Issue 34, 2018

Poly(arylene alkylene)s with pendant N-spirocyclic quaternary ammonium cations for anion exchange membranes

Abstract

Aromatic polymers functionalised with cycloaliphatic quaternary ammonium (QA) cations are currently emerging as base-stable anion exchange membranes (AEMs) for use in alkaline fuel cells and water electrolyzers. In the present work, we first prepared poly(biphenyl piperidine)s by superacid-mediated polycondensations, and then introduced different N-spirocyclic QA cations via cyclo-quaternisation of the piperidine rings. The resulting polymers and AEMs were free of diaryl ether linkages and benzylic C–H bonds, and showed very high thermal stability and hydroxide ion conductivity. Alkaline testing up to 120 °C implied that the alkaline stability of the spirocyclic cations was limited by distortions of the ring conformations caused by the rigid polymer backbone. As a consequence, the ring directly attached to the backbone degraded significantly faster by Hofmann β-elimination than the pendant ring in the spirocyclic cations. These results provide valuable insights towards the molecular design of highly thermochemically stable AEMs functionalised with N-spirocyclic QA cations.

Graphical abstract: Poly(arylene alkylene)s with pendant N-spirocyclic quaternary ammonium cations for anion exchange membranes

Supplementary files

Article information

Article type
Paper
Submitted
20 May 2018
Accepted
01 Aug 2018
First published
01 Aug 2018
This article is Open Access
Creative Commons BY-NC license

J. Mater. Chem. A, 2018,6, 16537-16547

Poly(arylene alkylene)s with pendant N-spirocyclic quaternary ammonium cations for anion exchange membranes

T. H. Pham, J. S. Olsson and P. Jannasch, J. Mater. Chem. A, 2018, 6, 16537 DOI: 10.1039/C8TA04699A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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