| 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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document
A high entropy oxide as high-activity electrocatalyst for water oxidation
Abstract
<jats:p>High entropy materials are a new pathway in the development of high-activity (electro )catalysts because of the inherent tunability and coexistence of multiple potential active sites, which may lead to earth-abundant catalyst materials for energy-efficient electrochemical energy storage. In this report, we identify how the multi-cation composition in high entropy perovskite oxides (HEO) contributes to high catalytic activity for the oxygen evolution reaction (OER), i.e. the key kinetically limiting half-reactions in several electrochemical energy conversion technologies, including green hydrogen generation. We compare the activity of the (001) facet of LaCr0.2Mn0.2Fe0.2Co0.2Ni0.2O3-δ with the parent compounds (single B-site in the ABO3 perovskite). While the single B-site perovskites roughly follow the expected volcano-type activity trends, the HEO clearly outperforms all of its parent compounds with 2.8 to 100 times higher currents at fixed overpotential. As all samples were grown as an epitaxial layer, our results indicate an intrinsic composition–function relationships, avoiding the effects of complex geometries or unknown surface composition. In-depth X-ray photoemission studies reveal a synergistic effect of simultaneous oxidation and reduction of different transition metal cations during adsorption of reaction intermediates. The surprisingly high OER activity demonstrates that HEOs are a highly attractive, earth-abundant new material class for high-activity OER electrocatalysts, possibly allowing fine-tuning the activity beyond the scaling limits of mono- or bimetallic oxides.</jats:p>