Issue 19, 2016

Electrochemical synthesis, optical, electrochemical and electrochromic characterizations of indene and 1,2,5-thiadiazole-based poly(2,5-dithienylpyrrole) derivatives

Abstract

Indene and benzothiadiazole units were incorporated to the central pyrrole ring of the poly(thienylpyrrole) backbone, and they are denoted PDIT and PBDTA, respectively. PDIT, PBDTA and their corresponding copolymers (P(DIT-co-DTP) and P(BDTA-co-DTP)) were electrochemically synthesized and their electrochromic properties are reported. The PDIT and PBDTA films were not only reversibly oxidized and reduced but also accompanied by obvious color change (yellow, green, and blue). Their corresponding P(DIT-co-DTP) and P(BDTA-co-DTP) copolymer films present multicolor electrochromism. ΔTmax of the P(DIT-co-DTP) and P(BDTA-co-DTP) films were measured as 45.3% at 1314 nm and 43.5% at 930 nm, respectively, in an ionic liquid solution, and the η of PBDTA and P(DIT-co-DTP) films were calculated to be 167.8 cm2 C−1 at 1070 nm and 177.4 cm2 C−1 at 1314 nm, respectively, in an ionic liquid solution. ECDs based on PDIT, PBDTA, P(DIT-co-DTP), and P(BDTA-co-DTP) as anodic polymers and poly(3,4-(2,2-diethylpropylenedioxy)thiophene) (PProDOT-Et2) as a cathodic polymer were constructed. PBDTA/PProDOT-Et2 ECD showed a high ΔTmax (43.8%) at 590 nm and satisfactory cyclic voltammetry stability, whereas P(BDTA-co-DTP)/PProDOT-Et2 ECD showed high ΔTmax (44.0%) and coloration efficiency (504.6 cm2 C−1) at 594 nm.

Graphical abstract: Electrochemical synthesis, optical, electrochemical and electrochromic characterizations of indene and 1,2,5-thiadiazole-based poly(2,5-dithienylpyrrole) derivatives

Supplementary files

Article information

Article type
Paper
Submitted
28 Dec 2015
Accepted
29 Jan 2016
First published
01 Feb 2016

RSC Adv., 2016,6, 15988-15998

Electrochemical synthesis, optical, electrochemical and electrochromic characterizations of indene and 1,2,5-thiadiazole-based poly(2,5-dithienylpyrrole) derivatives

T. Wu and J. Li, RSC Adv., 2016, 6, 15988 DOI: 10.1039/C5RA27902J

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.

Social activity

Spotlight

Advertisements