Reversible and Irreversible Cation Intercalation in NiFeO x Oxygen Evolution Catalysts in Alkaline Media.
Hanna TrzesniowskiNipon DekaOnno van der HeijdenRonny GolnakJie XiaoMarc T M KoperRobert SeidelRik Valentijn MomPublished in: The journal of physical chemistry letters (2023)
For electrocatalysts with a layered structure, ion intercalation is a common phenomenon. Gaining reliable information about the intercalation of ions from the electrolyte is indispensable for a better understanding of the catalytic performance of these electrocatalysts. Here, we take a holistic approach for following intercalation processes by studying the dynamics of the catalyst, water molecules, and ions during intercalation using operando soft X-ray absorption spectroscopy (XAS). Sodium and oxygen K-edge and nickel L-edge spectra were used to investigate the Na + intercalation in a Ni 0.8 Fe 0.2 O x electrocatalyst during the oxygen evolution reaction (OER) in NaOH (0.1 M). The Na K-edge spectra show an irreversible intensity increase upon initial potential cycling and a reversible intensity increase at the intercalation potential, 1.45 V RHE , coinciding with an increase in the Ni oxidation state. Simultaneously, the O K-edge spectra show that the Na + intercalation does not significantly impact the hydration of the catalyst.
Keyphrases
- metal organic framework
- ionic liquid
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- reduced graphene oxide
- high resolution
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- quantum dots
- density functional theory
- room temperature
- magnetic resonance imaging
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- computed tomography
- transition metal
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- nitric oxide
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- carbon nanotubes
- solid state
- water soluble