Issue 8, 2011

Electrochromic and electroluminescent devices based on a novel branched quasi-dendric fluorene-carbazole-2,5-bis(2-thienyl)-1H-pyrrole system

Abstract

We report here the synthesis of a novel branched quasi-dendric system, 9,9′-(9,9′-dihexylfluorene-2,7-diyl)bis[3,6-bis(2,5-bis(2-thienyl)pyrrol-1-yl)carbazole], (FCSNS), in four steps, followed by coating onto an ITO-coated glass surface by an electropolymerization process to give a very stable cross-linked polymeric film (poly-FCSNS). The yellowish-green color of this film in its neutral state changed reversibly to black upon oxidation. An electrochromic device, assembled in the sandwich configuration [ITO/anodically coloring polymer (poly-FCSNS)//gel electrolyte//cathodically coloring polymer/(PEDOT)/ITO], exhibited a relatively short response time (about 1 s), a high redox stability, and a high coloration efficiency (1624 cm2C−1). In addition to electrochromic studies, organic light-emitting diode (OLED) work was also carried out using FCSNS. A multilayer OLED having a configuration of ITO/PEDOT:PSS/FCSNS/Alq3/LiF : Al was fabricated, and it showed a turn-on voltage of approximately 6 V and exhibited a bright green emission with a luminance of 3700 cd m−2. The maximum luminous efficiency was found to be 2.0 cd A−1 at 14 V and 11.75 mA cm−2. The emitted light from the OLED device is green, and has the color coordinates of (x, y) (0.33, 0.54) according to CIE. Electrochemical and optical properties were also studied by using cyclic voltammetry, UV-Vis absorption and fluorescence spectroscopy, respectively.

Graphical abstract: Electrochromic and electroluminescent devices based on a novel branched quasi-dendric fluorene-carbazole-2,5-bis(2-thienyl)-1H-pyrrole system

Supplementary files

Article information

Article type
Paper
Submitted
22 Jul 2010
Accepted
11 Nov 2010
First published
10 Jan 2011

J. Mater. Chem., 2011,21, 2684-2693

Electrochromic and electroluminescent devices based on a novel branched quasi-dendric fluorene-carbazole-2,5-bis(2-thienyl)-1H-pyrrole system

S. Koyuncu, O. Usluer, M. Can, S. Demic, S. Icli and N. Serdar Sariciftci, J. Mater. Chem., 2011, 21, 2684 DOI: 10.1039/C0JM02366C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements