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Issue 14, 2018
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A full monolayer of superoxide: oxygen activation on the unmodified Ca3Ru2O7(001) surface

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Abstract

Activating the O2 molecule is at the heart of a variety of technological applications, most prominently in energy conversion schemes including solid oxide fuel cells, electrolysis, and catalysis. Perovskite oxides, both traditionally-used and novel formulations, are the prime candidates in established and emerging energy devices. This work shows that the as-cleaved and unmodified CaO-terminated (001) surface of Ca3Ru2O7, a Ruddlesden–Popper perovskite, supports a full monolayer of superoxide ions, O2, when exposed to molecular O2. The electrons for activating the molecule are transferred from the subsurface RuO2 layer. Theoretical calculations using both, density functional theory (DFT) and more accurate methods (RPA), predict the adsorption of O2 with Eads = 0.72 eV and provide a thorough analysis of the charge transfer. Non-contact atomic force microscopy (nc-AFM) and scanning tunnelling microscopy (STM) are used to resolve single molecules and confirm the predicted adsorption structures. Local contact potential difference (LCPD) and X-ray photoelectron spectroscopy (XPS) measurements on the full monolayer of O2 confirm the negative charge state of the molecules. The present study reports the rare case of an oxide surface without dopants, defects, or low-coordinated sites readily activating molecular O2.

Graphical abstract: A full monolayer of superoxide: oxygen activation on the unmodified Ca3Ru2O7(001) surface

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Publication details

The article was received on 09 Jan 2018, accepted on 04 Mar 2018 and first published on 05 Mar 2018


Article type: Paper
DOI: 10.1039/C8TA00265G
Citation: J. Mater. Chem. A, 2018,6, 5703-5713
  • Open access: Creative Commons BY-NC license
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    A full monolayer of superoxide: oxygen activation on the unmodified Ca3Ru2O7(001) surface

    D. Halwidl, W. Mayr-Schmölzer, M. Setvin, D. Fobes, J. Peng, Z. Mao, M. Schmid, F. Mittendorfer, J. Redinger and U. Diebold, J. Mater. Chem. A, 2018, 6, 5703
    DOI: 10.1039/C8TA00265G

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      [Original citation] - Published by The Royal Society of Chemistry.

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