Gold nanoparticles (AuNPs) are capable of localizing and enhancing light on a nano-sized scale, making these
particles a unique structure to overcome the diffraction limit to allow for higher optical resolution in photonic
devices. The optical response of AuNPs is controlled by their size, shape, and the refractive index contrast with
the surrounding medium. Using phase change materials (PCMs) in the AuNP design introduces a dynamic
tunability to the optical response without any modification to the geometrical properties. In this work, we have
studied the induced photothermal response of the vesicle nanoparticle (VNP) consisting of a vanadium dioxide
(VO2) core (80 nm), as a PCM, and an Au shell (10 nm) covered by Au-seeds (10 nm). When the VNP is irradiated
by a CW laser, the light energy absorbed by the particle provides enough heat for the VO2 core to undergo a
phase change from the semiconductor state to the metallic state. To do this, we simultaneously solve a selfconsistent
multiphysics problem consisting of electromagnetism and thermodynamics. Our calculations show
that the maximum tunability of the extinction cross section corresponds to the scattering part achieved at the
near-infrared wavelength of λ = 790 nm for the incident threshold intensity of 101.5 kW/cm2 at which the VO2
core experiences the semiconductor-metal phase change. We also show how the temperature is localized inside
the VNP at both the semiconductor and metal phases of the VO2 core. It is expected that our results will offer a
promising potential application in active photonic devices, near infrared imaging, detectors, and tunable
scatterers.