In situ 57Fe mössbauer study of a porphyrin based FeNC catalyst for ORR
FeNC catalysts are important substitutes for the oxygen reduction reaction (ORR) in fuel cells. This work reports on an in situ Mössbauer spectroelectrochemical study of a porphyrin-based catalyst. Activity and selectivity towards ORR were determined from rotating ring disc electrode (RRDE) experime...
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| Veröffentlicht in: | Electrochimica acta 2021-11, Vol.395, p.139200, Article 139200 |
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| container_title | Electrochimica acta |
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| creator | Ni, Lingmei Theis, Pascal Paul, Stephen Stark, Robert W. Kramm, Ulrike I. |
| description | FeNC catalysts are important substitutes for the oxygen reduction reaction (ORR) in fuel cells. This work reports on an in situ Mössbauer spectroelectrochemical study of a porphyrin-based catalyst. Activity and selectivity towards ORR were determined from rotating ring disc electrode (RRDE) experiments at different loadings in acidic electrolyte and accompanied by H2O2 oxidation reduction measurements in order to identify the contributions to the different ORR pathways as function of potential. The comparison to in situ 57Fe Mössbauer spectra enables an assignment of these contributions to the iron signatures. The results indicate that two different "onset potentials" for obtaining the deoxygenated state associated with two different iron environments can be identified and being associated with the selectivity data. Moreover, the in situ data enable the determination of mass-based site density and turn-over frequency data for ORR relevant conditions. As a consequence, this work sheds light on the oxygen reduction reaction mechanism involved in FeNC catalysts. |
| doi_str_mv | 10.1016/j.electacta.2021.139200 |
| format | Article |
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This work reports on an in situ Mössbauer spectroelectrochemical study of a porphyrin-based catalyst. Activity and selectivity towards ORR were determined from rotating ring disc electrode (RRDE) experiments at different loadings in acidic electrolyte and accompanied by H2O2 oxidation reduction measurements in order to identify the contributions to the different ORR pathways as function of potential. The comparison to in situ 57Fe Mössbauer spectra enables an assignment of these contributions to the iron signatures. The results indicate that two different "onset potentials" for obtaining the deoxygenated state associated with two different iron environments can be identified and being associated with the selectivity data. Moreover, the in situ data enable the determination of mass-based site density and turn-over frequency data for ORR relevant conditions. As a consequence, this work sheds light on the oxygen reduction reaction mechanism involved in FeNC catalysts.</description><identifier>ISSN: 0013-4686</identifier><identifier>EISSN: 1873-3859</identifier><identifier>DOI: 10.1016/j.electacta.2021.139200</identifier><language>eng</language><publisher>Oxford: Elsevier BV</publisher><subject>Acidic oxides ; Catalysts ; Deoxygenation ; Electrolytic cells ; Fuel cells ; Hydrogen peroxide ; Iron ; Iron 57 ; Mossbauer spectroscopy ; Oxidation ; Oxygen reduction reactions ; Porphyrins ; Reaction mechanisms ; Selectivity</subject><ispartof>Electrochimica acta, 2021-11, Vol.395, p.139200, Article 139200</ispartof><rights>Copyright Elsevier BV Nov 1, 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1790-bad6eeb89abae97fbb305f6f46088bb4201d97220ee7d240db79684c98b583743</citedby><cites>FETCH-LOGICAL-c1790-bad6eeb89abae97fbb305f6f46088bb4201d97220ee7d240db79684c98b583743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Ni, Lingmei</creatorcontrib><creatorcontrib>Theis, Pascal</creatorcontrib><creatorcontrib>Paul, Stephen</creatorcontrib><creatorcontrib>Stark, Robert W.</creatorcontrib><creatorcontrib>Kramm, Ulrike I.</creatorcontrib><title>In situ 57Fe mössbauer study of a porphyrin based FeNC catalyst for ORR</title><title>Electrochimica acta</title><description>FeNC catalysts are important substitutes for the oxygen reduction reaction (ORR) in fuel cells. This work reports on an in situ Mössbauer spectroelectrochemical study of a porphyrin-based catalyst. Activity and selectivity towards ORR were determined from rotating ring disc electrode (RRDE) experiments at different loadings in acidic electrolyte and accompanied by H2O2 oxidation reduction measurements in order to identify the contributions to the different ORR pathways as function of potential. The comparison to in situ 57Fe Mössbauer spectra enables an assignment of these contributions to the iron signatures. The results indicate that two different "onset potentials" for obtaining the deoxygenated state associated with two different iron environments can be identified and being associated with the selectivity data. Moreover, the in situ data enable the determination of mass-based site density and turn-over frequency data for ORR relevant conditions. As a consequence, this work sheds light on the oxygen reduction reaction mechanism involved in FeNC catalysts.</description><subject>Acidic oxides</subject><subject>Catalysts</subject><subject>Deoxygenation</subject><subject>Electrolytic cells</subject><subject>Fuel cells</subject><subject>Hydrogen peroxide</subject><subject>Iron</subject><subject>Iron 57</subject><subject>Mossbauer spectroscopy</subject><subject>Oxidation</subject><subject>Oxygen reduction reactions</subject><subject>Porphyrins</subject><subject>Reaction mechanisms</subject><subject>Selectivity</subject><issn>0013-4686</issn><issn>1873-3859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNo9kN9KwzAYxYMoOKfPYMDr1i9Jmz-XMpwThoOh1yFpv-DKttakveiL-QK-mB0T4cC5OZzD-RFyzyBnwORjk-Meq95NyjlwljNhOMAFmTGtRCZ0aS7JDICJrJBaXpOblBoAUFLBjKxejzTt-oGWaon08POdkncDRpr6oR5pG6ijXRu7zzHujtS7hDVd4tuCVq53-zH1NLSRbrbbW3IV3D7h3Z_Pycfy-X2xytabl9fF0zqrmDKQeVdLRK-N8w6NCt4LKIMMhQStvS84sNoozgFR1byA2isjdVEZ7UstVCHm5OHc28X2a8DU26Yd4nGatLycvipeKjal1DlVxTaliMF2cXdwcbQM7Ambbew_NnvCZs_YxC9EvmLS</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Ni, Lingmei</creator><creator>Theis, Pascal</creator><creator>Paul, Stephen</creator><creator>Stark, Robert W.</creator><creator>Kramm, Ulrike I.</creator><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>202111</creationdate><title>In situ 57Fe mössbauer study of a porphyrin based FeNC catalyst for ORR</title><author>Ni, Lingmei ; Theis, Pascal ; Paul, Stephen ; Stark, Robert W. ; Kramm, Ulrike I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1790-bad6eeb89abae97fbb305f6f46088bb4201d97220ee7d240db79684c98b583743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acidic oxides</topic><topic>Catalysts</topic><topic>Deoxygenation</topic><topic>Electrolytic cells</topic><topic>Fuel cells</topic><topic>Hydrogen peroxide</topic><topic>Iron</topic><topic>Iron 57</topic><topic>Mossbauer spectroscopy</topic><topic>Oxidation</topic><topic>Oxygen reduction reactions</topic><topic>Porphyrins</topic><topic>Reaction mechanisms</topic><topic>Selectivity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ni, Lingmei</creatorcontrib><creatorcontrib>Theis, Pascal</creatorcontrib><creatorcontrib>Paul, Stephen</creatorcontrib><creatorcontrib>Stark, Robert W.</creatorcontrib><creatorcontrib>Kramm, Ulrike I.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Electrochimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ni, Lingmei</au><au>Theis, Pascal</au><au>Paul, Stephen</au><au>Stark, Robert W.</au><au>Kramm, Ulrike I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In situ 57Fe mössbauer study of a porphyrin based FeNC catalyst for ORR</atitle><jtitle>Electrochimica acta</jtitle><date>2021-11</date><risdate>2021</risdate><volume>395</volume><spage>139200</spage><pages>139200-</pages><artnum>139200</artnum><issn>0013-4686</issn><eissn>1873-3859</eissn><abstract>FeNC catalysts are important substitutes for the oxygen reduction reaction (ORR) in fuel cells. This work reports on an in situ Mössbauer spectroelectrochemical study of a porphyrin-based catalyst. Activity and selectivity towards ORR were determined from rotating ring disc electrode (RRDE) experiments at different loadings in acidic electrolyte and accompanied by H2O2 oxidation reduction measurements in order to identify the contributions to the different ORR pathways as function of potential. The comparison to in situ 57Fe Mössbauer spectra enables an assignment of these contributions to the iron signatures. The results indicate that two different "onset potentials" for obtaining the deoxygenated state associated with two different iron environments can be identified and being associated with the selectivity data. Moreover, the in situ data enable the determination of mass-based site density and turn-over frequency data for ORR relevant conditions. 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| subjects | Acidic oxides Catalysts Deoxygenation Electrolytic cells Fuel cells Hydrogen peroxide Iron Iron 57 Mossbauer spectroscopy Oxidation Oxygen reduction reactions Porphyrins Reaction mechanisms Selectivity |
| title | In situ 57Fe mössbauer study of a porphyrin based FeNC catalyst for ORR |
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