001     10068
005     20240711085631.0
024 7 _ |2 DOI
|a 10.1149/1.3270047
024 7 _ |2 WOS
|a WOS:000273222700036
037 _ _ |a PreJuSER-10068
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Electrochemistry
084 _ _ |2 WoS
|a Materials Science, Coatings & Films
100 1 _ |0 P:(DE-HGF)0
|a Endler, C
|b 0
245 _ _ |a Time-dependent electrode performance changes in intermediate temperature solid oxide fuel cells
260 _ _ |a Pennington, NJ
|b Electrochemical Society
|c 2010
300 _ _ |a B292 - B298
336 7 _ |0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
|a Journal Article
336 7 _ |2 DataCite
|a Output Types/Journal article
336 7 _ |0 0
|2 EndNote
|a Journal Article
336 7 _ |2 BibTeX
|a ARTICLE
336 7 _ |2 ORCID
|a JOURNAL_ARTICLE
336 7 _ |2 DRIVER
|a article
440 _ 0 |0 3889
|a Journal of the Electrochemical Society
|v 157
|x 0013-4651
|y 2
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a This study gives evidence that the time-dependent performance changes in anode supported cells for intermediate-temperature solid oxide fuel cells is essentially influenced by the mixed ionic-electronic conducting (MIEC) cathode. The impedance spectra recorded during 700 h of operation at 750 degrees C were interpreted using an appropriate equivalent circuit model by (i) a distribution of relaxation time analysis followed by (ii) a complex nonlinear least squares fit. Four electrode polarization processes were separated by selective experimental parameters. The cathodic part, initially the smallest, is only discovered among the anodic contributions by a change in fuel gas composition from H-2-H2O to CO-CO2 and increases by 310% (15 m cm(2) at 11 h, 62 m cm(2) at 700 h). A Sr (and Co) depletion of the MIEC cathode composition La0.58Sr0.4Co0.2Fe0.8O3-delta possibly caused this degradation. The anodic polarization has a proportion of 92% at the start and decreases to 73% (168 m cm(2) at 11 h, 173 m cm(2) at 700 h). The anode charge-transfer reaction initially causes 60% of the total polarization losses and 50% after 700 h. This is assigned to a change in the triple phase boundary and/or a degradation in ionic conductivity in the anode functional layer. The gas diffusion polarization remains constant at 58 m cm(2).
536 _ _ |0 G:(DE-Juel1)FUEK402
|2 G:(DE-HGF)
|a Rationelle Energieumwandlung
|c P12
|x 0
536 _ _ |0 G:(DE-Juel1)SOFC-20140602
|a SOFC - Solid Oxide Fuel Cell (SOFC-20140602)
|c SOFC-20140602
|f SOFC
|x 1
588 _ _ |a Dataset connected to Web of Science
650 _ 7 |2 WoSType
|a J
653 2 0 |2 Author
|a cobalt compounds
653 2 0 |2 Author
|a electrochemical electrodes
653 2 0 |2 Author
|a ionic conductivity
653 2 0 |2 Author
|a lanthanum compounds
653 2 0 |2 Author
|a solid oxide fuel cells
653 2 0 |2 Author
|a strontium compounds
700 1 _ |0 P:(DE-HGF)0
|a Leonide, A.
|b 1
700 1 _ |0 P:(DE-HGF)0
|a Weber, A.
|b 2
700 1 _ |0 P:(DE-Juel1)129667
|a Tietz, F.
|b 3
|u FZJ
700 1 _ |0 P:(DE-HGF)0
|a Ivers-Tiffée, E.
|b 4
773 _ _ |0 PERI:(DE-600)2002179-3
|a 10.1149/1.3270047
|g Vol. 157, p. B292 - B298
|p B292 - B298
|q 157|t Journal of the Electrochemical Society
|v 157
|x 0013-4651
|y 2010
856 7 _ |u http://dx.doi.org/10.1149/1.3270047
856 4 _ |u https://juser.fz-juelich.de/record/10068/files/FZJ-10068_PV.pdf
|y Restricted
|z Published final document.
909 C O |o oai:juser.fz-juelich.de:10068
|p VDB
913 1 _ |0 G:(DE-Juel1)FUEK402
|b Energie
|k P12
|l Rationelle Energieumwandlung
|v Rationelle Energieumwandlung
|x 0
913 2 _ |0 G:(DE-HGF)POF3-135
|1 G:(DE-HGF)POF3-130
|2 G:(DE-HGF)POF3-100
|a DE-HGF
|b Forschungsbereich Energie
|l Speicher und vernetzte Infrastrukturen
|v Fuel Cells
|x 0
914 1 _ |y 2010
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |0 I:(DE-Juel1)VDB809
|d 30.09.2010
|g IEF
|k IEF-1
|l Werkstoffsynthese und Herstellungsverfahren
|x 0
970 _ _ |a VDB:(DE-Juel1)120236
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)IEK-1-20101013
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IMD-2-20101013
981 _ _ |a I:(DE-Juel1)IEK-1-20101013


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