Abstract

Realization of Fano resonance in plasmonic oligomers is often exploited to design efficient plasmonic substrates for surface-enhanced coherent anti-Stokes Raman scattering. Disk-type Fano-resonant plasmonic oligomers are widely used to enhance the Raman signal of the probe material. Generally, hot spots are generated in those oligomers at different spatial locations at different wavelengths and only a few spatially overlapping hot spots at multiple wavelengths can be achieved with oblique incidence of excitation light. In this work, we proposed hexagonal gold nanoparticle based Fano-resonant plasmonic oligomers that can yield higher number of spatially overlapped hot spots compared to the disk type oligomers even with the normal incidence of excitation light. The oligomers were numerically modelled and optimized for surface-enhanced coherent anti-Stokes Raman scattering with 780 nm pumping and 500–1800 cm− 1 Raman signature region. The Fano lineshape was engineered to ensure near-field energy coupling at pump while enhancing the coherent anti-Stokes Raman signal at the far field. Our computational studies explored the purely electric origin of Fano resonance in those oligomers and provided maximum Raman enhancements of 1012–1013 from them to enable single-molecular level applications. Our findings provide a way to realize fabrication-friendly nanostructures with higher number of spatially localized hotspots for improving the Raman detection sensitivity.

Highlights

  • The ability of Raman spectroscopy (RS) to provide accurate chemical ‘fingerprint’ of probed material [1,2,3] enables its utilization as a powerful analytical tool in different scientific and industrial fields [4, 5]

  • We achieved to engineer the lineshape of the Fano resonance (FR) in those oligomers so that the sub-radiant mode of FR would spectrally overlap with the pump to ensure energy coupling between the excitation light and the nanostructures while the super-radiant modes of FR would tune with the Stokes and coherent anti-Stokes Raman scattering (CARS) regimes to enhance far-field propagation of the output light

  • Our estimated Surface-enhanced CARS (SECARS) enhancements from the proposed oligomers were in the order of 1012–1013, which meet the requirement of single molecular level applications

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Summary

Introduction

The ability of Raman spectroscopy (RS) to provide accurate chemical ‘fingerprint’ of probed material [1,2,3] enables its utilization as a powerful analytical tool in different scientific and industrial fields [4, 5]. Biosensing at nanoscale [13,14,15] and single molecule detection [16,17,18,19] become realizable nowadays with the suitable application of SERS. Another approach of strengthening the Raman signal is coherent anti-Stokes Raman scattering (CARS) where the Raman response is amplified with the help of a nonlinear optical four-wave mixing (FWM) process, instead of a plasmonic substrate [20,21,22,23,24,25,26,27]. In CARS, two laser beams, the so-called pump (ωp) and Stokes (ωs), are focused into a sample and its molecular vibration

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