Core-shell of FePt@SiO2-Au magnetic nanoparticles for rapid SERS detection
In this study, multifunctional hybrid nanoparticles composed of iron platinum (FePt), silica (SiO 2 ), and gold nanoparticles (AuNPs) had been developed for surface-enhanced Raman scattering (SERS) application. Core-shell structure of SiO 2 and FePt nanoparticles (FePt@SiO 2 ) was fabricated through...
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Published in | Nanoscale research letters Vol. 10; no. 1; p. 412 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.12.2015
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | In this study, multifunctional hybrid nanoparticles composed of iron platinum (FePt), silica (SiO
2
), and gold nanoparticles (AuNPs) had been developed for surface-enhanced Raman scattering (SERS) application. Core-shell structure of SiO
2
and FePt nanoparticles (FePt@SiO
2
) was fabricated through sol-gel process and then immobilized gold nanoparticles onto the surface of FePt@SiO
2
, which displays huge Raman enhancement effect and magnetic separation capability. The resulting core-shell nanoparticles were subject to evaluation by transmission electron microscopy (TEM), Energy-dispersive X-ray spectroscopy (EDX), zeta potential measurement, and X-ray photoelectron spectroscopy (XPS). TEM observation revealed that the particle size of resultant nanoparticles displayed spherical structure with the size ~30 nm and further proved the successful immobilization of Au onto the surface of FePt@SiO
2
. Zeta potential measurement exhibited the successful reaction between FePt@SiO
2
and AuNPs. The rapid SERS detection and identification of small biomolecules (adenine) and microorganisms (gram-positive bacteria,
Staphylococcus aureus
) was conducted through Raman spectroscopy. In summary, the novel core-shell magnetic nanoparticles could be anticipated to apply in the rapid magnetic separation under the external magnetic field due to the core of the FePt superparamagnetic nanoparticles and label-free SERS bio-sensing of biomolecules and bacteria. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1931-7573 1556-276X |
DOI: | 10.1186/s11671-015-1111-0 |