STRUCTURE AND CATALYTIC ABILITY OF Sn-Co POWDERS TO OXYGEN REDUCTION REACTION IN A MODEL METAL-AIR BATTERY

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creativework.keywordsAlloy powders, Catalytic ability, Metal-air battery, Microstructure, Sn-co
creativework.publisherUniversity of Chemical Technology and Metallurgyen
dc.contributor.authorIgnatova K.
dc.contributor.authorPopov I.
dc.contributor.authorShipochka M.
dc.date.accessioned2024-07-16T11:16:51Z
dc.date.accessioned2024-07-16T11:19:25Z
dc.date.available2024-07-16T11:16:51Z
dc.date.available2024-07-16T11:19:25Z
dc.date.issued2022-01-01
dc.description.abstractComposition, microstructure, current efficiency and catalytic ability of Sn-Co powders, deposited by constant and pulse potential modes are investigated. SEM, EDS, XPS, XRD and BET methods were applied. It is shown that at higher potentials in stationary mode and at higher pulse frequencies in pulse mode (500-1000 Hz), Sn-Co powders with maximum specific surface area (21 - 23 m2 g-1) and cobalt content (56 wt. % in stationary and 75.5 wt. % in pulse mode) are obtained. XRD and XPS analysis showed that the powders obtained in both modes represent a mixture of amorphous and microcrystalline phases of tetragonal β-Sn, α-Co with hexagonal, hcp lattice, as well as phases of CoO, SnO2 and impurity phase of SnF2 only in stationary mode. It was found that the catalytic ability of Sn-Co powders to the oxygen reduction reaction, ORR in a model Metal-Air battery is better than that of the reference Ag catalyst at low current densities. It increases with an increase in the cobalt content and with an increase in the dispersity of the powders
dc.identifier.issn1314-7978
dc.identifier.issn1314-7471
dc.identifier.scopusSCOPUS_ID:85125238057en
dc.identifier.urihttps://rlib.uctm.edu/handle/123456789/1356
dc.language.isoen
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85125238057&origin=inward
dc.titleSTRUCTURE AND CATALYTIC ABILITY OF Sn-Co POWDERS TO OXYGEN REDUCTION REACTION IN A MODEL METAL-AIR BATTERY
dc.typeArticle
oaire.citation.issue2
oaire.citation.volume57
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