journal article·2018-02-26Open access

Molecular Design Strategy for a Two-Component Gel Based on a Thermally Activated Delayed Fluorescence Emitter

P. Rajamalli, Diego Rota Martir, Eli Zysman-Colman

ACS Applied Energy Materials· Volume 1· Issue 2

Abstract

Luminescent materials that can spontaneously assemble into highly ordered networks are essential to improve the quality of thin films in stacked device architectures and enhance the performances of solution-processed organic light emitting devices (OLEDs). Herein, we report two pyridine-decorated thermally activated delayed fluorescence (TADF) emitters, 3PyCzBP and 4PyCzBP. 4PyCzBP shows robust two-component gel formation in the presence of either tartaric acid or succinic acid along with significant emission enhancement. Morphology studies reveal that these gels consist of homogeneous nanofibers assembled in hierarchical supramolecular networks. Transient photoluminescence spectra confirm that the gels emit via a TADF mechanism, making them the first examples of TADF gels. These nanofibers are promising candidates as self-assembled emitting nanofibers in thin films in solution-processed OLEDs.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Conducting polymers and applications

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

Affiliations

Organic Semiconductor Centre, EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST, United Kingdom

Funding

Research Councils UK · Leverhulme Trust · European Commission

References (33)

Show source-provided references
1. 10.1039/C5TC03943F10.1039/C5TC03943F ↗
2. 10.1109/TED.2017.264796410.1109/TED.2017.2647964 ↗
3. 10.1021/acsami.7b0607610.1021/acsami.7b06076 ↗
4. 10.1002/adom.20160021710.1002/adom.201600217 ↗
5. 10.1002/adma.20150310810.1002/adma.201503108 ↗
6. 10.1021/am501207g10.1021/am501207g ↗
7. 10.1021/am301703a10.1021/am301703a ↗
8. 10.1002/adma.20140397310.1002/adma.201403973 ↗
9. 10.1039/b926348a10.1039/b926348a ↗
10. 10.1039/C6NR06654B10.1039/C6NR06654B ↗
11. 10.1002/adfm.20170217610.1002/adfm.201702176 ↗
12. 10.1039/C4CC04231J10.1039/C4CC04231J ↗
13. 10.1038/nchem.234710.1038/nchem.2347 ↗
14. 10.1039/c2cs35106d10.1039/c2cs35106d ↗
15. 10.1038/nchem.149610.1038/nchem.1496 ↗
16. 10.1021/ja503363v10.1021/ja503363v ↗
17. 10.1039/c3cc38419e10.1039/c3cc38419e ↗
18. 10.1038/nature1168710.1038/nature11687 ↗
19. 10.1002/adma.20160544410.1002/adma.201605444 ↗
20. 10.1039/C6CS00368K10.1039/C6CS00368K ↗
21. 10.1002/adma.20140253210.1002/adma.201402532 ↗
22. 10.1002/adfm.20150299510.1002/adfm.201502995 ↗
23. 10.1002/adma.20150449010.1002/adma.201504490 ↗
24. 10.1002/adma.20150109010.1002/adma.201501090 ↗
25. 10.1021/acsami.6b0481710.1021/acsami.6b04817 ↗
26. 10.1021/acs.langmuir.6b0337510.1021/acs.langmuir.6b03375 ↗
27. 10.1021/acs.chemrev.6b0022110.1021/acs.chemrev.6b00221 ↗
28. 10.1002/anie.20140299210.1002/anie.201402992 ↗
29. 10.1021/jacs.7b0384810.1021/jacs.7b03848 ↗
30. 10.1002/adma.20170276710.1002/adma.201702767 ↗
31. 10.1021/acsami.6b1067810.1021/acsami.6b10678 ↗
32. 10.1021/la104888p10.1021/la104888p ↗
33. 10.1002/chem.20080091510.1002/chem.200800915 ↗