Self‐Organized Buffer Layers in Organic Solar Cells
Self‐Organized Buffer Layers in Organic Solar Cells
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DOI:
10.1002/adma.200792876
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发表时间:
2008-06
影响因子:
29.4
通讯作者:
Qingshuo Wei;T. Nishizawa;K. Tajima;K. Hashimoto
中科院分区:
文献类型:
--
作者:
Qingshuo Wei;T. Nishizawa;K. Tajima;K. Hashimoto
The self-organization of organic molecules is an attractive approach for nanostructure fabrication.[1–4] The control of layered structures on the nanoscale is particularly desirable in thin-film organic devices because this largely affects the electrical, optical, and mechanical properties of the films. To spontaneously fabricate such multilayered structures, the careful control of driving forces such as phase separation, crystallization, or the surface energy of the materials is necessary. For example, Goffri et al. reported the spontaneous formation of bilayer structures between poly (3-hexylthiophene)(P3HT) and polyethylene in mixture films.[5] The crystallization of polyethylene induces the effective encapsulation of P3HT at the organicsemiconductor/dielectric interface, resulting in mechanically robust and high-performance thin-film transistors. Very recently, Krishnan et al. reported a new method of obtaining self-organized multilayer structures at the nanoscale level.[6] The spin-coated films from the mixtures of the nanoparticles and the polymers were simply annealed to achieve the accumulation of the nanoparticles to the substrate surface owing to the entropic and enthalpic driving forces. These pioneering studies proposed new attractive approaches for the fabrication of various organic thin-film devices. However, studies of the self-organized bilayer or multilayer structure of functional materials are still very limited and remain challenging. Moreover, their applications to actual electronic devices have been hardly explored.In the present work, we report a novel, simple approach to form layered structures in organic thin films by controlling the surface energy of the materials and its application to organic solar cells. It is well-known that materials having a low surface energy such as ffuorinated or silicone compounds prefer to migrate to the air/liquid interface during coating.[7–10] This is called surface segregation, which is driven by the total energy