Amorphous photonic structures exhibit interesting optical properties such as non-iridescent angle-independent structural colors and isotropic photonic band gaps. Here, we demonstrate colloidal assemblies of engineered amorphous photonic materials, using pigmentary α-Fe 2 O 3 /SiO 2 core/shell nanoparticles, exhibiting non-iridescent and tunable colors. The observed colors result from combination of colloidal particle arrangements, giving arises to the structural colors, along with the inherent pigmentary color of the α-Fe 2 O 3 /SiO 2 nanoparticles. Colloidal particle assemblies of α-Fe 2 O 3 /SiO 2 core/shell nanoparticles, and therefore the resulting colors, can be manipulated by shell thickness, particle concentration and external electrical stimuli. α-Fe 2 O 3 /SiO 2 nanoparticles based amorphous photonic structures exhibit short-range order on a length scale comparable to optical wavelengths and are weakly correlated to each other, as confirmed by ultra-small-angle X-ray scattering measurements. Dynamic tunability of α-Fe 2 O 3 /SiO 2 nanomaterials in the visible wavelengths is demonstrated using electrophoretic deposition process with a noticeable difference between transmitted and reflected colors. Amorphous structures have been investigated both theoretically and experimentally due to their unique properties as compared with perfectly ordered crystalline structures [1] . Prototypical A novel amorphous photonic structures using pigmentary α-Fe 2 O 3 /SiO 2 core/shell nanoparticles are succesfully fabricated. The resulting non-iridicent brilliant colors are in combination of pigmenary and structural colororation and manipulated by shell thickness, particle concentration and external electrical stimuli using electrophoretic deposition process. In the process, fully reversible and instantaneous color change as well as noticeable difference between transmitted and reflected colors is observed.