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dc.contributor.authorKasatkin, P. E.
dc.contributor.authorJäger, Rutha
dc.contributor.authorHärk, Eneli
dc.contributor.authorTeppor, Patrick
dc.contributor.authorTallo, Indrek
dc.contributor.authorJoost, Urmas
dc.contributor.authorŠmits, Krišjanis
dc.contributor.authorKanarbik, Rait
dc.contributor.authorLust, Enn I.
dc.date.accessioned2020-10-01T13:35:46Z
dc.date.available2020-10-01T13:35:46Z
dc.date.issued2017
dc.identifier.issn1388-2481
dc.identifier.urihttps://dspace.lu.lv/dspace/handle/7/52566
dc.descriptionThis work was supported by the projects TK141 “Advanced materials and high-technology devices for energy recuperation systems” (2014-2020.4.01.15-0011), NAMUR “Nanomaterials - research and applications” (3.2.0304.12-0397) and by the Estonian Institutional Research Grant No. IUT20-13.en_US
dc.description.abstractTwo different Fe-N/C(SiC) catalysts (Fe + Bipyr/C(SiC) and Fe + Phen/C(SiC)) for oxygen reduction based on silicon carbide derived carbon were synthesized and investigated in 0.1 M KOH aqueous solution by rotating disc electrode method. It was found that the electrocatalytic activity and stability are significantly influenced by the change of the nitrogen ligand in the catalyst. Comparable current density values obtained for 20%Pt-Vulcan electrode could be achieved for Fe + Bipyr/C(SiC) and Fe + Phen/C(SiC) catalysts in alkaline media. The durability tests (~ 150 h) showed that the decrease of the activity for Fe + Bipyr/C(SiC) and Fe + Phen/C(SiC) is only 0.5 mV h− 1 and 0.17 mV h− 1, respectively. The Fe + Bipyr/C(SiC) catalyst demonstrated higher activity in the RDE measurements, but during the long-term test the Fe + Phen/C(SiC) catalyst prove to be more stable than Fe + Bipyr/C(SiC).en_US
dc.description.sponsorshipTK141 2014-2020.4.01.15-0011; NAMUR 3.2.0304.12-0397; Estonian Institutional Research Grant No. IUT20-13; Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART²en_US
dc.language.isoengen_US
dc.publisherElsevier Inc.en_US
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/739508/EU/Centre of Advanced Material Research and Technology Transfer/CAMART²en_US
dc.relation.ispartofseriesElectrochemistry Communications;80
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES:Physicsen_US
dc.subjectCarbide derived carbonen_US
dc.subjectDurability testen_US
dc.subjectFe-N/C catalysten_US
dc.subjectOxygen reduction reactionen_US
dc.subjectRotating disc electrode methoden_US
dc.titleFe-N/C catalysts for oxygen reduction based on silicon carbide derived carbonen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.identifier.doi10.1016/j.elecom.2017.05.001


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