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dc.contributor.authorMuthuswamy, Navaneethan
dc.contributor.authorBuan, Marthe Emelie Melandsø
dc.contributor.authorWalmsley, John
dc.contributor.authorRønning, Magnus
dc.date.accessioned2017-12-05T09:57:36Z
dc.date.available2017-12-05T09:57:36Z
dc.date.created2017-12-04T09:06:31Z
dc.date.issued2018
dc.identifier.citationCatalysis Today. 2018, 301 11-16.nb_NO
dc.identifier.issn0920-5861
dc.identifier.urihttp://hdl.handle.net/11250/2469217
dc.description.abstractOxygen reduction on N-doped carbon nanomaterials is believed to take place at either N-centered active sites (C-Nx) or Fe-centered active sites (Fe-Nx). In this work the origin of the oxygen reduction on nitrogen-doped carbon nanofibers (N-CNFs) is investigated by removing nitrogen and iron from the N-CNF surface using high temperature KOH treatment. The activities for the oxygen reduction reaction (ORR) in 0.5 M H2SO4 are correlated with the XPS results and discussed with respect to the contribution from C-Nx and Fe-Nx active sites. Increasing the time and temperature of the KOH treatment decreased the iron and nitrogen content at the N-CNF surface. The contribution from Fe-Nx active sites was found to be minor compared to the C-Nx active sites as the KOH-treated N-CNFs with no iron in the surface still showed considerable ORR activity. Furthermore, the activity was maintained when the fraction of pyridinic-N was greatly reduced compared to quaternary-N. Finally, even when no iron or nitrogen could be detected by XPS, 50% of the initial oxygen reduction activity of the N-CNFs persisted. It is therefore suggested that there are active sites not originating from iron or nitrogen atoms, but rather from a distinct carbon environment.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleEvaluation of ORR active sites in nitrogen-doped carbon nanofibers by KOH post treatmentnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber11-16nb_NO
dc.source.volume301nb_NO
dc.source.journalCatalysis Todaynb_NO
dc.identifier.doi10.1016/j.cattod.2017.03.045
dc.identifier.cristin1522225
dc.relation.projectEC/FP7/280658nb_NO
dc.relation.projectNorges forskningsråd: 197405nb_NO
dc.description.localcode© 2017. This is the authors’ accepted and refereed manuscript to the article. LOCKED until 8.4.2019 due to copyright restrictions. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/nb_NO
cristin.unitcode194,66,30,0
cristin.unitcode194,66,20,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.unitnameInstitutt for fysikk
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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