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Ultrafast Spectroscopic Investigation of P3HT and Derivatives in Versatile Contexts: From Organic Solar Cells, via Perovskite Photovoltaics to Biosensing

机译:在多种情况下对P3HT及其衍生物的超快光谱研究:从有机太阳能电池到钙钛矿光伏再到生物传感

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In this talk, versatile results obtained for P3HT and related polythiophenes, using ultrafast spectroscopic techniques, will be overviewed. I will start with excited-state relaxation processes taking place in P3HT thin films and solutions [1], focusing on the importance of short-lived delocalized states. I will then move on to charge generation mechanisms in polythiophene:PCBM blends (organic photovoltaic materials). Here, particular emphasis will be on the influence of the phase morphology and microstructure on the generation and recombination of charges [2]. Next, I will talk about charge transfer dynamics from methyl ammonium lead iodide perovskites to P3HT hole transporting materials [3], and discuss why this is found to be particularly slow. Finally, the photophysical properties of a water-soluble cationic polythiophene derivative, used for DNA sensing [4], will be presented as a function of assembly with different single-stranded DNA sequences.
机译:在本次演讲中,将概述使用超快速光谱技术获得的P3HT和相关聚噻吩的通用结果。我将从P3HT薄膜和溶液中发生的激发态弛豫过程开始[1],重点是短期离域态的重要性。然后,我将继续介绍聚噻吩:PCBM混合物(有机光伏材料)中的电荷产生机理。在这里,将特别强调相形态和微观结构对电荷产生和复合的影响[2]。接下来,我将讨论从甲基铵碘化铅钙钛矿到P3HT空穴传输材料的电荷转移动力学[3],并讨论为什么发现这种方法特别慢。最后,用于DNA传感的水溶性阳离子聚噻吩衍生物的光物理性质[4],将作为不同单链DNA序列组装的函数。

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