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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/1094
DC FieldValueLanguage
dc.contributor.authorŠušić, M. V.en_US
dc.contributor.authorMentus, Slavkoen_US
dc.date.accessioned2022-12-16T17:30:06Z-
dc.date.available2022-12-16T17:30:06Z-
dc.date.issued1983-01-01-
dc.identifier.issn0167-2738en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/1094-
dc.description.abstractSolid electrolytes, the composition of which is 0.8AgI·o0.2Ag2MoO4 and 0.2Agl· ·0.8Ag2MoO4, were investigated by means of ac and dc electrochemical methods at room temperature and at elevated temperatures. Cyclovoltamograms of the both electrolytes on Pt and Ag electrodes are similar and show that fast Ag+ ⇋ Ag redox process and strong anodic passivation occur, due to which it seems that these electrolytes decomposition potential is much above the theoretical value. By means of Tafel analysis the equilibrium potentials, Ag+ ⇌ Ag redox process exchange currents, and the activation energy were determined. The nature of the electrode/electrolyte interface was investigated also on the basis of faradaic and capacitance currents measurements within 0.1 - 1 kHz frequency range. © 1983.en
dc.relation.ispartofSolid State Ionicsen
dc.titleElectrode processes at metal/Ag I-Ag<inf>2</inf>MoO<inf>4</inf> solid electrolyte interfaceen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/0167-2738(83)90314-4-
dc.identifier.scopus2-s2.0-0020905195-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0020905195-
dc.relation.firstpage683en
dc.relation.lastpage688en
dc.relation.issuePART 1en
dc.relation.volume9-10en
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
crisitem.author.orcid0000-0001-8155-8003-
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University of Belgrade
Faculty of Physical Chemistry
Studentski trg 12-16
11158 Belgrade 118
PAC 105305
SERBIA
University of Belgrade Faculty of Physical Chemistry