Large Increase in External Quantum Efficiency by Dihedral Angle Tuning in a Sky‐Blue Thermally Activated Delayed Fluorescence Emitter
Source abstract
Abstract
Abstract Efficient and stable blue emitters for organic light‐emitting diodes are urgently needed for next‐generation display and lighting applications. The discovery of thermally activated delayed fluorescence (TADF) has revealed a new class of promising candidates. After pairing the iminodibenzyl donor with the triazine acceptor via a phenylene linker, dihedral angle tuning is employed to regulate the difference between the energy levels of singlet and triplet excited states. Enhanced reverse intersystem crossing rates are observed in response to increased methylation at the phenylene linker. This behavior agrees with the density functional theory calculations. Photoluminescence quantum yields of up to 98% are achieved upon doping into a solid‐state matrix. When incorporated in devices, the maximum external quantum efficiency is 28.3% for the emitter with the most favorable trade‐off between singlet–triplet splitting and fluorescent oscillator strength. This result highlights the general applicability of dihedral angle tuning, a molecular design strategy that can be used to improve the performance of donor–acceptor type TADF emitters without significantly changing their emission spectra.
Source: crossref · Quality: baseline
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
Department of Chemistry Massachusetts Institute of Technology Cambridge MA 02139 USA
Beijing National Laboratory for Molecular Sciences College of Chemistry and Molecular Engineering Peking University Beijing 100871 P. R. China
Department of Electrical Engineering and Computer Science Massachusetts Institute of Technology Cambridge MA 02139 USA
Advanced Materials Lab (AML) Samsung Advanced Institute of Technology (SAIT) America Burlington MA 01803 USA
Funding
Samsung · U.S. Department of Energy
References (35)
Show source-provided references
1. 10.1002/978111918749310.1002/9781119187493 ↗
2. 10.1038/2595410.1038/25954 ↗
3. 10.1063/1.140958210.1063/1.1409582 ↗
4. 10.1002/978352762130910.1002/9783527621309 ↗
5. 10.1039/C7SC03905K10.1039/C7SC03905K ↗
6. 10.1109/JDT.2005.85280210.1109/JDT.2005.852802 ↗
7. 10.1088/1468-6996/15/3/03420110.1088/1468-6996/15/3/034201 ↗
8. 10.1038/nature1168710.1038/nature11687 ↗
9. 10.1038/nphoton.2014.1210.1038/nphoton.2014.12 ↗
10. 10.1038/nmat415410.1038/nmat4154 ↗
11. 10.1038/ncomms947610.1038/ncomms9476 ↗
12. 10.1103/PhysRevB.60.1442210.1103/PhysRevB.60.14422 ↗
13. 10.1038/nphoton.2012.3110.1038/nphoton.2012.31 ↗
14. 10.1002/cphc.20160066210.1002/cphc.201600662 ↗
15. 10.1038/ncomms1368010.1038/ncomms13680 ↗
16. 10.1039/C6TC04377A10.1039/C6TC04377A ↗
17. 10.1002/adma.20160167510.1002/adma.201601675 ↗
18. 10.1039/C5TC04057D10.1039/C5TC04057D ↗
19. 10.1021/acs.chemmater.7b0240310.1021/acs.chemmater.7b02403 ↗
20. 10.1039/C6CS00368K10.1039/C6CS00368K ↗
21. 10.1002/adma.20160544410.1002/adma.201605444 ↗
22. 10.1038/natrevmats.2018.2010.1038/natrevmats.2018.20 ↗
23. 10.1021/acs.chemmater.6b0532410.1021/acs.chemmater.6b05324 ↗
24. 10.1002/adma.20170276710.1002/adma.201702767 ↗
25. 10.1002/adfm.20170602310.1002/adfm.201706023 ↗
26. 10.1002/anie.20160945910.1002/anie.201609459 ↗
27. 10.1021/acs.chemmater.7b0349010.1021/acs.chemmater.7b03490 ↗
28. 10.1002/chem.20160344910.1002/chem.201603449 ↗
29. 10.1016/j.orgel.2015.10.01410.1016/j.orgel.2015.10.014 ↗
30. 10.1016/j.orgel.2011.02.00510.1016/j.orgel.2011.02.005 ↗
31. 10.1039/B517914A10.1039/B517914A ↗
32. 10.1063/1.46430410.1063/1.464304 ↗
33. 10.1007/BF0053348510.1007/BF00533485 ↗
34. 10.1002/jcc.1018910.1002/jcc.10189 ↗
35. 10.1002/adma.20170198710.1002/adma.201701987 ↗