Back to Search Start Over

One-pot synthesis of CoFe2O4/graphene oxide hybrids and their conversion into FeCo/graphene hybrids for lightweight and highly efficient microwave absorber.

Authors :
Li, Xinghua
Feng, Juan
Du, Yaping
Bai, Jintao
Fan, Haiming
Zhang, Haoli
Peng, Yong
Li, Fashen
Source :
Journal of Materials Chemistry A; 2015, Vol. 3 Issue 10, p5535-5546, 12p
Publication Year :
2015

Abstract

CoFe<subscript>2</subscript>O<subscript>4</subscript>/graphene oxide hybrids have been successfully fabricated via a facile one-pot polyol route, followed by chemical conversion into FeCo/graphene hybrids under H<subscript>2</subscript>/NH<subscript>3</subscript> atmosphere. These magnetic nanocrystals were uniformly decorated on the entire graphene nanosheets without aggregation. The morphology, chemical composition and crystal structure have been characterized in detail. In particular, FeCo/graphene hybrids show significant improvement in both permeability and permittivity due to the combination of the high magnetocrystalline anisotropy of metallic FeCo and high conductivity of light-weight graphene. This leads to remarkable enhancement in microwave absorption properties. The maximum reflection loss of FeCo/graphene hybrids reaches −40.2 dB at 8.9 GHz with a matching thickness of only 2.5 mm, and the absorption bandwidth with reflection loss exceeding −10 dB is in the 3.4–18 GHz range for the absorber thickness of only 1.5–5 mm. Moreover, the experimental relationship between matching thickness and frequency is found to obey the quarter-wavelength matching model, facilitating the design of FeCo/graphene hybrid film for practical application. The results suggest that the FeCo/graphene hybrids developed here can serve as an ideal candidate for the manufacture of light-weight and high-efficiency microwave-absorbing devices. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20507488
Volume :
3
Issue :
10
Database :
Complementary Index
Journal :
Journal of Materials Chemistry A
Publication Type :
Academic Journal
Accession number :
101195671
Full Text :
https://doi.org/10.1039/c4ta05718j