TY - JOUR
T1 - Fe-Ce0.1Zr0.9O2-Ag electrode for one-step methane synthesis in solid oxide electrolyser
AU - Biswas, Saheli
AU - Kulkarni, Aniruddha P.
AU - Seeber, Aaron
AU - Greaves, Mark
AU - Giddey, Sarbjit
AU - Bhattacharya, Sankar
N1 - Funding Information:
This research is funded by the Research and Development Program (Renewable Hydrogen for Export) of the Australian Renewable Energy Agency (ARENA). Additional support has been received from CSIRO Hydrogen Energy Systems Future Science Platform and CSIRO Research Office. The funders were not involved in the experimental design or the collection, analysis and interpretation of data, or writing of the manuscript, or the decision to submit it for publication.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/1
Y1 - 2021/1
N2 - A novel mixed oxide material, Fe-Ce0.1Zr0.9O2-Ag, has been tested as cathode, for the very first time, for one-step methane synthesis in a single temperature solid oxide electrolyser by electrolysing a H2/CO2 (4:1 v/v) mixture at 500 °C. Maximum methane selectivity and yield were 6.67 % and 2.66 %, respectively, at an applied potential of 1.6 V (corresponding to a current density of 3.94 mAcm-2). CO2 conversion (~ 40 %) was independent of the applied voltage. However, upon increasing the potential, CO% dropped monotonically with a commensurate increase in methane%. Calculations based on oxide ion removal as a function of current density confirmed that under loaded conditions steam generated in situ (via reverse water gas shift and methanation reactions) got electrolysed to H2, which reacted with CO producing more methane. Such excess methane produced purely electrolytically under loaded conditions matched well with the values predicted theoretically assuming that the decrease in CO% was solely due to enhanced methanation.
AB - A novel mixed oxide material, Fe-Ce0.1Zr0.9O2-Ag, has been tested as cathode, for the very first time, for one-step methane synthesis in a single temperature solid oxide electrolyser by electrolysing a H2/CO2 (4:1 v/v) mixture at 500 °C. Maximum methane selectivity and yield were 6.67 % and 2.66 %, respectively, at an applied potential of 1.6 V (corresponding to a current density of 3.94 mAcm-2). CO2 conversion (~ 40 %) was independent of the applied voltage. However, upon increasing the potential, CO% dropped monotonically with a commensurate increase in methane%. Calculations based on oxide ion removal as a function of current density confirmed that under loaded conditions steam generated in situ (via reverse water gas shift and methanation reactions) got electrolysed to H2, which reacted with CO producing more methane. Such excess methane produced purely electrolytically under loaded conditions matched well with the values predicted theoretically assuming that the decrease in CO% was solely due to enhanced methanation.
KW - Ceria-zirconia mixed oxide cathode
KW - CO methanation
KW - One-step methane synthesis
KW - Oxide ion removal
UR - https://www.scopus.com/pages/publications/85117620581
U2 - 10.1007/s11581-021-04330-4
DO - 10.1007/s11581-021-04330-4
M3 - Article
AN - SCOPUS:85117620581
SN - 0947-7047
VL - 28
SP - 329
EP - 340
JO - Ionics
JF - Ionics
ER -