Water Oxidation Promoted by Proximity-Induced Magnetism under Dzyaloshinskii–Moriya Interaction
Spin polarization governs the kinetics of multielectron water oxidation, yet benchmark catalysts like IrO<sub>2</sub> lack intrinsic ferromagnetism at ambient temperature, precluding spin control. Here, we exploit the interfacial Dzyaloshinskii-Moriya interaction (DMI) in Co/IrO<sub>2</sub> bilayers to induce spin-polarized states in the surface IrO<sub>2</sub>. This DMI-driven spin polarization boosts intrinsic oxygen evolution reaction activity by 1 order of magnitude, achieving a turnover frequency of 4.17 s<sup>-1</sup> at 300 mV overpotential. Ferromagnetic resonance spectroscopy quantifies strong interfacial spin polarization via a 100% increase in the Gilbert damping. Spin-polarized DFT shows that DMI stabilizes a ferromagnetic ground state in IrO<sub>2</sub> and reveals that spin ordering alters the adsorption configurations and lowers reaction barriers for *OH dehydrogenation and O-O coupling. Inserting a Cu spacer eliminates DMI, quenching both magnetism and catalytic enhancement. Our results establish interfacial DMI as a general strategy to activate hidden spin states in nonmagnetic oxides, offering a new route to surpass the activity limits in water-oxidation catalysis.
Authors
- Xingjie Peng
- Zhichuan Xu
- Tianze Wu (ORCID: https://orcid.org/0000-0001-7123-6844)
- Xiaotian Zhao (ORCID: https://orcid.org/0000-0002-0482-4758)
- Shixuan Du
- L. Tao
- R. Sun
- Ding Ma
- Xiao Ren
- Wu Zhou
Institutions
- Nanyang Technological University (SG)
- Chinese Academy of Sciences (CN)
- Peking University (CN)
- FZU ‒ Institute of Physics of the Academy of Sciences of the Czech Republic (CZ)
- Technical Institute of Physics and Chemistry (CN)
- National Laboratory for Superconductivity (CN)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-02-09
- DOI
- https://doi.org/10.1021/jacs.5c17778
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00