Angle-Independent Plasmonic Substrates for Multi-Mode Vibrational Strong Coupling with Molecular Thin Films
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Date
2021-03-09
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Citation of Original Publication
Zachary T. Brawley, S. David Storm, Diego A. Contreras Mora, Matthew Pelton, and Matthew Sheldon, "Angle-independent plasmonic substrates for multi-mode vibrational strong coupling with molecular thin films", J. Chem. Phys. 154, 104305 (2021) https://doi.org/10.1063/5.0039195
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Attribution 4.0 International (CC BY 4.0)
Attribution 4.0 International (CC BY 4.0)
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Abstract
Strong vibrational 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 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.