Nanostructure design for surface-enhanced Raman spectroscopy -prospects and limits

Abstract

Surface-enhanced Raman spectroscopy (SERS) allows single-molecule detection due to the strong field localization occurring at sharp bends or kinks of the metal-vacuum interface. An important question concerns the limits of the signal enhancement that can be achieved via a judicious design of the surface. By using a specific example of a technologically realizable nanopatterned surface, we demonstrate that while very high enhancement factors (≈ 1012) can be found for an ideal surface, these are unlikely to be achieved in laboratory samples, because even a minute, inevitable rounding-off strongly suppresses the enhancement, as well as shifts the optimal frequency. Our simulations indicate that the geometric enhancement factors are unlikely to exceed ≈ 108 for real samples, and that it is necessary to consider the geometric uncertainty to reliably predict the frequency for maximum enhancement.