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 cm(2) 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

Zambianchi M;Benvenuti E;Bettini C;Gentili D;Cavallini M;Muccini M;Toffanin S;Melucci M
2016

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 cm(2) 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.
2016
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
Istituto per lo Studio dei Materiali Nanostrutturati - ISMN
design and synthesis
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/326645
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 28
  • ???jsp.display-item.citation.isi??? ND
social impact