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-Pérot 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 allow 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 Rabi splitting from 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.
Highlights
Strong coupling of molecular vibrational modes to optical cavities has been explored increasingly in recent years as an avenue to modify the intrinsic vibrational response of molecular systems and, thereby, the chemical properties associated with the vibrating bond.[1,2,3,4,5] When molecules are inside an optical cavity, the two systems can coherently exchange radiative energy if the frequency of the cavity resonance is tuned to the molecular vibrational mode
We demonstrate that the plasmonic substrate provides strong coupling with the C==O vibrational stretch of deposited films of PMMA
We show that the large linewidths of the plasmon resonance allow 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
Summary
Strong coupling of molecular vibrational modes to optical (infrared) cavities has been explored increasingly in recent years as an avenue to modify the intrinsic vibrational response of molecular systems and, thereby, the chemical properties associated with the vibrating bond.[1,2,3,4,5] When molecules are inside an optical cavity, the two systems can coherently exchange radiative energy if the frequency of the cavity resonance is tuned to the molecular vibrational mode. By establishing this spectral design feature, we hypothesized that our system would demonstrate similar Rabi splitting as described in prior work.[19,24,27,49] due to the angle-independent resonance, nearly 100% of the molecules within the optical near-field could strongly couple to the plasmonic substrate, regardless of molecular orientation.
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