Photocurrent in bulk heterojunction solar cells

被引:74
作者
Limpinsel, M. [1 ]
Wagenpfahl, A. [1 ]
Mingebach, M. [1 ]
Deibel, C. [1 ]
Dyakonov, V. [1 ,2 ]
机构
[1] Julius Maximilians Univ Wurzburg, D-97074 Wurzburg, Germany
[2] Bavarian Ctr Appl Energy Res ZAE Bayern, Funct Mat Energy Technol, D-97074 Wurzburg, Germany
来源
PHYSICAL REVIEW B | 2010年 / 81卷 / 08期
关键词
CURRENT-VOLTAGE; RECOMBINATION; POLYMER; DISSOCIATION; IONS;
D O I
10.1103/PhysRevB.81.085203
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We investigated the photocurrent in poly (3-hexylthiophene-2,5-diyl)(P3HT):[6,6]-phenyl-C(61) butyric acid methyl ester solar cells by applying a pulsed measurement technique. For annealed samples, a point of optimal symmetry with a corresponding voltage V(POS) of 0.52-0.64 V could be determined. Based on macroscopic simulations and results from capacitance-voltage measurements, we identify this voltage with flat band conditions in the bulk of the cell but not the built-in voltage as proposed by Ooi et al., J. Mater. Chem. 18, 1644 (2008). We calculated the field-dependent polaron pair dissociation after Onsager-Braun and the voltage-dependent extraction of charge carriers after Sokel and Hughes with respect to this point of symmetry. Our analysis allows to explain the experimental photocurrent in both forward and reverse directions. Also, we observed a voltage-independent offset of the photocurrent. As this offset is crucial for the device performance, we investigated its dependence on cathode material and thermal treatment. From our considerations we gain insight into the photocurrent's voltage dependence and the limitations of device efficiency.
引用
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页数:6
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