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  • 1
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2017
    In:  ECS Transactions Vol. 77, No. 10 ( 2017-05-03), p. 149-156
    In: ECS Transactions, The Electrochemical Society, Vol. 77, No. 10 ( 2017-05-03), p. 149-156
    Materialart: Online-Ressource
    ISSN: 1938-6737 , 1938-5862
    Sprache: Englisch
    Verlag: The Electrochemical Society
    Publikationsdatum: 2017
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2011
    In:  ECS Meeting Abstracts Vol. MA2011-02, No. 4 ( 2011-08-01), p. 180-180
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2011-02, No. 4 ( 2011-08-01), p. 180-180
    Kurzfassung: Abstract not Available.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2011
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2006
    In:  ECS Meeting Abstracts Vol. MA2005-01, No. 30 ( 2006-02-22), p. 1047-1047
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2005-01, No. 30 ( 2006-02-22), p. 1047-1047
    Kurzfassung: Abstract not Available.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2006
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Online-Ressource
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    The Electrochemical Society ; 2017
    In:  ECS Meeting Abstracts Vol. MA2017-03, No. 1 ( 2017-07-01), p. 279-279
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2017-03, No. 1 ( 2017-07-01), p. 279-279
    Kurzfassung: Although continuous progress is achieved with respect to lifetime and performance improvements, solid oxide fuel cells (SOFC) continue to struggle with commercialization. One important factor to possibly reduce overall costs of SOFC systems would be the omission of desulfurization units during the fuel processing. However, sulfur-containing impurities in the most common fuels such as natural gas and biogas lead to significant performance drops upon exposure to Ni-based anodes. In this regard, it has been shown that Ni/gadolinium-doped ceria (CGO) anodes display lower performance drops upon short-time sulfur exposure than Ni/YSZ. However, their long-term resistivity towards sulfur exposure has not been investigated so far, although this is likely to be the most vital factor determining SOFC lifetime. This work presents the first in-depth analysis of long-term degradation due to sulfur poisoning of Ni/CGO10-based SOFC. A parameter study of the sulfur-induced long-term degradation of commercial, high-performance single cells was conducted with an accumulated cell testing time of more than one year. The long-term degradation behavior is investigated at 900 °C for different H 2 S concentrations and varying H 2 /H 2 O/N 2 fuel gas atmospheres. The sulfur poisoning periods of the different cells varied from 100 up to 1500 h. The progress of the degradation during the experiments was monitored by means of electrochemical impedance spectroscopy. It is shown that Ni/CGO anodes can be exposed to 10 ppm H 2 S and operated without significant irreversible degradation at a current density of 0.5 A·cm –2 for 1500 h for certain fuel gas mixtures, demonstrating their promising long-term stability. However, for reduced hydrogen partial pressures in the fuel gas, the same H 2 S concentration leads to a considerable voltage decrease that is reflected by an increase in anode charge transfer and ohmic resistance. Furthermore, the microstructural evolution of the Ni/CGO is examined ex-situ by means of SEM and correlated to the anode performance degradation. The existence of a stable operating regime for Ni/CGO anodes under sulfur exposure is clearly shown and the critical operating parameters are outlined. The presented results give important insights into the degradation processes occurring during long-term operation of Ni/CGO anodes as well as strategies for stable SOFC operation. Moreover, the results encourage to further optimize the performance and sulfur tolerance of Ni/CGO anodes.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2017
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    In: ECS Transactions, The Electrochemical Society, Vol. 91, No. 1 ( 2019-07-10), p. 1751-1760
    Materialart: Online-Ressource
    ISSN: 1938-6737 , 1938-5862
    Sprache: Englisch
    Verlag: The Electrochemical Society
    Publikationsdatum: 2019
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2015
    In:  ECS Transactions Vol. 68, No. 1 ( 2015-06-02), p. 1373-1382
    In: ECS Transactions, The Electrochemical Society, Vol. 68, No. 1 ( 2015-06-02), p. 1373-1382
    Kurzfassung: An elementary kinetic model is developed to predict the influence of sulfur on Ni/YSZ anodes of solid oxide fuel cells (SOFC) performance. A multi-step reaction mechanism describing the formation and oxidation of sulfur on the Ni surface is coupled with gas transport in the channel and porous phase, and charge-transfer processes. A thermodynamic and kinetic data set of sulfur formation and oxidation is derived based upon various literature sources including a coverage-dependent description of the enthalpy of surface-adsorbed sulfur. The validity of the model is demonstrated on two SOFC operation modes, namely H 2 /H 2 O/H 2 S and CH 4 /H 2 /H 2 O/H 2 S fuel mixtures, at different operating conditions using various electrochemical literature experiments. The first concern is the influence of adsorbed sulfur on charge-transfer processes and the second concern is the effect of adsorbed sulfur on complex methane reforming chemistry. The results reveal that sulfur surface coverage increases with current density demonstrating a low sulfur oxidation rate.
    Materialart: Online-Ressource
    ISSN: 1938-5862 , 1938-6737
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2015
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 7
    Online-Ressource
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    The Electrochemical Society ; 2015
    In:  ECS Transactions Vol. 68, No. 1 ( 2015-06-02), p. 3553-3561
    In: ECS Transactions, The Electrochemical Society, Vol. 68, No. 1 ( 2015-06-02), p. 3553-3561
    Kurzfassung: Within a joint project of German Aerospace Center (DLR) and Forschungszentrum JÜLICH solid oxide fuel cells have been electrochemically characterized and the influence of the current density and fuel gas humidity on the long-term stability of electrolysis operation have been investigated. In order to observe the time- dependent change in electrochemical behaviour of the fuel electrode supported cells, in-situ analysis with a special focus on impedance spectroscopy was utilized. DRT-analysis was applied to validate assumptions made for equivalent circuit fitting and to improve fitting quality and reliability. Four rate limiting processes (electrolyte, cathode, anode and mass transport) could be separated and it was possible to track their development during the 1000 h experiments, showing their individual degradation behaviour under the applied operating conditions. This information was used for a dependence study, while additionally post mortem analysis methods were applied.
    Materialart: Online-Ressource
    ISSN: 1938-5862 , 1938-6737
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2015
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2019
    In:  ECS Transactions Vol. 91, No. 1 ( 2019-07-10), p. 1985-1992
    In: ECS Transactions, The Electrochemical Society, Vol. 91, No. 1 ( 2019-07-10), p. 1985-1992
    Materialart: Online-Ressource
    ISSN: 1938-6737 , 1938-5862
    Sprache: Englisch
    Verlag: The Electrochemical Society
    Publikationsdatum: 2019
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 9
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2017
    In:  ECS Meeting Abstracts Vol. MA2017-01, No. 33 ( 2017-04-15), p. 1610-1610
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2017-01, No. 33 ( 2017-04-15), p. 1610-1610
    Kurzfassung: The presence of fuel impurities, such as sulfur, siloxane and phosphorus, in biogas, diesel and natural gas can cause Solid Oxide Fuel Cell (SOFC) degradation due to surface poisoning of Ni-containing anodes. In this regard, Ni/CGO anodes were shown to display higher sulfur tolerance than Ni/YSZ anodes and a comparable high performance. In order to allow for a more profound understanding of the processes underlying sulfur poisoning, this study presents an extensive experimental investigation of commercial Ni/CGO-based SOFC operating on H 2 /H 2 O gas and reformate fuel mixtures with trace amounts of hydrogen sulfide (H 2 S). The short-term poisoning behavior of high-performance electrolyte-supported Ni/CGO10-based cells was systematically investigated by means of transient voltage stability experiments and electrochemical impedance measurements for a wide range of operating conditions. The effects of temperature (800 – 950 °C) and current density (OCV – 0.75 A·cm ‒2 ) on the extent of sulfur poisoning (1 – 20 ppm H 2 S) was evaluated. The poisoning behavior was shown to be completely reversible for short exposure times in all cases. By means of equivalent circuit modeling, the chemical capacitance of Ni/CGO10 anodes was demonstrated to be strongly dependent on temperature and gas phase composition reflecting a changing Ce 3+ /Ce 4+ ratio in the CGO phase. Using a model reformate as fuel gas, it was shown that CO can still be electrochemically converted under sulfur exposure. Furthermore, long-term experiments of 1000 h were conducted at 900 °C and 0.5 A·cm ‒2 with and without sulfur exposure and the degradation progress was monitored by impedance spectroscopy. Moreover, comprehensive post-mortem analysis including FIB/SEM, TEM and XRF was carried out in order to identify the nature and location of the occurring microstructural changes.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2017
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 10
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2015
    In:  ECS Meeting Abstracts Vol. MA2015-03, No. 1 ( 2015-07-15), p. 418-418
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2015-03, No. 1 ( 2015-07-15), p. 418-418
    Kurzfassung: A special measurement setup with the ability to measure four cells simultaneously in reversible SOEC/SOFC mode was implemented. As preliminary experiment extensive characterization of anode supported Ni-YSZ|YSZ|CGO|LSCF cells provided by Forschungszentrum Jülich was conducted including polarization curves and impedance measurements in the range from 750 °C to 850 °C and fuel gas humidifications from 40 mol% H 2 O to 80 mol% H 2 O in SOFC and SOEC mode. Core of this work is the systematic investigation of the influence of the operating parameters temperature , fuel gas humidification and current density on SOEC long-term degradation and its underlying individual processes. In order to obtain this information a series of five 1000 h experiments with an operating temperature between 750 °C to 850 °C and fuel gas humidification between 40 mol% H 2 O to 80 mol% H 2 O was devised. During each measurement over 1000 h four cells are measured simultaneously under identical conditions with the exception of current density where each cell runs galvanostatically with a fixed value between 0 A/cm 2 and 1.5 A/cm 2 .  The progress of degradation was monitored in-situ approximately every 150 h by impedance spectroscopy. It was possible to isolate fuel electrode processes R 1+2 , an oxygen electrode process R 3 , a mass transport limitation on the fuel electrode R 4 and the electrolyte resistance R 0 . It could be shown that the processes R 0 and R 1+2 show a strong correlation between current density and degradation; however the processes R 3 and R 4 exhibit degradation behavior completely independent of the applied current. Furthermore it could be shown that the oxygen electrode process R 3 demonstrates rapid degradation during the first approximately 500 h dominating the overall cell degradation, however slowing down to be negligible after 1000 h. Post-mortem investigations are being conducted in order to localize and identify the rate limiting processes R 0 to R 4 . In this way we will be able to explain the observed degradation for each process and also validate the observed dependencies ex-situ. Additionally, the remaining long-term experiments are being conducted in order to complete this study and clarify the correlation between degradation processes and fuel gas humidity as well as operating temperature.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2015
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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