Raman Scattering Enhancements Due to Super- and Subradiant Collective Plasmon Modes on Large-Area 2D-Au Arrays.

Ordered metal nanoparticle (MNP) arrays with ultrasmall interparticle gaps exhibit strong enhancement of the electromagnetic (EM) near-field, known as hotspots, for surface-enhanced Raman spectroscopy (SERS) sensing. These arrays, with uniform gap sizes, are also essential for studying nonlinear Raman scattering effects and surface selection rules. Optical characterization of the fabricated large-area Au arrays with ≪ , where is the MNP radius, revealed the excitation of hybridized-collective plasmon modes with giant EM near-field enhancement. We found that the SERS enhancement associated with a subradiant plasmon mode depends primarily on the interparticle gap distance , rather than on the ordering of MNPs into arrays. However, arranging MNPs in the form of arrays influenced the far-field scattering of the super-radiant mode excited at a longer wavelength, resulting in lower but highly anisotropic SERS enhancements that depend on the far-field excitation polarization angle σ. This study on ordered MNP arrays with ultrasmall interparticle gaps ≪ highlights the roles of S and MNP ordering in SERS enhancement of an analyte. This understanding is pivotal for designing SERS substrates with very small interparticle gaps, as they generate a large number of intense and well-distributed SERS hotspots. Furthermore, an anisotropy-induced SERS dichroism effect was observed. Polarization-dependent SERS intensities varied based on the excitation wavelength λ and its corresponding Stokes wavelength positions related to the excited plasmon mode. As a result, the SERS dichroism of lower-frequency Stokes-shifted peaks exhibited a cos(σ) dependence, whereas higher-frequency Stokes-shifted peaks exhibited a sin(σ) dependence. This observation validates the EM near-field mechanism of SERS. The fabricated large-area 2D-Au arrays meet most of the essential requirements for efficient, robust, and reliable large-area SERS sensing.