A series of Fe(II)-based metallo-supramolecular polymers with three-dimensional (3-D) structures were synthesized by the stepwise complexation of an Fe(II) salt with different ratios of a linear bis(terpyridine) ligand and a branched tris(terpyridine) ligand. Atomic force microscopy images of the polymer films showed a drastic change in the surface morphology upon varying the amount of the branched ligand. The surface of a designed 3-D construction film showed a highly porous structure (pore size: approximately 30−50 nm in diameter), probably due to the formation of a hyperbranched polymer structure. All the 3-D polymers had a blue color based on the metal-to-ligand charge-transfer (MLCT) absorption and exhibited excellent electrochromic properties. The most highly porous 3-D-structured film showed the best electrochromic performance; as compared with a 1-D linear polymer, the switching times were improved 38.7% for the coloring (0.31 → 0.19 s) and 37.9% for the bleaching (0.58 → 0.36 s). The transmittance change (ΔT) increased 21.8% (41.6 → 50.7%). Also, the coloration efficiency (η) was enhanced 45.3% (263.8 → 383.4 cm 2 C −1 ). The redox in the 3-D film was diffusion-controlled, as supported by the linear relationship between the current and square root of the scan rate. It is considered that the porous structure of the 3-D polymer films contributed to smooth ionic transfer during the redox and to the improved electrochromic properties.
The InGaZnO taken as switching layer in resistive nonvolatile memory is proposed in this paper. The memory cells composed of Ti/InGaZnO/TiN reveal the bipolar switching behavior that keeps stable resistance ratio of 102 with switching responses over 100 cycles. The resistance switching is ascribed to the formation/disruption of conducting filaments upon electrochemical reaction near/at the bias-applied electrode. The influence of electrode material on resistance switching is investigated through Pt/InGaZnO/TiN devices, which perform the unipolar and bipolar behavior as applying bias on Pt and TiN electrode, respectively. Experimental results demonstrate that the switching behavior is selective by the electrode.
In this study, electrochemical responses of inkjet-printed multicolored electrochromic devices (ECD) were studied to evaluate the feasibility of presenting multiple colors in one ECD. Metallo-supramolecular polymers (MEPE) solutions with two primary colors were inkjet-printed on flexible electrodes. By digitally controlling print dosages of each species, the colors of the printed EC thin film patterns can be adjusted directly without premixing or synthesizing new materials. The printed EC thin films were then laminated with a solid transparent thin film electrolyte and a transparent conductive thin film to form an ECD. After applying a dc voltage, the printed ECDs exhibited great contrast with a transmittance change (ΔT) of 40.1% and a high coloration efficiency of 445 cm(2) C(-1) within a short darkening time of 2 s. The flexible ECDs also showed the same darkening time of 2 s and still had a high ΔT of 30.1% under bending condition. This study demonstrated the feasibility to fabricate display devices with different color setups by an all-solution process and can be further extended to other types of displays.
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