English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Paper

Molecular polaritonics in dense mesoscopic disordered ensembles

MPS-Authors
/persons/resource/persons223674

Sommer,  Christian
Genes Research Group, Research Groups, Max Planck Institute for the Science of Light, Max Planck Society;

/persons/resource/persons223667

Reitz,  Michael
Genes Research Group, Research Groups, Max Planck Institute for the Science of Light, Max Planck Society;
International Max Planck Research School, Max Planck Institute for the Science of Light, Max Planck Society;

/persons/resource/persons223672

Mineo,  Francesca
International Max Planck Research School, Max Planck Institute for the Science of Light, Max Planck Society;
Genes Research Group, Research Groups, Max Planck Institute for the Science of Light, Max Planck Society;

/persons/resource/persons216190

Genes,  Claudiu
Genes Research Group, Research Groups, Max Planck Institute for the Science of Light, Max Planck Society;

External Resource
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Sommer, C., Reitz, M., Mineo, F., & Genes, C. (2020). Molecular polaritonics in dense mesoscopic disordered ensembles. arXiv: 2010.07155.


Cite as: https://hdl.handle.net/21.11116/0000-0007-4258-C
Abstract
We study the dependence of the vacuum Rabi splitting (VRS) on frequency disorder, vibrations, near-field effects and density in molecular polaritonics. In the mesoscopic limit, static frequency disorder introduces a loss mechanism from polaritonic states into a dark state reservoir, which we
quantitatively describe, providing an analytical scaling of the VRS on the level of disorder. The combination of disorder, vibronic coupling, dipole-dipole interactions and vibrational relaxation induces an incoherent FRET (Forster resonance energy transfer) migration of excitations from
donor-type to acceptor-type molecules within the collective molecular state. This is equivalent to a dissipative disorder and has the effect of saturating and even reducing the VRS in the mesoscopic, high-density limit.