journal article·2006-02

Sharp and red “single-chain” luminescence from poly[2,5-dialkoxy-1,4-phenylene vinylene] locked in ordered host matrix

Kang-Yung Peng, Show-An Chen

Synthetic Metals· Volume 156· Issue 2-4
Publisher page

Abstract

Abstract We found that the luminescence profile of poly[2,5-di(3′,7′-dimethyloctyloxy)-1,4-phenylene vinylene] (OC 10 C 10 -PPV), which originally is an orange-emitting polymer, can red-shift significantly by ca. 30 nm ( λ max : from 585 to 614 nm) and become very narrow (full width at half maximum: 30 nm) when doped into poly{2-[ m -(3′,7′-dimethyloctyloxy)phenyl]-1,4-phenylene vinylene} ( m -Ph-PPV). Due to the ordered structure of the host polymer, the effective conjugation length of the guest polymer is extended as if the chains were frozen. Surprisingly, the OC 10 C 10 -PPV chains can even be more tightly locked in the ordered m -Ph-PPV matrix than in the cooled neat OC 10 C 10 -PPV film at 5 K.
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Research context

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

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References (20)

Show source-provided references
1. Burroughes · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
2. Friend · 1998 · vol. 2 · 823
3. Brédas · Chem. Phys. Lett. · 1994 · 217 · 50710.1016/0009-2614(93)E1421-C ↗
4. Gettinger · J. Chem. Phys. · 1994 · 101 · 167310.1063/1.468438 ↗
5. Sato · T. J. Am. Chem. Soc. · 1999 · 121 · 1065810.1021/ja9922983 ↗
6. Herz · Phys. Rev. B · 2001 · 64 · 19520310.1103/PhysRevB.64.195203 ↗
7. H. Mattoussi, H. Murata, C. D. Merritt, Z. H. Kafafi, in: Zakya H. Kafafi (Ed.), Organic Light-Emitting Materials and Devices II, Proceedings of SPIE, vol. 3476, 1998, p. 49.10.1117/12.332634 ↗
8. Tasch · Phys. Rev. B · 1997 · 56 · 447910.1103/PhysRevB.56.4479 ↗
9. Hu · J. Appl. Phys. · 1998 · 83 · 600210.1063/1.367502 ↗
10. Lee · Synth. Met. · 2002 · 131 · 12910.1016/S0379-6779(02)00175-3 ↗
11. Chin · Appl. Phys. Lett. · 2004 · 84 · 177710.1063/1.1651644 ↗
12. Chao · Appl. Phys. Lett. · 1998 · 73 · 42610.1063/1.121888 ↗
13. Lee · Appl. Phys. Lett. · 2001 · 79 · 30810.1063/1.1385586 ↗
14. H. Spreitzer, W. Kreuder, H. Becker, H. Schoo, R. Demandt, PCT Patent Application, WO 98 27136 (1996).
15. Peng · J. Phys. Chem. B · 2005 · 109 · 936810.1021/jp044243f ↗
16. Nguyen · Science · 2000 · 288 · 65210.1126/science.288.5466.652 ↗
17. Yu · Appl. Phys. Lett. · 2002 · 81 · 201410.1063/1.1506209 ↗
18. Halger · Phys. Rev. B · 1991 · 44 · 865210.1103/PhysRevB.44.8652 ↗
19. Gaab · J. Phys. Chem. B · 2004 · 108 · 461910.1021/jp036120l ↗
20. Netravali · 1995