材料科学
激子
四烯
纳米纤维
化学物理
表面改性
纳米
纳米技术
无定形固体
分子
扩散
纳米尺度
超分子化学
光电子学
结晶学
化学工程
凝聚态物理
复合材料
化学
物理
有机化学
工程类
热力学
作者
Martin H. C. van Son,Anton Matthijs Berghuis,Bas F. M. de Waal,Felix A. Wenzel,Klaus Kreger,Hans‐Werner Schmidt,Jaime Gómez Rivas,Ghislaine Vantomme,E. W. Meijer
标识
DOI:10.1002/adma.202300891
摘要
Efficient energy transport over long distances is essential for optoelectronic and light-harvesting devices. Although self-assembled nanofibers of organic molecules are shown to exhibit long exciton diffusion lengths, alignment of these nanofibers into films with large, organized domains with similar properties remains a challenge. Here, it is shown how the functionalization of C3 -symmetric carbonyl-bridged triarylamine trisamide (CBT) with oligodimethylsiloxane (oDMS) side chains of discrete length leads to fully covered surfaces with aligned domains up to 125 × 70 µm2 in which long-range exciton transport takes place. The nanoscale morphology within the domains consists of highly ordered nanofibers with discrete intercolumnar spacings within a soft amorphous oDMS matrix. The oDMS prevents bundling of the CBT fibers, reducing the number of defects within the CBT columns. As a result, the columns have a high degree of coherence, leading to exciton diffusion lengths of a few hundred nanometers with exciton diffusivities (≈0.05 cm2 s-1 ) that are comparable to those of a crystalline tetracene. These findings represent the next step toward fully covered surfaces of highly aligned nanofibers through functionalization with oDMS.
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