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Journal article

Electrolysis of carbon dioxide in Solid Oxide Electrolysis Cells

From

Electrochemical Evaluation, Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark1

Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark2

Risø National Laboratory for Sustainable Energy, Technical University of Denmark3

Electrochemistry, Fuel Cells and Solid State Chemistry Division, Risø National Laboratory for Sustainable Energy, Technical University of Denmark4

Carbon dioxide electrolysis was studied in Ni/YSZ electrode supported Solid Oxide Electrolysis Cells (SOECs) consisting of a Ni-YSZ support, a Ni-YSZ electrode layer, a YSZ electrolyte, and a LSM-YSZ O2 electrode (YSZ = Yttria Stabilized Zirconia). The results of this study show that long term CO2 electrolysis is possible in SOECs with nickel electrodes.The passivation rate of the SOEC was between 0.22 and 0.44 mV h−1 when operated in mixtures of CO2/CO = 70/30 or CO2/CO = 98/02 (industrial grade) at 850 °C and current densities between −0.25 and −0.50 A cm−2.

The passivation rate was independent of the current density and irreversible when operated at conditions that would oxidise carbon. This clearly shows that the passivation was not caused by coke formation. On the other hand, the passivation was partly reversible when introducing hydrogen. The passivation may be a consequence of impurities in the gas stream, most likely sulphur, adsorbing on some specific nickel sites in the cathode of the SOEC.

Activation can be carried out by hydrogen reacting with adsorbed sulphur to form the volatile compound H2S. Because adsorption of sulphur is site specific, only a part of the nickel sites were passivated and long-time operation of CO2 electrolysis in these Ni/YSZ electrode supported Solid Oxide Electrolysis Cells seems therefore feasible.

Language: English
Year: 2009
Pages: 349-358
ISSN: 18732755 and 03787753
Types: Journal article
DOI: 10.1016/j.jpowsour.2009.02.093
ORCIDs: Mogensen, Mogens Bjerg

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