journal article·2021-06-02

Planar Chiral [2.2]Paracyclophane-Based Thermally Activated Delayed Fluorescent Materials for Circularly Polarized Electroluminescence

Chen Liao, Yu Zhang, Shang-Hui Ye, Wen-Hua Zheng

ACS Applied Materials & Interfaces· Volume 13· Issue 21
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Abstract

This work describes the construction of a novel planar chiral [2.2]paracyclophane-based thermally activated delayed fluorescence (TADF)-active molecule with circularly polarized luminescence (CPL). The combination of the bulky planar chiral phenoxazinephane (PXZp) donor based [2.2]paracyclophane and triazine acceptor enables the highly efficient luminescence performances and excellent CPL properties. The enantiomers exhibit excellent TADF activities, the energy difference (ΔEST) between singlet and triplet of the molecule is only 0.03 eV. Notably, through solution-process, a yellow CP-OLEDs based on the molecule as the emitting layers displays high maximum brightness (Lmax) up to 34 293 cd m–2, maximum external quantum efficiency (EQEmax) up to 7.8% and remarkable CP-EL signal with gEL factor up to 4.6 × 10–3.
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Research context

OpenAlex topics: Synthesis and Properties of Aromatic Compounds · Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials

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

Affiliations

State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, 163 Xianlin Avenue, Nanjing 210023, Jiangsu China

Key Laboratory for Organic Electronics & Information Displays (KLOEID) and Institute of Advanced Materials, National Synergistic Innovation Center for Advanced Materials (SICAM), Nanjing University of Posts and Telecommunications, Nanjing 210023, China

References (46)

Show source-provided references
1. 10.1063/1.12313810.1063/1.123138 ↗
2. 10.1002/anie.20180124810.1002/anie.201801248 ↗
3. 10.1002/anie.20180383310.1002/anie.201803833 ↗
4. 10.1039/c3cc42323a10.1039/c3cc42323a ↗
5. 10.1021/cr400477t10.1021/cr400477t ↗
6. Kim D.-Y. · J. Korean Phys. Soc. · 2006 · 49 · 505
7. 10.1021/ja971912c10.1021/ja971912c ↗
8. 10.1002/(SICI)1521-4095(200003)12:5<362::AID-ADMA362>3.0.CO;2-P10.1002/(SICI)1521-4095(200003)12:5<362::AID-ADMA362>3.0.CO;2-P ↗
9. 10.1021/ja037733e10.1021/ja037733e ↗
10. 10.1002/adma.20120496110.1002/adma.201204961 ↗
11. 10.1002/adma.20170090710.1002/adma.201700907 ↗
12. 10.1021/acsnano.7b0739010.1021/acsnano.7b07390 ↗
13. 10.1039/C8CC05153D10.1039/C8CC05153D ↗
14. 10.1002/chem.20200372110.1002/chem.202003721 ↗
15. 10.1002/anie.20180019810.1002/anie.201800198 ↗
16. 10.1002/adfm.20180005110.1002/adfm.201800051 ↗
17. 10.1021/acs.orglett.8b0362010.1021/acs.orglett.8b03620 ↗
18. 10.1002/adma.20190052410.1002/adma.201900524 ↗
19. 10.1039/C9TC01632E10.1039/C9TC01632E ↗
20. 10.1039/C9TC04941J10.1039/C9TC04941J ↗
21. 10.1021/acsami.9b0700510.1021/acsami.9b07005 ↗
22. 10.1002/anie.20191424910.1002/anie.201914249 ↗
23. 10.1063/5.002112710.1063/5.0021127 ↗
24. 10.1002/adfm.20200483810.1002/adfm.202004838 ↗
25. 10.1002/advs.20200080410.1002/advs.202000804 ↗
26. 10.1021/jacs.0c0898010.1021/jacs.0c08980 ↗
27. 10.1002/adom.20210001710.1002/adom.202100017 ↗
28. 10.1002/anie.20201541110.1002/anie.202015411 ↗
29. 10.1002/adma.20140489110.1002/adma.201404891 ↗
30. 10.1038/srep1491210.1038/srep14912 ↗
31. 10.1021/jacs.6b0246310.1021/jacs.6b02463 ↗
32. 10.1002/adom.20170035910.1002/adom.201700359 ↗
33. 10.1002/adfm.20160371910.1002/adfm.201603719 ↗
34. 10.1039/C9CS00680J10.1039/C9CS00680J ↗
35. 10.1002/adfm.20201028110.1002/adfm.202010281 ↗
36. 10.1038/nature1168710.1038/nature11687 ↗
37. 10.1002/adma.20160544410.1002/adma.201605444 ↗
38. 10.1021/acs.chemmater.6b0532410.1021/acs.chemmater.6b05324 ↗
39. 10.1039/C6CS00368K10.1039/C6CS00368K ↗
40. 10.1021/jacs.6b0085010.1021/jacs.6b00850 ↗
41. 10.1021/acs.orglett.8b0299510.1021/acs.orglett.8b02995 ↗
42. 10.1039/C9SC01821B10.1039/C9SC01821B ↗
43. 10.1021/acs.orglett.8b0071110.1021/acs.orglett.8b00711 ↗
44. 10.1039/c2cc36237f10.1039/c2cc36237f ↗
45. 10.1002/adma.20070234310.1002/adma.200702343 ↗
46. 10.1002/anie.20060409410.1002/anie.200604094 ↗