001     1038448
005     20250203103335.0
037 _ _ |a FZJ-2025-01444
100 1 _ |a Uecker, Jan
|0 P:(DE-Juel1)187524
|b 0
|e Corresponding author
111 2 _ |a SOFC: Eighteenth International Symposium on Solid Oxide Fuel Cells (SOFC-XVIII)
|c Boston
|d 2023-07-02 - 2023-07-07
|w USA
245 _ _ |a Electrochemical Activity and Stability of Pure Gadolinium Doped Ceria as Fuel Electrode in Solid Oxide Electrolysis Cell
260 _ _ |c 2023
336 7 _ |a Abstract
|b abstract
|m abstract
|0 PUB:(DE-HGF)1
|s 1738243583_31342
|2 PUB:(DE-HGF)
336 7 _ |a Conference Paper
|0 33
|2 EndNote
336 7 _ |a INPROCEEDINGS
|2 BibTeX
336 7 _ |a conferenceObject
|2 DRIVER
336 7 _ |a Output Types/Conference Abstract
|2 DataCite
336 7 _ |a OTHER
|2 ORCID
520 _ _ |a The state-of-the-art fuel electrode materials for solid oxide electrolysis cells (SOECs) are Ni-cermets due to their high electro-catalytic activity, high electrical conductivity and the low price. However, one major concern that must be solved for a widespread commercialisation is their poor degradation behaviour during electrolysis operation caused by for example Ni migration, depletion and agglomeration in the fuel electrode. One strategy to improve the durability of SOECs is the usage of alternative fuel electrode materials. For instance, completely Ni-free fuel electrodes may solve the problems of morphological degradation during operation and further could enhance redox cycling stability. Within possible candidates, gadolinium doped ceria (GDC) is an interesting material due to good stability towards carbon deposition and the possibility to host electro catalysis in electrolysis reactions [1, 2]. Furthermore, GDC (Ce0.8Gd0.2O2-δ) shows electronic conducting (700 °C, 0.028 S·cm-1) and ionic conducting (700 °C, 0.47 S·cm-1) properties at low partial pressures of oxygen and high temperatures [3]. Hence, in this work we have prepared electrolyte supported single cells with GDC (Ce0.8Gd0.2O2-δ) as single phase fuel electrode for their use as SOEC. The single cells (GDC//8YSZ//GDC//LSCF) were characterized by electrochemical impedance spectroscopy (EIS) and current-voltage characteristics in steam electrolysis, co-electrolysis and CO2 electrolysis conditions exhibiting 70 % of the performance compared to similar produced Ni-GDC fuel electrode single cells at 900 °C [4]. Furthermore, the results include process analysis by EIS, long term stability experiments for steam electrolysis and CO2 electrolysis conditions of at least 1000 hours and post characterization of the degraded cells by EIS, SEM and EDX analysis.[1] Nakmura et al. Journal of the Electrochemical Society155 (2008) B563.[2] Chueh et al. Nature Materials11 (2012) 155-161.[3] Maricle et al. Solid State Ionics52 (1992) 173-182.[4] Unachukwu et al. Journal of Power Sources556 (2023) 232436.
536 _ _ |a 1232 - Power-based Fuels and Chemicals (POF4-123)
|0 G:(DE-HGF)POF4-1232
|c POF4-123
|f POF IV
|x 0
536 _ _ |a HITEC - Helmholtz Interdisciplinary Doctoral Training in Energy and Climate Research (HITEC) (HITEC-20170406)
|0 G:(DE-Juel1)HITEC-20170406
|c HITEC-20170406
|x 1
700 1 _ |a Vibhu, Vaibhav
|0 P:(DE-Juel1)169490
|b 1
700 1 _ |a Unachukwu, Ifeanyichukwu Daniel
|0 P:(DE-Juel1)180285
|b 2
700 1 _ |a Vinke, Izaak C.
|0 P:(DE-Juel1)129936
|b 3
700 1 _ |a de Haart, L. G. J.
|0 P:(DE-Juel1)129952
|b 4
700 1 _ |a Eichel, Rüdiger-A.
|0 P:(DE-Juel1)156123
|b 5
|u fzj
856 4 _ |u https://iopscience.iop.org/article/10.1149/MA2023-0154276mtgabs
909 C O |o oai:juser.fz-juelich.de:1038448
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910 1 _ |a Forschungszentrum Jülich
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910 1 _ |a Forschungszentrum Jülich
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910 1 _ |a RWTH Aachen
|0 I:(DE-588b)36225-6
|k RWTH
|b 5
|6 P:(DE-Juel1)156123
913 1 _ |a DE-HGF
|b Forschungsbereich Energie
|l Materialien und Technologien für die Energiewende (MTET)
|1 G:(DE-HGF)POF4-120
|0 G:(DE-HGF)POF4-123
|3 G:(DE-HGF)POF4
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|v Chemische Energieträger
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914 1 _ |y 2024
920 _ _ |l yes
920 1 _ |0 I:(DE-Juel1)IEK-9-20110218
|k IEK-9
|l Grundlagen der Elektrochemie
|x 0
980 _ _ |a abstract
980 _ _ |a VDB
980 _ _ |a I:(DE-Juel1)IEK-9-20110218
980 _ _ |a UNRESTRICTED


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