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Complexions at the Electrolyte/Electrode Interface in Solid Oxide Cells

MPS-Authors
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Türk,  Hanna
Theory, Fritz Haber Institute, Max Planck Society;
Chair for Theoretical Chemistry and Catalysis Research Center, Department of Chemistry, Technische Universität München;

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Schmidt,  Franz
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Department of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion;

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Götsch,  Thomas
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Girgsdies,  Frank
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Hammud,  Adnan
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Ivanov,  Danail
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Reuter,  Karsten
Theory, Fritz Haber Institute, Max Planck Society;
Chair for Theoretical Chemistry and Catalysis Research Center, Department of Chemistry, Technische Universität München;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Department of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion;

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Knop-Gericke,  Axel
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Department of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion;

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Scheurer,  Christoph
Theory, Fritz Haber Institute, Max Planck Society;
Chair for Theoretical Chemistry and Catalysis Research Center, Department of Chemistry, Technische Universität München;

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Lunkenbein,  Thomas
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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admi.202100967.pdf
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Citation

Türk, H., Schmidt, F., Götsch, T., Girgsdies, F., Hammud, A., Ivanov, D., et al. (2021). Complexions at the Electrolyte/Electrode Interface in Solid Oxide Cells. Advanced Materials Interfaces, 8(18): 2100967. doi:10.1002/admi.202100967.


Cite as: https://hdl.handle.net/21.11116/0000-0009-1CAB-8
Abstract
Rapid deactivation presently limits a wide spread use of high-temperature solid oxide cells (SOCs) as otherwise highly efficient chemical energy converters. With deactivation triggered by the ongoing conversion reactions, an atomic-scale understanding of the active triple-phase boundary between electrolyte, electrode, and gas phase is essential to increase cell performance. Here, a multi-method approach is used comprising transmission electron microscopy and first-principles calculations and molecular simulations to untangle the atomic arrangement of the prototypical SOC interface between a lanthanum strontium manganite (LSM) anode and a yttria-stabilized zirconia (YSZ) electrolyte in the as-prepared state after sintering. An interlayer of self-limited width with partial amorphization and strong compositional gradient is identified, thus exhibiting the characteristics of a complexion that is stabilized by the confinement between two bulk phases. This offers a new perspective to understand the function of SOCs at the atomic scale. Moreover, it opens up a hitherto unrealized design space to tune the conversion efficiency.