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Comparison of new photorefractive composites based on a poly(phenylene vinylene) derivative with traditional poly(n-vinylcarbazole) composites

机译:基于聚亚苯基亚乙烯基衍生物的新型光折变复合材料与传统聚(n-乙烯基咔唑)复合材料的比较

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摘要

The performances of two classes of photorefractive polymer composites with low glass-transition temperatures (about 10-5 °C) are compared. One is based on the commonly used photoconductor poly(N-vinylcarbazole) (PVK), i.e., containing isolated charge-transport moieties for hopping. The other is based on the π-conjugated poly[1,4-phenylene-1,2-di(4-benzyloxyphenyl)vinylene] (DBOP-PPV), promising faster response times. The steady-state performance of the DBOP-PPV-based composites was found to be superior owing to (i) the larger internal free volume, allowing more efficient poling of the chromophores, and (ii) the slightly stronger space-charge field as a result of an increased trap density. By contrast, the dynamic response in a four-wave mixing experiment was similar to that of PVK-based composites despite the higher hole-drift mobility in conjugated PPV homopolymers than PVK. It was demonstrated that this is mainly a result of the poor charge-carrier generation efficiency.
机译:比较了两类具有低玻璃化转变温度(约10-5°C)的光折变聚合物复合材料的性能。一种是基于常用的光电导体聚(N-乙烯基咔唑)(PVK),即包含用于跳跃的分离的电荷传输部分。另一种是基于π-共轭的聚[1,4-亚苯基-1,2-二(4-苄氧基苯基)亚乙烯基](DBOP-PPV),有望实现更快的响应时间。发现基于DBOP-PPV的复合材料的稳态性能优异,这是由于(i)较大的内部自由体积,允许发色团更有效地极化,以及(ii)作为陷阱密度增加的结果。相比之下,尽管共轭PPV均聚物中的空穴漂移迁移率比PVK高,但四波混合实验中的动态响应与基于PVK的复合材料相似。已经证明,这主要是由于电荷载流子产生效率差的结果。

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