Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4940
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dc.contributor.authorDe, Joydip-
dc.contributor.authorPal, Santanu-
dc.date.accessioned2023-08-21T08:29:37Z-
dc.date.available2023-08-21T08:29:37Z-
dc.date.issued2021-
dc.identifier.citationOptical Materials, 120, 111410.en_US
dc.identifier.urihttps://doi.org/10.1016/j.optmat.2021.111410-
dc.identifier.urihttp://hdl.handle.net/123456789/4940-
dc.descriptionOnly IISERM authors are available in the record.en_US
dc.description.abstractSolution 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.en_US
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.subjectWeten_US
dc.subjectprocessen_US
dc.subjectfeasibleen_US
dc.subjectfluorene-baseden_US
dc.subjectmolecularen_US
dc.subjecttransportingen_US
dc.titleWet process feasible novel fluorene-based molecular hole transporting layer for phosphorescent organic light emitting diodesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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