Приказ основних података о документу

dc.creatorAnastasijević, Nikola A.
dc.creatorŠtrbac, Svetlana
dc.creatorAdžić, Radoslav R.
dc.date.accessioned2021-03-12T15:09:34Z
dc.date.available2021-03-12T15:09:34Z
dc.date.issued1988
dc.identifier.issn1572-6657
dc.identifier.issn0022-0728
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4355
dc.description.abstractOxygen reduction was studied for the first time using a single crystal electrode in a rotating disc-ring arrangement. The Au (311) surface shows a complex behaviour, with a very high activity in certain potential regions. The first electron transfer is rate determining in the region of 4-electron reduction. As with Au (100), a 4 e- reduction changes into a 2 e- process, which reverts back to a 4 e-reaction at very negative potentials. Based on a general reaction scheme of O2 reduction, a map of the operating potential dependent reaction pathways was constructed. Nearly 60% of the mass flux of O2 undergoes a direct reduction to OH- in the region of mixed control. The high activity of Au (311) was ascribed to a high step density and AuOH present on its surface.sr
dc.language.isoensr
dc.publisherElseviersr
dc.rightsrestrictedAccesssr
dc.sourceJournal of Electroanalytical Chemistrysr
dc.subjectoxygensr
dc.subjectOxygen reductionsr
dc.subjectelectron transfersr
dc.subjectElectrochemistrysr
dc.subjectsingle crystal electrodesr
dc.titleOxygen reduction on the Au (311) electrode surface in alkaline electrolytesr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractAджић, Радослав Р.; Aнастасијевић, Никола A.; Штрбац, Светлана;
dc.citation.volume240
dc.citation.issue1-2
dc.citation.spage239
dc.citation.epage252
dc.identifier.doi10.1016/0022-0728(88)80326-7
dc.identifier.scopus2-s2.0-0023827036
dc.type.versionpublishedVersionsr


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Приказ основних података о документу