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This research demonstrates that quadruply bonded Mo₂ molecules function as intrinsic emitter-resonator systems capable of trapping photons in free space without external cavities. By exhibiting vacuum Rabi splitting under ambient conditions, the study bridges molecular physics with quantum electrodynamics, offering a new platform for scalable quantum optical experiments using standard spectroscopic tools.
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Quadruply Bonded Mo2 Molecules: An Innate Emitter-Resonator Quantum System in Free Space

arXiv3 min read

arXiv:2607.27683v1 Announce Type: new Abstract: In recent decades, significant progress has been made in constructing and studying individual quantum systems based on two level atoms (molecules) and photons. Here we demonstrate that the quadruply bonded Mo2 unit, with a MoMo bond distance as short as 2.1A, functions as an innate emitter resonator molecular quantum system capable of trapping visible light photons between the two molybdenum atoms under ambient conditions, thereby generating an intense quantized local electromagnetic field with an extremely small mode volume. The resonance fluorescence spectra of three Mo2 complexes indicate that the intermetallic Mo-Mo charge transfer transition is coherently coupled to the local scattering field, exhibiting vacuum Rabi splitting and Mollow triplets. Resonant coupling of single molecules and N-molecule ensembles to the scattered light through sideband excitation produces a sequence of discrete optical modes spanning a broad wavelength range, with polaritonic transitions identical to those observed in Ni2 based systems. These results establish the Mo2 molecule as an independent emitter resonator integrated quantum system that enables quantum optical experiments in free space using conventional spectroscopic instrumentation. This work extends quantum electrodynamics into molecular science, providing new insights into metal metal bonding, molecular physics, and light matter interactions.

Abstract:In recent decades, significant progress has been made in constructing and studying individual quantum systems based on two level atoms (molecules) and photons. Here we demonstrate that the quadruply bonded Mo2 unit, with a MoMo bond distance as short as 2.1A, functions as an innate emitter resonator molecular quantum system capable of trapping visible light photons between the two molybdenum atoms under ambient conditions, thereby generating an intense quantized local electromagnetic field with an extremely small mode volume. The resonance fluorescence spectra of three Mo2 complexes indicate that the intermetallic Mo-Mo charge transfer transition is coherently coupled to the local scattering field, exhibiting vacuum Rabi splitting and Mollow triplets. Resonant coupling of single molecules and N-molecule ensembles to the scattered light through sideband excitation produces a sequence of discrete optical modes spanning a broad wavelength range, with polaritonic transitions identical to those observed in Ni2 based systems. These results establish the Mo2 molecule as an independent emitter resonator integrated quantum system that enables quantum optical experiments in free space using conventional spectroscopic instrumentation. This work extends quantum electrodynamics into molecular science, providing new insights into metal metal bonding, molecular physics, and light matter interactions.

Quantum Physics (quant-ph); Chemical Physics (physics.chem-ph)

arXiv:2607.27683 [quant-ph]

(or arXiv:2607.27683v1 [quant-ph] for this version)

https://doi.org/10.48550/arXiv.2607.27683 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 291 words

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