We have investigated the dynamics of strongly coupled modes of surface plasmon polaritons (SPPs) and fluorescent molecules by analyzing their scattered emission polarization. While the scattered emission of SPPs is purely transverse magnetic (TM) polarized, the strong coupling with molecules induces transverse electric (TE) polarized emission via the partial molecular nature of the formed SPP–molecule polariton mode. We observe that the TM/TE ratio of the polariton emission follows the contribution of the molecular excited states in this hybrid mode. By using several types of molecules, we observe that, in addition to the coupling strength, which determines the contribution of the molecular excited states, also the Stokes shift of the molecule fluorescence influences the polarization of the emission: the larger the shift, the lower the TE-polarized emission. We argue that due to random orientation of the molecules, the emission of a fully coherent SPP–molecule polariton should be purely TM-polarized, like SPP. However, as a result of the unique microenvironments of the molecules in combination with thermal motion, this symmetry may break for individual excitations, providing a route to TE emission. The experimental results agree qualitatively with this model, including the symmetry breaking. Furthermore, the relaxation rate of the polariton correlates with the Stokes shift, so that TE emission can occur only if the Stokes shift is small and consequently the lifetime is long. Our results suggest that taking into account microscopic details of the molecules in SPP–molecule polaritons is important for a thorough understanding of the molecular dynamics of molecules under strong coupling with light modes. Theoretical models that include these details will be essential to systematically exploit strong coupling for plasmonics or even controlling chemical reactions.

We demonstrate a strong coupling between surface plasmon polaritons and Sulforhodamine 101 dye molecules. Dispersion curves for surface plasmon polaritons on samples with a thin layer of silver covered with Sulforhodamine 101 molecules embedded in SU-8 polymer are obtained experimentally by reflectometry measurements and compared to the dispersion of samples without molecules. Clear Rabi splittings, with energies up to 360 and 190 meV, are observed at the positions of the dye absorption maxima. The split energies are dependent on the number of Sulforhodamine 101 molecules involved in the coupling process. Transfer matrix and coupled oscillator methods are used to model the studied multilayer structures with a great agreement with the experiments. Detection of the scattered radiation after the propagation provides another way to obtain the dispersion relation of the surface plasmon polaritons and, thus, provides insight into dynamics of the surface plasmon polariton/dye interaction, beyond the refrectometry measurements.PACS: 42.50.Hz, 33.80.-b, 78.67.-n

In this article we experimentally demonstrate the strong coupling between surface plasmon polaritons (SPP) and the S 2 state of β-carotene. The SPPs are excited by prism coupling technique on a thin silver film with β-carotene embedded in a polymer layer on top of that. Rabi splittings with energies 80 and 130 meV are observed in the recorded dispersion relations. Both coupled oscillator model and transfer matrix method are used to fit the experimental results. The scattered radiation of the propagating strongly coupled SPP-S 2 hybrids is collected and an increase of the low energy splitting to 120 meV is observed compared to the reflectivity data. In addition, we performed molecule excitation by laser and analyzed the emission patterns revealing clear surface plasmon coupled fluorescence of β-carotene. By increasing the concentration of β-carotene we are able to collect also surface plasmon coupled Raman scattering. This study substantially extends the SPP-molecular excitation strong coupling studies to biomolecules, and energy transfer and coupling properties of excited states of carotenoids.

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