Electronic Behavior of Ba0.5Sr0.5Co0.8Fe0.2O3-d and SrCo0.9Nb0.1O3-d

2011 ◽  
Vol 1331 ◽  
Author(s):  
Robert E. Usiskin ◽  
Richard Y. Wang ◽  
Sossina M. Haile

ABSTRACTThe perovskite Ba0.5Sr0.5Co0.8Fe0.2O3-d (BSCF 5582) has attracted great interest as an oxygen reduction catalyst for solid oxide fuel cells and as an oxygen permeation membrane material. Mixed ionic and electronic conductivity is essential to the high catalytic activity it exhibits, however its electronic behavior and overall defect chemistry are not well understood. The related material SrCo0.9Nb0.1O3-d (SCN 091) is another promising composition that may have comparable performance, but with defect chemistry that is simpler to study. From a combination of thermogravimetric, impedance, and diffraction measurements we find SCN 091 to exhibit somewhat smaller oxygen nonstoichiometry, five times higher electronic conductivity, lower enthalpy of hole migration, and greater structural stability than BSCF 5582. We also observe that the enthalpy of hole migration in such materials tends to increase as oxygen content decreases; the origins of this behavior are unclear.

2020 ◽  
Vol 8 (44) ◽  
pp. 23313-23322
Author(s):  
Seo Ju Kim ◽  
Ja Yang Koo ◽  
Taeeun Mun ◽  
Mingi Choi ◽  
Wonyoung Lee

Engineering the defect chemistry at the interface between the electrolyte and the electrode is crucial to facilitate oxygen reduction reaction, thereby improve the electrochemical performance of intermediate temperature solid oxide fuel cells.


2019 ◽  
Vol 108 ◽  
pp. 01019 ◽  
Author(s):  
Anna Niemczyk ◽  
Konrad Świerczek

One of major goals in the development of solid oxide fuel cells and its reversible mode, solid oxide electrolyzer cells, is related to a decrease of the operating temperature, down to the intermediate range (600-800 °C) or even lower temperatures. However, this reduction causes an increase of the polarization resistance, especially for the air electrode, which results in a significant decline of the efficiency of the device. Therefore, it is essential to obtain new, thermally and chemically stable materials with the high ionic-electronic conductivity and good catalytic activity for the oxygen reduction reaction working in the decreased temperature range. At the same time, environmental and economic aspects have to be considered in the development of the new compounds. Promising cobalt-free electrode materials can be Cu-based oxides with the perovskite and perovskite-related structures.


2017 ◽  
Vol 121 (28) ◽  
pp. 15017-15027 ◽  
Author(s):  
Mårten E. Björketun ◽  
Ivano E. Castelli ◽  
Jan Rossmeisl ◽  
Thomas Olsen ◽  
Kenji Ukai ◽  
...  

Ionics ◽  
2020 ◽  
Vol 26 (11) ◽  
pp. 5641-5649
Author(s):  
Patrick Stanley ◽  
A. Mohammed Hussain ◽  
Yi-Lin Huang ◽  
J. Evans Gritton ◽  
Eric D. Wachsman

2020 ◽  
Vol 8 (16) ◽  
pp. 7792-7800 ◽  
Author(s):  
Tian Gan ◽  
Xinqiang Fan ◽  
Ye Liu ◽  
Chengyu Wang ◽  
Haoran Mei ◽  
...  

Ni/3DOM Ce0.8Sm0.2O1.9 shows a high catalytic activity as the anode material of CH3OH fueled SOFCs.


2008 ◽  
Vol 1126 ◽  
Author(s):  
Wenquan Gong ◽  
Manoj Yadav ◽  
Allan J. Jacobson

AbstractThe segregated vacancies in the A site-ordered oxygen-deficient double perovskites REBaCo2O5+x (RE = La, Pr, Nd, Sm, Eu) (RBCO) are thought to greatly enhance the diffusivity of oxide ions in the bulk of these materials and possibly supply surface defect sites with enhanced reactivity towards molecular oxygen. Some materials in this family of REBaCo2O5+x compounds, such as PrBaCo2O5+x, (PBCO), have already demonstrated high electronic conductivity, rapid oxygen ion diffusion and surface exchange kinetics. Therefore, the family of REBaCo2O5+x compounds were synthesized and evaluated as cathode materials for intermediate temperature solid oxide fuel cells (SOFCs) based on gadolinium doped ceria (CGO) electrolytes. The electrochemical performance of symmetrical cells (REBaCo2O5+x + CGO composite cathodes on the CGO electrolytes) was evaluated by using AC impedance spectroscopy. The area specific resistance (ASR) performance was measured as a function of temperature as well as oxygen partial pressure.


2013 ◽  
Vol 1542 ◽  
Author(s):  
Matthew C Schrandt ◽  
Praveen Kolla ◽  
A. Smirnova

ABSTRACTPt catalysts are the leading catalysts for use in ORR. However, Pt is an expensive catalyst and with limited supply can not be considered a sustainable material for feasible application that is scalable in the economy. This calls for new solutions for catalyst materials that either mitigate the amount of Pt used in catalysts by developing hybrid catalysts, or to replace Pt altogether with a material with similar or better catalytic activity. Perovskite LSCF and Fluorite GDC materials with proven catalytic activity in solid oxide fuel cells are herein explored for their catalytic reduction of oxygen for use at low temperatures. Since the materials lack electronic conductivity at low temperatures, we have improved their conductivity with graphene. The resulting materials are compared to Pt in their ORR catalytic capabilities and electronic conductivity.


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