journal article·2009-10-26

Effect of Molecular Morphology on Amplified Spontaneous Emission of Bis‐Styrylbenzene Derivatives

Ryota Kabe, Hajime Nakanotani, Tomo Sakanoue, Masayuki Yahiro, Chihaya Adachi

Advanced Materials· Volume 21· Issue 40
Publisher page

Abstract

Molecular aggregation greatly affects the fluorescence quantum efficiency, transient lifetime, and amplified spontaneous emission (ASE) of bis-styrylbenzene derivatives. We compare the optical properties for various morphologies (solution, film, doped film, and single crystalline state) (see figure) and demonstrate that ambipolar operation of a 1,4-bis(4-methylstyryl) benzene layer in field-effect transistors leads to intense blue electroluminescence with a rather sharp emission width.
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Photochemistry and Electron Transfer Studies · Photochromic and Fluorescence Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (32)

Show source-provided references
1. 10.1038/3869310.1038/38693 ↗
2. 10.1063/1.12066910.1063/1.120669 ↗
3. 10.1063/1.186755510.1063/1.1867555 ↗
4. 10.1038/382695a010.1038/382695a0 ↗
5. 10.1126/science.273.5283.183310.1126/science.273.5283.1833 ↗
6. 10.1063/1.149447310.1063/1.1494473 ↗
7. 10.1063/1.193800110.1063/1.1938001 ↗
8. 10.1063/1.210599610.1063/1.2105996 ↗
9. 10.1063/1.239064410.1063/1.2390644 ↗
10. 10.1126/science.109419610.1126/science.1094196 ↗
11. 10.1002/adma.1997009151210.1002/adma.19970091512 ↗
12. 10.1016/S0301-0104(97)00215-210.1016/S0301-0104(97)00215-2 ↗
13. 10.1063/1.12128410.1063/1.121284 ↗
14. 10.1002/(SICI)1521-4095(199903)11:3<234::AID-ADMA234>3.0.CO;2-B10.1002/(SICI)1521-4095(199903)11:3<234::AID-ADMA234>3.0.CO;2-B ↗
15. 10.1063/1.12431410.1063/1.124314 ↗
16. 10.1063/1.143579710.1063/1.1435797 ↗
17. 10.1002/1521-4095(20020116)14:2<119::AID-ADMA119>3.0.CO;2-710.1002/1521-4095(20020116)14:2<119::AID-ADMA119>3.0.CO;2-7 ↗
18. 10.1002/adma.20039004810.1002/adma.200390048 ↗
19. 10.1002/adma.20030481610.1002/adma.200304816 ↗
20. 10.1063/1.213836110.1063/1.2138361 ↗
21. 10.1002/cphc.20050066910.1002/cphc.200500669 ↗
22. 10.1021/ja050872710.1021/ja0508727 ↗
23. 10.1039/B612732K10.1039/B612732K ↗
24. 10.1063/1.272029810.1063/1.2720298 ↗
25. 10.1063/1.274808610.1063/1.2748086 ↗
26. 10.1063/1.288468710.1063/1.2884687 ↗
27. 10.1002/adfm.20070006910.1002/adfm.200700069 ↗
28. 10.1016/S0022-0248(98)00034-710.1016/S0022-0248(98)00034-7 ↗
29. 10.1103/PhysRevLett.96.01740410.1103/PhysRevLett.96.017404 ↗
30. 10.1021/jp807684m10.1021/jp807684m ↗
31. 10.1143/APEX.1.09180110.1143/APEX.1.091801 ↗
32. 10.1063/1.294240110.1063/1.2942401 ↗