Abstract
A series of red fluorescent materials (compounds 1-4), which each contain the symmetric fluorene-thiophene-BT-thiophene-fluorene core, is presented along with their performance in solution-processed OLED devices. Extending the molecular conjugation through end-capping with additional fluorene units (compound 2), or through incorporation of donor functionalities (compounds 3 and 4) improves OLED performance relative to the parent compound 1. Notably, incorporating triphenylamine donor groups in compound 3 led to solution-processed OLED devices operating with a peak luminance of 2888 cd m −2 and a low turn-on voltage (3.6 V).
| Original language | English |
|---|---|
| Pages (from-to) | 3934-3944 |
| Number of pages | 11 |
| Journal | Journal of Materials Chemistry C |
| Volume | 7 |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - 4 Mar 2019 |
Funding
NJF, JC and AK thank the EPSRC for funding (EP/R03480X/1, EP/P02744X/2 and EP/N009908/2). We acknowledge the EPSRC UK National Mass Spectrometry Facility (NMSF) at Swansea University for HRMS data.
Keywords
- end group functionalisation
- small molecules
- organic light-emitting diodes
- fluorene–thiophene–benzothiadiazole motif
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