A spin polarization porous transport layer for anion exchange membrane water electrolyzers with a current density of 11.5 A cm−2

Abstract

Alkaline anion exchange membrane water electrolyzers (AEMWEs) are a promising technology for hydrogen production from renewable energy sources. However, their performance is far lower than that of proton exchange membrane water electrolyzers and traditional alkaline water electrolyzers. Here, we demonstrate that chiral catalysts embedded in the porous transport layer (PTL) can enhance AEMWE performance. The chiral CoOx-based PTL achieves a current density of 8.21 A cm−2 at 2.0 V in AEMWEs, which is higher than that of the achiral meso-CoOx-PTL (5.42 A cm−2). The chiral CoOx-PTL provides additional active sites and facilitates interfacial charge transfer between the catalyst and electrolyte, thereby increasing the current density during electrocatalysis. Electrochemical analysis and measurement of H2O2 byproduct concentration confirmed that the chiral CoOx-PTL suppresses H2O2 formation even after surface reconstruction, supporting the persistence of the spin polarization. Extending this strategy to bimetallic systems, the chiral NiFe-based PTL achieves a remarkable current density of 11.5 A cm−2 at 2.0 V and exceptional operational stability, maintaining 1 A cm−2 for over 1000 hours in 1 M KOH. These results demonstrate the potential of spin-engineered catalysts for advancing AEMWEs toward industrial-scale hydrogen production.

Graphical abstract: A spin polarization porous transport layer for anion exchange membrane water electrolyzers with a current density of 11.5 A cm−2

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Article information

Article type
Paper
Submitted
02 Oct 2025
Accepted
10 Nov 2025
First published
10 Nov 2025

Sustainable Energy Fuels, 2026, Advance Article

A spin polarization porous transport layer for anion exchange membrane water electrolyzers with a current density of 11.5 A cm−2

T. H. Kim, C. Hu, H. K. Cho, S. H. Jae, S. Lee, B. Yeom, Y. M. Lee and Y. Kim, Sustainable Energy Fuels, 2026, Advance Article , DOI: 10.1039/D5SE01313E

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