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◆ Journal of the American Chemical Society2026-01-02· X-ray absorption spectroscopy

Operando HERFD-XAS of Bimetallic Perovskite Thin Film Interfaces

Qijun Che, Iris C. G. van den Bosch, Jelle R. H. Ruiters, Yuang Piao, Christoph Baeumer, Glatzel Pieter, Danilo Kühn, Frank M. F. de Groot

原始摘要(英文原文)· Original abstract
We investigated the valence dynamics of thin films during the electrocatalytic oxygen evolution reaction using operando high-energy-resolution fluorescence-detected (HERFD) X-ray absorption spectroscopy (XAS) in a 0.1 M KOH solution under an applied potential. We show that it is possible to measure the 10 unit cell (∼4 nm) bimetallic perovskite oxide La 2 CoMnO 6 thin film grown on Pt-covered SiN x membranes. Operando Co and Mn K-edge HERFD XAS spectra on the active surface species were recorded from the backside of the SiN x membrane. The HERFD XAS Co K-edge spectra reveal a (partial) increase in the oxidation state from Co 2+ in ex situ conditions to mainly Co 3+ in the solid–liquid open-circuit voltage (OCV). Voltage-dependent Co K-edge HERFD XAS white line intensities show that Co is oxidized toward the higher oxidation state, while Mn remains Mn 4+ . Interestingly, the Co and Mn main edge shifts with the average valence change of 0.20; the valence of Mn is constant, implying that the valence of Co increases by 0.40. The OCV spectra were reversible when switching off the potentials. These observations clearly identify element-specific valence dynamics in the intrinsic oxygen evolution reaction.
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