Nanoscale Analysis of LSM/YSZ Interfaces within Composite Cathodes for Commercial Solid Oxide Fuel Cells

Y. N. Picard, J. D. Poplawsky, S. Lee, H. W. Abernathy

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

1 Scopus citations

Abstract

Atom probe tomography (APT) was utilized to probe composition at the nanoscale across cathode/electrolyte interfaces for anodesupported commercial SOFCs. These SOFCs contained a porous composite cathode layer, consisting of sintered (La0.8Sr0.2)0.95MnO3 (LSM) and yttria-stabilized zirconia (YSZ). SOFCs were operated up to a 500 h duration at a 0.75 A/cm2 current density and 800°C. The measured cell voltage increased over the first 100 hours of operation, followed by a steady and linear drop in cell voltage that translated to a 5.35% performance loss per 1000 h. Cation migration behavior was extrapolated through comparisons of compositional profiles acquired by APT across LSM/YSZ particle interfaces for as-sintered, operated and thermally aged conditions. The results show that operation drives La/Sr away from the LSM nanoparticle surface and Y depletion at the YSZ nanoparticle surface. Energy dispersive spectroscopy (EDS) inside a scanning transmission electron microscope (STEM) provided additional insights regarding Mn aggregation behavior during operation.

Original languageEnglish
Title of host publication17th International Symposium on Solid Oxide Fuel Cells, SOFC 2021
PublisherIOP Publishing Ltd
Pages1351-1362
Number of pages12
Edition1
ISBN (Electronic)9781607685395
DOIs
StatePublished - 2021
Event17th International Symposium on Solid Oxide Fuel Cells, SOFC 2021 - Stockholm, Sweden
Duration: Jul 18 2021Jul 23 2021

Publication series

NameECS Transactions
Number1
Volume103
ISSN (Print)1938-6737
ISSN (Electronic)1938-5862

Conference

Conference17th International Symposium on Solid Oxide Fuel Cells, SOFC 2021
Country/TerritorySweden
CityStockholm
Period07/18/2107/23/21

Funding

 This manuscript has been authored by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). The US government retains and the publisher, by accepting the article for publication, acknowledges that the US government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan). This project was funded by the United States Department of Energy, National Energy Technology Laboratory, in part, through a site support contract. Neither the United States Government nor any agency thereof, nor any of their employees, nor the support contractor, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof.

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