Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/98608
DC FieldValue
dc.titleX-ray photoelectron spectroscopy studies on PEOnMBr2 (M = Co, Ni, Zn) solid electrolytes
dc.contributor.authorMartin-Vosshage, D.
dc.contributor.authorChowdari, B.V.R.
dc.date.accessioned2014-10-16T09:49:16Z
dc.date.available2014-10-16T09:49:16Z
dc.date.issued1995-05
dc.identifier.citationMartin-Vosshage, D.,Chowdari, B.V.R. (1995-05). X-ray photoelectron spectroscopy studies on PEOnMBr2 (M = Co, Ni, Zn) solid electrolytes. Solid State Ionics 78 (1-2) : 9-17. ScholarBank@NUS Repository.
dc.identifier.issn01672738
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/98608
dc.description.abstractPEOnMBr2 (M = Co, Ni, Zn) electrolytes were prepared at room temperature with values of n ranging from 128 to 8. X-ray photoelectron spectroscopy studies for each electrolyte system indicate a characteristic interaction of the CH2CH2Ochain of PEO with the divalent cations. While in PEO there is only one kind of carbon, these interactions have led to the formation of inequivalent carbons in all three electrolyte systems with increased salt concentration. Strongest cation interaction is identified for all systems at a salt concentration corresponding to n ≅ 16. Whereas the cations are found to change their coordination with varying salt concentration, the anions of each system are found to have nearly unchanged coordination. These results reveal the PEOn MBr2 systems with M = Co, Ni and Zn as complexes formed by the ether oxygen of PEO and each cation and an effective cross-linking between the CH2CH2O chain and the anion of the salt. © 1995.
dc.sourceScopus
dc.subjectCation interaction
dc.subjectPEOnMBr2 electrolyte
dc.subjectSpectroscopy
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.description.sourcetitleSolid State Ionics
dc.description.volume78
dc.description.issue1-2
dc.description.page9-17
dc.description.codenSSIOD
dc.identifier.isiutNOT_IN_WOS
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