Dissolving a monomer in an UV-curable liquid electrolyte, followed by exposure to UV light, results in a solid electrolyte matrix. [28,29] Frisbie and co-workers and others formed solid-state electrolytes by dissolving viologen derivatives with a copolymer and ionic liquids. [30-36] Such methods require the EC monomers to have good solubility in liquid-gel electrolytes. ECDs, based on solid polymer electrolytes (SPEs), have a long switching time and relatively low redox stability. [19,26-36] These problems might be due to the low ionic conductivities created by a large interfacial resistance at the electrode or the electrolyte's interface as well as poor contact with the electrodes. [37] In order to advance the application of these ECDs, it is necessary to optimize the working electrode-electrolyte combination to form structurally simplified and highly stable ECDs. Here, we demonstrated solid-state multicolor ECDs based on metallo-organic coatings and a layered architecture. Spraycoated layers of electrochromic metal complexes (1, 2) [38] on transparent conducting metal oxides (TCOs) were covered by dropcasting an electrolyte salt embedded in a UV-cured matrix (Figures 1 and 2). [28,29] These ECDs are thermally robust (100 °C, 24 h), have a redox stability of â4500 cycles, and switching times of t = 0.4-2.8 s. The device performance does not require a dedicated ion-storage layer, which is common for analogous devices that use a liquid gel-type electrolyte. [38] The multicolor ECDs reported here are formed by using a mixture of two isostructural iron and osmium complexes in one coating. The solid-polymer electrolyte-based architecture offers a new generation of thermally and electrochemically stable devices based on metallo-organic assemblies.