Abstract

Abstract Enhancing the circular dichroism signals of chiral plasmonic nanostructures is vital for realizing miniaturized functional chiroptical devices, such as ultrathin wave plates and high-performance chiral biosensors. Rationally assembling individual plasmonic metamolecules into coupled nanoclusters or periodic arrays provides an extra degree of freedom to effectively manipulate and leverage the intrinsic circular dichroism of the constituent structures. Here, we show that sophisticated manipulation over the geometric parameters of a plasmonic stereo-metamolecule array enables selective excitation of its surface lattice resonance mode either by left- or right-handed circularly polarized incidence through diffraction coupling, which can significantly amplify the differential absorption and hence the intrinsic circular dichroism. In particular, since the diffraction coupling requires no index-matching condition and its handedness can be switched by manipulating the refractive index of either the superstrate or the substrate, it is therefore possible to achieve dynamic tuning and active control of the intrinsic circular dichroism response without the need of modifying structure parameters. Our proposed system provides a versatile platform for ultrasensitive chiral plasmonics biosensing and light field manipulation.

Highlights

  • Circular dichroism (CD) characterized by the differential absorption of left-handed (LCP) and right-handed circularly polarized (RCP) light is an intrinsic property of chiral compounds, which provides a powerful spectroscopy tool for structural and conformational analyses of complex biomolecules [1, 2]

  • We investigate the chiroptical response of a plasmonic stereo-metamolecule array and show that the CD resonance strength can be significantly leveraged by selectively exciting surface lattice resonance (SLR) modes

  • We have shown that the excitation of SLRs can significantly enhance the chiroptical response of plasmonic metamaterials up to 10 times, with a maximum of CD around 0.7

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Summary

Introduction

Circular dichroism (CD) characterized by the differential absorption of left-handed (LCP) and right-handed circularly polarized (RCP) light is an intrinsic property of chiral compounds, which provides a powerful spectroscopy tool for structural and conformational analyses of complex biomolecules [1, 2]. The extraordinary CD responses of plasmonic chiral nanostructures have gained considerable attention, where the excitation of localized surface plasmon resonances (LSPRs) significantly enhances the light-structure interaction strength due to their extremely large dipole moments, and the generated CD signals are orders of magnitude larger than that of natural compounds [9,10,11,12,13,14,15,16,17]. Strong intrinsic CD responses have been observed in threedimensional plasmonic helixes [20,21,22,23,24,25,26,27,28,29,30], spirals [31,32,33], nanopillars [34], twisted nanoparticles (e. g., split-ring resonators (SRRs) [35, 36], gammadions [37], arcs [38], and

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