Abstract

Chalcogenide phase-change materials (PCMs) offer a unique feature that can be used to dynamically control the response of the photonic devices and achieve fast, nonvolatile, reversible, multilevel, and specific optical modulation. The phase-change material ${\rm Ge} _{2}{\rm Sb}_2{\rm Se} _{4}{\rm Te}_1$ (GSST) has recently received a lot of attention due to the large index contrast between its amorphous and crystalline states with significantly low optical loss in the optical to near-IR spectrum. In this paper, we propose a tunable and reconfigurable hybrid PCM plasmonic nanostructure composed of a spacer layer of GSST sandwiched between a Ag back reflector and a 1D Ag Fabry–Perot grating structure. We use the finite element method (FEM) to numerically calculate the light absorption, absorption contrast, and figure of merit of the plasmonic nanostructure for both the amorphous and crystalline state of the GSST. Our calculations show that with constant structural variation the observed multimode absorption is drastically modified when the GSST undergoes a phase change from the amorphous to the crystalline state. The absorption contrast spectrum, which is defined as the absorption difference between the amorphous and crystalline state of GSST, shows four extrema modes between 70% and 89%. The figure of merit spectrum shows two large values of 44.39 and 37.78 at the 1502 nm and 2063 nm wavelengths, respectively. We also address the observed modes in the absorption contrast spectrum through spatial representation of the enhanced electric field distribution at their corresponding wavelengths. We show how the phase change in the GSST spacer can control the coupling between the optical cavity modes and the Ag surface plasmon resonance modes in the cavities and GSST spacer strip boundaries. The findings in this paper may open new avenues toward the design of next-generation photonic systems such as thermal emission controllers, sensors, ranging holograms, modulators and optical detection devices.

© 2021 Optical Society of America

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