Article
Towards multiple readout application of plasmonic arrays.
Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich-Schiller-University Jena, Helmholtzweg 4, 07743 Jena, Germany.
Beilstein Journal of Nanotechnology (impact factor:
0.79).
01/2011;
2:501-8.
DOI:10.3762/bjnano.2.54
pp.501-8
Source: PubMed
- Citations (2)
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Cited In (0)
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Article: Surface enhanced Raman scattering (SERS) by molecules adsorbed at spherical particles: errata.
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ABSTRACT: A model for Raman scattering by a molecule adsorbed at the surface of a spherical particle is articulated by treating the molecule as a classical electric dipole. This follows Moskovits's suggestion [J. Chem. Phys. 69, 4159 (1978)] and the experiments by Creighton et al. [J. Chem. Soc. Faraday Trans. II, 75, 790 (1979)] that such a system may exhibit SERS similar to that at roughened electrode surfaces. The molecule is stimulated by a primary field comprised of the incident and near-scattered fields. Emission consists of the dipole field plus a scattered field, each at the shifted frequency. Addition of feedback terms between the dipole and the particle makes only a negligible contribution to the fields. For pyridine adsorbed at the surface of a silver sphere, the 1010-cm(-1) band is enhanced by ~10(6) if the radius is much less than the wavelengths and the excitation wavelength is ~382 nm, a wavelength for which the relative refractive index of silver is close to m = radical2i. Detailed results are given for the effect upon the angular distribution and the polarization of the Raman emission of particle size, distance from the surface, excitation wavelength, and location of the molecule upon the surface. These results simulate those observed at roughened silver electrodes and suggest that the mechanism of SERS at those electrodes may resemble the electromagnetic mechanism elucidated here. We predict that comparable effects should be observed for fluorescent scattering.Applied Optics 12/1980; 19(24):4159-74. · 1.41 Impact Factor -
Article: Dependence of fluorescence intensity on the spectral overlap between fluorophores and plasmon resonant single silver nanoparticles.
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ABSTRACT: We investigate the fluorescence from dyes coupled to individual DNA-functionalized metal nanoparticles. We use single-particle darkfield scattering and fluorescence microscopy to correlate the fluorescence intensity of the dyes with the localized surface plasmon resonance (LSPR) spectra of the individual metal nanoparticles to which they are attached. For each of three different dyes, we observe a strong correlation between the fluorescence intensity of the dye and the degree of spectral overlap with the plasmon resonance of the nanoparticle. On average, we observe the brightest fluorescence from dyes attached to metal nanoparticles that have a LSPR scattering peak approximately 40-120 meV higher in energy than the emission peak of the fluorophore. These results should prove useful for understanding and optimizing metal-enhanced fluorescence.Nano Letters 04/2007; 7(3):690-6. · 13.20 Impact Factor
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Keywords
advantages
bioanalytics
careful adjustment
different distances
DNA detection scheme
efficient SERS enhancement
fabrication
flexible use
fluorescent molecules
metallic surface
nanostructured gold surface
open
optical behavior
plasmonic arrays
SERS
specific Raman fingerprint
surface-enhanced Raman spectroscopy
unique design
various gold nanostructured arrays