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This is a In Vitro Study study.

August 19, 2025

Interfacial Trapping of Reactive Water and Concurrent Stabilization of Lattice Oxygen for Efficient Acidic Oxygen Evolution

ZWZhongfeng WangAllen Institute for Brain Science MWMingming WangTianjin University XLXinyi LiHong Kong Polytechnic University

Key Points

Al-RuO2 catalyst achieves a 10-fold higher turnover frequency than RuO2, significantly improving performance.
The new catalyst maintains operation for over 600 hours at 1.0 A cm-2, showcasing long-lasting stability.
Design incorporates strong Al-O bonding to inhibit Ru dissolution, optimized through altering the oxygen evolution pathway.
Dynamic trapping of reactive water enhances catalytic activity without compromising the structural integrity of the catalyst.

Abstract

RuO2 surpasses IrO2 in both activity and cost efficiency for the acidic oxygen evolution reaction (OER), yet its rapid degradation in membrane electrode assemblies (MEAs) under industrial current densities severely limits practical application. To resolve this activity-stability dilemma, we designed a dual-functional Al-RuO2 catalyst that simultaneously suppresses lattice oxygen oxidation and traps interfacial reactive water. Through strong Al-O bonding, Al dopants lock lattice oxygen and shift the OER pathway from the mixed adsorbate evolution mechanism (AEM) and lattice oxygen mechanism (LOM) on RuO2 to an exclusive AEM on Al-RuO2. This mechanistic transition inhibits Ru dissolution and preserves the structural integrity. Surface -OH and/or Lewis acidic Al sites dynamically trap free water via H-bonding and/or Lewis acid-base interactions to enhance the OER activity without sacrificing stability. Consequently, this Al-RuO2 achieves a 10-fold higher turnover frequency than RuO2 and high MEA performance (1.528 V@1.0 A cm-2, operation >600 h@1.0 A cm-2).

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