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Photoconductivity of Organic Semiconductor Polymers Studied by Time-resolved THz-TDS

机译:通过时间分辨Thz-TDS研究的有机半导体聚合物的光电导性

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This study employs optical-pump terahertz-probe time-domain spectroscopy to measure relative carrier mobilities of semiconductor organic polymer films of poly-3-hexylthiophene (P3HT) and poly(2,5-bis(3-tetradecylthiophen-2-yl)thieno[3,2-b]thiophene) (PBTTT) polymers and these results directly correlate to recently reported electrical device mobility measurements. An approximately four-fold increase in mobility of P3HT is observed with molecular weight increase from c.a. 18 kD to 150 kD where the intrinsic film mobility saturates for molecular weight > 70 kD. The decay dynamics studies of these polymers showed almost no dependence on the molecular weight of the polymer. The studies also showed an order of magnitude increase in mobility between as cast P3HT films and annealed PBTTT films supporting a strong conjugation length effect. We also measured the mobility dependence on the film quality that is affected by regularity of the polymer, dispersing solvent, electron acceptor traps, and other film growth related parameters relevant to device manufacturing.
机译:本研究采用光学泵太赫兹 - 探针时域光谱,以测量聚-3-己烯烯(P3HT)和聚(2,5-双(3-四癸酰噻吩-2-基)Thieno的半导体有机聚合物膜的相对载体迁移率[3,2-B]噻吩)(PBTTT)聚合物,这些结果与最近报道的电气设备迁移率测量直接相关。观察到P3HT的迁移率的大约四倍增加,从C.a的分子量增加。 18kd至150kd,其中固有薄膜迁移率为分子量饱和> 70kd。这些聚合物的衰变动力学研究几乎没有对聚合物的分子量的依赖性。研究还表明,随着支撑强缀合长度效应的铸造P3HT薄膜和退火的PBTTT薄膜之间的迁移率增加了级别。我们还测量了对由聚合物规律性影响的薄膜质量,分散溶剂,电子受体捕集器和与装置制造相关的其他薄膜生长相关参数影响的薄膜质量的迁移依赖性。

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