Issue 43, 2014

Correlating on-substrate prepared electrochromes with their solution processed counterparts – towards validating polyazomethines as electrochromes in functioning devices

Abstract

A series of polyazomethines prepared from complementary triphenylamine diamines and thiophene dialdehydes by both solution step-growth and on-substrate polymerizations were examined. The absorbance, electrochemical, and spectroelectrochemical properties of the solution processable polyazomethines were compared to their on-substrate prepared counterparts that were immobilized on ITO coated glass substrates. The on-substrate prepared polymers were found to have enhanced optical and spectroelectrochemical properties compared to their solution processed counterparts. The optoelectronic properties were also contingent on the substitution of the triphenylamine repeating unit with electron donating and withdrawing groups. The on-substrate prepared polyazomethines offered many advantages compared to their counterparts prepared by conventional solution step-growth polymerization, including shorter polymerization times, simpler reaction conditions, straightforward purification, extended duty cycle in simulated electrochromic devices, and enhanced colors, among many others. More importantly, the on-substrate prepared polyazomethines were consistently immobilized on the device electrodes without delamination with extended oxidation/neutralization switching cycles between the neutral and oxidized states.

Graphical abstract: Correlating on-substrate prepared electrochromes with their solution processed counterparts – towards validating polyazomethines as electrochromes in functioning devices

Supplementary files

Article information

Article type
Paper
Submitted
14 May 2014
Accepted
18 Jul 2014
First published
08 Aug 2014

J. Mater. Chem. C, 2014,2, 9099-9108

Correlating on-substrate prepared electrochromes with their solution processed counterparts – towards validating polyazomethines as electrochromes in functioning devices

M. E. Mulholland, D. Navarathne, M. L. Petrus, T. J. Dingemans and W. G. Skene, J. Mater. Chem. C, 2014, 2, 9099 DOI: 10.1039/C4TC01003E

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