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We report the synthetic methodology for silver nanorings with controlled nanoscale morphology. The morphology of Ag nanorings was kinetically controlled by electrochemical potential tuning of Ag deposition using halide counter-ions, which resulted in concentric PtAu@Ag nanorings (i.e., Ag homogeneously wrapped around the Pt nanorings) and eccentric PtAu@Ag nanorings (i.e., Ag selectively deposited at the inner boundary of the Pt nanorings). The resulting high quality of each Ag nanoring allowed us to systematically investigate their corresponding localized surface plasmon resonance (LSPR) profiles as a function of their geometrical parameters. Additionally, we evaluated the application of the samples as surface-enhanced Raman spectroscopy (SERS) substrates composed of 2D monolayers of varied compositions of Ag and Au nanorings, which showed a different extent of enhancement depending on the adsorption characteristics of the analytes. [ABSTRACT FROM AUTHOR]

The development of a stepwise synthetic strategy for Au ring-in-a-triangle nanoframes with a high degree of structural solidity is essential to the advancement of highly amplified near-field focusing. This strategy leads to the formation of an inscribed nanoring in a triangular metal frame with stability to withstand elevated temperatures and an oxidizing environment, which is critical for successful single-particle surface-enhanced Raman scattering (SERS). The existence of inscribed nanorings plays an important role in enhancing the so-called "lightning rod effect," whereby the electromagnetic near-field enhancement occurs on the highly curved curvature of a metallic interface. We evaluated the corresponding single-particle SERS as a function of the thickness of the rims and then constructed two-dimensional (2D) bulk SERS substrates, wherein an ensemble of hotspots exists. The synergic contribution from both inter- and intrahotspots allowed the outstanding linearity of the calibration curve and the lowest limit of detection, ∼10 -18 M for the analyte concentration.

We designed complex Au nanorings with intertwined triple rings (ANITs) in a single entity to amplify the efficacy of near-field focusing. Such a complex and unprecedented morphology at the nanoscale was realized through on-demand multistepwise reactions. Triangular nanoprisms were first sculpted into circular nanorings, followed by a series of chemical etching and deposition reactions eventually leading to ANITs wherein thin metal bridges hold the structure together without any linker molecules. In the multistepwise reaction, the well-faceted growth pattern of Au, which induces the growth of two distinctive flat facets in a lateral direction, is important to evolve the morphology from single to multiple nanorings. Although our synthesis proceeds through multiple steps in one batch without purification steps, it shows a remarkably high yield (>∼90%) at the final stage. The obtained high degree of homogeneity (in both shape and size) of the resulting ANITs allowed us to systematically investigate the corresponding localized surface plasmon resonance (LSPR) coupling with varying nanoring arrangements and observe their single-particle surface enhanced Raman scattering (SERS). Surprisingly, individual ANITs exhibited an enormously large enhancement factor (∼10 9 ), which confirms their superior near-field focusing relative to other reported nanoparticles.