No Arabic abstract
We study theoretically the optical response of a nanohybrid comprising a symmetric quantum dimer emitter coupled to a metal nanoparticle (MNP). The interactions between the exitonic transitions in the dimer and the plasmons in the MNP lead to novel effects in the composites input-output characteristics for the light intensity and the absorption spectrum, which we study in the linear and nonlinear regimes. We fnd that the exciton-plasmon hybridization leads to optical bistability and hysteresis for the one-exciton transition and enhancement of excitation for the two-exciton transition. The latter leads to a signifcant decrease of the field strength needed to saturate the system. In the linear regime, the absortion spectrum has a dispersive (Fano-like) line shape. The spectral position and shape of this spectrum depend on the detuning of the dimers one-exciton resonance relative to the plasmon resonance. Upon increasing the applied field intensity to the nonlinear regime, the Fano-like singularities in the absorption spectra are smeared and they disappear due to the saturation of the dimer, which leads to the MNP dominating the spectrum. The above effects, for which we provide physical explanations, allow one to tailor the Fano-like shape of the absorption spectrum, by changing either the detuning or the input power.
Hybrid molecular-plasmonic nanostructures have demonstrated their potential for surface enhanced spectroscopies, sensing or quantum control at the nanoscale. In this work, we investigate the strong coupling regime and explicitly describe the hybridization between the localized plasmons of a metal nanoparticle and the excited state of a quantum emitter, offering a simple and precise understanding of the energy exchange in full analogy with cavity quantum electrodynamics treatment and dressed atom picture. Both near field emission and far field radiation are discussed, revealing the richness of such optical nanosources.
We present a theoretical study of the resonance fluorescence spectra of an optically driven quantum dot placed near a single metal nanoparticle. The metallic reservoir coupling is calculated for an 8-nm metal nanoparticle using a time-convolutionless master equation approach where the exact photon reservoir function is included using Green function theory. By exciting the system coherently near the nanoparticle dipole mode, we show that the driven Mollow spectrum becomes highly asymmetric due to internal coupling effects with higher-order plasmons. We also highlight regimes of resonance squeezing and broadening as well as spectral reshaping through light propagation. Our master equation technique can be applied to any arbitrary material system, including lossy inhomogeneous structures, where mode expansion techniques are known to break down.
We consider the coupling of a single mode microwave resonator to a tunnel junction whose contacts are at thermal equilibrium. We derive the quantum master equation describing the evolution of the resonator field in the strong coupling regime, where the characteristic impedance of the resonator is larger than the quantum of resistance. We first study the case of a normal-insulator-normal junction and show that a dc driven single photon source can be obtained. We then consider the case of a superconductor-insulator-normal and superconductor-insulator-superconductor junction. There, we show that the Lamb shift induced by the junction gives rise to a nonlinear spectrum of the resonator even when the junction induced losses are negligible. We discuss the resulting dynamics and consider possible applications including quantum Zeno dynamics and the realization of a qubit.
We present a theoretical study of the optical response of a nonlinear oscillator formed by coupling a metal nanoparticle local surface plasmon resonance to excitonic degrees of freedom in a monolayer transition-metal dichalcogenide. We show that the combined system should exhibit strong anharmonicity in its low-lying states, predicting for example a seven order-of-magnitude increase in nonlinearity relative to a silicon photonic crystal cavity. Then, we demonstrate that such system exhibits strong quantum features such as antibunching and non-Gaussianity. Arrays of such nanoscale nonlinear oscillators could be used to realize novel optical metamaterials; alternatively, an individual nanoparticle-monolayer construct could be coupled to an optical resonator to mediate efficient input-output coupling to propagating fields.
We demonstrate reversible strain-tuning of a quantum dot strongly coupled to a photonic crystal cavity. We observe an average redshift of 0.45 nm for quantum dots located inside the cavity membrane, achieved with an electric field of 15 kV/cm applied to a piezo-electric actuator. Using this technique, we demonstrate the ability to tune a quantum dot into resonance with a photonic crystal cavity in the strong coupling regime, resulting in a clear anti-crossing. The bare cavity resonance is less sensitive to strain than the quantum dot and shifts by only 0.078 nm at the maximum applied electric field.