Atomic-level Ru-Ir mixing in rutile-type (RuIr)O<sub>2</sub> for efficient and durable oxygen evolution catalysis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39794326.
- Also identified by DOI 10.1038/s41467-025-55910-1 and PMC identifier 11723980.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The success of proton exchange membrane water electrolysis (PEMWE) depends on active and robust electrocatalysts to facilitate oxygen evolution reaction (OER). Heteroatom-doped-RuO<sub>x</sub> has emerged as a promising electrocatalysts because heteroatoms suppress lattice oxygen participation in the OER, thereby preventing the destabilization of surface Ru and catalyst degradation. However, identifying suitable heteroatoms and achieving their atomic-scale coupling with Ru atoms are nontrivial tasks. Herein, to steer the reaction pathway away from the involvement of lattice oxygen, we integrate OER-active Ir atoms into the RuO<sub>2</sub> matrix, which maximizes the synergy between stable Ru and active Ir centers, by leveraging the changeable growth behavior of Ru/Ir atoms on lattice parameter-modulated templates. In PEMWE, the resulting (RuIr)O<sub>2</sub>/C electrocatalysts demonstrate notable current density of 4.96 A cm<sup>-2</sup> and mass activity of 19.84 A mg<sub>Ru+Ir</sub><sup>-1</sup> at 2.0 V. In situ spectroscopic analysis and computational calculations highlight the importance of the synergistic coexistence of Ru/Ir-dual-OER-active sites for mitigating Ru dissolution via the optimization of the binding energy with oxygen intermediates and stabilization of Ru sites.