Chromic materials exhibiting reversible changes in optical properties under external stimuli represent an important class of smart materials with applications in smart windows, sensors, and optoelectronic devices. Transition-metal oxides (TMOs) provide a versatile platform for chromic functionality due to their coupled structural, electronic, and optical properties. In this review, the chromic response of selected TMO thin films is analyzed using both microscopic and phenomenological approaches. The microscopic description is based on many-body theory, including Green’s function methods and correlation effects, while the macroscopic optical response is described using Drude–Lorentz and Tauc–Lorentz models within the effective medium approximation. Chromic behavior in TMOs is shown to originate from two principal mechanisms: (i) electronic and structural reconstruction driven by Peierls–Mott metal–insulator phase transitions, leading to thermochromism (notably in VO2 and V2O3), and (ii) formation of localized states driven by small-polaron injection, giving rise to electrochromism, gasochromism, and photochromism. The models are applied to representative systems, including VO2, WO3, NiO, and TiO2, demonstrating the chromic changes in the dielectric function spectra. These results highlight chromism in TMOs as a multiscale phenomenon linking microscopic interactions with macroscopic optical response.
Varzari et al. (Wed,) studied this question.