期刊
ADVANCED FUNCTIONAL MATERIALS
卷 29, 期 21, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201805058
关键词
dye aggregates; exciton coupling; merocyanine dyes; pigments; narrow bandwidth; organic photodiodes
类别
资金
- Bavarian State Ministry of Education, Science and the Arts
- Bavarian Polymer Institute (BPI) at the Center for Nanosystems Chemistry in Wurzburg
Ultranarrowband organic photodiodes (OPDs) are demonstrated for thin film solid state materials composed of tightly packed dipolar merocyanine dyes. For these dyes the packing arrangement can be controlled by the bulkiness of the donor substituent, leading to either strong H- or strong J-type exciton coupling in the interesting blue (H-aggregate) and NIR (J-aggregate) spectral ranges. Both bands are shown to arise from one single exciton band according to fluorescence measurements and are not just a mere consequence of different polymorphs within the same thin film. By fabrication of organic thin-film transistors, these dyes are demonstrated to exhibit hole transport behavior in spin-coated thin films. Moreover, when used as organic photodiodes in planar heterojunctions with C-60 fullerene, they show wavelength-selective photocurrents in the solid state with maximum external quantum efficiencies of up to 11% and ultranarrow bandwidths down to 30 nm. Thereby, narrowing the linewidths of optoelectronic functional materials by exciton coupling provides a powerful approach to produce ultranarrowband organic photodiodes.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据