In this paper, we present an in-depth examination of the absorption dynamics of a silver plasmonic grating incorporating Kerr-type nonlinear graphene-oxide (GO) nanoslits and a Ge2Sb2Se4Te1 (GSST) phase-change material, both in linear and nonlinear regimes. Linear absorption approaches unity at the resonant wavelength when GSST is amorphous. Upon exposure to a nanosecond Gaussian pulse laser irradiation with appropriate fluences, the amorphous GSST partially crystallizes through a thermoplasmonic-induced process, resulting in a significant reduction of the linear on-resonance absorption in the form of a step-like curve. Additionally, the weak off-resonance linear absorption of the system can be enhanced owing to the non-uniform phase-transition within the GSST. Transitioning to a nonlinear regime, considering the third-order nonlinearity of GO nanoslits, reveals distinct absorption behaviors. Temporal analysis reveals that at the on-resonance wavelength, the unit absorption decreases with increasing laser intensity, reaching a minimum at the pulse peak due to the Kerr nonlinearity in the GO. Intriguingly, the absorption exhibits a U-shaped curve at lower fluences, while at higher fluences, it stabilizes at a lower value post-pulse peak where the amorphous GSST undergoes a thermally driven partially crystallization phase transformation. In the off-resonance mode, the weak absorption enhances dramatically by increasing the fluence, tracing an imperfect parabolic trajectory that reaches nearly unit at the trailing edge of the pulse, attributed to the Kerr nonlinearity within the GO nanoslits. By further increasing the laser fluence, the photothermal response of the GSST emerges as the dominant factor, diminishing the unity absorption observed at the trailing edge of the pulse. These findings underscore the dynamic responsiveness of the proposed grating to pulsed laser illumination, driven by the nonlinear Kerr effect and GSST reconfigurability, offering promising opportunities for developing active optical switching devices.
