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Springer eBooks

The Signature of a Single Molecule

Partha Pratim Mondal, Samuel Hess

Published Jan 1, 2026• 0 citations
Publisher
DOI
10.1007/978-3-032-13442-4_8

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Strong light-matter coupling offers exciting opportunities for controlling molecular properties, yet resolving single-molecule behavior from collective effects remains a challenge. Recent experiments in scanning tunneling microscope break junctions (STM-BJs) have demonstrated strong light-matter coupling at the single-molecule level. Because STM-BJs provide direct access to molecular-junction currents, we investigate whether strong coupling leaves a measurable fingerprint in transport, potentially probing polaritonic states beyond optical spectroscopy. Using a semiclassical mapping approach for nonequilibrium quantum transport, we find that steady-state current indeed carries a direct signature of single-molecule strong coupling. We test the robustness of this signature against electrode connectivity, nuclear motion, spatially structured electromagnetic modes, and solvent effects. While environmental factors and nuclear motion reshape the signature, the current is not a passive response but is actively influenced by coupled molecular dynamics. Our work establishes current as a tool to interpret and control strong light-matter interactions in nanoscale junctions.

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Strong light-matter coupling offers exciting opportunities for controlling molecular properties, yet resolving single-molecule behavior from collective effects remains a challenge. Recent experiments in scanning tunneling microscope break junctions (STM-BJs) have demonstrated strong light-matter coupling at the single-molecule level. Because STM-BJs provide direct access to molecular-junction currents, we investigate whether strong coupling leaves a measurable fingerprint in transport, potentially probing polaritonic states beyond optical spectroscopy. Using a semiclassical mapping approach for nonequilibrium quantum transport, we find that steady-state current indeed carries a direct signature of single-molecule strong coupling. We test the robustness of this signature against electrode connectivity, nuclear motion, spatially structured electromagnetic modes, and solvent effects. While environmental factors and nuclear motion reshape the signature, the current is not a passive response but is actively influenced by coupled molecular dynamics. Our work establishes current as a tool to interpret and control strong light-matter interactions in nanoscale junctions.
We built an interferometer where one of the two slits of a classical Young's setup is replaced by a single molecule embedded in a solid matrix. This enabled direct measurement of the first order coherence of the 0-0 single-molecule emission, which at high excitation powers proves to be split in coherent and incoherent parts. We demonstrate an order of magnitude higher precision in axial localization of single molecules in comparison with that of confocal microscopy. These experiments open a possibility for single-molecule holography. Detection of single molecules with low luminescence quantum yields could be another application of this technique.