Phase-Transition-Driven Hyperbolic Optical Response and Directional Polaritons in Epitaxial VO2 Thin Films

Abstract

Optical anisotropy in crystalline solids enables direction-dependent light-matter interactions and underpins a variety of advanced photonic functionalities. In this context, Vanadium dioxide (VO2) represents a prototypical material that undergoes a reversible MIT near 67°C, accompanied by pronounced electronic, structural, and optical modifications. The MIT not only dramatically modifies the VO2 electrical conductivity but also reshapes its anisotropic optical response, making VO2 an exceptional platform for dynamically tunable photonic and optoelectronic devices. In this work, we investigate how the intrinsic crystalline anisotropy of VO2 induces a hyperbolic optical behavior in the metallic rutile phase. We study two epitaxial VO2 thin films of different thicknesses grown on (110) oriented MgF2 substrates. Broadband polarized spectroscopic measurements, spanning the infrared to UV spectral range, are employed to independently investigate the optical response in both the monoclinic and rutile phases. From these measurements, we extract the optical conductivity and the dielectric function, revealing a pronounced anisotropy in the rutile metallic phase, with an enhanced free-carrier response along the rutile c axis. Our data show that, within a narrow near-infrared spectral window, the real parts of the dielectric tensor components along the two principal axes acquire opposite signs, indicating the emergence of a hyperbolic type-II dispersion. The hyperbolic response is quantitatively evaluated through the quality factor and the degree of dielectric anisotropy, enabling a systematic assessment of VO2 as a thermally switchable, hyperbolic optical medium. These findings expand the understanding of anisotropy-driven optical phenomena in phase-change materials and highlight VO2 thin films as a promising platform for tunable and reconfigurable photonic applications.