Separating Charges at Organic Interfaces: Effects of Disorder, Hot States, and Electric Field

被引:61
作者
Nayak, Pabitra K. [1 ]
Narasimhan, K. L. [2 ]
Cahen, David [1 ]
机构
[1] Weizmann Inst Sci, Dept Mat & Interfaces, IL-76100 Rehovot, Israel
[2] Tata Inst Fundamental Res, Dept Condensed Matter & Mat Sci, Bombay 400005, Maharashtra, India
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2013年 / 4卷 / 10期
关键词
HETEROJUNCTION SOLAR-CELLS; EXCITON DISSOCIATION; TRANSIENT ABSORPTION; PHOTOVOLTAIC DIODES; EXCIPLEX FORMATIONS; BAND-GAP; RECOMBINATION; ENERGY; EFFICIENCY; BLENDS;
D O I
10.1021/jz4002339
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
Charge separation at organic-organic (O-O) interfaces is crucial to how many organic-based optoelectronic devices function. However, the mechanism of formation of spatially separated charge carriers and the role of geminate recombination remain topics of discussion and research. We review critically the contributions of the various factors, including electric fields, long-range order, and excess energy (beyond the minimum needed for photoexcitation), to the probability that photogenerated charge carriers will be separated. Understanding the processes occurring at the O/O interface and their relative importance for effective charge separation is crucial to design efficient solar cells and photodetectors. We stress that electron and hole delocalization after photoinduced charge transfer at the interface is important for efficient free carrier generation. Fewer defects at the interface and long-range order in the materials also improve overall current efficiency in solar cells. In efficient organic cells, external electric fields play only a small role for charge separation.
引用
收藏
页码:1707 / 1717
页数:11
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