Highly active and stable A-site Pr-doped LaSrCrMnO-based fuel electrode for direct CO2 solid oxide electrolyzer cells

Direct CO2 electrolysis has been explored as a means to store renewable energy and produce renewable fuels. La chromate-based perovskite oxides have attracted great attention as fuel electrode materials for solid oxide electrolyzer cells. However, the electrochemical catalytic activity of such oxide...

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Published inInternational journal of hydrogen energy Vol. 45; no. 29; pp. 14648 - 14659
Main Authors Pan, Zehua, Shi, Hongqi, Wang, Shun, Jiang, Huaguo, Zheng, Yifeng
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 26.05.2020
Subjects
CO2 utilization and upgrade
Direct CO2 electrolysis
Pr-doped La0.75Sr0.25Cr0.5Mn0.5O3-δ
Short-term stability
Solid oxide electrolysis cells
Solid oxide electrolysis cells
Direct CO2 electrolysis
Pr-doped La0.75Sr0.25Cr0.5Mn0.5O3-δ
CO2 utilization and upgrade
Short-term stability
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Abstract Direct CO2 electrolysis has been explored as a means to store renewable energy and produce renewable fuels. La chromate-based perovskite oxides have attracted great attention as fuel electrode materials for solid oxide electrolyzer cells. However, the electrochemical catalytic activity of such oxides is relatively low, and their stability has not been confirmed. In this study, Pr is doped into La0.75Sr0.25Cr0.5Mn0.5O3-δ (LSCM) and the applicability of the resulting fuel electrode to direct CO2 electrolysis is investigated. The polarization resistance of the resulting electrode at 800 °C is decreased by 25%. Distribution function of relaxation times analysis indicates that the observed improvements may be attributed to increased oxygen ion conductivity. A full cell of Pr-doped LSCM-gadolinium-doped ceria (GDC)|scandia-stabilized zirconia|La0.6Sr0.4Co0.2Fe0.8O3-δ-GDC achieves an electrolysis current of 0.5 A cm−2 at 1.36 V and a Faradaic efficiency close to 100%. Short-term (210 h) stability testing of the cell under an electrolysis current of 0.5 A cm−2 at 800 °C with pure CO2 as the feedstock reveals a decrease in applied voltage at a rate of 7 mV kh−1, thereby indicating excellent stability. Thus, given its satisfactory performance and stability, the Pr-doped LSCM electrode may be considered a promising candidate material for direct CO2 electrolysis. •Pr was doped into LSCM to develop an effective fuel electrode for CO2 electrolysis.•Polarization resistance in CO2 at 800 °C was reduced by 25% by doping Pr into LSCM.•Full cell with Pr-doped LSCM cathode, ScSZ electrolyte, LSCF-GDC anode was tested.•Full cell showed 0.5 A cm−2 at 1.36 V at 800 °C and Faradaic efficiency nearly 100%.•Full cell showed excellent stability in short-term test with 0.5 A cm−2 at 800 °C.
AbstractList Direct CO2 electrolysis has been explored as a means to store renewable energy and produce renewable fuels. La chromate-based perovskite oxides have attracted great attention as fuel electrode materials for solid oxide electrolyzer cells. However, the electrochemical catalytic activity of such oxides is relatively low, and their stability has not been confirmed. In this study, Pr is doped into La0.75Sr0.25Cr0.5Mn0.5O3-δ (LSCM) and the applicability of the resulting fuel electrode to direct CO2 electrolysis is investigated. The polarization resistance of the resulting electrode at 800 °C is decreased by 25%. Distribution function of relaxation times analysis indicates that the observed improvements may be attributed to increased oxygen ion conductivity. A full cell of Pr-doped LSCM-gadolinium-doped ceria (GDC)|scandia-stabilized zirconia|La0.6Sr0.4Co0.2Fe0.8O3-δ-GDC achieves an electrolysis current of 0.5 A cm−2 at 1.36 V and a Faradaic efficiency close to 100%. Short-term (210 h) stability testing of the cell under an electrolysis current of 0.5 A cm−2 at 800 °C with pure CO2 as the feedstock reveals a decrease in applied voltage at a rate of 7 mV kh−1, thereby indicating excellent stability. Thus, given its satisfactory performance and stability, the Pr-doped LSCM electrode may be considered a promising candidate material for direct CO2 electrolysis. •Pr was doped into LSCM to develop an effective fuel electrode for CO2 electrolysis.•Polarization resistance in CO2 at 800 °C was reduced by 25% by doping Pr into LSCM.•Full cell with Pr-doped LSCM cathode, ScSZ electrolyte, LSCF-GDC anode was tested.•Full cell showed 0.5 A cm−2 at 1.36 V at 800 °C and Faradaic efficiency nearly 100%.•Full cell showed excellent stability in short-term test with 0.5 A cm−2 at 800 °C.
Author Wang, Shun
Zheng, Yifeng
Pan, Zehua
Shi, Hongqi
Jiang, Huaguo
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Keywords Solid oxide electrolysis cells
Direct CO2 electrolysis
Pr-doped La0.75Sr0.25Cr0.5Mn0.5O3-δ
CO2 utilization and upgrade
Short-term stability
Language English
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Snippet Direct CO2 electrolysis has been explored as a means to store renewable energy and produce renewable fuels. La chromate-based perovskite oxides have attracted...
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StartPage 14648
SubjectTerms CO2 utilization and upgrade
Direct CO2 electrolysis
Pr-doped La0.75Sr0.25Cr0.5Mn0.5O3-δ
Short-term stability
Solid oxide electrolysis cells
Title Highly active and stable A-site Pr-doped LaSrCrMnO-based fuel electrode for direct CO2 solid oxide electrolyzer cells
URI https://dx.doi.org/10.1016/j.ijhydene.2020.03.224
Volume 45
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