TY - JOUR
T1 - Polarization-Driven Reversible Switching between Weak and Strong Coupling in Plasmonic Nanocavities
AU - Wang, Yueweiying
AU - Wei, Xuetong
AU - Tian, Xiaoshuang
AU - Lu, Fanfan
AU - Gao, Feng
AU - Mei, Ting
AU - Zhang, Wending
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/3/19
Y1 - 2026/3/19
N2 - Achieving dynamic control of light–matter coupling regimes in plasmonic nanocavities at room temperature is pivotal for quantum technologies but remains challenging due to limitations in polarization-selective excitation efficiency. Here, we demonstrate a polarization-driven reversible switch between weak and strong coupling at the vertical incidence. Leveraging radial vector beam (RVB’s) cylindrical symmetry, we generate a confined longitudinal electric field that directly couples to nanoparticle-on-mirror plasmonic modes without sample tilting. This strategy enhances the local electric field by 327-fold (71% higher than linearly polarized beam, LPB) and compresses the mode field volume, amplifying the coupling strength to g = 107 meV, surpassing the strong coupling criterion. Using Rhodamine 800 as a quantum emitter, we demonstrate reversible all-optical switching between a Purcell-enhanced weak coupling regime (under LPB) and a strong coupling regime with 32.8 meV Rabi splitting (under RVB) within the molecule–nanocavity coupling system characterized by highly resolved Rabi splitting in the fluorescence spectra. Further optimization via Au nanoparticle size (R = 40 nm) and collective molecular coupling (N ≥ 5) establishes a ternary synergy for robust quantum control. This noninvasive, polarization-mediated platform enables on-demand manipulation of quantum states for reconfigurable nanophotonic devices.
AB - Achieving dynamic control of light–matter coupling regimes in plasmonic nanocavities at room temperature is pivotal for quantum technologies but remains challenging due to limitations in polarization-selective excitation efficiency. Here, we demonstrate a polarization-driven reversible switch between weak and strong coupling at the vertical incidence. Leveraging radial vector beam (RVB’s) cylindrical symmetry, we generate a confined longitudinal electric field that directly couples to nanoparticle-on-mirror plasmonic modes without sample tilting. This strategy enhances the local electric field by 327-fold (71% higher than linearly polarized beam, LPB) and compresses the mode field volume, amplifying the coupling strength to g = 107 meV, surpassing the strong coupling criterion. Using Rhodamine 800 as a quantum emitter, we demonstrate reversible all-optical switching between a Purcell-enhanced weak coupling regime (under LPB) and a strong coupling regime with 32.8 meV Rabi splitting (under RVB) within the molecule–nanocavity coupling system characterized by highly resolved Rabi splitting in the fluorescence spectra. Further optimization via Au nanoparticle size (R = 40 nm) and collective molecular coupling (N ≥ 5) establishes a ternary synergy for robust quantum control. This noninvasive, polarization-mediated platform enables on-demand manipulation of quantum states for reconfigurable nanophotonic devices.
UR - https://www.scopus.com/pages/publications/105033145112
U2 - 10.1021/acs.jpca.6c00422
DO - 10.1021/acs.jpca.6c00422
M3 - 文章
AN - SCOPUS:105033145112
SN - 1089-5639
VL - 130
SP - 2422
EP - 2429
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 11
ER -