Strong Coupling in Infrared Plasmonic Cavities.

Controlling molecular spectroscopy and even chemical behavior in a cavity environment is a subject of intense experimental and theoretical interest. In Fabry-Pérot cavities, strong (radiation-matter) coupling phenomena without an intense radiation field often rely on the number of chromophore molecules collectively interacting with a cavity mode. For plasmonic cavities, the cavity field-matter coupling can be strong enough to manifest strong coupling involving even a single molecule. To this end, infrared plasmonic cavities can be particularly useful in understanding vibrational strong coupling. Here we present a procedure for estimating the radiation-matter coupling and, equivalently, the mode volume as well as the mode lifetime and quality factor for plasmonic cavities of arbitrary shapes and use it to estimate these quantities for infrared cavities of two particularly relevant geometries comprising several n-doped semiconductors. Our calculations demonstrate very high field confinement and low mode volumes of these cavities despite having relatively low quality factors, which is often the case for plasmonic cavities.

Coupling, lifetimes, and "strong coupling" maps for single molecules at plasmonic interfaces.

The interaction between excited states of a molecule and excited states of a metal nanostructure (e.g., plasmons) leads to hybrid states with modified optical properties. When plasmon resonance is swept through molecular transition frequency, an avoided crossing may be observed, which is often regarded as a signature of strong coupling between plasmons and molecules. Such strong coupling is expected to be realized when 2|⟨U⟩|/â„Γ > 1, where ⟨U⟩ and Γ are the molecule-plasmon coupling and the spectral width of the optical transition, respectively. Because both ⟨U⟩ and Γ strongly increase with decreasing distance between a molecule and a plasmonic structure, it is not obvious that this condition can be satisfied for any molecule-metal surface distance. In this work, we investigate the behavior of ⟨U⟩ and Γ for several geometries. Surprisingly, we find that if the only contributions to Γ are lifetime broadenings associated with the radiative and nonradiative relaxation of a single molecular vibronic transition, including effects on molecular radiative and nonradiative lifetimes induced by the metal, the criterion 2|⟨U⟩|/â„Γ > 1 is easily satisfied by many configurations irrespective of the metal-molecule distance. This implies that the Rabi splitting can be observed in such structures if other sources of broadening are suppressed. Additionally, when the molecule-metal surface distance is varied keeping all other molecular and metal parameters constant, this behavior is mitigated due to the spectral shift associated with the same molecule-plasmon interaction, making the observation of Rabi splitting more challenging.