TY - JOUR
T1 - ZrO2 atomic layer deposition into Sr0.5Sm0.5CoO3-: δ-Ce0.9Gd0.1O2- δ solid oxide fuel cell cathodes: Mechanisms of stability enhancement
AU - Schmauss, Travis A.
AU - Railsback, Justin G.
AU - Lu, Matthew Y.
AU - Zhao, Kevin Y.
AU - Barnett, Scott A.
N1 - Funding Information:
This work was mainly supported by the US Department of Energy Office of Science, award number DE-SC0016965 and the National Science Foundation, award OISE-1545907, that supported some of the microstructural characterization. Travis Schmauss was partially supported by a graduate fellowship provided by the Institute for Sustainability and Energy at Northwestern. Dr Roberto Scipioni assisted with the electrochemical impedance modeling. The authors would also like to thank John Pieterse, Hongqian Wang, Kunli Yang, and Shanlin Zhang for experimental advice and assistance. This work utilized Northwestern University Micro/Nano Fabrication Facility (NUFAB) and the Northwestern University Integrated Molecular Structure Education and Research Center (IMSERC), which are partially supported by So and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205), the Materials Research Science and Engineering Center (NSF DMR-1720139), the State of Illinois, and Northwestern University; the EPIC and Keck-II facilities of the NUANCE Center at Northwestern University, which has received support from the MRSEC Program (NSF DMR-1121262) at the Materials Research Center, the International Institute of Nanotechnology (IIN), the Keck Foundation, and the State of Illinois, through the IIN; and the J. B. Cohen X-Ray Diffraction Facility supported by the MRSEC Program of the National Science Foundation (DMR-1720139) at the Materials Research Center of Northwestern University and the So and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205.) Metal analysis was performed at the Northwestern University Quantitative Bio-element Imaging Center.
Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - The application of atomic layer deposition (ALD) on solid oxide fuel cell (SOFC) cathodes has previously yielded mixed results and has been seen to depend on the ALD species, catalyst chemistry, catalyst morphology, and the conditions for deposition. Characterized here is the effect of an ALD zirconia coating within an SOFC oxygen electrode: Sr0.5Sm0.5CoO3-δ infiltrated into Gd-doped ceria, Ce0.9Gd0.1O2-δ, scaffolds (SSC-GDC). Island-like ALD-ZrO2 coatings with approximately monolayer coverage initially yield a higher electrode polarization resistance, RP, but thereafter the coated electrodes show lower RP and slower degradation. For example, after ∼1000 hour accelerated ageing tests carried out at 750 °C, SSC-GDC coated with ∼0.3 nm of ALD-ZrO2 showed an RP increase of 18% compared to 30% for uncoated SSC-GDC. Strontium surface segregation was not found to be a significant degradation factor. At 750 °C, a reaction between the Zr-overlayer and the SSC was observed, producing SrZrO3, Co3O4, and SmCoO3. The low RP values achieved suggest that the reactant products were thin enough to be discontinuous and thus not hinder the oxygen surface exchange process, and yet they acted as a barrier to SSC particle coarsening.
AB - The application of atomic layer deposition (ALD) on solid oxide fuel cell (SOFC) cathodes has previously yielded mixed results and has been seen to depend on the ALD species, catalyst chemistry, catalyst morphology, and the conditions for deposition. Characterized here is the effect of an ALD zirconia coating within an SOFC oxygen electrode: Sr0.5Sm0.5CoO3-δ infiltrated into Gd-doped ceria, Ce0.9Gd0.1O2-δ, scaffolds (SSC-GDC). Island-like ALD-ZrO2 coatings with approximately monolayer coverage initially yield a higher electrode polarization resistance, RP, but thereafter the coated electrodes show lower RP and slower degradation. For example, after ∼1000 hour accelerated ageing tests carried out at 750 °C, SSC-GDC coated with ∼0.3 nm of ALD-ZrO2 showed an RP increase of 18% compared to 30% for uncoated SSC-GDC. Strontium surface segregation was not found to be a significant degradation factor. At 750 °C, a reaction between the Zr-overlayer and the SSC was observed, producing SrZrO3, Co3O4, and SmCoO3. The low RP values achieved suggest that the reactant products were thin enough to be discontinuous and thus not hinder the oxygen surface exchange process, and yet they acted as a barrier to SSC particle coarsening.
UR - http://www.scopus.com/inward/record.url?scp=85076640575&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076640575&partnerID=8YFLogxK
U2 - 10.1039/c9ta09214e
DO - 10.1039/c9ta09214e
M3 - Article
AN - SCOPUS:85076640575
SN - 2050-7488
VL - 7
SP - 27585
EP - 27593
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 48
ER -