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Fast electrochromic polymers based on new poly(3,4-alkylenedioxythiophene) derivatives

机译:基于新型聚(3,4-亚烷基二氧噻吩)衍生物的快速电致变色聚合物

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摘要

A series of new poly(3,4-alkylenedioxythiophene)swere electrosynthesized using 3,4-alkylenedioxythiophenederivative monomers where either the size of the alkylenedioxyring, or the nature of the pendant group, was varied.Optoelectrochemical experiments revealed that electronic bandgaps for all polymers are approximately 1.7 eV(730 nm). Thesecathodically coloring polymers switch from a relativelytransmissive light green in the oxidized form to an opaque darkblue in the reduced form. Multiple switching studies, monitoringthe electrochromic contrast, showed that Ca. 300 mm thickpolymer films could be fully switched between their reduced andoxidized forms in 0.8-2.2 5 with A%T of 44-63%. In situconductivity studies carried out on relatively thick polymer films(2.7-9.5 ~m) deposited between large gap (200 mm) lateral growthelectrodes demonstrated the low potential turn on for thesematerials and relative maximum conductivities of 0.2-12.1 S/cm were affained.
机译:使用3,4-亚烷基二氧基噻吩基的去离子基单体电合成了一系列新的聚(3,4-亚烷基二氧基噻吩基),其中亚烷基二氧基环的大小或侧基的性质均发生了变化。光电化学实验表明,所有聚合物的电子带隙均是约1.7 eV(730 nm)。这些具有阴极色的聚合物从氧化形式的相对透射的浅绿色转换为还原形式的不透明的深蓝色。多次切换研究,监测电致变色对比度,显示出Ca。 300 mm厚的聚合物薄膜可以在0.8-2.2 5的还原和氧化形式之间完全转换,A%T为44-63%。在较大间隙(200 mm)侧向生长电极之间沉积的相对较厚的聚合物膜(2.7-9.5μm)上进行的原位电导率研究表明,这些材料的电势较低,相对最大电导率为0.2-12.1 S / cm。

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