Improvement of a single-chamber solid-oxide fuel cell and evaluation of new cell designs
The performance of a single-chamber solid-oxide fuel cell (SOFC) made from a YSZ solid electrolyte with a 25 wt% Ce0.8Gd0.2O1.9 (GDC)-containing Ni anode and a 15 wt% MnO2-containing La0.8Sr0.2MnO3 cathode was found to be significantly enhanced by the deposition of Mn, Ga, Cr, Ce, and Lu oxide layer...
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Veröffentlicht in: | Journal of the Electrochemical Society 2000-04, Vol.147 (4), p.1338-1343 |
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description | The performance of a single-chamber solid-oxide fuel cell (SOFC) made from a YSZ solid electrolyte with a 25 wt% Ce0.8Gd0.2O1.9 (GDC)-containing Ni anode and a 15 wt% MnO2-containing La0.8Sr0.2MnO3 cathode was found to be significantly enhanced by the deposition of Mn, Ga, Cr, Ce, and Lu oxide layers on the YSZ surface. In particular, the deposition of the Mn oxide layer increased the maximum power density from 161 to 213 mW/cm2 in a mixture of methane and air having a CH4/O2 volume ratio of 1/1 at a flow rate of 300 mL/min, and at an operating temperature of 950 C. This effect was the result of the promoted anodic and cathodic reactions. Two types of cell designs were examined for the single-chamber SOFC; the two electrodes were deposited on opposite surfaces (A-type cell) and on the same face (B-type cell) of the solid electrolyte. The A-type cell showed increasing power density with decreasing electrolyte thickness. The maximum power density was 256 mW/cm2 at a solid electrolyte thickness of 0.3 mm. The B-type cell showed an increased power density for a decreased gap between the electrodes. The maximum power density was 143 mW/cm2 for a gap of 0.5 mm. The long-term stability of the SOFC was also studied and found to have a direct relationship with carbon deposition on the GDC-containing Ni electrode. 18 refs. |
doi_str_mv | 10.1149/1.1393359 |
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In particular, the deposition of the Mn oxide layer increased the maximum power density from 161 to 213 mW/cm2 in a mixture of methane and air having a CH4/O2 volume ratio of 1/1 at a flow rate of 300 mL/min, and at an operating temperature of 950 C. This effect was the result of the promoted anodic and cathodic reactions. Two types of cell designs were examined for the single-chamber SOFC; the two electrodes were deposited on opposite surfaces (A-type cell) and on the same face (B-type cell) of the solid electrolyte. The A-type cell showed increasing power density with decreasing electrolyte thickness. The maximum power density was 256 mW/cm2 at a solid electrolyte thickness of 0.3 mm. The B-type cell showed an increased power density for a decreased gap between the electrodes. The maximum power density was 143 mW/cm2 for a gap of 0.5 mm. The long-term stability of the SOFC was also studied and found to have a direct relationship with carbon deposition on the GDC-containing Ni electrode. 18 refs.</description><identifier>ISSN: 0013-4651</identifier><identifier>EISSN: 1945-7111</identifier><identifier>DOI: 10.1149/1.1393359</identifier><identifier>CODEN: JESOAN</identifier><language>eng</language><publisher>Pennington, NJ: Electrochemical Society</publisher><subject>30 DIRECT ENERGY CONVERSION ; Applied sciences ; Direct energy conversion and energy accumulation ; Electrical engineering. Electrical power engineering ; Electrical power engineering ; Electrochemical conversion: primary and secondary batteries, fuel cells ; Exact sciences and technology ; MANGANESE OXIDES ; POWER DENSITY ; SOLID OXIDE FUEL CELLS ; YTTRIUM ; ZIRCONATES</subject><ispartof>Journal of the Electrochemical Society, 2000-04, Vol.147 (4), p.1338-1343</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-b2aa65e7305fd5d7826a8feb2cf6487e282d8bf69870dc343f0ecde10ecabe3e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1323856$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/20075608$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><contributor>WCA</contributor><creatorcontrib>HIBINO, T</creatorcontrib><creatorcontrib>TSUNEKAWA, H</creatorcontrib><creatorcontrib>TANIMOTO, S</creatorcontrib><creatorcontrib>SANO, M</creatorcontrib><creatorcontrib>National Industrial Research Inst. of Nagoya (JP)</creatorcontrib><title>Improvement of a single-chamber solid-oxide fuel cell and evaluation of new cell designs</title><title>Journal of the Electrochemical Society</title><description>The performance of a single-chamber solid-oxide fuel cell (SOFC) made from a YSZ solid electrolyte with a 25 wt% Ce0.8Gd0.2O1.9 (GDC)-containing Ni anode and a 15 wt% MnO2-containing La0.8Sr0.2MnO3 cathode was found to be significantly enhanced by the deposition of Mn, Ga, Cr, Ce, and Lu oxide layers on the YSZ surface. In particular, the deposition of the Mn oxide layer increased the maximum power density from 161 to 213 mW/cm2 in a mixture of methane and air having a CH4/O2 volume ratio of 1/1 at a flow rate of 300 mL/min, and at an operating temperature of 950 C. This effect was the result of the promoted anodic and cathodic reactions. Two types of cell designs were examined for the single-chamber SOFC; the two electrodes were deposited on opposite surfaces (A-type cell) and on the same face (B-type cell) of the solid electrolyte. The A-type cell showed increasing power density with decreasing electrolyte thickness. The maximum power density was 256 mW/cm2 at a solid electrolyte thickness of 0.3 mm. The B-type cell showed an increased power density for a decreased gap between the electrodes. The maximum power density was 143 mW/cm2 for a gap of 0.5 mm. The long-term stability of the SOFC was also studied and found to have a direct relationship with carbon deposition on the GDC-containing Ni electrode. 18 refs.</description><subject>30 DIRECT ENERGY CONVERSION</subject><subject>Applied sciences</subject><subject>Direct energy conversion and energy accumulation</subject><subject>Electrical engineering. Electrical power engineering</subject><subject>Electrical power engineering</subject><subject>Electrochemical conversion: primary and secondary batteries, fuel cells</subject><subject>Exact sciences and technology</subject><subject>MANGANESE OXIDES</subject><subject>POWER DENSITY</subject><subject>SOLID OXIDE FUEL CELLS</subject><subject>YTTRIUM</subject><subject>ZIRCONATES</subject><issn>0013-4651</issn><issn>1945-7111</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LxDAQhoMouK4e_AcFRfDQNR9Nmh5l8QsWvCh4C2ky2Y20ydq0q_57u3TBywzDPO_LzIvQJcELQorqjiwIqxjj1RGakargeUkIOUYzjAnLC8HJKTpL6XMciSzKGfp4abdd3EELoc-iy3SWfFg3kJuNbmvoshQbb_P44y1kboAmM9A0mQ42g51uBt37GPbCAN_TykLy65DO0YnTTYKLQ5-j98eHt-Vzvnp9elner3LDuOjzmmotOJQMc2e5LSUVWjqoqXGikCVQSa2snahkia1hBXMYjAUyVl0DAzZHV5NvTL1XyfgezMbEEMD0imJccoHlSN1M1Pjs1wCpV61P-3N1gDgkRUteSUrpCN5OoOliSh04te18q7tfRbDaJ6yIOiQ8stcHU52Mblyng_HpX8Aok1ywP_G9em8</recordid><startdate>20000401</startdate><enddate>20000401</enddate><creator>HIBINO, T</creator><creator>TSUNEKAWA, H</creator><creator>TANIMOTO, S</creator><creator>SANO, M</creator><general>Electrochemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QQ</scope><scope>8FD</scope><scope>JG9</scope><scope>OTOTI</scope></search><sort><creationdate>20000401</creationdate><title>Improvement of a single-chamber solid-oxide fuel cell and evaluation of new cell designs</title><author>HIBINO, T ; TSUNEKAWA, H ; TANIMOTO, S ; SANO, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-b2aa65e7305fd5d7826a8feb2cf6487e282d8bf69870dc343f0ecde10ecabe3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>30 DIRECT ENERGY CONVERSION</topic><topic>Applied sciences</topic><topic>Direct energy conversion and energy accumulation</topic><topic>Electrical engineering. Electrical power engineering</topic><topic>Electrical power engineering</topic><topic>Electrochemical conversion: primary and secondary batteries, fuel cells</topic><topic>Exact sciences and technology</topic><topic>MANGANESE OXIDES</topic><topic>POWER DENSITY</topic><topic>SOLID OXIDE FUEL CELLS</topic><topic>YTTRIUM</topic><topic>ZIRCONATES</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HIBINO, T</creatorcontrib><creatorcontrib>TSUNEKAWA, H</creatorcontrib><creatorcontrib>TANIMOTO, S</creatorcontrib><creatorcontrib>SANO, M</creatorcontrib><creatorcontrib>National Industrial Research Inst. of Nagoya (JP)</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>OSTI.GOV</collection><jtitle>Journal of the Electrochemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HIBINO, T</au><au>TSUNEKAWA, H</au><au>TANIMOTO, S</au><au>SANO, M</au><au>WCA</au><aucorp>National Industrial Research Inst. of Nagoya (JP)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improvement of a single-chamber solid-oxide fuel cell and evaluation of new cell designs</atitle><jtitle>Journal of the Electrochemical Society</jtitle><date>2000-04-01</date><risdate>2000</risdate><volume>147</volume><issue>4</issue><spage>1338</spage><epage>1343</epage><pages>1338-1343</pages><issn>0013-4651</issn><eissn>1945-7111</eissn><coden>JESOAN</coden><abstract>The performance of a single-chamber solid-oxide fuel cell (SOFC) made from a YSZ solid electrolyte with a 25 wt% Ce0.8Gd0.2O1.9 (GDC)-containing Ni anode and a 15 wt% MnO2-containing La0.8Sr0.2MnO3 cathode was found to be significantly enhanced by the deposition of Mn, Ga, Cr, Ce, and Lu oxide layers on the YSZ surface. In particular, the deposition of the Mn oxide layer increased the maximum power density from 161 to 213 mW/cm2 in a mixture of methane and air having a CH4/O2 volume ratio of 1/1 at a flow rate of 300 mL/min, and at an operating temperature of 950 C. This effect was the result of the promoted anodic and cathodic reactions. Two types of cell designs were examined for the single-chamber SOFC; the two electrodes were deposited on opposite surfaces (A-type cell) and on the same face (B-type cell) of the solid electrolyte. The A-type cell showed increasing power density with decreasing electrolyte thickness. The maximum power density was 256 mW/cm2 at a solid electrolyte thickness of 0.3 mm. The B-type cell showed an increased power density for a decreased gap between the electrodes. The maximum power density was 143 mW/cm2 for a gap of 0.5 mm. The long-term stability of the SOFC was also studied and found to have a direct relationship with carbon deposition on the GDC-containing Ni electrode. 18 refs.</abstract><cop>Pennington, NJ</cop><pub>Electrochemical Society</pub><doi>10.1149/1.1393359</doi><tpages>6</tpages></addata></record> |
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subjects | 30 DIRECT ENERGY CONVERSION Applied sciences Direct energy conversion and energy accumulation Electrical engineering. Electrical power engineering Electrical power engineering Electrochemical conversion: primary and secondary batteries, fuel cells Exact sciences and technology MANGANESE OXIDES POWER DENSITY SOLID OXIDE FUEL CELLS YTTRIUM ZIRCONATES |
title | Improvement of a single-chamber solid-oxide fuel cell and evaluation of new cell designs |
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