Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells

Detalhes bibliográficos
Autor(a) principal: Yaremchenko, Aleksey
Data de Publicação: 2022
Outros Autores: Boiba, Dziyana, Merkulov, Oleg, Lisenkov, Aleksey
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/10773/34190
Resumo: Long-term degradation remains the main issue for the viability of solid oxide electrolysis cell (SOEC) technology as a practical hydrogen production system. The principle of the so-called fuel-assisted electrolysis cell is to supply the low-grade fuel to the anode where it can react with oxygen, thus bringing down the oxygen chemical potential at the electrolyte/anode interface and improving its stability. The present work is aimed at the evaluation of Sr0.7Ce0.3MnO3-d perovskite for potential application as an anode in fuel-assisted SOEC. Sr0.7Ce0.3MnO3-d was synthesized by the glycine-nitrate technique with repeated calcinations at 900-1300°C to obtain phase-pure perovskite material. Ceramic samples were sintered in air at 1450°C. The oxide exhibits negligible variations of oxygen content under oxidizing conditions while reducing p(O2) below 10-4 atm at 750-900°C results in oxygen losses and reduction of Mn cations. The low-p(O2) stability boundary of the perovskite phase at 800°C corresponds to ~3×10-17 atm. Sr0.7Ce0.3MnO3-d shows good thermomechanical compatibility with solid electrolytes under oxidizing conditions; however, reduction at operation temperatures (800°C) leads to undesirable chemical expansion. The electrical conductivity of Sr0.7Ce0.3MnO3 ceramics is p-type electronic and decreases with reducing p(O2) but still exceeds 40 S/cm under anticipated oxygen electrode operation conditions. The electrochemical activity of Sr0.7Ce0.3MnO3 electrodes was evaluated in contact with YSZ solid electrolyte as a function of relevant parameters. The best performance was obtained for the cells with a CGO buffer layer and Sr0.7Ce0.3MnO3 electrodes infiltrated with PrOy (load of ~ 30 wt.%) that can show anodic overpotentials of ~50 mV under 400 mA/cm2 at 800°C in air.
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spelling Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cellsSolid oxide electrolysis cellLong-term degradation remains the main issue for the viability of solid oxide electrolysis cell (SOEC) technology as a practical hydrogen production system. The principle of the so-called fuel-assisted electrolysis cell is to supply the low-grade fuel to the anode where it can react with oxygen, thus bringing down the oxygen chemical potential at the electrolyte/anode interface and improving its stability. The present work is aimed at the evaluation of Sr0.7Ce0.3MnO3-d perovskite for potential application as an anode in fuel-assisted SOEC. Sr0.7Ce0.3MnO3-d was synthesized by the glycine-nitrate technique with repeated calcinations at 900-1300°C to obtain phase-pure perovskite material. Ceramic samples were sintered in air at 1450°C. The oxide exhibits negligible variations of oxygen content under oxidizing conditions while reducing p(O2) below 10-4 atm at 750-900°C results in oxygen losses and reduction of Mn cations. The low-p(O2) stability boundary of the perovskite phase at 800°C corresponds to ~3×10-17 atm. Sr0.7Ce0.3MnO3-d shows good thermomechanical compatibility with solid electrolytes under oxidizing conditions; however, reduction at operation temperatures (800°C) leads to undesirable chemical expansion. The electrical conductivity of Sr0.7Ce0.3MnO3 ceramics is p-type electronic and decreases with reducing p(O2) but still exceeds 40 S/cm under anticipated oxygen electrode operation conditions. The electrochemical activity of Sr0.7Ce0.3MnO3 electrodes was evaluated in contact with YSZ solid electrolyte as a function of relevant parameters. The best performance was obtained for the cells with a CGO buffer layer and Sr0.7Ce0.3MnO3 electrodes infiltrated with PrOy (load of ~ 30 wt.%) that can show anodic overpotentials of ~50 mV under 400 mA/cm2 at 800°C in air.2022-07-18T14:54:27Z2022-07-01T00:00:00Z2022-07conference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10773/34190engYaremchenko, AlekseyBoiba, DziyanaMerkulov, OlegLisenkov, Alekseyinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-06T04:38:29Zoai:ria.ua.pt:10773/34190Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:15:20.859224Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
title Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
spellingShingle Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
Yaremchenko, Aleksey
Solid oxide electrolysis cell
title_short Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
title_full Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
title_fullStr Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
title_full_unstemmed Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
title_sort Sr0.7Ce0.3MnO3-d as anode material for fuel-assisted solid oxide electrolysis cells
author Yaremchenko, Aleksey
author_facet Yaremchenko, Aleksey
Boiba, Dziyana
Merkulov, Oleg
Lisenkov, Aleksey
author_role author
author2 Boiba, Dziyana
Merkulov, Oleg
Lisenkov, Aleksey
author2_role author
author
author
dc.contributor.author.fl_str_mv Yaremchenko, Aleksey
Boiba, Dziyana
Merkulov, Oleg
Lisenkov, Aleksey
dc.subject.por.fl_str_mv Solid oxide electrolysis cell
topic Solid oxide electrolysis cell
description Long-term degradation remains the main issue for the viability of solid oxide electrolysis cell (SOEC) technology as a practical hydrogen production system. The principle of the so-called fuel-assisted electrolysis cell is to supply the low-grade fuel to the anode where it can react with oxygen, thus bringing down the oxygen chemical potential at the electrolyte/anode interface and improving its stability. The present work is aimed at the evaluation of Sr0.7Ce0.3MnO3-d perovskite for potential application as an anode in fuel-assisted SOEC. Sr0.7Ce0.3MnO3-d was synthesized by the glycine-nitrate technique with repeated calcinations at 900-1300°C to obtain phase-pure perovskite material. Ceramic samples were sintered in air at 1450°C. The oxide exhibits negligible variations of oxygen content under oxidizing conditions while reducing p(O2) below 10-4 atm at 750-900°C results in oxygen losses and reduction of Mn cations. The low-p(O2) stability boundary of the perovskite phase at 800°C corresponds to ~3×10-17 atm. Sr0.7Ce0.3MnO3-d shows good thermomechanical compatibility with solid electrolytes under oxidizing conditions; however, reduction at operation temperatures (800°C) leads to undesirable chemical expansion. The electrical conductivity of Sr0.7Ce0.3MnO3 ceramics is p-type electronic and decreases with reducing p(O2) but still exceeds 40 S/cm under anticipated oxygen electrode operation conditions. The electrochemical activity of Sr0.7Ce0.3MnO3 electrodes was evaluated in contact with YSZ solid electrolyte as a function of relevant parameters. The best performance was obtained for the cells with a CGO buffer layer and Sr0.7Ce0.3MnO3 electrodes infiltrated with PrOy (load of ~ 30 wt.%) that can show anodic overpotentials of ~50 mV under 400 mA/cm2 at 800°C in air.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-18T14:54:27Z
2022-07-01T00:00:00Z
2022-07
dc.type.driver.fl_str_mv conference object
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