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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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Haug, Leander
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Publications (4/4 displayed)
- 2024How defects in lanthanum iron manganite perovskite structures promote the catalytic reduction of NO by CO
- 2023Pivotal Role of Ni/ZrO2 Phase Boundaries for Coke-Resistant Methane Dry Reforming Catalysts
- 2023Electrocatalytic Enhancement of CO Methanation at the Metal–Electrolyte Interface Studied Using In Situ X-ray Photoelectron Spectroscopy
- 2022Atomic-Scale Insights into Nickel Exsolution on LaNiO 3 Catalysts via In Situ Electron Microscopycitations
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article
Electrocatalytic Enhancement of CO Methanation at the Metal–Electrolyte Interface Studied Using In Situ X-ray Photoelectron Spectroscopy
Abstract
<jats:p>For the direct reduction of CO2 and H2O in solid oxide electrolysis cells (SOECs) with cermet electrodes toward methane, a fundamental understanding of the role of elemental carbon as a key intermediate within the reaction pathway is of eminent interest. The present synchrotron-based in situ near-ambient-pressure X-ray photoelectron spectroscopy (NAP-XPS) study shows that alloying of Ni/yttria-stabilized-zirconia (YSZ) cermet electrodes with Cu can be used to control the electrochemical accumulation of interfacial carbon and to optimize its reactivity toward CO2. In the presence of syngas, sufficiently high cathodic potentials induce excess methane on the studied Ni/yttria-stabilized-zirconia (YSZ)-, NiCu/YSZ- and Pt/gadolinium-doped-ceria (GDC) cermet systems. The hydrogenation of carbon, resulting from CO activation at the triple-phase boundary of Pt/GDC, is most efficient.</jats:p>