Issue 31, 2018

N-Alkyl substituted 1H-benzimidazoles as improved n-type dopants for a naphthalene-diimide based copolymer

Abstract

Doped polymer semiconductors are actively studied for opto- and micro-electronic applications including thermoelectric generators, where a high electrical conductivity is a key factor. In general, n-type doping is more challenging to achieve than p-type doping. Here we study n-type doping of a commonly used electron transporting naphthalene-diimide bithiophene copolymer with a series of air-stable and solution-processable benzimidazole dopants. To understand the role of dopant structure on miscibility and the resulting conductivity, benzimidazoles with different linear and branched alkyl substituents were synthesized, and their doping efficacy compared through combined morphological, electrical and thermoelectric characterization. We observe a clear dependence of the nature of the alkyl substituent on dopant intercalation into the semicrystalline morphology. By increasing the length or the steric hindrance of the alkyl substituents, the miscibility between dopant and copolymer is enhanced leading to optimized electrical conductivity.

Graphical abstract: N-Alkyl substituted 1H-benzimidazoles as improved n-type dopants for a naphthalene-diimide based copolymer

Supplementary files

Article information

Article type
Paper
Submitted
25 May 2018
Accepted
11 Jul 2018
First published
19 Jul 2018

J. Mater. Chem. A, 2018,6, 15294-15302

Author version available

N-Alkyl substituted 1H-benzimidazoles as improved n-type dopants for a naphthalene-diimide based copolymer

B. Saglio, M. Mura, M. Massetti, F. Scuratti, D. Beretta, X. Jiao, C. R. McNeill, M. Sommer, A. Famulari, G. Lanzani, M. Caironi and C. Bertarelli, J. Mater. Chem. A, 2018, 6, 15294 DOI: 10.1039/C8TA04901G

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