| Home > Publications database > Complexions at the Electrolyte/Electrode Interface in Solid Oxide Cells |
| Journal Article | FZJ-2021-05750 |
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2021
Wiley-VCH
Weinheim
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Please use a persistent id in citations: http://hdl.handle.net/2128/29849 doi:10.1002/admi.202100967
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.
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