Morphology of polymer/fullerene bulk heterojunction solar cells

被引:1206
作者
Hoppe, H [1 ]
Sariciftci, NS [1 ]
机构
[1] Johannes Kepler Univ Linz, LIOS, A-4040 Linz, Austria
关键词
D O I
10.1039/b510618b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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.
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收藏
页码:45 / 61
页数:17
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