材料科学
异质结
富勒烯
激子
聚合物太阳能电池
有机太阳能电池
接受者
聚合物
相(物质)
载流子
光活性层
混合太阳能电池
有机半导体
太阳能电池
纳米技术
光电子学
化学物理
扩散
化学
凝聚态物理
复合材料
有机化学
热力学
物理
作者
Harald Hoppe,Niyazi Serdar Sariçiftçi
摘要
Within the different organic photovoltaic devices the conjugated polymer/fullerene bulk heterojunction approach is one of the foci of today's research interest. These devices are highly dependent on the solid state nanoscale morphology of the two components (donor/acceptor) in the photoactive layer. The need for finely phase separated polymer–fullerene blends is expressed by the limited exciton diffusion length present in organic semiconductors. Typical distances that these photo-excitations can travel within a pristine material are around 10–20 nm. In an efficient bulk heterojunction the scale of phase separation is therefore closely related to the respective exciton diffusion lengths of the two materials involved. Once the excitons reach the donor/acceptor interface, the photoinduced charge transfer results in the charge separation. After the charges have been separated they require percolated pathways to the respective charge extracting electrodes in order to supply an external direct current. Thus also an effective charge transport relies on the development of a suitable nanomorphology i.e. bicontinuous interpenetrating phase structures within these blend films. The present feature article combines and summarizes the experimental findings on this nanomorphology–efficiency relationship.
科研通智能强力驱动
Strongly Powered by AbleSci AI