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Shaping of the temporal distribution of the ultrashort pulses, compensation of pulse deformations due to phase shift in transmission and amplification are of interest in various optical applications. To address these problems, in this study, we have demonstrated an ultra-thin reconfigurable localized surface plasmon (LSP) band-stop optical filter driven by insulator-metal phase transition of vanadium dioxide. A Joule heating mechanism is proposed to control the thermal phase transition of the material. The resulting permittivity variation of vanadium dioxide tailors spectral response of the transmitted pulse from the stack. Depending on how the pulse’s spectrum is located with respect to the resonance of the band-stop filter, the thin film stack can dynamically compress/expand the output pulse span up to 20% or shift its phase up to 360°. Multi-stacked filters have shown the ability to dynamically compensate input carrier frequency shifts and pulse span variations besides their higher span expansion rates.

Vanadium dioxide (VO2) has attracted interest due to its phase transition from the insulating to the metallic states for potential use in a variety of optical and photonic applications. Here, we propose a VO2/Si core-shell structure to improve switching in band-selective reflection properties of the composite. Mie scattering formulation is used to analyze the structure before and after phase transition to show the impact of resonance quality on the mid-infrared light back-scattering. After investigating the effect of various VO2 nano-sphere radius sizes in both phases on light reflectivity, a VO2/Si core-shell structure is proposed to boost reflectivity and improve light controllability. Randomly distributed nanoparticles are studied to illustrate how these composites have similar behavior to their deterministic-distributed counterpart. Our results indicate that up to two-thirds of incident light power can be controlled by embedding proper core-shells in a polymer host material.

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The chimera state is the concurrent combination of synchronous and incoherent oscillations in a set of identical oscillators. In this study, we demonstrate the states for optical nanoresonators where the oscillators are designed based on a plasmonic dimer cavity. This resonator interchanges radiative energy with an active medium located at its hotspot, and therefore forms an amplitude-mediated oscillating system. Finite-difference time-domain (FDTD)-based numerical analysis of a circular array of the coupled oscillators reveals that regardless of identical nature, oscillator phase is not concordant over time for all members. The effect of coupling strength on the phase escape/synchronization of the oscillators is investigated for the plasmonic nanoresonator system. It is shown that for identical oscillators, which are placed symmetrically over the perimeter of a disc, the array can be divided to several subgroups of concurrent coherent and incoherent members. While the oscillator of each subgroup seems to be locked together, one member can escape from synchronization for a while and return to coherency, or it can sync with the other groups. The effect of coupling strength and number of oscillators on the phase-escape pace is studied for this system, and strong coupling is shown to force the array members to fully synchronize while weaker coupling causes chimera states in the array.