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Electrocatalysis for oxygen electrodes in fuel cells and water electrolyzers for space applicationsIn most instances separate electrocatalysts are needed to promote the reduction of O2 in the fuel cell mode and to generate O2 in the energy storage-water electrolysis mode in aqueous electrochemical systems operating at low and moderate temperatures (T greater than or equal to 200 C). Interesting exceptions are the lead and bismuth ruthenate pyrochlores in alkaline electrolytes. These catalysts on high area carbon supports have high catalytic activity for both O2 reduction and generation. Rotating ring-disk electrode measurements provide evidence that the O2 reduction proceeds by a parallel four-electron pathway. The ruthenates can also be used as self-supported catalysts to avoid the problems associated with carbon oxidation, but the electrode performance so far achieved in the research at Case Western Reserve University (CWRU) is considerably less. At the potentials involved in the anodic mode the ruthenate pyrochlores have substantial equilibrium solubility in concentrated alkaline electrolyte. This results in the loss of catalyst into the bulk solution and a decline in catalytic activity. Furthermore, the hydrogen generation counter electrode may become contaminated with reduction products from the pyrochlores (lead, ruthenium).
Document ID
19900011152
Acquisition Source
Legacy CDMS
Document Type
Conference Paper
Authors
Prakash, Jai
(Case Western Reserve Univ. Cleveland, OH, United States)
Tryk, Donald
(Case Western Reserve Univ. Cleveland, OH, United States)
Yeager, Ernest
(Case Western Reserve Univ. Cleveland, OH, United States)
Date Acquired
September 6, 2013
Publication Date
December 1, 1989
Publication Information
Publication: NASA, Lewis Research Center, Space Electrochemical Research and Technology (SERT), 1989
Subject Category
Energy Production And Conversion
Accession Number
90N20468
Funding Number(s)
CONTRACT_GRANT: NAG3-964
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.
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