Abstract
Herein, we report the synthesis and electrochemical oxygen evolution experiments for a graphene-supported Ni3MnO4 catalyst. The changes that occur at the Ni active sites during the electrocatalyic oxygen evolution reaction (OER) were elucidated by a combination of operando Ni L-edge X-ray absorption spectroscopy (XAS) and Ni 2p3d resonant inelastic X-ray scattering (RIXS). These data are compared to reference measurements on NiO, β-Ni(OH)2, β-NiOOH, and γ-NiOOH. Through this comparative analysis, we are able to show that under alkaline conditions (0.1 M KOH), the oxides of the Ni3MnO4 catalyst are converted to hydroxides. At the onset of catalysis (1.47 V), the β-Ni(OH)2-like phase is oxidized and converted to a dominantly γ-NiOOH phase. The present study thus challenges the notion that the β-NiOOH phase is the active phase in OER and provides further evidence that the γ-NiOOH phase is catalytically active. The ability to use Ni L-edge XAS and 2p3d RIXS to provide a rational basis for structure-activity correlations is highlighted.
Highlights
The ability to use sunlight to split water into H2 and O2 is an attractive target toward realizing a renewable energy economy
The electrocatalytic characterization shows that the Ni3MnO4 catalyst shows an ∼20−30% decrease in catalytic current and almost one-third of the turnover frequency (TOF) on NiO
Operando Ni L-edge X-ray absorption spectroscopy (XAS) and 2p3d RIXS were utilized to follow the evolution of the Ni site during the activation and oxygen evolution reaction (OER) conditions
Summary
The ability to use sunlight to split water into H2 and O2 is an attractive target toward realizing a renewable energy economy. To obtain more detailed insights into the changes in an electronic structure upon incorporation of Mn into the nickel oxide-based material, we measured Ni 2p3d RIXS In this experiment, the features, which appear on the energy transfer (ET) axis, correspond to d−d excitations (at energies
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