A new anthracene-based twisted oligomer combining a rigid anthracene-xylene core with diphenylamine ends 4,4′-(anthracene-9,10-diyl)bis(2,5-dimethyl-N,N-diphenylaniline), DiPAXA, is herein presented as an efficient and deep blue emitter material. By exploiting DiPAXA as an emissive layer and 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT) as a p-type semiconducting layer, we realize a blue emitting unipolar light emitting transistor (OLET) with a maximum external quantum efficiency (EQE) of 0.13%, a charge mobility up to 0.32 cm2 V-1 s-1 and CIE color coordinates of (0.18, 0.21), i.e. closer to currently available standards (PAL, NTSC). Moreover, comparison with other anthracene-based blue emitters highlights the suitability of this family of twisted anthracene-xylene compounds for unipolar blue OLET applications as a result of the enhanced performances in terms of CIE coordinates and light emission output of newly synthesized DiPAXA.

Anthracene-based molecular emitters for non-doped deep-blue organic light emitting transistors

ZANARDI, Chiara;
2016-01-01

Abstract

A new anthracene-based twisted oligomer combining a rigid anthracene-xylene core with diphenylamine ends 4,4′-(anthracene-9,10-diyl)bis(2,5-dimethyl-N,N-diphenylaniline), DiPAXA, is herein presented as an efficient and deep blue emitter material. By exploiting DiPAXA as an emissive layer and 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT) as a p-type semiconducting layer, we realize a blue emitting unipolar light emitting transistor (OLET) with a maximum external quantum efficiency (EQE) of 0.13%, a charge mobility up to 0.32 cm2 V-1 s-1 and CIE color coordinates of (0.18, 0.21), i.e. closer to currently available standards (PAL, NTSC). Moreover, comparison with other anthracene-based blue emitters highlights the suitability of this family of twisted anthracene-xylene compounds for unipolar blue OLET applications as a result of the enhanced performances in terms of CIE coordinates and light emission output of newly synthesized DiPAXA.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/5012142
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