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

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Summary

■ INTRODUCTION

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

■ CONCLUSIONS
■ ACKNOWLEDGMENTS
Findings
■ REFERENCES

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