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dc.creatorDražić, Dragutin M.
dc.creatorLedinski, Z. V.
dc.creatorZečević, Strahinja K.
dc.date.accessioned2021-04-09T09:58:25Z
dc.date.available2021-04-09T09:58:25Z
dc.date.issued1983
dc.identifier.issn0021-891X
dc.identifier.issn1572-8838
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4427
dc.description.abstractPorous carbon air-electrodes activated by CoPC, FePHP, PdPC, PtPC and metal-free PC were studied in 2 mol dm-3 NaCl electrolyte. The activity of heat-treated carbon activated by CoPC was compared to carbon activated by in situ formed Co oxide. All the results show that the main catalytic activity of the catalyst used comes from the central metal atom used, while the chelate or oxide structures serve predominantly to keep the metal in the stable form at the carbon surface. Metal-free phthalocyanine does not show any catalytic activity for oxygen reduction.sr
dc.language.isoensr
dc.publisherSpringer Naturesr
dc.rightsrestrictedAccesssr
dc.sourceJournal of Applied Electrochemistrysr
dc.subjectelectrodesr
dc.subjectElectrolytessr
dc.subjectcatalysissr
dc.subjectoxygen reductionsr
dc.subjectphthalocyaninessr
dc.titleTransition metal catalysts for porous carbon air-electrodes in neutral chloride electrolytessr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractЛедински, З. В.; Зечевић, Страхиња К.; Дражић, Драгутин М.;
dc.citation.volume13
dc.citation.issue3
dc.citation.spage337
dc.citation.epage340
dc.identifier.doi10.1007/BF00941605
dc.identifier.scopus2-s2.0-0020749726
dc.type.versionpublishedVersionsr


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Приказ основних података о документу