Abstract

Efficient substrates for surface-enhanced Raman spectroscopy (SERS) are under constant development, since time-consuming and costly fabrication routines are often an issue for high-throughput spectroscopy applications. In this research, we use a two-step fabrication method to produce self-organized parallel-oriented plasmonic gold nanostructures. The fabrication routine is ready for wafer-scale production involving only low-energy ion beam irradiation and metal deposition. The optical spectroscopy features of the resulting structures show a successful bidirectional plasmonic response. The localized surface plasmon resonances (LSPRs) of each direction are independent from each other and can be tuned by the fabrication parameters. This ability to tune the LSPR characteristics allows the development of optimized plasmonic nanostructures to match different laser excitations and optical transitions for any arbitrary analyte. Moreover, in this study, we probe the polarization and wavelength dependence of such bidirectional plasmonic nanostructures by a complementary spectroscopic ellipsometry and Raman spectroscopy analysis. We observe a significant signal amplification by the SERS substrates and determine enhancement factors of over a thousand times. We also perform finite element method-based calculations of the electromagnetic enhancement for the SERS signal provided by the plasmonic nanostructures. The calculations are based on realistic models constructed using the same particle sizes and shapes experimentally determined by scanning electron microscopy. The spatial distribution of electric field enhancement shows some dispersion in the LSPR, which is a direct consequence of the semi-random distribution of hotspots. The signal enhancement is highly efficient, making our SERS substrates attractive candidates for high-throughput chemical sensing applications in which directionality, chemical stability, and large-scale fabrication are essential requirements.

Highlights

  • Raman spectroscopy is a well-established method in a wide eld of chemical sensing applications.[1]

  • We show that the position of the localized surface plasmon resonance (LSPR) depends on the gold nanoparticle geometry, which allows tuning the localized surface plasmon resonances (LSPRs) from the visible (VIS) to the near-infrared (NIR) spectral range

  • Until know we presented the development of LSPR and SERS enhancement for different gold thicknesses deposited on rippled templates

Read more

Summary

Introduction

Self-assembled SERS systems with bidirectionally excitable LSPRs offer a strategy to overcome this limitation. Noble metal nanoparticle chains on rippled templates have the potential for SERS with bidirectional independent tuneable LSPRs.[13,28,29,30] It is understandable that SERS substrates that are plasmonically active under multiple excitation wavelengths have signi cant potential for multipurpose chemical and biochemical sensing applications. This kind of SERS structures can be produced at a largescale with a two-step fabrication routine. We visualize the plasmonic hotspots by the nite element method (FEM) simulations using the exact nanoparticle size, geometry, and con guration experimentally determined from the SEM and TEM analysis

Sample fabrication
Morphological characterization
Optical characterization and Raman spectroscopy
Results
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call