Photochemical origins of burn-in degradation in small molecular weight organic photovoltaic cells

被引:63
作者
Burlingame, Quinn [1 ]
Tong, Xiaoran [2 ]
Hankett, Jeanne [3 ]
Slootsky, Michael [4 ]
Chen, Zhan [3 ]
Forrest, Stephen R. [1 ,2 ,4 ]
机构
[1] Univ Michigan, Dept Elect Engn & Comp Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
基金
美国能源部;
关键词
SOLAR-CELLS; DISSOCIATION; SPECTRA; C-120; DIMER;
D O I
10.1039/c4ee03444a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using a combination of Fourier transform infrared (FTIR) spectroscopy and physics-based degradation models, we find that the early aging of small molecular weight organic photovoltaic (OPV) cells is due to photochemical degradation of the C-60 acceptor layer. Planar and mixed boron subphthalocyanine chloride (SubPc)-donor/C-60-acceptor heterojunctions show significant changes in their IR absorption spectra after aging under illumination, which we find is due to exciton-mediated photo-oligomerization of C-60. The consequent decrease in exciton diffusion length in the C-60 layer results from a decreased exciton lifetime for C-60 oligomers (e.g. C-120 and C-180) compared to that of the monomer. The model describes the short-circuit current reduction in planar SubPc/C-60 OPV cells during early aging, and explains the lack of degradation in analogous mixed heterojunctions.
引用
收藏
页码:1005 / 1010
页数:6
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