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Coupled mode theory (CMT) is a powerful framework for decomposing interactions between electromagnetic waves and scattering bodies into resonances and their couplings with power-carrying channels. It has widespread use in few-resonance, weakly coupled resonator systems across nanophotonics, but cannot be applied to the complex scatterers of emerging importance. We use quasinormal modes to develop an exact, ab initio generalized coupled mode theory from Maxwells equations. This quasinormal coupled mode theory, which we denote QCMT, enables a direct, mode-based construction of scattering matrices without resorting to external solvers or data. We consider canonical scattering bodies, for which we show that a CMT model will necessarily be highly inaccurate, whereas QCMT exhibits near-perfect accuracy.
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Despite the several novel features arising from the dissipative optomechanical coupling, such effect remains vastly unexplored due to the lack of a simple formalism that captures non-Hermiticity in optomechanical systems. In this Letter, we show that quasinormal-mode-based perturbation theory is capable of correctly predicting both dispersive and dissipative optomechanical couplings. We validate our model through simulations and also by comparison with experimental results reported in the literature. Finally, we apply this formalism to plasmonic systems, used for molecular optomechanics, where strong dissipative coupling signatures in the amplification of vibrational modes are observed.
We report a self-consistent quasinormal mode theory for nanometer scale electromagnetism where the possible nonlocal and quantum effects are treated through quantum surface responses. With Feibelmans frequency-dependent textit{d} parameters to describe the quantum surface responses, we formulate the source-free Maxwells equations into a generalized linear eigenvalue problem to define the quasinormal modes. We then construct an orthonormal relation for the modes and consequently unlock the powerful toolbox of modal analysis. The orthonormal relation is validated by the reconstruction of the full numerical results through modal contributions. Significant changes in the landscape of the modes are observed due to the incorporation of the quantum surface responses for a number of nanostructures. Our semi-analytical modal analysis enables transparent physical interpretation of the spontaneous emission enhancement of a dipolar emitter as well as the near-field and far-field responses of planewave excitations in the nanostructures.
In this paper, we analyze a chain-linked triple-cavity photonic molecule (TCPM) with controllable coupling strengths between the cavities on their spectral properties and field (energy) distributions by solving eigenvalues and eigenvectors of the Hamiltonian matrix based on coupled mode theory. Phase transition is extended from double-cavity photonic molecules (DCPMs) to TCPMs, and evolutions of the supermode frequencies and linewidths are analyzed, which have synchronous relations with the degree of coherence between adjacent optical microcavities and energy distributions in the three cavities, respectively. We develop a superposition picture for the three supermodes of the TCPM, as interferences between supermodes of sub-DCPMs. In particular, we demonstrate the abnormal properties of the central supermode in TCPMs, such as dark state in middle cavity and phase shift when energy flowing between side cavities, which are promising in information processing and remote control of energy. General properties of TCPMs are summarized and limitation on linewidths are given. Finally, we make an interesting analog to intracavity electromagnetically induced transparency in multi-level atomic systems using the flexible TCPM platform under appropriate conditions.
We present a design methodology and analysis of a cavity optomechanical system in which a localized GHz frequency mechanical mode of a nanobeam resonator is evanescently coupled to a high quality factor (Q>10^6) optical mode of a separate nanobeam optical cavity. Using separate nanobeams provides flexibility, enabling the independent design and optimization of the optics and mechanics of the system. In addition, the small gap (approx. 25 nm) between the two resonators gives rise to a slot mode effect that enables a large zero-point optomechanical coupling strength to be achieved, with g/2pi > 300 kHz in a Si3N4 system at 980 nm and g/2pi approx. 900 kHz in a Si system at 1550 nm. The fact that large coupling strengths to GHz mechanical oscillators can be achieved in SiN is important, as this material has a broad optical transparency window, which allows operation throughout the visible and near-infrared. As an application of this platform, we consider wide-band optical frequency conversion between 1300 nm and 980 nm, using two optical nanobeam cavities coupled on either side to the breathing mode of a mechanical nanobeam resonator.
The number of eigenmodes in plasmonic nanostructures increases with complexity due to mode hybridization, raising the need for efficient mode characterization and selection. Here we experimentally demonstrate direct imaging and selective excitation of the bonding and antibonding plasmon mode in symmetric dipole nanoantennas using confocal two-photon photoluminescence mapping. Excitation of a high-quality-factor antibonding resonance manifests itself as a two-lobed pattern instead of the single spot observed for the broad bonding resonance, in accordance with numerical simulations. The two-lobed pattern is observed due to the fact that excitation of the antibonding mode is forbidden for symmetric excitation at the feedgap, while concomitantly the mode energy splitting is large enough to suppress excitation of the bonding mode. The controlled excitation of modes in strongly coupled plasmonic nanostructures is mandatory for efficient sensors, in coherent control as well as for implementing well-defined functionalities in complex plasmonic devices.
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