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Optical and electrochemical properties of polyether derivatives of perylenediimides adsorbed on nanocrystalline metal oxide films

机译:ylene二酰亚胺聚醚衍生物在纳米晶金属氧化物薄膜上的光学和电化学性质

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摘要

We report optical and electrochemical properties of polyether derivatives of perylenediimides (PDIs) thin films formed in various materials (semiconductor, insulator, amorphousand self-assembly). Perylenediimides adsorbed on nanocrystalline TiO2(NT) nanocrystalline alumina (NA), amorphous silicon (PS) and neat self-assemblied (SA) films wereprepared and characterized based on spectroscopic, electrochemical, spectro-electrochemical techniques. The absorption and fluorescence spectra of PDIs in chloroform exhibit vibronic features. The fluorescence quantum yields (Uf) of PDIs with end amino substituentsin chloroform solutions are over 0.95, while the quantum yield of triethoxyphenyl substituted PDIUfvalue is 0.024 in solution. Optical spectroscopy proves that PDIs in metal oxidethin films form aggregated type complexes. An electrochromism, a color change from redto blue/violet, is observed on metal oxide films, that indicates existence of mono and dianion forms of PDIs. Reversibility of electrochemical reductions in NT film depends on thescanning rate. However, electrochromism in NA films is stable and reversibility is independent from scanning rate. Stable mono and diaionic species are formed on NA films. SA filmsshow broad absorption peaks during the voltammetric scan. On the other hand, the firstreduction onset potentials of PDIs are almost equal to the onset potential of capacitive current of TiO2which lead to low efficiency in dye-sensitized solar cells.
机译:我们报告了在各种材料(半导体,绝缘体,非晶和自组装)中形成的per二酰亚胺(PDI)薄膜的聚醚衍生物的光学和电化学性质。基于光谱,电化学,光谱电化学技术,制备并表征了吸附在纳米TiO2(NT),纳米晶氧化铝(NA),非晶硅(PS)和纯自组装(SA)膜上的二酰亚胺。氯仿中PDI的吸收光谱和荧光光谱具有振动特征。在氯仿溶液中具有末端氨基取代基的PDI的荧光量子产率(Uf)超过0.95,而在溶液中三乙氧基苯基取代的PDIUf的量子产率为0.024。光谱学证明,金属氧化物薄膜中的PDI形成聚集型络合物。在金属氧化物膜上观察到电致变色,颜色从红色变为蓝色/紫色,表明存在PDI的单离子和双阴离子形式。 NT薄膜中电化学还原的可逆性取决于扫描速率。但是,NA膜中的电致变色是稳定的,并且可逆性与扫描速率无关。在NA膜上形成稳定的单离子和离子离子物质。 SA膜在伏安扫描中显示出宽的吸收峰。另一方面,PDI的首次还原起始电势几乎等于TiO2电容电流的起始电势,这导致染料敏化太阳能电池效率低下。

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