Strong Exciton-Photon Coupling in a Nanographene Filled Microcavity
arXiv:1709.04499 · doi:10.1021/acs.nanolett.7b02211
Abstract
Dibenzo[\emph{hi,st}]ovalene (DBOV) - a quasi-zero-dimensional `nanographene' - displays strong, narrow, and well-defined optical-absorption transitions at room temperature. On placing a DBOV-doped polymer film into an optical microcavity, we demonstrate strong coupling of the \textbf{0 0'} electronic and \textbf{0 1'} vibrational transitions to a confined cavity mode, with coupling energies of 104 meV and 40 meV, respectively. Photoluminescence measurements indicate that the polariton population is distributed between the lower and middle polariton branches at energies approximately coincident with the emission of the DBOV, indicating polariton population via an optical pumping mechanism.
arXiv commentA peer reviewed, updated and corrected version of this article appears in Nano Letters
References in corpus (9)
- Energy Band Gap Engineering of Graphene Nanoribbons
- Biased bilayer graphene: semiconductor with a gap tunable by electric field effect
- Strong light-matter coupling in two-dimensional atomic crystals
- Microcavity-integrated graphene photodetector
- Quantum-fluid dynamics of microcavity polaritons
- Light-matter interaction in a microcavity-controlled graphene transistor
- Semiconducting graphene from highly ordered substrate interactions
- Microscopic Theory of Polariton Lasing via Vibronically Assisted Scattering
- Exciton-phonon scattering and photo-excitation dynamics in J-aggregate microcavities
Cited by in corpus (4)
- Pump-Push-Probe for Ultrafast All-Optical Switching: The Case of a Nanographene Molecule
- Strong coupling between magnons confined in a single magnonic cavity
- Conformational Control of Exciton-Polariton Physics in Metal - Poly(9,9-dioctylfluorene) - Metal Cavities
- Chiral Flat-Band Optical Cavity with Atomically Thin Mirrors