Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2010
Title: Plasmofluidic single-molecule surface-enhanced Raman scattering from dynamic assembly of plasmonic nanoparticles
Authors: Patra, Partha Pratim
Chikkaraddy, Rohit
TRIPATHI, RAVI P. N.
Dasgupta, Arindam
KUMAR, G. V. PAVAN
Dept. of Physics
Keywords: Plasmofluidic
Raman scattering
Plasmonic nanoparticles
Optical excitation
Combining plasmonic
Raman scattered
2014
Issue Date: Jul-2014
Publisher: Nature Publishing Group
Citation: Nature Communications, 5, 4357.
Abstract: Single-molecule surface-enhanced Raman scattering (SM-SERS) is one of the vital applications of plasmonic nanoparticles. The SM-SERS sensitivity critically depends on plasmonic hot-spots created at the vicinity of such nanoparticles. In conventional fluid-phase SM-SERS experiments, plasmonic hot-spots are facilitated by chemical aggregation of nanoparticles. Such aggregation is usually irreversible, and hence, nanoparticles cannot be re-dispersed in the fluid for further use. Here, we show how to combine SM-SERS with plasmon polariton-assisted, reversible assembly of plasmonic nanoparticles at an unstructured metal–fluid interface. One of the unique features of our method is that we use a single evanescent-wave optical excitation for nanoparticle assembly, manipulation and SM-SERS measurements. Furthermore, by utilizing dual excitation of plasmons at metal–fluid interface, we create interacting assemblies of metal nanoparticles, which may be further harnessed in dynamic lithography of dispersed nanostructures. Our work will have implications in realizing optically addressable, plasmofluidic, single-molecule detection platforms.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2010
https://doi.org/10.1038/ncomms5357
ISSN: 2041-1723
Appears in Collections:JOURNAL ARTICLES

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.