journal article·2018-12

Interface Exciplex Anchoring the Color Stability of Solution‐Processed Thermally Activated Delayed Fluorescent White Organic Light‐Emitting Diodes

Yanwei Liu, Xiaofang Wei, Zhiyi Li, Jianjun Liu, Ruifang Wang, Xiaoxiao Hu, Pengfei Wang, Ting Qi, Ying Wang

Advanced Optical Materials· Volume 6· Issue 23
Publisher page

Abstract

Abstract Spectral stability and high color rendering index (CRI) remain challenges to high‐performance, solution‐processed white organic light‐emitting devices (WOLEDs) based on two complementary colors. The solution‐processed WOLED based on two thermally activated delayed fluorescence emitters with complementary color, i.e., the orange–red 2‐[4‐(diphenylamino) phenyl]‐10,10‐dioxide‐9H‐thioxanthen‐9‐one emitter and the blue 4,4′‐bis(carbazol‐9‐yl)‐2,2′‐dimethylbiphenyl:4,6‐bis(3,5‐di(pyridin‐4‐yl)phenyl)‐2‐phenylpyrimidine interface exciplex, is reported here. Poly[(9,9‐dioctylfluorenyl‐2,7‐diyl)‐co‐(4,4′‐(N‐(4‐sec‐butylphenyl)) diphenylamine)] is doped with 30 wt% cross‐linkable N,N′‐(4,4′‐(cyclohexane‐1,1‐diyl)bis(4,1‐phenylene))bis(N‐(4‐(6‐(2‐ethyloxetan‐2‐yloxy)hexyl)phenyl)‐3,4,5‐trifluoroaniline) to form a smooth hole transportation layer with outstanding solvent resistance ability and efficient hole transporting/injection ability. The position of interface exciplex and exciton management in the emitting layer can be tuned, thus anchoring the color stability. The device displays a maximum external quantum efficiency of 10.02% and a high CRI of 85 with Commission Internationale de l'Eclairage (CIE) color coordinates of (0.32, 0.33) at the luminescence of 1000 cd m−2. These results are among the best of solution‐processed WOLEDs based on two complementary chromophores.
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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.

Affiliations

School of Chemical Sciences University of Chinese Academy of Sciences Beijing 100049 China

Key Laboratory of Photochemical Conversion and Optoelectronic Materials Technical Institute of Physics and Chemistry Chinese Academy of Sciences Beijing 100049 China

School of Future Technology University of Chinese Academy of Sciences Beijing 100049 China

Funding

National Natural Science Foundation of China

References (53)

Show source-provided references
1. 10.1002/adma.20110475810.1002/adma.201104758 ↗
2. 10.1002/adma.20150186610.1002/adma.201501866 ↗
3. 10.1002/cplu.20170046510.1002/cplu.201700465 ↗
4. Zhang D. D. · ACS Appl. Mater. Interfaces · 2016 · 8 · 2319723203
5. 10.1021/acsphotonics.7b0137910.1021/acsphotonics.7b01379 ↗
6. 10.1021/acsphotonics.7b0121310.1021/acsphotonics.7b01213 ↗
7. 10.1039/C7TC05196D10.1039/C7TC05196D ↗
8. 10.1039/C5SC04902D10.1039/C5SC04902D ↗
9. 10.1002/adma.20150289710.1002/adma.201502897 ↗
10. 10.1016/j.orgel.2017.07.00910.1016/j.orgel.2017.07.009 ↗
11. 10.1002/adma.20100225410.1002/adma.201002254 ↗
12. 10.1021/acsami.6b1008710.1021/acsami.6b10087 ↗
13. 10.1038/nature1168710.1038/nature11687 ↗
14. 10.1002/adma.20170496110.1002/adma.201704961 ↗
15. 10.1002/adom.20180038510.1002/adom.201800385 ↗
16. 10.1002/adfm.20180203110.1002/adfm.201802031 ↗
17. 10.1002/adfm.20160250710.1002/adfm.201602507 ↗
18. 10.1002/adma.20140506210.1002/adma.201405062 ↗
19. 10.1002/adom.20170041510.1002/adom.201700415 ↗
20. 10.1002/anie.20180448310.1002/anie.201804483 ↗
21. 10.1021/acsami.5b1056110.1021/acsami.5b10561 ↗
22. 10.1021/acsami.6b0762910.1021/acsami.6b07629 ↗
23. 10.1021/acsami.7b1503410.1021/acsami.7b15034 ↗
24. 10.1021/acsenergylett.8b0071110.1021/acsenergylett.8b00711 ↗
25. 10.1039/C2TC00270A10.1039/C2TC00270A ↗
26. 10.1021/cm102405210.1021/cm1024052 ↗
27. 10.1002/adma.20140139310.1002/adma.201401393 ↗
28. 10.1002/adfm.20120119710.1002/adfm.201201197 ↗
29. 10.1021/ja026358810.1021/ja0263588 ↗
30. 10.1016/j.cplett.2006.01.08210.1016/j.cplett.2006.01.082 ↗
31. 10.1002/adom.20170041510.1002/adom.201700415 ↗
32. 10.1039/C7TC04025C10.1039/C7TC04025C ↗
33. 10.1002/adma.20160096510.1002/adma.201600965 ↗
34. 10.1002/adma.20110431610.1002/adma.201104316 ↗
35. 10.1002/adma.20140272610.1002/adma.201402726 ↗
36. 10.1038/nmat481810.1038/nmat4818 ↗
37. 10.1021/acsaem.7b0013110.1021/acsaem.7b00131 ↗
38. 10.1021/acsami.6b0519710.1021/acsami.6b05197 ↗
39. 10.1002/aelm.20160051910.1002/aelm.201600519 ↗
40. 10.1002/adfm.20170100210.1002/adfm.201701002 ↗
41. 10.1021/acsami.7b1469510.1021/acsami.7b14695 ↗
42. 10.1021/am501207g10.1021/am501207g ↗
43. 10.1002/cplu.20170046510.1002/cplu.201700465 ↗
44. 10.1039/C7TC03134C10.1039/C7TC03134C ↗
45. 10.1039/C7TC04969B10.1039/C7TC04969B ↗
46. 10.1016/j.orgel.2017.07.00910.1016/j.orgel.2017.07.009 ↗
47. 10.1039/C7TC05196D10.1039/C7TC05196D ↗
48. 10.1002/adma.20130477910.1002/adma.201304779 ↗
49. 10.1039/C8SC00282G10.1039/C8SC00282G ↗
50. 10.1021/acsami.8b0941810.1021/acsami.8b09418 ↗
51. 10.1039/C5TC03793J10.1039/C5TC03793J ↗
52. 10.1002/adom.20180016510.1002/adom.201800165 ↗
53. 10.1002/adma.20150026710.1002/adma.201500267 ↗