2008
DOI: 10.1039/b802918k
|View full text |Cite
|
Sign up to set email alerts
|

Plasmon-controlled fluorescence: a new paradigm in fluorescence spectroscopy

Abstract: Fluorescence spectroscopy is widely used in biological research. Until recently, essentially all fluorescence experiments were performed using optical energy which has radiated to the far-field. By far-field we mean at least several wavelengths from the fluorophore, but propagating far-field radiation is usually detected at larger macroscopic distances from the sample. In recent years there has been a growing interest in the interactions of fluorophores with metallic surfaces or particles. Near-field interacti… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

16
649
2
4

Year Published

2009
2009
2017
2017

Publication Types

Select...
4
3

Relationship

0
7

Authors

Journals

citations
Cited by 570 publications
(671 citation statements)
references
References 196 publications
16
649
2
4
Order By: Relevance
“…9-fold decrease in average lifetime suggests that enhancement results from strong interactions between the fluorophore and surface plasmons. [27] In addition, the shorter and longer lifetimes may be attributed respectively to the strongly (bright) and weakly (dim) enhanced regions (Fig. 3c, bottom).…”
mentioning
confidence: 92%
See 3 more Smart Citations
“…9-fold decrease in average lifetime suggests that enhancement results from strong interactions between the fluorophore and surface plasmons. [27] In addition, the shorter and longer lifetimes may be attributed respectively to the strongly (bright) and weakly (dim) enhanced regions (Fig. 3c, bottom).…”
mentioning
confidence: 92%
“…This technique utilizes metallic nanostructures in which the plasmons resonate with the fluorophores to reduce their excited state lifetimes and simultaneously increase their fluorescence emission intensities. [27] Silver island films are often used to meet such a requirement, and the typically ca. 10-fold enhancement has been applied to improve detection of DNA hybridization [28] and immunoassay.…”
mentioning
confidence: 99%
See 2 more Smart Citations
“…In the case of FRET in D−A QD pairs (as in Figure 2a), the emission enhancement factor for the donor and acceptor is given by (details are in Supporting Information: FRET in QDs pair) where γ D(A),exc is the exciton recombination rate of the donor (acceptor) and γ NRET = γ D,exc (R 0 /r) 6 is the Forster-type D−A transfer rate. Here, R 0 is the Forster radius, 27 and r is the separation distance between the D and the A. Parameters used in these calculations are provided in the Supporting Information: Numerical Results.…”
mentioning
confidence: 99%