SERS表面增强拉曼

Surface-enhanced Raman spectroscopy

From Wikipedia, the free encyclopedia

(Redirected from Surface-enhanced Raman scattering)

Raman spectrum of liquid 2-mercaptoethanol (below) and SERS spectrum of 2-mercaptoethanol monolayer formed on roughened silver (above). Spectra are scaled and shifted for clarity. A difference in selection rules is visible: Some bands appear only in the bulk-phase Raman spectrum or only in the SERS spectrum.

Surface-enhanced Raman spectroscopy or surface-enhanced Raman scattering (SERS) is a surface-sensitive technique that enhances Raman

scattering by molecules adsorbed on rough metal surfaces or by nanostructures such as plasmonic-magnetic silica nanotubes.[1] The enhancement factor can be as much as 1010 to 1011,[2][3] which means the technique may detect single molecules.[4][5]

Contents

[hide]

•1History

•2Mechanisms

o 2.1Electromagnetic theory

o 2.2Chemical theory

•3Surfaces

•4Applications

o 4.1Oligonucleotide targeting

•5Selection rules

•6References

History[edit]

SERS from pyridine adsorbed on electrochemically roughened silver was first observed by Martin Fleischmann, Patrick J. Hendra and A. James McQuillan at the Department of Chemistry at the University of Southampton, Southampton, UK in 1973.[6] This initial publication has been cited over 4000 times. The 40th Anniversary of the first observation of the SERS effect has been marked by the Royal Society of Chemistry by the award of a National Chemical Landmark plaque to the University of Southampton. In 1977, two groups independently noted that the concentration of scattering species could not account for the enhanced signal and each proposed a mechanism for the observed enhancement. Their theories are still accepted as explaining the SERS effect. Jeanmaire and Van Duyne[7] proposed an electromagnetic effect, while Albrecht and Creighton[8] proposed a charge-transfer effect. Rufus Ritchie, of Oak Ridge National Laboratory's Health Sciences Research Division, predicted the existence of the surface plasmon.[9]

Mechanisms[edit]

The exact mechanism of the enhancement effect of SERS is still a matter of debate in the literature. There are two primary theories and while their mechanisms differ substantially, distinguishing them experimentally has not been straightforward.

The electromagnetic theory proposes the excitation of localized surface plasmons, while the chemical theory proposes the formation of charge-transfer complexes. The chemical theory applies only for species that have formed a chemical bond with the surface, so it cannot explain the observed signal enhancement in all cases, whereas the electromagnetic theory can apply even in those cases where the specimen

is physisorbed only to the surface. It has been shown recently that SERS enhancement can occur even when an excited molecule is relatively far apart from the surface which hosts metallic nanoparticles enabling surface plasmon phenomena.[10] This observation provides a strong support for the electromagnetic theory of SERS. Research in 2015 on a more powerful extension of the SERS technique called SLIPSERS (Slippery

Liquid-Infused Porous SERS)[11] has further supported the EM theory.[12] Electromagnetic theory[edit]

The increase in intensity of the Raman signal for adsorbates on particular surfaces occurs because of an enhancement in the electric field provided by the surface. When the incident light in the experiment strikes the surface, localized surface plasmons are excited. The field enhancement is greatest when the plasmon frequency, ωp, is in resonance with the radiation. In order for scattering to occur, the plasmon oscillations must be perpendicular to the surface; if they are in-plane with the surface, no scattering will occur. It is because of this requirement that roughened surfaces or arrangements

of nanoparticles are typically employed in SERS experiments as these surfaces provide an area on which these localized collective oscillations can occur.[13]

The light incident on the surface can excite a variety of phenomena in the surface, yet the complexity of this situation can be minimized by surfaces with features much smaller than