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Photopatternable Electrochromic Materials from Oxetane Precursors

机译:氧杂环丁烷前体的可光致图案化电致变色材料

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Conjugated thiophenoazomethine triads containing an acid sensitive oxetane group were prepared. The solution processable monomers were immobilized on glass and ITO coated glass substrates by photoacid induced cationic ring-opening polymerization (CROP) of the oxetane moiety. Photolithography using a photoacid generator and photo-sensitizer were used to pattern an electroactive polymer. Micro- and macroscale patterns ranging between 20 μm and 50 mm were possible with the electrochromic materials. The photopolymerized azomethine remained electroactive, and it could be repeatedly switched eleqtrochemically between its neutral (mauve, λ_(max) = 535 nm) and oxidized (blue, λ_(max) = 585 nm) states without degradation. The electrochromic properties were evaluated in a simulated device where the colors were successfully cycled between blue (oxidized) and purple (neutral) states with applied biases of +0.6 V and —0.6 V vs Fc/Fc~+ under ambient conditions without significant color fatigue or degradation.
机译:制备了含有酸敏感性氧杂环丁烷基团的共轭噻吩甲亚胺三联体。通过光酸诱导的氧杂环丁烷部分的阳离子开环聚合(CROP),将可溶液处理的单体固定在玻璃和ITO涂覆的玻璃基板上。使用光致产酸剂和光敏剂的光刻用于图案化电活性聚合物。电致变色材料可以在20μm和50 mm之间的范围内进行微观和宏观的图案化。光聚合的偶氮甲碱保持电活性,可以在其中性(紫红色,λ_(最大)= 535 nm)和氧化(蓝色,λ_(最大)= 585 nm)状态之间反复电化学转化而不会降解。在模拟设备中评估电致变色性能,其中在环境条件下,在不显着的颜色疲劳的情况下,相对于Fc / Fc〜+施加的偏压为+0.6 V和-0.6 V,成功地在蓝色(氧化)状态和紫色(中性)状态之间循环了颜色或退化。

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