6  Real part of permittivity ε(a), imaginary part of permittivity ε″ (b), tangent angle of dielectric loss tanδε (c), real part of permeability μ(d), imaginary part of permeability μ(e) and tangent angle of magnetic loss tanδμ (f) for samples
Fig.7  Cole-Cole curves of S0 (a), S1 (b), S2 (c) and S3 (d)
Fig.8  C0 values of S0, S1, S2 and S3 in the range of 2-18 GHz
Fig.9  Impedance matching for the S0 (a), S1 (b), S2 (c) and S3 (d)
Fig.10  Attenuation constants (α) of S0, S1, S2 and S3 samples in the range of 2-18 GHz
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