Efficient red electroluminescence from diketopyrrolopyrrole copolymerised with a polyfluorene
Source abstract
Abstract
We report the synthesis, characterization, and device incorporation of copolymers based on a common green-emitting polyfluorene but containing a small proportion of a low energy gap donor-acceptor-donor unit for red emission in photo- and electro-luminescence. At just 1%–3% random incorporation, the low-gap unit is not present on all chains, yet we demonstrate that efficient charge and energy transfer can yield electroluminescent devices with 1% quantum efficiency and a color that can be tuned by adjusting the density of low-gap units to achieve primary red (National Television System Committee). The high current density tail off in the efficiency is reduced by replacing the hole-injection layer with a photochemically cross-linked electron‑blocking layer.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
University College London 1 Department of Physics and Astronomy and London Centre for Nanotechnology, , Gower Street, London WC1E 6BT, United Kingdom
Chalmers University of Technology 2 Department of Chemical and Biological Engineering, , 412 96 Gothenburg, Sweden
University College London 3 Department of Electronic and Electrical Engineering, , Gower Street, London WC1E 6BT, United Kingdom
References (70)
Show source-provided references
1. Angew. Chem., Int. Ed. · 1998 · 37 · 40210.1002/(SICI)1521-3773(19980302)37:4<402::AID-ANIE402>3.0.CO;2-9 ↗
2. Jpn. J. Appl. Phys. · 1991 · 30 · L194110.1143/JJAP.30.L1941 ↗
3. Adv. Mater. · 1992 · 4 · 3610.1002/adma.19920040107 ↗
4. Synth. Met. · 1997 · 84 · 43710.1016/S0379-6779(97)80820-X ↗
5. Adv. Mater. · 2000 · 12 · 173710.1002/1521-4095(200012)12:23<1737::AID-ADMA1737>3.0.CO;2-N ↗
6. Sol. Energy Mater. Sol. Cells · 2007 · 91 · 95410.1016/j.solmat.2007.01.015 ↗
7. Nature Mater. · 2003 · 2 · 67810.1038/nmat978 ↗
8. J. Am. Chem. Soc. · 2007 · 129 · 347210.1021/ja0683537 ↗
9. Adv. Funct. Mater. · 2010 · 20 · 314310.1002/adfm.201000840 ↗
10. Phys. Rev. B · 1997 · 56 · 447910.1103/PhysRevB.56.4479 ↗
11. J. Phys. Chem. C · 2009 · 113 · 158910.1021/jp809568a ↗
12. Appl. Phys. Lett. · 2008 · 93 · 16330510.1063/1.3006059 ↗
13. Chem. Phys. Lett. · 2000 · 325 · 55210.1016/S0009-2614(00)00725-9 ↗
14. Nano Lett. · 2011 · 11 · 245110.1021/nl2008778 ↗
15. Appl. Phys. Lett. · 2006 · 89 · 08350610.1063/1.2335275 ↗
16. Appl. Phys. Lett. · 2001 · 78 · 212210.1063/1.1359782 ↗
17. Nano Lett. · 2010 · 10 · 115410.1021/nl903212y ↗
18. J. Mod. Opt. · 2005 · 52 · 95510.1080/09500340512331327589 ↗
19. Science · 2002 · 295 · 150610.1126/science.1068153 ↗
20. J. Appl. Phys. · 2009 · 106 · 04450910.1063/1.3204947 ↗
21. Chem. Commun. · 2011 · 47 · 882010.1039/c1cc12752g ↗
22. Macromol. Rapid Commun. · 2013 · 34 · 99010.1002/marc.201300240 ↗
23. Chem. Phys. Lett. · 2010 · 489 · 9210.1016/j.cplett.2010.02.049 ↗
24. Appl. Phys. Lett. · 1999 · 75 · 138010.1063/1.124700 ↗
25. Nature Photon. · 2013 · 7 · 1310.1038/nphoton.2012.328 ↗
26. Org. Electron. · 2012 · 13 · 92510.1016/j.orgel.2012.01.026 ↗
27. Adv. Mater. · 2011 · 23 · 272110.1002/adma.201100405 ↗
28. J. Am. Chem. Soc. · 1982 · 104 · 63010.1021/ja00366a051 ↗
29. Mol. Phys. · 1970 · 18 · 14510.1080/00268977000100171 ↗
30. J. Appl. Phys. · 1998 · 83 · 234310.1063/1.366977 ↗
31. Curr. Appl. Phys. · 2005 · 5 · 22210.1016/j.cap.2003.11.090 ↗
32. Chem. Soc. Rev. · 1997 · 26 · 20310.1039/cs9972600203 ↗
33. Macromolecules · 2008 · 41 · 728710.1021/ma801376r ↗
34. Dyes Pigm. · 2013 · 97 · 19810.1016/j.dyepig.2012.12.005 ↗
35. Org. Lett. · 2012 · 14 · 267010.1021/ol300674v ↗
36. J. Mater. Chem. · 2012 · 22 · 1281710.1039/c2jm31189e ↗
37. Org. Lett. · 2010 · 12 · 332010.1021/ol101081m ↗
38. Adv. Mater. · 2013 · 25 · 185910.1002/adma.201201795 ↗
39. Synth. Met. · 2010 · 160 · 154410.1016/j.synthmet.2010.05.019 ↗
40. Polymer · 2010 · 51 · 101610.1016/j.polymer.2009.12.044 ↗
41. Polymer · 2010 · 51 · 572610.1016/j.polymer.2010.09.046 ↗
42. Macromolecules · 2006 · 39 · 834710.1021/ma0615349 ↗
43. J. Polym. Sci., Pol. Chem. · 2006 · 44 · 239510.1002/pola.21354 ↗
44. Macromolecules · 2007 · 40 · 698110.1021/ma0710941 ↗
45. Synth. Met. · 2002 · 130 · 11510.1016/S0379-6779(02)00058-9 ↗
46. Synth. Met. · 2010 · 160 · 213510.1016/j.synthmet.2010.07.044 ↗
47. Nature (London) · 1997 · 388 · 13110.1038/40532 ↗
48. Macromolecules · 2006 · 39 · 825010.1021/ma061024e ↗
49. Nature (London) · 2005 · 434 · 19410.1038/nature03376 ↗
50. Adv. Mater. · 2006 · 18 · 270810.1002/adma.200601080 ↗
51. Adv. Mater. · 2003 · 15 · 98810.1002/adma.200304150 ↗
52. J. Phys. Chem. Lett. · 2012 · 3 · 244210.1021/jz301013u ↗
53. See supplementary material at http://dx.doi.org/10.1063/1.4820433 for experimental details, synthetic information, and further materials characterisation.
54. Adv. Mater. · 1997 · 9 · 23010.1002/adma.19970090308 ↗
55. Adv. Mater. · 2008 · 20 · 321810.1002/adma.200800007 ↗
56. J. Chem. Phys. · 2009 · 130 · 04490310.1063/1.3054142 ↗
57. J. Mater. Chem. · 2007 · 17 · 138710.1039/b614789e ↗
58. J. Polym. Sci., Part B: Polym. Phys. · 2003 · 41 · 264910.1002/polb.10647 ↗
59. Adv. Mater. · 2009 · 21 · 145010.1002/adma.200802893 ↗
60. J. Appl. Phys. · 2003 · 93 · 615910.1063/1.1562739 ↗
61. Phys. Rev. Lett. · 1996 · 76 · 190010.1103/PhysRevLett.76.1900 ↗
62. Appl. Phys. Lett. · 1996 · 69 · 108010.1063/1.117064 ↗
63. Appl. Phys. Lett. · 1999 · 75 · 167910.1063/1.124789 ↗
64. Appl. Phys. Lett. · 2012 · 100 · 05330910.1063/1.3680606 ↗
65. Appl. Phys. Lett. · 2008 · 92 · 10330810.1063/1.2892685 ↗
66. Phys. Chem. Chem. Phys. · 2009 · 11 · 345510.1039/b819200f ↗
67. Appl. Phys. Lett. · 2005 · 87 · 24330510.1063/1.3668093 ↗
68. Appl. Phys. Lett. · 2011 · 99 · 24330510.1063/1.3668093 ↗
69. Org. Electron. · 2009 · 10 · 83410.1016/j.orgel.2009.04.004 ↗
70. Nature Mater. · 2010 · 9 · 15210.1038/nmat2594 ↗