Issue 43, 2020

Molecular hot spots in surface-enhanced Raman scattering

Abstract

The chemical and electromagnetic (EM) enhancements both contribute to surface-enhanced Raman scattering (SERS). It is well-known that the EM enhancement is induced by the intense local field of surface plasmon resonance (SPR). This report shows that the polarizability of the molecules adsorbed on the metal surface can lead to another channel for the EM field enhancement. When aromatic molecules are covalently bonded to the Au surface, they strongly interact with the plasmon, leading to a modification of the absorption spectrum and a strong SERS signal. The effect is seen in both 3 nm-Au nanoparticles with a weak SPR and 15 nm-Au nanoparticles with a strong SPR, suggesting that the coupling is through both EM field and chemical means. Linear-chain molecules on the 3 nm-Au nanoparticles do not have a SERS signal. However, when the aromatic and linear molecules are co-adsorbed, the strong SPR/molecular polarizability interaction spatially extends the local EM field, leading to a strong SERS signal from the linear-chain molecules. The results show that aromatic molecules immobilized on Au can create “hot spots” just like plasmonic nanostructures.

Graphical abstract: Molecular hot spots in surface-enhanced Raman scattering

Supplementary files

Article information

Article type
Communication
Submitted
12 Ndz 2020
Accepted
23 Nhl 2020
First published
26 Nhl 2020

Nanoscale, 2020,12, 22036-22041

Molecular hot spots in surface-enhanced Raman scattering

M. Li, S. K. Cushing, G. Zhou and N. Wu, Nanoscale, 2020, 12, 22036 DOI: 10.1039/D0NR06579J

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