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Extreme Polaritonic Interactions in a Room-Temperature Designable Sub-Nanocavity Quantum Electrodynamic Platform

  • Huatian Hu
  • , Xin Shu
  • , Zhiwei Hu
  • , Di Zheng
  • , Ruiqian Zhang
  • , Ximin Cui
  • , Wei Dai
  • , Xiang Lan
  • , Xiaobo Han*
  • , Wen Chen*
  • , Hongxing Xu*
  • *Corresponding author for this work
  • Wuhan Institute of Technology
  • Italian Institute of Technology
  • East China Normal University
  • Shenzhen University
  • Wuhan University
  • Donghua University
  • Henan Academy of Sciences

Research output: Contribution to journalArticlepeer-review

Abstract

Pushing nanoscale optical confinement to its ultimate limits defines the regime of nano-cavity quantum electrodynamics (nano-cQED), where light-matter interactions approach the fundamental quantum limits of individual atoms, e.g., picocavities. However, realizing such extreme confinement in a stable and controllable manner remains a key challenge. Here, we introduce a van der Waals material-based nano-cQED platform by coupling monolayer (Formula presented.) excitons to plasmonic sub-nanocavities formed via assembly of ultrasmall gold clusters (3–5 nm) in the nanogap of a nanoparticle-on-mirror nanocavity. These clusters emulate the field-confining role of atomic protrusions of the picocavities through a resonance-insensitive lightning-rod effect, achieving deep-subwavelength mode volumes. In this nano-cQED testbed, we observe pronounced multi-branch Rabi splittings ((Formula presented.) meV, (Formula presented.)) and ultrastrong lower-branch polaritonic photoluminescence with up to 10 (Formula presented.) -fold enhancement. This architecture provides a controllable pathway to access picocavity-like behavior and opens new opportunities for single-molecule spectroscopy and the exploration of nano-cQED.

Original languageEnglish
JournalAdvanced Science
DOIs
StateAccepted/In press - 2026

Keywords

  • nanoseed
  • strong coupling
  • sub-nanocavity
  • transition metal dichalcogenides

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