| People | Locations | Statistics |
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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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Gunkel, Felix
Forschungszentrum Jülich
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (24/24 displayed)
- 2024Structural, magnetic and electrical properties of oxygendeficientLa(0.6)Sr(0.4)CoO(3-δ) thin films
- 2024Space charge governs the kinetics of metal exsolutioncitations
- 2023Separating the Effects of Band Bending and Covalency in Hybrid Perovskite Oxide Electrocatalyst Bilayers for Water Electrolysis
- 2023Enhanced metal exsolution at the non-polar (001) surfaces of multi-faceted epitaxial thin filmscitations
- 2023A High-Entropy Oxide as High-Activity Electrocatalyst for Water Oxidationcitations
- 2023A High-Entropy Oxide as High-Activity Electrocatalyst for Water Oxidationcitations
- 2022Atomistic Insights into Activation and Degradation of La0.6Sr0.4CoO3-δElectrocatalysts under Oxygen Evolution Conditionscitations
- 2022Separating the Effects of Band Bending and Covalency in Hybrid Perovskite Oxide Electrocatalyst Bilayers for Water Electrolysiscitations
- 2022A high entropy oxide as high-activity electrocatalyst for water oxidation
- 2022Quantitative Determination of Native Point‐Defect Concentrations at the ppm Level in Un‐Doped BaSnO 3 Thin Filmscitations
- 2022Atomistic Insights into Activation and Degradation of La0.6Sr0.4CoO3−δ Electrocatalysts under Oxygen Evolution Conditionscitations
- 2022Activity-Stability Relationships in Oxide Electrocatalysts for Water Electrolysiscitations
- 2021Carbonate formation lowers the electrocatalytic activity of perovskite oxides for water electrolysiscitations
- 2021Identifying Ionic and Electronic Charge Transfer at Oxide Heterointerfacescitations
- 2020SrTiO3 termination controlcitations
- 2020Effect of Cationic Interface Defects on Band Alignment and Contact Resistance in Metal/Oxide Heterojunctionscitations
- 2019Electrolysis of Water at Atomically Tailored Epitaxial Cobaltite Surfacescitations
- 2017Unraveling the enhanced Oxygen Vacancy Formation in Complex Oxides during Annealing and Growthcitations
- 2016Defect-control of conventional and anomalous electron transport at complex oxide interfacescitations
- 2016Dynamics of the metal-insulator transition of donor-doped SrTi O $_{3}$citations
- 2015Surface Termination Conversion during SrTiO$_{3}$ Thin Film Growth Revealed by X-ray Photoelectron Spectroscopycitations
- 2015The influence of the local oxygen vacancy concentration on the piezoresponse of strontium titanate thin filmscitations
- 2015Surface Termination Conversion during SrTiO3 Thin Film Growth Revealed by X-ray Photoelectron Spectroscopycitations
- 2013The role of defects at functional interfaces between polar and non-polar perovskite oxides
Places of action
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article
Enhanced metal exsolution at the non-polar (001) surfaces of multi-faceted epitaxial thin films
Abstract
<jats:title>Abstract</jats:title><jats:p>Metal exsolution is a dynamic process driven under a reducing atmosphere and at elevated temperatures that results in the self-assembly of nanoparticles at the surface of complex perovskite catalysts. The nanoparticle characteristics of metal exsolution catalysts can be subject to considerable inhomogeneity, and the anisotropic surface properties of ceramic oxides have been identified to have a major influence on the exsolution behavior. We systematically reveal the orientation-dependent anisotropy of the exsolution behavior of Ni in SrTi<jats:sub>0.9</jats:sub>Nb<jats:sub>0.05</jats:sub>Ni<jats:sub>0.05</jats:sub>O<jats:sub>3−δ</jats:sub> using multi-faceted epitaxial thin films that represent a material system with properties in between functional ceramics and single-crystalline perovskite thin film model systems. Using an approach of combined orientation mapping and surface imaging we study the exsolution behavior with particular focus on the initial exsolution response, i.e. after short annealing times. We find orientation-specific variations in the surface morphology of the thin film facets. In the as-prepared state, surface reconstructions cause the formation of patterned surface structures for all thin film facets apart from (001) surfaces, which exhibit a plain surface morphology as well as an enhanced exsolution response. Surface reconstructions and their inherent energy landscape may hence cause an additional energy barrier for the exsolution reaction that results in orientation-dependent differences in the exsolution kinetics.</jats:p>