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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Sun, Zhaozong
Aarhus University
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (15/15 displayed)
- 2023Steering carbon dioxide reduction toward C–C coupling using copper electrodes modified with porous molecular filmscitations
- 2022Can the CO 2 Reduction Reaction Be Improved on Cu:Selectivity and Intrinsic Activity of Functionalized Cu Surfacescitations
- 2022The cobalt oxidation state in preferential CO oxidation on CoO x /Pt(111) investigated by operando X-ray photoemission spectroscopycitations
- 2022The cobalt oxidation state in preferential CO oxidation on CoOx/Pt(111) investigated by operando X-ray photoemission spectroscopycitations
- 2022Can the CO2Reduction Reaction Be Improved on Cucitations
- 2021Nanoscale Chevrel-Phase Mo 6 S 8 Prepared by a Molecular Precursor Approach for Highly Efficient Electrocatalysis of the Hydrogen Evolution Reaction in Acidic Mediacitations
- 2021Nanoscale Chevrel-Phase Mo6S8Prepared by a Molecular Precursor Approach for Highly Efficient Electrocatalysis of the Hydrogen Evolution Reaction in Acidic Mediacitations
- 2021Nanoscale Chevrel Phase Mo6S8 Prepared by a Molecular Precursor Approach for Highly Efficient Electrocatalysis of the Hydrogen Evolution Reaction in Acidic Media
- 2021Nanoscale Chevrel Phase Mo6S8 Prepared by a Molecular Precursor Approach for Highly Efficient Electrocatalysis of the Hydrogen Evolution Reaction in Acidic Media
- 2020Cubes on a string:a series of linear coordination polymers with cubane-like nodes and dicarboxylate linkerscitations
- 2019Anisotropic iron-doping patterns in two-dimensional cobalt oxide nanoislands on Au(111)citations
- 2019Structural and electronic properties of Fe dopants in cobalt oxide nanoislands on Au(111)citations
- 2018Phase Transitions of Cobalt Oxide Bilayers on Au(111) and Pt(111):The Role of Edge Sites and Substrate Interactionscitations
- 2018Phase Transitions of Cobalt Oxide Bilayers on Au(111) and Pt(111)citations
- 2017Phase Transitions of Cobalt Oxide Bilayers on Au(111) and Pt(111): The Role of Edge Sites and Substrate Interactions.citations
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article
Phase Transitions of Cobalt Oxide Bilayers on Au(111) and Pt(111)
Abstract
<p>Well-characterized metal oxides supported on single crystal surfaces serve as valuable model systems to study fundamental chemical properties and reaction mechanisms in heterogeneous catalysis or as new thin film metal oxide catalysts in their own right. Here, we present scanning tunneling microscopy and X-ray photoelectron spectroscopy results for cobalt oxide nanoislands that reveal the detailed atomistic mechanisms leading to transitions between Co-O bilayer and O-Co-O trilayer, induced by oxidation in O<sub>2</sub> and reductive vacuum annealing treatments, respectively. By comparing between two different noble metal substrates, Au(111) and Pt(111), we further address the influence of the substrate. Overall, nanoisland edges act to initiate both the oxidation and reduction processes on both substrates. However, important influences of the choice of substrate were found, as the progress of oxidation includes intermediate steps on Au(111) not observed on Pt(111), where the oxidation on the other hand takes place at a significantly higher rate. During reductive treatment of trilayer, the bilayer structure gradually reappears on Pt(111), but not on Au(111) where the reduction rather results in the appearance of a stacked cobalt oxide morphology. These observations point to strong differences in the catalytic behavior between Au and Pt supported cobalt oxides, despite the otherwise strong structural similarities.</p>