Electropolymerization of an EDOT-Quinoxaline Monomer for Green Electrochromic Thin Films and Devices.

In this study, we present a 5,8-bis(3,4-ethylenedioxythiophene)quinoxaline monomer with two 4-(octyloxy)phenyl side chains (EDOTPQ) that can be electropolymerized on ITO glass in standard electrolytes containing lithium salts and propylene carbonate as solvent. The electrochemically deposited PEDOTPQ layers show very good adhesion and homogeneity on ITO. The green-colored polymer thin films exhibit promising electrochromic (EC) properties and are interesting for applications such as adaptive camouflage, as well as smart displays, labels, and sensors.

Flexible Electrochromic Device on Polycarbonate Substrate with PEDOT:PSS and Color-Neutral TiO as Ion Storage Layer.

Electrochromic (EC) windows on glass for thermal and glare protection in buildings, often referred to as smart (dimmable) windows, are commercially available, along with rearview mirrors or windows in aircraft cabins. Plastic-based applications, such as ski goggles, visors and car windows, that require lightweight, three-dimensional (3D) geometry and high-throughput manufacturing are still under development. To produce such EC devices (ECDs), a flexible EC film could be integrated into a back injection molding process, where the films are processed into compact 3D geometries in a single automized step at a low processing time.

Avoiding Voltage-Induced Degradation in PET-ITO-Based Flexible Electrochromic Devices.

The cycling stability of flexible electrochromic devices (ECDs) under humid atmospheres is limited by irreversible indium tin oxide (ITO) reduction. A strategy to limit this degradation was developed and tested for model ECDs based on a sidechain-modified poly(3,4-ethylene dioxythiophene) (PEDOT) derivative and Prussian blue (PB). This work reveals that the cycling stability is reduced by dissolution of the ITO thin films and formation of metallic indium particles on the surface of the ITO layers.

Detailed study of layer-by-layer self-assembled and dip-coated electrochromic thin films based on metallo-supramolecular polymers.

Electrochromic thin films of metallo-supramolecular polyelectrolytes based on Fe(OAc)2 and 1,4-bis(2,2':6',2″-terpyridin-4'-yl)benzene are readily prepared by layer-by-layer (LbL) deposition or dip-coating on transparent conducting electrode surfaces. By applying a potential, we can switch the color of the films from blue to colorless. Because of the strong absorption and the fast switching speed, the color change can be observed with the eye.

Thermally induced structural rearrangement of the Fe(II) coordination geometry in metallo-supramolecular polyelectrolytes.

Rigid rod-type metallo-supramolecular coordination polyelectrolytes with Fe(II) centres (Fe-MEPEs) are produced via the self-assembly of the ditopic ligand 1,4-bis(2,2':6',2''-terpyridine-4'-yl)benzene (tpy-ph-tpy) and Fe(II) acetate. Fe-MEPEs exhibit remarkable electrochromic properties; they change colour from blue to transparent when an electric potential is applied. This electrochemical process is generally reversible.