Deep Energetic Trap States in Organic Photovoltaic Devices

被引:60
作者
Shuttle, Christopher G. [1 ]
Treat, Neil D. [1 ]
Douglas, Jessica D. [2 ,3 ]
Frechet, Jean M. J. [2 ,3 ,4 ]
Chabinyc, Michael L. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[4] King Abdullah Univ Sci & Technol, Thuwal 23955, Saudi Arabia
关键词
solar cells; disorder; trapping; charge transport; PCBM; FIELD-EFFECT TRANSISTORS; SOLAR-CELLS; MOBILITY; SELENIUM; SOLIDS;
D O I
10.1002/aenm.201100541
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
The nature of energetic disorder in organic semiconductors is poorly understood. In photovoltaics, energetic disorder leads to reductions in the open circuit voltage and contributes to other loss processes. In this work, three independent optoelectronic methods were used to determine the long-lived carrier populations in a high efficiency N-alkylthieno[3,4-c]pyrrole-4,6-dione (TPD) based polymer: fullerene solar cell. In the TPD co-polymer, all methods indicate the presence of a long-lived carrier population of similar to 10(15) cm-3 on timescales = 100 mu s. Additionally, the behavior of these photovoltaic devices under optical bias is consistent with deep energetic lying trap states. Comparative measurements were also performed on high efficiency poly-3-hexylthiophene (P3HT): fullerene solar cells; however a similar long-lived carrier population was not observed. This observation is consistent with a higher acceptor concentration (doping) in P3HT than in the TPD-based copolymer.
引用
收藏
页码:111 / 119
页数:9
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