Issue 44, 2015

Sandwich-structured Fe2O3@SiO2@Au nanoparticles with magnetoplasmonic responses

Abstract

We report a method for the fabrication of relatively uniform sandwich-like core-interlayer-shell nanostructures by using γ-Fe2O3 as the inner core, SiO2 as the interlayer, and relatively uniform gold (Au) as the outer shell. The resulting novel hybrid nanoparticle combines the intense local fields of nanorods with the highly tunable plasmon resonances of nanoshells. The length and diameter of the resulting nanoparticles can be tuned by the aspect ratio of α-Fe2O3, the interlayer of SiO2 and the outer layer of Au. After calcination under H2 and then exposure to air, α-Fe2O3 was transformed into γ-Fe2O3, which provides the hybrid particle magnetic tunability. This metal oxide (γ-Fe2O3) dielectric core, the SiO2 interlayer and the Au shell spindle nanoparticle resemble a grain of Au nanorice (γ-Fe2O3@SiO2@Au ellipsoids). The core-interlayer-shell geometry possesses greater structural and magnetic tunability than a nanorod or a nanoshell. The plasmon resonance of this novel γ-Fe2O3@SiO2@Au geometry is believed to arise from a hybridization of the primitive plasmons of an ellipsoidal cavity inside a continuous Au shell. The unique magnetoplasmonic properties of this γ-Fe2O3@SiO2@Au nanostructure are highly attractive for applications such as surface plasmon resonance sensing because of the dipole resonance of the resultant nanostructure and recyclable catalysts arising from the outer Au layer and the inner magnetic γ-Fe2O3 core.

Graphical abstract: Sandwich-structured Fe2O3@SiO2@Au nanoparticles with magnetoplasmonic responses

Supplementary files

Article information

Article type
Paper
Submitted
05 May 2015
Accepted
09 Oct 2015
First published
09 Oct 2015

J. Mater. Chem. C, 2015,3, 11645-11652

Author version available

Sandwich-structured Fe2O3@SiO2@Au nanoparticles with magnetoplasmonic responses

Z. Cai, E. S. P. Leong, Z. Wang, W. Niu, W. Zhang, S. Ravaine, N. L. Yakovlev, Y. J. Liu, J. Teng and X. Lu, J. Mater. Chem. C, 2015, 3, 11645 DOI: 10.1039/C5TC01259G

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