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Proton uptake into the protonic cathode material BaCo^sub 0.4^Fe^sub 0.4^Zr^sub 0.2^O^sub 3-d^ and comparison to protonic electrolyte materials
Proton uptake in mixed-conducting cathode materials is of particular interest as it allows the oxygen reduction reaction to proceed via the bulk path in proton conducting ceramic fuel cells (PCFC). This work investigates the proton concentration of BaCo0.4 Fe0.4 Zr0.2 O3-d (BCFZr) and the predominan...
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Published in: | Solid state ionics 2017-01, Vol.299, p.64 |
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description | Proton uptake in mixed-conducting cathode materials is of particular interest as it allows the oxygen reduction reaction to proceed via the bulk path in proton conducting ceramic fuel cells (PCFC). This work investigates the proton concentration of BaCo0.4 Fe0.4 Zr0.2 O3-d (BCFZr) and the predominant proton uptake reactions using thermogravimetry. Based on the obtained proton concentrations increasing from 0.5 mol% at 400 °C to 1.5 mol% at 200 °C, the bulk path is expected to be active for BCFZr. The variation of proton concentrations with the concentration of electronic defects indicates nonideal behavior with detrimental interactions between protons and (trapped) holes. The comparison of BCFZr with other materials emphasizes that several factors determine the proton concentration such as oxide ion basicity, B-site cations and their oxidation state and B-O covalency. |
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This work investigates the proton concentration of BaCo0.4 Fe0.4 Zr0.2 O3-d (BCFZr) and the predominant proton uptake reactions using thermogravimetry. Based on the obtained proton concentrations increasing from 0.5 mol% at 400 °C to 1.5 mol% at 200 °C, the bulk path is expected to be active for BCFZr. The variation of proton concentrations with the concentration of electronic defects indicates nonideal behavior with detrimental interactions between protons and (trapped) holes. The comparison of BCFZr with other materials emphasizes that several factors determine the proton concentration such as oxide ion basicity, B-site cations and their oxidation state and B-O covalency.</description><identifier>ISSN: 0167-2738</identifier><identifier>EISSN: 1872-7689</identifier><language>eng</language><publisher>Amsterdam: Elsevier BV</publisher><subject>Basicity ; Cathodes ; Electrode materials ; Electrolytic cells ; Iron ; Oxidation ; Protons ; Thermodynamics ; Thermogravimetric analysis ; Thermogravimetry ; Valence ; Zirconium</subject><ispartof>Solid state ionics, 2017-01, Vol.299, p.64</ispartof><rights>Copyright Elsevier BV Jan 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Zohourian, R</creatorcontrib><creatorcontrib>Merkle, R</creatorcontrib><creatorcontrib>Maier, J</creatorcontrib><title>Proton uptake into the protonic cathode material BaCo^sub 0.4^Fe^sub 0.4^Zr^sub 0.2^O^sub 3-d^ and comparison to protonic electrolyte materials</title><title>Solid state ionics</title><description>Proton uptake in mixed-conducting cathode materials is of particular interest as it allows the oxygen reduction reaction to proceed via the bulk path in proton conducting ceramic fuel cells (PCFC). This work investigates the proton concentration of BaCo0.4 Fe0.4 Zr0.2 O3-d (BCFZr) and the predominant proton uptake reactions using thermogravimetry. Based on the obtained proton concentrations increasing from 0.5 mol% at 400 °C to 1.5 mol% at 200 °C, the bulk path is expected to be active for BCFZr. The variation of proton concentrations with the concentration of electronic defects indicates nonideal behavior with detrimental interactions between protons and (trapped) holes. The comparison of BCFZr with other materials emphasizes that several factors determine the proton concentration such as oxide ion basicity, B-site cations and their oxidation state and B-O covalency.</description><subject>Basicity</subject><subject>Cathodes</subject><subject>Electrode materials</subject><subject>Electrolytic cells</subject><subject>Iron</subject><subject>Oxidation</subject><subject>Protons</subject><subject>Thermodynamics</subject><subject>Thermogravimetric analysis</subject><subject>Thermogravimetry</subject><subject>Valence</subject><subject>Zirconium</subject><issn>0167-2738</issn><issn>1872-7689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNjbsOgkAQRTdGE_HxD5NYY5Y3tBKNnRZWFpAVxogCi7tD4Vf4y26M0dbqnsydOTNglhNHrh2FcTJkFnfCyHYjLx6zidZXznnoxaHFnnslSbbQdyRuCFVLEuiC0L3HVQGFoIssERpBqCpRw0qkMtP9CfjSzzb4xaP6oJvt3uTZZQaiLaGQTSdUpc0bY_-ascaClKwf9LPrGRudTeD8k1O22KwP6dY2Z_ceNeVX2avWVLmTBAH3Ezfwvf-2Xu6pVlk</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Zohourian, R</creator><creator>Merkle, R</creator><creator>Maier, J</creator><general>Elsevier BV</general><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20170101</creationdate><title>Proton uptake into the protonic cathode material BaCo^sub 0.4^Fe^sub 0.4^Zr^sub 0.2^O^sub 3-d^ and comparison to protonic electrolyte materials</title><author>Zohourian, R ; Merkle, R ; Maier, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_19550492543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Basicity</topic><topic>Cathodes</topic><topic>Electrode materials</topic><topic>Electrolytic cells</topic><topic>Iron</topic><topic>Oxidation</topic><topic>Protons</topic><topic>Thermodynamics</topic><topic>Thermogravimetric analysis</topic><topic>Thermogravimetry</topic><topic>Valence</topic><topic>Zirconium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zohourian, R</creatorcontrib><creatorcontrib>Merkle, R</creatorcontrib><creatorcontrib>Maier, J</creatorcontrib><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Solid state ionics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zohourian, R</au><au>Merkle, R</au><au>Maier, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proton uptake into the protonic cathode material BaCo^sub 0.4^Fe^sub 0.4^Zr^sub 0.2^O^sub 3-d^ and comparison to protonic electrolyte materials</atitle><jtitle>Solid state ionics</jtitle><date>2017-01-01</date><risdate>2017</risdate><volume>299</volume><spage>64</spage><pages>64-</pages><issn>0167-2738</issn><eissn>1872-7689</eissn><abstract>Proton uptake in mixed-conducting cathode materials is of particular interest as it allows the oxygen reduction reaction to proceed via the bulk path in proton conducting ceramic fuel cells (PCFC). This work investigates the proton concentration of BaCo0.4 Fe0.4 Zr0.2 O3-d (BCFZr) and the predominant proton uptake reactions using thermogravimetry. Based on the obtained proton concentrations increasing from 0.5 mol% at 400 °C to 1.5 mol% at 200 °C, the bulk path is expected to be active for BCFZr. The variation of proton concentrations with the concentration of electronic defects indicates nonideal behavior with detrimental interactions between protons and (trapped) holes. The comparison of BCFZr with other materials emphasizes that several factors determine the proton concentration such as oxide ion basicity, B-site cations and their oxidation state and B-O covalency.</abstract><cop>Amsterdam</cop><pub>Elsevier BV</pub></addata></record> |
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subjects | Basicity Cathodes Electrode materials Electrolytic cells Iron Oxidation Protons Thermodynamics Thermogravimetric analysis Thermogravimetry Valence Zirconium |
title | Proton uptake into the protonic cathode material BaCo^sub 0.4^Fe^sub 0.4^Zr^sub 0.2^O^sub 3-d^ and comparison to protonic electrolyte materials |
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