Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jpowsour.2003.08.011
DC FieldValue
dc.titleVisualization of particle distribution in composite polymer electrolyte systems
dc.contributor.authorZhang, S.
dc.contributor.authorLee, J.Y.
dc.contributor.authorHong, L.
dc.date.accessioned2014-10-09T07:05:47Z
dc.date.available2014-10-09T07:05:47Z
dc.date.issued2004-02-16
dc.identifier.citationZhang, S., Lee, J.Y., Hong, L. (2004-02-16). Visualization of particle distribution in composite polymer electrolyte systems. Journal of Power Sources 126 (1-2) : 125-133. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jpowsour.2003.08.011
dc.identifier.issn03787753
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/90482
dc.description.abstractA simple visualization method is developed to enable the imaging of the distribution and agglomeration of ceramic fillers in composite polymer electrolytes by scanning electron microscopy (SEM). Solvent-free composite electrolytes based on poly(ethylene oxide) (PEO), LiBF4 and SiO 2 particles are used as examples. The SiO2 particles are stained by a heavy element (Pb) to enhance the imaging contrast between the particles and their surroundings. Modified SiO2 from a silanization reaction where most of the surface OH groups has been replaced by Si-phenyl groups is also used to reduce the Lewis acid-base interactions between the ceramic fillers, the polymer and the Li salt. Although nearly the same particle size and particle distribution are found for SiO2 and modified SiO2 in PEO, the two composite electrolyte systems exhibit remarkably different electrochemical transport properties. The difference can, therefore, be unambiguously attributed to the benefit of Lewis acid-base interactions. © 2003 Elsevier B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.jpowsour.2003.08.011
dc.sourceScopus
dc.subjectCeramic filler
dc.subjectLithium batteries
dc.subjectMorphology
dc.subjectPoly(ethylene) oxide
dc.subjectPolymer electrolyte
dc.subjectSurface groups
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1016/j.jpowsour.2003.08.011
dc.description.sourcetitleJournal of Power Sources
dc.description.volume126
dc.description.issue1-2
dc.description.page125-133
dc.description.codenJPSOD
dc.identifier.isiut000188947000017
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