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Oxidation resistant cerium oxide styrene-ethylene-propylene-styrene (SEPS) composite anion exchange membranes for water electrolysis

Lookup NU author(s): Dr Balakondareddy SanaORCiD, Dr Simon DohertyORCiD, Professor Mohamed MamloukORCiD

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

This study investigates the reinforcement of quaternised styrene-ethylene-propylene-styrene (QSEPS) ionomers using a porous PTFE matrix (1 μm pore size and 70% porosity) and cerium oxide (CeO2) nanoparticles as a strategy to balance mechanical durability, ionic conductivity, and oxidative stability of the anion exchange membrane in a water electrolyser (AEMWE). Vacuum filtration achieved 69 wt.% QSEPS loading in PTFE, with 72.5 wt.% infiltrating pores (60.1 v.% pore occupancy) and 27.5 wt.% forming an 8 μm surface layer. The composite QSEPS/PTFE exhibited reduced ionic conductivity of 0.025 S/cm at 20°C compared with 0.038 S/cm for neat QSEPS, corresponding to a 32% reduction. This has been attributed to geometric constraints and tortuous ion pathways of PTFE alongside limited hydration (16% lower water uptake than QSEPS). Incorporating 6 wt.% CeO2 nanoparticles enhanced oxidative stability via radical scavenging, using the Ce3+/Ce4+ redox cycle to neutralize hydroxyl radicals. Despite a lower initial conductivity (35 mS/cm at 60°C, 73% of QSEPS/PTFE), QSEPS/CeO2/PTFE achieved higher tensile strength (21.04 MPa) and retained 246 mA/cm2 current density after 900 hrs of electrolysis (24.2% higher than QSEPS/PTFE). Solid-state 13C NMR cross-polarization total sideband suppression (CPTOSS) of residual solid membranes and solution 1H and 13C NMR of the residual Fenton solution is consistent with the "two-segment" fragmentation model, which explained post-degradation soluble/insoluble residue formation. Solution 1H and 13C NMR identified identical soluble byproducts in both composites which include carbonyl species such as aldehydes and carboxylates as well as ammonium salts possible resulting from nucleophilic substitution. While CeO2 mitigated backbone oxidation it failed to protect quaternary ammonium (QA) groups, highlighting a trade-off between mechanical reinforcement and QA stability. In other words, CeO2 only mitigates hydroxyl radical flux, which decreased the degradation rate.


Publication metadata

Author(s): Mohanraj C, Atout HAE, Sana B, Doherty S, Mamlouck M

Publication type: Article

Publication status: Published

Journal: International Journal of Hydrogen Energy

Year: 2026

Volume: 215

Print publication date: 06/03/2026

Online publication date: 09/02/2026

Acceptance date: 20/01/2026

Date deposited: 04/02/2026

ISSN (print): 0360-3199

ISSN (electronic): 1879-3487

Publisher: Elsevier Ltd

URL: https://doi.org/10.1016/j.ijhydene.2026.153643

DOI: 10.1016/j.ijhydene.2026.153643

Data Access Statement: The datasets underpinning this publication have been archived in the Newcastle University Data Repository and are available at: https://doi. org/10.25405/data.ncl.31272838


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Funding

Funder referenceFunder name
EP/T00939X/1
EPSRC
Horizon Europe Guarantee scheme under grant reference number (10042301)
UKRI

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