Garnet
structure Ga-based oxides are reported here as a new host
for inorganic reversible thermochromic materials. Doping of 3d transition
metal elements at the Ga site could be an efficient route for controlling
the electronic spectrum. Multicolored reversible thermochromic materials
have been prepared with Cr3+/Mn3+/Fe3+/Co3+-doped Er3Ga5O12 by a high-temperature solid state reaction method and investigated
by X-ray diffraction, Raman spectroscopy, and ultraviolet–visible–near-infrared
spectroscopy. The color and CIE-L*ab parameters as a function of temperature
were explored from room temperature to 460 °C. The color distinction
at room temperature was attributed to the unique optical characteristics,
and the color for Cr3+- and Mn3+-doped samples
arose from Cr3+ d–d transitions at ∼2.8 and
∼2.0 eV and the Mn3+ d–d transition at ∼2.5
eV, respectively. In addition to the d–d transition for Fe3+/Co3+, charge transfer of ligand–metal
in the visible region was the primary cause of the color of Fe3+/Co3+-substituted samples. As the temperature
increased, a continuous change in color was perceived, and the color
recovered when the temperature decreased to room temperature. The
thermochromic effect originated from the alteration of the energy
required for the d–d transition or charge transfer with temperature,
resulting in a characteristic shift and deformation of these absorption
bands.