Relationship between Crystalline Order and Exciton Diffusion Length in Molecular Organic Semiconductors

被引:299
作者
Lunt, Richard R. [1 ,2 ,3 ]
Benziger, Jay B. [3 ]
Forrest, Stephen R. [1 ,2 ]
机构
[1] Univ Michigan, Dept Phys Elect Engn & Comp Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[3] Princeton Univ, Dept Chem Engn, Princeton, NJ 08544 USA
关键词
THIN-FILMS; TRIPLET EXCITONS; ENERGY-TRANSFER; TETRACENE; SINGLET; FLUORESCENCE; ABSORPTION; TRANSISTORS; MECHANISMS; EXCITATION;
D O I
10.1002/adma.200902827
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The effect of crystalline order on the exciton diffusion length (L-D) is shown for the archetypal organic semiconductor 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA; see figure). L-D increases from similar to 6.5 nm in the amorphous limit to similar to 25 nm for single crystals. These changes in diffusion length are connected to changes in the fluorescence quantum yield, which is useful for understanding where crystal-size-dependant diffusion trends are likely to be observed for other organic materials.
引用
收藏
页码:1233 / +
页数:5
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