Probing the effect of relative molecular orientation on the photovoltaic device performance of an organic bilayer heterojunction using soft x-ray spectroscopies

被引:15
|
作者
Cho, S. W. [1 ]
DeMasi, A. [1 ]
Preston, A. R. H. [1 ]
Smith, K. E. [1 ]
Piper, L. F. J. [2 ]
Chauhan, K. V. [3 ]
Jones, T. S. [3 ]
机构
[1] Boston Univ, Dept Phys, Boston, MA 02215 USA
[2] SUNY Binghamton, Dept Phys Appl Phys & Astron, Binghamton, NY 13902 USA
[3] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
SOLAR-CELLS; ELECTRONIC-STRUCTURE; INTERFACES; PENTACENE; MOBILITY; FILMS;
D O I
10.1063/1.4731197
中图分类号
O59 [应用物理学];
学科分类号
摘要
The orientation of the constituent molecules in organic thin film devices can affect significantly their performance due to the highly anisotropic nature of pi-conjugated molecules. We report here an angle dependent x-ray absorption study of the control of such molecular orientation using well-ordered interlayers for the case of a bilayer heterojunction of chloroaluminum phthalocyanine (ClAlPc) and C-60. Furthermore, the orientation-dependent energy level alignment of the same bilayer heterojunction has been measured in detail using synchrotron radiation-excited photoelectron spectroscopy. Regardless of the orientation of the organic interlayer, we find that the subsequent ClAlPc tilt angle improves the pi-pi interaction at the interface, thus leading to an improved short-circuit current in photovoltaic devices based on ClAlPc/C-60. The use of the interlayers does not change the effective band gap at the ClAlPc/C-60 heterointerface, resulting in no change in open-circuit voltage. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4731197]
引用
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页数:4
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