Fabrication and magnetic-induced aggregation of Fe^sub 3^O^sub 4^-noble metal composites for superior SERS performances
Fe^sub 3^O^sub 4^-noble metal composites were obtained by combining Au, Ag nanoparticles (NPs) with 3-aminopropyltrimethoxysilane-functionalized Fe^sub 3^O^sub 4^ NPs. UV-Visible absorption spectroscopy demonstrates the obtained Fe^sub 3^O^sub 4^ -noble metal composites inherit the typical surface p...
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Veröffentlicht in: | Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2013-11, Vol.15 (11), p.1 |
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Sprache: | eng |
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Zusammenfassung: | Fe^sub 3^O^sub 4^-noble metal composites were obtained by combining Au, Ag nanoparticles (NPs) with 3-aminopropyltrimethoxysilane-functionalized Fe^sub 3^O^sub 4^ NPs. UV-Visible absorption spectroscopy demonstrates the obtained Fe^sub 3^O^sub 4^ -noble metal composites inherit the typical surface plasmon resonance bands of Au, Ag at 533 and 453 nm, respectively. Magnetic measurements also indicated that the superparamagnetic Fe^sub 3^O^sub 4^ -noble metal composites have excellent magnetic response behavior. A magnetic-induced idea was introduced to change their aggregated states and take full advantage of their surface-enhanced Raman scattering (SERS) performances. Under the induction of an external magnetic field, the bifunctional Fe^sub 3^O^sub 4^ -noble metal aggregates exhibit the unique superiority in SERS detection of Rhodamine 6G (R6G), compared with the naturally dispersed Au, Ag NPs. Especially, the detection limit of the Fe^sub 3^O^sub 4^-Ag aggregates for R6G is as low as 10^sup -14^ M, and the calculated EF reaches up to 1.2 × 10^sup 6^, which meets the requirements for trace detection of analytes. Furthermore, the superiority could be extended to sensitive detection of other organic molecules, such as 4-mercaptopyridine. This work provides a new insight for active adjustment of the aggregated states of SERS substrates and the optimization of SERS performances.[PUBLICATION ABSTRACT] |
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ISSN: | 1388-0764 1572-896X |
DOI: | 10.1007/s11051-013-1954-1 |