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Synthesis of Fe3O4/SiO2 nanocomposites via click chemistry and electromagnetic wave absorption properties.

Authors :
Ji, Xiaoli
Qiao, Ruochen
Xu, Zhihao
Liu, Jian
Ma, Qianqian
Yuan, Haoze
Xing, Honglong
Source :
Journal of Materials Science: Materials in Electronics; May2024, Vol. 35 Issue 15, p1-18, 18p
Publication Year :
2024

Abstract

Fe<subscript>3</subscript>O<subscript>4</subscript>/SiO<subscript>2</subscript> nanocomposites (NCs) were prepared by the interaction of alkyne-functionalized ferric oxide (Fe<subscript>3</subscript>O<subscript>4</subscript>-Alk) nanoparticles (NPs) and azide-functionalized silicon dioxide (SiO<subscript>2</subscript>-N<subscript>3</subscript>) NPs via the click reaction. The morphology and structure of the Fe<subscript>3</subscript>O<subscript>4</subscript>/SiO<subscript>2</subscript> NCs were investigated using scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and infrared analyses, and the electromagnetic parameters were measured using a vector network analyzer. For the Fe<subscript>3</subscript>O<subscript>4</subscript>/SiO<subscript>2</subscript> nanocomposites obtained via the click reaction, the minimum reflection loss reached − 37.15 dB at 16.68 GHz and a matching thickness of 5.0 mm, and the bandwidth below − 10 dB ranged from 3.2 to 6.7 GHz and 15.7 to 17.6 GHz. The Fe<subscript>3</subscript>O<subscript>4</subscript>/SiO<subscript>2</subscript> composites synthesized via the click reaction exhibited better microwave absorption performance than the physically blended sample. This is mainly because Fe<subscript>3</subscript>O<subscript>4</subscript> and SiO<subscript>2</subscript> are covalently bonded through the click reaction in the composites, creating multiple heterogeneous interfaces, which enhance dielectric loss and impedance matching. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09574522
Volume :
35
Issue :
15
Database :
Complementary Index
Journal :
Journal of Materials Science: Materials in Electronics
Publication Type :
Academic Journal
Accession number :
177641855
Full Text :
https://doi.org/10.1007/s10854-024-12766-3