journal article·2006-06

Optical gain in fluorenyl-thiophene co-oligomer thin films

S. Lattante, M. Anni, M. Salerno, L. Lagonigro, R. Cingolani, G. Gigli, M. Pasini, S. Destri, W. Porzio

Optical Materials· Volume 28· Issue 8-9
Publisher page

Abstract

We report on the emission properties of thin films of a fluorenyl-thiophene co-oligomer under strong optical excitation. A clear line narrowing is observed in the emission spectra as a function of the excitation density, due to a Stimulated Emission band attributed to Amplified Spontaneous Emission (ASE). The ASE threshold of about 150 lJ cm_2 is comparable with the best values reported for other oligomeric and/or co-oligomeric films or crystals. A maximum gain value of about 8 cm_1 is obtained for an excitation density of about 940 lJ cm_2. These results propose fluorene-thiophene co-oligomers as interesting materials for high performance optically pumped laser devices.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials

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

References (33)

Show source-provided references
1. Schweitzer · Phys. Rev. B · 1999 · 59 · 411210.1103/PhysRevB.59.4112 ↗
2. Zenz · Appl. Phys. Lett. · 1997 · 71 · 256610.1063/1.119332 ↗
3. Hide · Science · 1996 · 273 · 183310.1126/science.273.5283.1833 ↗
4. Henari · J. Appl. Phys. · 2003 · 93 · 187110.1063/1.1537463 ↗
5. Manaa · J. Opt. A: Pure Appl. Opt. · 2003 · 5 · 34110.1088/1464-4258/5/4/306 ↗
6. Anni · Appl. Phys. Lett. · 2001 · 78 · 267910.1063/1.1369392 ↗
7. Quochi · Appl. Phys. Lett. · 2004 · 84 · 445410.1063/1.1759384 ↗
8. Brouwer · Appl. Phys. Lett. · 1998 · 73 · 70810.1063/1.121975 ↗
9. Garnier · Appl. Phys. Lett · 1998 · 72 · 208710.1063/1.121284 ↗
10. Lawrence · Opt. Lett. · 2004 · 29 · 86910.1364/OL.29.000869 ↗
11. Barbarella · J. Am. Chem. Soc · 2000 · 122 · 1197110.1021/ja002037p ↗
12. Barbarella · Adv. Mater. · 1998 · 10 · 55110.1002/(SICI)1521-4095(199805)10:7<551::AID-ADMA551>3.0.CO;2-Y ↗
13. Anni · Appl. Phys. Lett. · 2000 · 77 · 245810.1063/1.1314886 ↗
14. Pisignano · Appl. Phys. Lett. · 2002 · 81 · 353410.1063/1.1519735 ↗
15. Anni · Symp. Mater. Res. Soc. Symp. Proc. · 2002 · 665 · 29
16. Zavelani-Rossi · Appl. Phys. Lett · 2001 · 79 · 408210.1063/1.1426686 ↗
17. Heliotis · Appl. Phys. Lett. · 2002 · 81 · 41510.1063/1.1494473 ↗
18. Xia · Appl. Phys. Lett. · 2003 · 82 · 359910.1063/1.1576906 ↗
19. Heliotis · Appl. Phys. Lett. · 2003 · 83 · 211810.1063/1.1612903 ↗
20. Heliotis · J. Appl. Phys. · 2004 · 96 · 695910.1063/1.1811374 ↗
21. Heliotis · Adv. Funct. Mater. · 2004 · 14 · 9110.1002/adfm.200305504 ↗
22. Setayesh · J. Am. Chem. Soc. · 2001 · 123 · 94610.1021/ja0031220 ↗
23. Kreyenschimdt · Macromolecules · 1998 · 31 · 109910.1021/ma970914e ↗
24. Donat-Bouillud · Chem. Mater. · 2000 · 12 · 193110.1021/cm0001298 ↗
25. Liu · Macromolecules · 2000 · 33 · 894510.1021/ma000866p ↗
26. Destri · Synth. Met. · 2003 · 135–136 · 40910.1016/S0379-6779(02)00665-3 ↗
27. Nagawa · Appl. Phys. Lett. · 2002 · 80 · 54410.1063/1.1435797 ↗
28. Ichikawa · Adv. Mater. · 2003 · 15 · 21310.1002/adma.200390048 ↗
29. Zhu · Adv. Mater. · 2003 · 15 · 90610.1002/adma.200304816 ↗
30. Svelto · 1989
31. Anni · Appl. Phys. Lett. · 2003 · 83 · 275410.1063/1.1616645 ↗
32. Frolov · Phys. Rev. B · 1998 · 57 · 914110.1103/PhysRevB.57.9141 ↗
33. Shaklee · Appl. Phys. Lett. · 1971 · 18 · 47510.1063/1.1653501 ↗