Tailoring Structure-Property Relationships in π-Conjugated Heterocyclic Poly(arylene alkylene) Anion-Exchange Membranes for High-Performance Water Electrolysis
(2026) In Advanced Science- Abstract
- Anion-exchange membrane water electrolysis (AEMWE) is a promising technology for sustainable hydrogen production, but practical applications are limited by the trade-off between hydroxide conductivity and alkaline stability of anion-exchange membranes (AEMs). Here, we report a molecular design strategy that regulates ion transport pathways and membrane stability by tethering quaternary ammonium cations via flexible side chains to π-conjugated heterocyclic backbone polymers. Durable cationic copolymers containing p-terphenyl with dibenzofuran (DBF) or dibenzothiophene (DBT) units are synthesized. Combined experimental and theoretical studies establish structure-property relationships linking heteroatom chemistry to the hydration,... (More)
- Anion-exchange membrane water electrolysis (AEMWE) is a promising technology for sustainable hydrogen production, but practical applications are limited by the trade-off between hydroxide conductivity and alkaline stability of anion-exchange membranes (AEMs). Here, we report a molecular design strategy that regulates ion transport pathways and membrane stability by tethering quaternary ammonium cations via flexible side chains to π-conjugated heterocyclic backbone polymers. Durable cationic copolymers containing p-terphenyl with dibenzofuran (DBF) or dibenzothiophene (DBT) units are synthesized. Combined experimental and theoretical studies establish structure-property relationships linking heteroatom chemistry to the hydration, microphase morphology, and ion transport. DBF-units promote dense hydrogen bonding networks, whereas DBT-units strengthen ion-dipole interactions and induce more pronounced microphase separation. Consequently, optimized DBF- and DBT-based membranes exhibit hydroxide conductivities exceeding 180 and 200 mS cm−1, respectively, at 80°C. In AEMWEs using non-precious-metal catalysts, these membranes deliver current densities above 4.1 and 5.1 A cm−2 at 2 V, respectively. The DBT-based membrane also maintains stable operation for over 1600 h at 1 A cm−2 and 60°C. This work establishes structure-performance relationships and provides a practical molecular design strategy for highly conductive, durable AEMs based on π-conjugated heterocyclic backbone units. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/60b0783d-87d3-4f35-ab53-914fb38ad96e
- author
- Wang, Qian
; Huang, Riyang
; Zhao, Wenzhe
; Chen, Si
LU
; Guo, Yunpeng
; Wu, Yang
; Zhao, Yun
; Jannasch, Patric
LU
and Yang, Jingshuai
LU
- organization
- publishing date
- 2026
- type
- Contribution to journal
- publication status
- epub
- subject
- in
- Advanced Science
- article number
- e77491
- pages
- 16 pages
- publisher
- John Wiley & Sons Inc.
- ISSN
- 2198-3844
- DOI
- 10.1002/advs.77491
- language
- English
- LU publication?
- yes
- id
- 60b0783d-87d3-4f35-ab53-914fb38ad96e
- date added to LUP
- 2026-04-03 12:48:12
- date last changed
- 2026-09-02 15:00:12
@article{60b0783d-87d3-4f35-ab53-914fb38ad96e,
abstract = {{Anion-exchange membrane water electrolysis (AEMWE) is a promising technology for sustainable hydrogen production, but practical applications are limited by the trade-off between hydroxide conductivity and alkaline stability of anion-exchange membranes (AEMs). Here, we report a molecular design strategy that regulates ion transport pathways and membrane stability by tethering quaternary ammonium cations via flexible side chains to π-conjugated heterocyclic backbone polymers. Durable cationic copolymers containing <i>p</i>-terphenyl with dibenzofuran (DBF) or dibenzothiophene (DBT) units are synthesized. Combined experimental and theoretical studies establish structure-property relationships linking heteroatom chemistry to the hydration, microphase morphology, and ion transport. DBF-units promote dense hydrogen bonding networks, whereas DBT-units strengthen ion-dipole interactions and induce more pronounced microphase separation. Consequently, optimized DBF- and DBT-based membranes exhibit hydroxide conductivities exceeding 180 and 200 mS cm<sup>−1</sup>, respectively, at 80°C. In AEMWEs using non-precious-metal catalysts, these membranes deliver current densities above 4.1 and 5.1 A cm<sup>−2</sup> at 2 V, respectively. The DBT-based membrane also maintains stable operation for over 1600 h at 1 A cm<sup>−2</sup> and 60°C. This work establishes structure-performance relationships and provides a practical molecular design strategy for highly conductive, durable AEMs based on π-conjugated heterocyclic backbone units.}},
author = {{Wang, Qian and Huang, Riyang and Zhao, Wenzhe and Chen, Si and Guo, Yunpeng and Wu, Yang and Zhao, Yun and Jannasch, Patric and Yang, Jingshuai}},
issn = {{2198-3844}},
language = {{eng}},
publisher = {{John Wiley & Sons Inc.}},
series = {{Advanced Science}},
title = {{Tailoring Structure-Property Relationships in π-Conjugated Heterocyclic Poly(arylene alkylene) Anion-Exchange Membranes for High-Performance Water Electrolysis}},
url = {{http://dx.doi.org/10.1002/advs.77491}},
doi = {{10.1002/advs.77491}},
year = {{2026}},
}