A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells

© 2017 The Electrochemical Society. All rights reserved. The interfaces between cathode and electrolyte in solid oxide fuel cells (SOFCs) play a critical role in the overall performance and durability, and are generally formed by pre-sintering at high temperatures, e.g., ~1150°C in the case of La 0....

Full description

Bibliographic Details
Main Authors: He, Shuai, Chen, K., Saunders, M., Li, J., Cui, C., Jiang, San Ping
Format: Journal Article
Published: The Electrochemical Society, Inc 2017
Online Access:http://purl.org/au-research/grants/arc/DP150102044
http://hdl.handle.net/20.500.11937/66202
_version_ 1848761263584182272
author He, Shuai
Chen, K.
Saunders, M.
Li, J.
Cui, C.
Jiang, San Ping
author_facet He, Shuai
Chen, K.
Saunders, M.
Li, J.
Cui, C.
Jiang, San Ping
author_sort He, Shuai
building Curtin Institutional Repository
collection Online Access
description © 2017 The Electrochemical Society. All rights reserved. The interfaces between cathode and electrolyte in solid oxide fuel cells (SOFCs) play a critical role in the overall performance and durability, and are generally formed by pre-sintering at high temperatures, e.g., ~1150°C in the case of La 0.8 Sr 0.2 MnO 3 (LSM) cathodes. Here the interface between LSM and yttria-stabilized zirconia (YSZ) or Gd-doped ceria (GDC) electrolytes formed under high temperature sintering is studied using Focused Ion Beam and Scanning Transmission Electron Microscope (FIB-STEM) techniques. In the case of LSM/YSZ interface, there is a significant cation interdiffusion, particularly Mn 2+ into YSZ electrolyte in the convex contact ring region and Mn, La and Y cation diffusion along the grain boundary of YSZ electrolyte also occurs. For LSM/GDC interface, no cation interdiffusion was observed. The results indicate the formation of semi-coherent interface, i.e., an atom-by-atom matching only exists locally in regions along the interface, but orientation relationship and lattice mismatch factor between electrode and electrolyte crystallographic planes at the LSM/YSZ and LSM/GDC interfaces vary significantly. Lattice disorientation and misfit of the crystallographic planes occur within a narrow region of 0.10–0.5 nm wide with no amorphous or solid solution formation. The results demonstrate that cation interdiffusion is not an essential requirement for the formation of heterointerfaces for LSM electrode, and disorientation and dislocation of the crystallographic planes at the interface does not impede the oxygen diffusion and incorporation process for the O 2 reduction reaction.
first_indexed 2025-11-14T10:28:54Z
format Journal Article
id curtin-20.500.11937-66202
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T10:28:54Z
publishDate 2017
publisher The Electrochemical Society, Inc
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-662022022-10-12T07:16:16Z A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells He, Shuai Chen, K. Saunders, M. Li, J. Cui, C. Jiang, San Ping © 2017 The Electrochemical Society. All rights reserved. The interfaces between cathode and electrolyte in solid oxide fuel cells (SOFCs) play a critical role in the overall performance and durability, and are generally formed by pre-sintering at high temperatures, e.g., ~1150°C in the case of La 0.8 Sr 0.2 MnO 3 (LSM) cathodes. Here the interface between LSM and yttria-stabilized zirconia (YSZ) or Gd-doped ceria (GDC) electrolytes formed under high temperature sintering is studied using Focused Ion Beam and Scanning Transmission Electron Microscope (FIB-STEM) techniques. In the case of LSM/YSZ interface, there is a significant cation interdiffusion, particularly Mn 2+ into YSZ electrolyte in the convex contact ring region and Mn, La and Y cation diffusion along the grain boundary of YSZ electrolyte also occurs. For LSM/GDC interface, no cation interdiffusion was observed. The results indicate the formation of semi-coherent interface, i.e., an atom-by-atom matching only exists locally in regions along the interface, but orientation relationship and lattice mismatch factor between electrode and electrolyte crystallographic planes at the LSM/YSZ and LSM/GDC interfaces vary significantly. Lattice disorientation and misfit of the crystallographic planes occur within a narrow region of 0.10–0.5 nm wide with no amorphous or solid solution formation. The results demonstrate that cation interdiffusion is not an essential requirement for the formation of heterointerfaces for LSM electrode, and disorientation and dislocation of the crystallographic planes at the interface does not impede the oxygen diffusion and incorporation process for the O 2 reduction reaction. 2017 Journal Article http://hdl.handle.net/20.500.11937/66202 10.1149/2.1061713jes http://purl.org/au-research/grants/arc/DP150102044 The Electrochemical Society, Inc restricted
spellingShingle He, Shuai
Chen, K.
Saunders, M.
Li, J.
Cui, C.
Jiang, San Ping
A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells
title A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells
title_full A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells
title_fullStr A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells
title_full_unstemmed A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells
title_short A FIB-STEM study of La0.8Sr0.2MnO3 Cathode and Y2O3-ZrO2/Gd2O3-CeO2 electrolyte interfaces of solid oxide fuel cells
title_sort fib-stem study of la0.8sr0.2mno3 cathode and y2o3-zro2/gd2o3-ceo2 electrolyte interfaces of solid oxide fuel cells
url http://purl.org/au-research/grants/arc/DP150102044
http://hdl.handle.net/20.500.11937/66202