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Trap Generation Dynamics in Photo-Oxidised DEH Doped Polymers

机译:光氧化DEH掺杂的聚合物的陷阱产生动力学

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A series of polyester films doped with a hole transport molecule, p-diethylaminobenzaldehyde-1,1'-diphenylhydrazone (DEH), have been systematically exposed to ultraviolet radiation with a peak wavelength of about 375 nm. The electronic performance of the films, evaluated using time-of-flight and space-charge current injection methods, is observed to continuously degrade with increasing ultraviolet exposure. The degradation is attributed to photo cyclic oxidation of DEH that results in the creation of indazole (IND) molecules which function as bulk hole traps. A proposed model for the generation dynamics of the IND traps is capable of describing both the reduction in current injection and the associated time-of-flight hole mobility provided around 1% of the DEH population produce highly reactive photo-excited states which are completely converted to indazole during the UV exposure period. The rapid reaction of these states is incompatible with bulk oxygen diffusion-reaction kinetics within the films and is attributed to the creation of excited states within the reaction radius of soluble oxygen. It is suggested that encapsulation strategies to preserve the electronic integrity of the films should accordingly focus upon limiting the critical supply of oxygen for photo cyclic reaction.
机译:一系列掺杂有空穴传输分子对二乙氨基苯甲醛-1,1'-二苯hydr(DEH)的聚酯薄膜已系统性地暴露于峰值波长约为375 nm的紫外线辐射下。观察到使用飞行时间和空间电荷电流注入方法评估的薄膜的电子性能会随着紫外线暴露的增加而持续下降。降解归因于DEH的光环氧化,导致形成吲唑(IND)分子,该分子起着空穴陷阱的作用。提出的IND陷阱生成动力学模型可以描述电流注入的减少以及相关的飞行时间空穴迁移率,前提是大约1%的DEH人口产生了高反应性的光激发态,这些光激发态被完全转换在紫外线照射期间会产生吲唑。这些状态的快速反应与膜内的大量氧扩散反应动力学不相容,并且归因于在可溶性氧的反应半径内产生激发态。建议用于保持膜的电子完整性的包封策略应相应地集中于限制用于光环反应的氧气的关键供应。

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