Study of the influence of the molecular organization on single-layer OLEDs' performances

被引:20
作者
Aubouy, Laurent
Gerbier, Philippe
Guerin, Christian
Huby, Nolwenn
Hirsch, Lionel
Vignau, Laurence
机构
[1] Univ Montpellier 2, Inst Charles Gerhardt, UMR 5253, F-34095 Montpellier, France
[2] Univ Bordeaux 1, Federat Rech SyMe, CNRS FR 2648, F-33405 Talence, France
关键词
silole derivatives; single-layer OLEDs; pi-stacking; LIGHT-EMITTING-DIODES; SILOLE; ELECTROLUMINESCENCE;
D O I
10.1016/j.synthmet.2006.12.012
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We have synthesized three new silole derivatives with incrementally flexible structure to tune their packing ability and therefore study the influence of the molecular organization in single-layer OLEDs. This architecture was chosen since the absence of organic layers interfaces allows a better evaluation of the role of the molecular arrangement in the active layer. The examination of the EL properties gives evidences of the prominent role of the molecular organization on the OLED efficiency. A crystalline-like organization of the molecules allows high current density but low luminance efficiency since an excessive electron current flow is involved compared to the hole one, and the recombination rate is poor. On the contrary, disordered assemblies of molecules allows better performances by avoiding unfavourable Tr-stacking, while keeping good intermolecular orbital overlaps to support charge carrier transport. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 97
页数:7
相关论文
共 26 条
[21]   Structural optimization of 2,5-diarylsiloles as excellent electron-transporting materials for organic electroluminescent devices [J].
Uchida, M ;
Izumizawa, T ;
Nakano, T ;
Yamaguchi, S ;
Tamao, K ;
Furukawa, K .
CHEMISTRY OF MATERIALS, 2001, 13 (08) :2680-2683
[22]   Toward the ideal organic light-emitting diode. The versatility and utility of interfacial tailoring by cross-linked siloxane interlayers [J].
Veinot, JGC ;
Marks, TJ .
ACCOUNTS OF CHEMICAL RESEARCH, 2005, 38 (08) :632-643
[23]   Modification of the electronic structure of silole by the substituents on the ring silicon [J].
Yamaguchi, S ;
Jin, RZ ;
Tamao, K .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1998, 559 (1-2) :73-80
[24]  
Yamaguchi S, 2000, CHEM-EUR J, V6, P1683, DOI 10.1002/(SICI)1521-3765(20000502)6:9<1683::AID-CHEM1683>3.3.CO
[25]  
2-D
[26]   Silole-containing σ- and π-conjugated compounds [J].
Yamaguchi, S ;
Tamao, K .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1998, (22) :3693-3702