Published March 2017 | Version v1
Journal article

Investigation of structural and electrochemical properties of LaSrCo1−xSbxO4 (0≤x≤0.20) as potential cathode materials in intermediate-temperature solid oxide fuel cells

Description

The structural and electrochemical properties of the layered perovskite oxides LaSrCo1−xSbxO4 (0≤x≤0.20) were investigated to study the effects of substituting Sb for Co for application as cathode materials in intermediate temperature solid oxide fuel cells (IT-SOFCs). The results of crystal structure analyses show the maximum content of Sb in LaSrCo1−xSbxO4 to be 0.05 as a pure single phase. XPS shows that Co and Sb in LaSrCo0.95Sb0.05O4 may possess mixed-oxidation states. The electrical conductivity increased greatly after Sb substitution. An improvement in the cathode polarization (Rp) values is observed from the Sb-doped sample with respect to the undoped samples. For example, Rp of LaSrCo0.95Sb0.05O4 on LSGM was observed to be 0.16 Ω cm2 at 800 °C in air. The main rate-limiting step for LaSrCo0.95Sb0.05O4 cathode is charge transfer of oxygen atoms. These results indicate that Sb can be incorporated into LaSrCo1−xSbxO4 based materials and can have a beneficial effect on the performance, making them potentially suitable for use as cathode materials in IT-SOFCs. - Graphical abstract: The oxygen partial pressure dependence of polarization resistances for a new layered perovskite cathode LaSrCo0.95Sb0.05O4 at various temperatures was measured. - Highlights: • The maximum content of Sb was 0.05 mol in LaSrCo1−xSbxO4. • The maximum electrical conductivity is 194 S cm−1for LaSrCo0.95Sb0.05O4 at 800 °C. • A rate-limiting process of charge transfer presented.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2016.11.038

Additional details

Identifiers

DOI
10.1016/j.jssc.2016.11.038;
PII
S0022-4596(16)30476-5;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
247
Journal Page Range
p. 24-30
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.