Angle-Independent Plasmonic Substrates for Multi-Mode Vibrational Strong Coupling with Molecular Thin Films

TL;DR

This paper introduces an angle-independent plasmonic nanodisk substrate capable of simultaneously strongly coupling with multiple vibrational modes in molecular thin films, overcoming orientation limitations of traditional cavities and enabling advanced chemical manipulation.

Contribution

The study presents a novel angle-independent plasmonic substrate that achieves multi-mode vibrational strong coupling regardless of molecular orientation, with tunable plasmon resonance via nanodisk diameter.

Findings

Strong coupling with C=O vibrational stretch of PMMA.

Simultaneous strong coupling to water vibrational modes.

Tunable plasmon resonance through nanodisk diameter.

Abstract

Vibrational strong coupling of molecules to optical cavities based on plasmonic resonances has been explored recently, because plasmonic near-fields can provide strong coupling in sub-diffraction limited volumes. Such field localization maximizes coupling strength, which is crucial for modifying the vibrational response of molecules and, thereby, manipulating chemical reactions. Here, we demonstrate an angle-independent plasmonic nanodisk substrate that overcomes limitations of traditional Fabry-Perot optical cavities, because the design can strongly couple with all molecules on the surface of the substrate regardless of molecular orientation. We demonstrate that the plasmonic substrate provides strong coupling with the C=O vibrational stretch of deposited films of PMMA. We also show that the large linewidths of the plasmon resonance allows for simultaneous strong coupling to two, orthogonal water symmetric and asymmetric vibrational modes in a thin film of copper sulfate monohydrate deposited on the substrate surface. A three-coupled-oscillator model is developed to analyze the coupling strength of the plasmon resonance with these two water modes. With precise control over the nanodisk diameter, the plasmon resonance is tuned systematically through the modes, with the coupling strength to both modes varying as a function of the plasmon frequency, and with strong coupling to both modes achieved simultaneously for a range of diameters. This work may aid further studies into manipulation of the ground-state chemical landscape of molecules by perturbing multiple vibrational modes simultaneously and increasing the coupling strength in sub-diffraction limited volumes.