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Electrochromic device response controlled by an in situ polymerized ionic liquid based gel electrolyte

机译:原位聚合的离子液体基凝胶电解质控制电致变色器件响应

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摘要

Polymer electrolytes were synthesized by two different approaches and applied to electrochromicuddevices based on electrodeposited tungsten oxide (WO3) or poly(3,4-ethylenedioxythiophene)ud(PEDOT) films as the cathode, and a Prussian blue (PB) film as the anode. The first method involvedudthe entrapping of an ionic liquid in a polymer host (poly(methylmethacrylate) or PMMA) and theudsecond approach relied on the in situ thermal polymerization of methylmethacrylate (MMA) in theudhydrophobic ionic liquid, yielding a solidified transparent gel. The effect of in situ solid polymerudelectrolyte formation on device performance characteristics was realized in terms of a largerudcoloration efficiency of 119 cm2 C21 (l = 550 nm) achieved for the WO3–PB (MMA) device, asudcompared to a value of 54 cm2 C21 obtained for the WO3–PB (PMMA) device. Similar enhancementsudin electrochromic coloring efficiency, reflectance contrast, and faster switching kinetics were obtainedudfor the PEDOT–PB (MMA) device. The strategy of introducing an electrolyte to the electrochromicuddevice in a liquid state and then subjecting the same to gradual polymerization allows greaterudaccessibility of the electrolyte ions to the active sites on the electrochromic electrodes and superiorudinterfacial contact. As a consequence, larger optical contrast and faster kinetics are achieved in theudMMA based devices. While PEDOT films were amorphous, PB films were semi-crystalline but only inudthe case of WO3; the hexagonal structure of WO3, equipped with three/four/six-coordinated voids wasudfound to affect bleaching kinetics favorably. The performance of PMMA based electrolyte is limitedudby high resistance at the electrode–electrolyte interface, and a smaller number of ions available forudoxidation and reduction. Large area (y10 cm 6 4 cm) devices were also fabricated using this simpleudwet chemistry method and their ability to color uniformly without any pinholes was demonstrated.
机译:通过两种不同的方法合成高分子电解质,并将其应用于以电沉积氧化钨(WO3)或聚(3,4-乙撑二氧噻吩) ud(PEDOT)薄膜为阴极,以普鲁士蓝(PB)薄膜为电沉积的电致变色 ud器件中。阳极。第一种方法涉及将离子液体截留在聚合物主体(聚(甲基丙烯酸甲酯)或PMMA)中,第二种方法依赖于在超疏水离子液体中进行甲基丙烯酸甲酯(MMA)的原位热聚合,从而产生固化的透明凝胶。与WO3–PB(MMA)器件相比,实现了原位固体聚合物 ud电解质形成对器件性能特性的影响,因为WO3-PB(MMA)器件实现了更高的119 cm2 C21(l = 550 nm)的脱色效率。 WO3-PB(PMMA)设备获得的C21值为54 cm2。对于PEDOT-PB(MMA)器件,获得了类似的增强效果 udin电致变色着色效率,反射率对比度和更快的切换动力学。将电解质以液态引入到电致变色器件中然后使其逐渐聚合的策略允许电解质离子更易进入电致变色电极上的活性部位,并且具有优越的/界面接触性。结果,在基于udMMA的设备中实现了更大的光学对比度和更快的动力学。尽管PEDOT膜是非晶态的,而PB膜却是半结晶的,但仅在WO3的情况下。没有发现WO3的六边形结构具有三个/四个/六个配位的空隙,从而有利地影响了漂白动力学。基于PMMA的电解质的性能受到电极与电解质界面处的高电阻的限制,并且可用于过氧化和还原的离子数量较少。还使用这种简单的 udwet化学方法制造了大面积(y10 cm 6 4 cm)器件,并且证明了它们均匀着色而没有任何针孔的能力。

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