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Journal article

Assessment of the cathode contribution to the degradation of anode-supported solid oxide fuel cells

From

Electrochemistry, Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark1

Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark2

Risø National Laboratory for Sustainable Energy, Technical University of Denmark3

Microstructures and Interfaces, Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark4

Electroceramics, Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark5

The degradation of anode-supported cells was studied over 1500 h as a function of cell polarization either in air or oxygen on the cathode side. Based on impedance analysis, contributions of the anode and cathode to the increase of total resistance were assigned. Accordingly, the degradation rates of the cathode were strongly dependent on the pO(2).

Microstructural analysis of the cathode/electrolyte interface carried out after removal of the cathode showed craters on the electrolyte surface where the lanthanum strontium manganite (LSM) particles had been located. The changes of shape and size of these craters observed after testing correlated with the cell voltage degradation rates.

The results can be interpreted in terms of element redistribution at the cathode/electrolyte interface and formation of foreign phases giving rise to a weakening of local contact points of the LSM cathode and yttria-stabilized zirconia electrolyte and consequently a reduced three-phase boundary length. (C) 2008 The Electrochemical Society.

Language: English
Publisher: The Electrochemical Society
Year: 2008
Pages: B1047
ISSN: 19457111 and 00134651
Types: Journal article
DOI: 10.1149/1.2960938
ORCIDs: Hagen, Anke and Hendriksen, Peter Vang

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