We have investigated the influence of Rabi splitting tuning on the dynamics of strongly coupled J-aggregate/surface plasmon polariton systems. In particular, the Rabi splitting was tuned by modifying the J-aggregate molecule concentration while a polaritonic system was provided by a nanostructure formed by holes array in a golden layer. From the periodic and concentration changes we have identified, through numerical and experimental steady-state analyses, the best geometrical configuration for maximizing Rabi splitting, which was then used for transient absorption measurements. It was found that in transient absorption spectra, under upper band excitation, two bleaching peaks appear when a nanostructured polaritonic pattern is used. Importantly, their reciprocal distance increases upon increase of J-aggregate concentration, a result confirmed by steady-state analysis. In a similar manner it was also found that the lifetime of the upper band is intimately related to the coupling strength. In particular, we argue that with strong coupling strength, i.e. high J-aggregate concentration, a short lifetime of the upper band has to be expected due to the suppression of the bottleneck effect. This result supports the idea that the dynamics of hybrid systems is profoundly dependent on Rabi splitting.
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http://dx.doi.org/10.1039/c6nr01588c | DOI Listing |
Philos Trans A Math Phys Eng Sci
December 2024
Department of Physics and Astronomy, University of Exeter, Exeter, Devon EX4 4QL, UK.
Room-temperature cavity quantum electrodynamics with molecular materials in optical cavities offers exciting prospects for controlling electronic, nuclear and photonic degrees of freedom for applications in physics, chemistry and materials science. However, achieving strong coupling with molecular ensembles typically requires high molecular densities and substantial electromagnetic-field confinement. These conditions usually involve a significant degree of molecular disorder and a highly structured photonic density of states.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Guangdong Provincial Key Laboratory of Optoelectronic Information Processing Chips and Systems, School of Microelectronics Science and Technology, Sun Yat-sen University, Zhuhai 519082, China.
The strong coupling between infrared photonic resonances and vibrational transitions of organic molecules is called vibrational strong coupling (VSC), which presents attractive prospects for modifying molecular chemical characteristics and behaviors. Currently, VSC studies suffer from limited bandwidth or enormous mode volumes. In addition, in certain instances, the absorption spectrum of VSC is weaker, thus impeding the effective monitoring of the VSC effect.
View Article and Find Full Text PDFNanophotonics
June 2024
Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093, USA.
The vacuum Rabi splitting (VRS) in molecular polaritons stands as a fundamental measure of collective light-matter coupling. Despite its significance, the impact of molecular disorder on VRS is not fully understood yet. This study delves into the complexities of VRS amidst various distributions and degrees of disorder.
View Article and Find Full Text PDFNanophotonics
June 2024
Department of Chemistry, University of Rochester, 120 Trustee Road, Rochester, NY 14627, USA.
We present a theory that explains the resonance effect of the vibrational strong coupling (VSC) modified reaction rate constant at the normal incidence of a Fabry-Pérot (FP) cavity. This analytic theory is based on a mechanistic hypothesis that cavity modes promote the transition from the ground state to the vibrational excited state of the reactant, which is the rate-limiting step of the reaction. This mechanism for a single molecule coupled to a single-mode cavity has been confirmed by numerically exact simulations in our recent work in [J.
View Article and Find Full Text PDFNanophotonics
June 2024
Department of Materials Science and Engineering, National Cheng Kung University, Tainan, Taiwan.
The realization of higher coupling strengths between coupled resonant modes enables exploration of compelling phenomena in diverse fields of physics and chemistry. In this study, we focus on the modal coupling between localized surface plasmon resonance (LSPR) of Au nanoparticles (Au-NPs) and Fabry-Pérot mode (p-NiO/Au film). The effects of nanoparticle size, projected surface coverage (PSC), interparticle distance (IPD), and arrangement to the coupling strength between the two modes are theoretically investigated using finite-difference time-domain (FDTD) method.
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