journal article·2021-10

Wet process feasible novel fluorene-based molecular hole transporting layer for phosphorescent organic light emitting diodes

Sujith Sudheendran Swayamprabha, Gintare Krucaite, Deepak Kumar Dubey, Kiran Kishore Kesavan, Joydip De, Mangey Ram Nagar, Hsun Lee, Simona Sutkuviene, Santanu Pal, Sun-Zen Chen, Raminta Beresneviciute, Saulius Grigalevičius, Jwo-Huei Jou

Optical Materials· Volume 120
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Abstract

Abstract Solution processable hole transporting materials (HTMs) are indispensable component for the cost-effective and large-area roll-to-roll fabrication of organic light emitting diodes (OLEDs). Hole transport layers should display high triplet energy, good hole injection properties along with potential electron blocking capability. In this paper, we report a series of novel fluorene-based HTMs, 9,9-diethyl-2,7-bis(2-(trifluoromethyl)phenyl)-9H-fluorene (3), 9,9-diethyl-2,7-bis(3-(trifluoromethyl)phenyl)-9H-fluorene (4) and 9,9- diethyl-2,7-bis(4-(trifluoromethyl)phenyl)-9H-fluorene (5) containing symmetrical and asymmetrical substitution of trifluoromethyl pendants at different positions. The synthesized HTMs have an exceptional solubility in common organic solvents such as THF (tetrahydrofuran), o-Xylene, etc. and possess good thermal stability to form morphologically stable films. The suitable molecular energy level alignment (HOMO-LUMO) for barrier free injection, adequate ionization potential (6.12, 6.20, and 6.23 eV) and high triplet energies (3.12,3.17, and 3.13 eV) for compound 3, 4, and 5, these suitable characteristics promote materials performance as a good hole transporting layer (HTL). Solution-processed yellow phosphorescent OLEDs fabricated by utilizing these HTMs with a conventional yellow emitter Iridium (III)bis (4-phenylthieno [3,2-c]pyridinato-N,C2′)acetylacetonate (PO-01) doped in 4,4′-bis(N-carbazolyl)-1,1′-biphenyl (CBP) host. The best device with molecule 4 showed an improvement of 54 % in current efficiency (CE) from 23.3 to 35.8 cd/A and 14 % in external quantum efficiency (EQE) from 11.3 to 12.9 %, compared to reference device containing N, N′-Bis(naphthalen-1-yl)-N,N′-bis(phenyl)benzidine (NPB) as HTL. Compounds 3 and 5 based devices also showed a competitive performance with the reference device. The effect of solvent was also studied. These outcomes recommend that this type of solution processable HTMs will be promising contender for high-efficiency OLED devices.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Catalytic Cross-Coupling Reactions

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

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