Electrolyte-Supported Fuel Cell: Co-Sintering Effects of Layer Deposition on Biaxial Strength
The mechanical reliability of reversible solid oxide cell (SOC) components is critical for the development of highly efficient, durable, and commercially competitive devices. In particular, the mechanical integrity of the ceramic cell, also known as membrane electrolyte assembly (MEA), is fundamenta...
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description | The mechanical reliability of reversible solid oxide cell (SOC) components is critical for the development of highly efficient, durable, and commercially competitive devices. In particular, the mechanical integrity of the ceramic cell, also known as membrane electrolyte assembly (MEA), is fundamental as its failure would be detrimental to the performance of the whole SOC stack. In the present work, the mechanical robustness of an electrolyte-supported cell was determined via ball-on-3-balls flexural strength measurements. The main focus was to investigate the effect of the manufacturing process (i.e., layer by layer deposition and their co-sintering) on the final strength. To allow this investigation, the electrode layers were screen-printed one by one on the electrolyte support and thus sintered. Strength tests were performed after every layer deposition and the non-symmetrical layout was taken into account during mechanical testing. Obtained experimental data were evaluated with the help of Weibull statistical analysis. A loss of mechanical strength after every layer deposition was usually detected, with the final strength of the cell being significantly smaller than the initial strength of the uncoated electrolyte (
₀ ≈ 800 MPa and
₀ ≈ 1800 MPa, respectively). Fractographic analyses helped to reveal the fracture behavior changes when individual layers were deposited. It was found that the reasons behind the weakening effect can be ascribed to the presence and redistribution of residual stresses, changes in the crack initiation site, porosity of layers, and pre-crack formation in the electrode layers. |
doi_str_mv | 10.3390/ma12020306 |
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₀ ≈ 800 MPa and
₀ ≈ 1800 MPa, respectively). Fractographic analyses helped to reveal the fracture behavior changes when individual layers were deposited. It was found that the reasons behind the weakening effect can be ascribed to the presence and redistribution of residual stresses, changes in the crack initiation site, porosity of layers, and pre-crack formation in the electrode layers.</description><identifier>ISSN: 1996-1944</identifier><identifier>EISSN: 1996-1944</identifier><identifier>DOI: 10.3390/ma12020306</identifier><identifier>PMID: 30669404</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Barrier layers ; Ceramics ; Cermets ; Commercialization ; Complex systems ; Component reliability ; Crack initiation ; Deposition ; Efficiency ; Electrodes ; Electrolytes ; Flexural strength ; Fracture mechanics ; Fuel cells ; Interfacial bonding ; Investigations ; Load ; Mechanical properties ; Mechanical tests ; Operating temperature ; Oxidation ; Porosity ; Residual stress ; Screen printing ; Sintering ; Sintering (powder metallurgy) ; Statistical analysis ; Thermal expansion ; Thickness</subject><ispartof>Materials, 2019-01, Vol.12 (2), p.306</ispartof><rights>2019. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-b94c5cb831feb5e90a8efe5e3f075e56e44980c303c99184cbc8e6ddccea7f713</citedby><cites>FETCH-LOGICAL-c434t-b94c5cb831feb5e90a8efe5e3f075e56e44980c303c99184cbc8e6ddccea7f713</cites><orcidid>0000-0002-6117-240X ; 0000-0002-8053-8489</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356930/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356930/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30669404$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masini, Alessia</creatorcontrib><creatorcontrib>Strohbach, Thomas</creatorcontrib><creatorcontrib>Šiška, Filip</creatorcontrib><creatorcontrib>Chlup, Zdeněk</creatorcontrib><creatorcontrib>Dlouhý, Ivo</creatorcontrib><title>Electrolyte-Supported Fuel Cell: Co-Sintering Effects of Layer Deposition on Biaxial Strength</title><title>Materials</title><addtitle>Materials (Basel)</addtitle><description>The mechanical reliability of reversible solid oxide cell (SOC) components is critical for the development of highly efficient, durable, and commercially competitive devices. In particular, the mechanical integrity of the ceramic cell, also known as membrane electrolyte assembly (MEA), is fundamental as its failure would be detrimental to the performance of the whole SOC stack. In the present work, the mechanical robustness of an electrolyte-supported cell was determined via ball-on-3-balls flexural strength measurements. The main focus was to investigate the effect of the manufacturing process (i.e., layer by layer deposition and their co-sintering) on the final strength. To allow this investigation, the electrode layers were screen-printed one by one on the electrolyte support and thus sintered. Strength tests were performed after every layer deposition and the non-symmetrical layout was taken into account during mechanical testing. Obtained experimental data were evaluated with the help of Weibull statistical analysis. A loss of mechanical strength after every layer deposition was usually detected, with the final strength of the cell being significantly smaller than the initial strength of the uncoated electrolyte (
₀ ≈ 800 MPa and
₀ ≈ 1800 MPa, respectively). Fractographic analyses helped to reveal the fracture behavior changes when individual layers were deposited. It was found that the reasons behind the weakening effect can be ascribed to the presence and redistribution of residual stresses, changes in the crack initiation site, porosity of layers, and pre-crack formation in the electrode layers.</description><subject>Barrier layers</subject><subject>Ceramics</subject><subject>Cermets</subject><subject>Commercialization</subject><subject>Complex systems</subject><subject>Component reliability</subject><subject>Crack initiation</subject><subject>Deposition</subject><subject>Efficiency</subject><subject>Electrodes</subject><subject>Electrolytes</subject><subject>Flexural strength</subject><subject>Fracture mechanics</subject><subject>Fuel cells</subject><subject>Interfacial bonding</subject><subject>Investigations</subject><subject>Load</subject><subject>Mechanical properties</subject><subject>Mechanical tests</subject><subject>Operating temperature</subject><subject>Oxidation</subject><subject>Porosity</subject><subject>Residual stress</subject><subject>Screen printing</subject><subject>Sintering</subject><subject>Sintering (powder metallurgy)</subject><subject>Statistical analysis</subject><subject>Thermal expansion</subject><subject>Thickness</subject><issn>1996-1944</issn><issn>1996-1944</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kV1LXDEQhkOxVNnuTX9ACXgjwmnzdT7ihaDr2goLXqy9LCEnO1kjZ0-OSY50_30ja6164TAwA_PwMi8vQl8o-ca5JN83mjLCCCfVB3RApawKKoXYe7Hvo2mMdyQX57Rh8hPaz3QlBREH6Pe8A5OC77YJiuU4DD4kWOHLETo8g647wTNfLF2fILh-jefWZjxib_FCbyHgCxh8dMn5Huc-d_qP0x1epgD9Ot1-Rh-t7iJMn-YE_bqc38x-FovrH1ezs0VhBBepaKUwpWkbTi20JUiiG7BQArekLqGsQAjZEMMJN1LSRpjWNFCtVsaArm1N-QSd7nSHsd3AykCfgu7UENxGh63y2qnXl97dqrV_UBUvK5l1J-joSSD4-xFiUhsXTfave_BjVIzWUlBW0iajh2_QOz-GPttTjHPGakIoe5dilNVlTas6U8c7ygQfYwD7_DIl6jFe9T_eDH99afIZ_Rcm_wuKlp-3</recordid><startdate>20190118</startdate><enddate>20190118</enddate><creator>Masini, Alessia</creator><creator>Strohbach, Thomas</creator><creator>Šiška, Filip</creator><creator>Chlup, Zdeněk</creator><creator>Dlouhý, Ivo</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6117-240X</orcidid><orcidid>https://orcid.org/0000-0002-8053-8489</orcidid></search><sort><creationdate>20190118</creationdate><title>Electrolyte-Supported Fuel Cell: Co-Sintering Effects of Layer Deposition on Biaxial Strength</title><author>Masini, Alessia ; Strohbach, Thomas ; Šiška, Filip ; Chlup, Zdeněk ; Dlouhý, Ivo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-b94c5cb831feb5e90a8efe5e3f075e56e44980c303c99184cbc8e6ddccea7f713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Barrier layers</topic><topic>Ceramics</topic><topic>Cermets</topic><topic>Commercialization</topic><topic>Complex systems</topic><topic>Component reliability</topic><topic>Crack initiation</topic><topic>Deposition</topic><topic>Efficiency</topic><topic>Electrodes</topic><topic>Electrolytes</topic><topic>Flexural strength</topic><topic>Fracture mechanics</topic><topic>Fuel cells</topic><topic>Interfacial bonding</topic><topic>Investigations</topic><topic>Load</topic><topic>Mechanical properties</topic><topic>Mechanical tests</topic><topic>Operating temperature</topic><topic>Oxidation</topic><topic>Porosity</topic><topic>Residual stress</topic><topic>Screen printing</topic><topic>Sintering</topic><topic>Sintering (powder metallurgy)</topic><topic>Statistical analysis</topic><topic>Thermal expansion</topic><topic>Thickness</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masini, Alessia</creatorcontrib><creatorcontrib>Strohbach, Thomas</creatorcontrib><creatorcontrib>Šiška, Filip</creatorcontrib><creatorcontrib>Chlup, Zdeněk</creatorcontrib><creatorcontrib>Dlouhý, Ivo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masini, Alessia</au><au>Strohbach, Thomas</au><au>Šiška, Filip</au><au>Chlup, Zdeněk</au><au>Dlouhý, Ivo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrolyte-Supported Fuel Cell: Co-Sintering Effects of Layer Deposition on Biaxial Strength</atitle><jtitle>Materials</jtitle><addtitle>Materials (Basel)</addtitle><date>2019-01-18</date><risdate>2019</risdate><volume>12</volume><issue>2</issue><spage>306</spage><pages>306-</pages><issn>1996-1944</issn><eissn>1996-1944</eissn><abstract>The mechanical reliability of reversible solid oxide cell (SOC) components is critical for the development of highly efficient, durable, and commercially competitive devices. In particular, the mechanical integrity of the ceramic cell, also known as membrane electrolyte assembly (MEA), is fundamental as its failure would be detrimental to the performance of the whole SOC stack. In the present work, the mechanical robustness of an electrolyte-supported cell was determined via ball-on-3-balls flexural strength measurements. The main focus was to investigate the effect of the manufacturing process (i.e., layer by layer deposition and their co-sintering) on the final strength. To allow this investigation, the electrode layers were screen-printed one by one on the electrolyte support and thus sintered. Strength tests were performed after every layer deposition and the non-symmetrical layout was taken into account during mechanical testing. Obtained experimental data were evaluated with the help of Weibull statistical analysis. A loss of mechanical strength after every layer deposition was usually detected, with the final strength of the cell being significantly smaller than the initial strength of the uncoated electrolyte (
₀ ≈ 800 MPa and
₀ ≈ 1800 MPa, respectively). Fractographic analyses helped to reveal the fracture behavior changes when individual layers were deposited. It was found that the reasons behind the weakening effect can be ascribed to the presence and redistribution of residual stresses, changes in the crack initiation site, porosity of layers, and pre-crack formation in the electrode layers.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>30669404</pmid><doi>10.3390/ma12020306</doi><orcidid>https://orcid.org/0000-0002-6117-240X</orcidid><orcidid>https://orcid.org/0000-0002-8053-8489</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Barrier layers Ceramics Cermets Commercialization Complex systems Component reliability Crack initiation Deposition Efficiency Electrodes Electrolytes Flexural strength Fracture mechanics Fuel cells Interfacial bonding Investigations Load Mechanical properties Mechanical tests Operating temperature Oxidation Porosity Residual stress Screen printing Sintering Sintering (powder metallurgy) Statistical analysis Thermal expansion Thickness |
title | Electrolyte-Supported Fuel Cell: Co-Sintering Effects of Layer Deposition on Biaxial Strength |
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