Spectral correlation between surface-enhanced resonant Raman and far field scattering destructed by dipole quadrupole coupled plasmon resonance
arXiv:2207.02513 · doi:10.1021/acs.jpcc.3c00106
Abstract
The spectral relationships between surface enhanced resonant Raman scattering (SERRS) and plasmon resonance observed in far field scattering cross are investigated using single silver nanoparticle dimers with focusing on the lowest energy (superradiant) plasmon resonance. We find that these relationships can be classified into two types. The first is SERRS spectral envelopes with spectral shapes similar to those of plasmon resonance spectra. The second is SERRS envelopes exhibiting higher energy shifts from the plasmon resonance spectra. These results are examined as an effect of degree of morphological asymmetry in dimers based on an electromagnetic (EM) mechanism. The analysis of the first and second types reveals that dipole-dipole and dipole-quadrupole coupled plasmon resonance (subradiant Fano resonance) respectively determine the EM enhancement. This mechanism is commonly important for the development of plasmonic nanostructures for various surface enhanced spectroscopies.
43 pages, 15 figures
References in corpus (3)
- Surface-enhanced Raman scattering and fluorescence near metal nanoparticles
- Absorption cross-section spectroscopy of single strong coupling system between plasmon and molecular exciton resonance using single silver nanoparticle dimer generating surface enhanced resonant Raman scattering
- Propagation mechanism of surface-enhanced resonant Raman scattering light through one-dimensional plasmonic hotspot along silver nanowire dimer junction
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- Plasmon-enhanced two photon excited emission from edges of one-dimensional plasmonic hotspots with continuous-wave laser excitation
- Ultrabroad resonance of localized plasmon on a nanoparticle coupled with surface plasmon on a nanowire enabling two-photon excited emission via continuous-wave laser
- Electromagnetic coupling between subradiant plasmons and dye molecular excitons analyzed by spectral changes in ultrafast surface-enhanced fluorescence