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Structure formation in perfluoropentacene:diindenoperylene blends and its impact on transient effects in the optical properties studied in real-time during growth

机译:全氟并五苯:二茚并戊二烯共混物中的结构形成及其对生长过程中实时研究的光学性质的瞬态效应的影响

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We discuss the result of the competing effects of favourable intermolecular interactions and steric incompatibilities due to the size mismatch of perfluoropentacene (PFP) and diindenoperylene (DIP) on the structure formation and associated optical properties in mixed films. Using real-time grazing incidence X-ray diffraction we investigate the size of coherently scattering islands l_s as a function of film thickness and mixing ratio. We find that for PFP:DIP 1:2 blends l_s is by a factor of ~4 smaller than in pure DIP films, while l_s of the PFP:DIP 2:1 blends is not significantly reduced compared with pure PFP. Yet, we observe an increase in l_s with film thickness for all of the samples, independent on the mixing ratio. In parallel with the structural characterization we investigate the evolution of the absorption spectra in the visible spectral range and its dependence on l_s in situ during film growth using differential reflectance spectroscopy. We observe a surprisingly strong effect of changes in the structural order on the shape of ε_(2, xy)(E), evident by a pronounced evolution of characteristic peaks in the thickness range from 1.6 nm to 9.6 nm. The combined results of the real-time experiments allow to identify the thickness dependent crystal grain size as the origin of the observed transient effects in the absorption spectra.
机译:我们讨论了由于全氟并五苯(PFP)和二茚并戊二烯(DIP)的尺寸不匹配对混合膜的结构形成和相关光学性能的有利分子间相互作用和空间不相容性竞争效应的结果。使用实时掠入射X射线衍射,我们研究了相干散射岛ls的大小与膜厚和混合比的关系。我们发现,对于PFP:DIP 1:2混合物,l_s比纯DIP膜小ls约4倍,而与纯PFP相比,PFP:DIP 2:1混合物的l_s没有显着降低。然而,我们观察到所有样品的薄膜厚度均随膜厚的增加而增加,而与混合比无关。在进行结构表征的同时,我们使用差分反射光谱研究了在可见光谱范围内吸收光谱的演变及其在薄膜生长过程中对原位ls的依赖性。我们观察到结构顺序变化对ε_(2,xy)(E)的形状产生了令人惊讶的强大影响,这可以从1.6 nm至9.6 nm厚度范围内的特征峰的明显演变中看出。实时实验的综合结果可以确定厚度相关的晶粒尺寸,将其作为吸收光谱中观察到的瞬态效应的起源。

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