Please use this identifier to cite or link to this item: https://doi.org/10.1002/pat.1994.220050305
DC FieldValue
dc.titleX-ray photoelectron spectroscopic studies of charge transfer interactions in electroactive polyaniline
dc.contributor.authorTan, K.L.
dc.contributor.authorKang, E.T.
dc.contributor.authorNeoh, K.G.
dc.date.accessioned2014-10-09T08:22:26Z
dc.date.available2014-10-09T08:22:26Z
dc.date.issued1994-03
dc.identifier.citationTan, K.L.,Kang, E.T.,Neoh, K.G. (1994-03). X-ray photoelectron spectroscopic studies of charge transfer interactions in electroactive polyaniline. Polymers for Advanced Technologies 5 (3) : 171-177. ScholarBank@NUS Repository. <a href="https://doi.org/10.1002/pat.1994.220050305" target="_blank">https://doi.org/10.1002/pat.1994.220050305</a>
dc.identifier.issn10427147
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91800
dc.description.abstractFour modes of charge transfer interactions in polyaniline (PAN), viz. acid protonation, self-doping, charge transfer interactions with organic acceptors, and charge transfer interactions with surface grafted functional polymers have been studied by X-ray photoelectron spectroscopy (XPS). In the case of acid protonation, the protonation behavior of volatile and non-volatile acid differs. The structures of sulfonated leucomeraldine (LM) and nigraniline (NA) are similar to those of sulfonated and self-protonated emeraldine (EM). A substantially higher degree of charge transfer interaction with the organic acceptors is observed for EM film that has been subjected to one cycle of acid/base treatment. The charge transfer interactions with the organic acceptors have proceeded further than the pure formation of molecular complexes. Both pristine and Ar plasma or O3 pretreated EM films are susceptible to surface modifications by graft copolymerization. The protonic acid functional groups of the graft readily give rise to a self-protonated EM surface.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/pat.1994.220050305
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL ENGINEERING
dc.contributor.departmentPHYSICS
dc.description.doi10.1002/pat.1994.220050305
dc.description.sourcetitlePolymers for Advanced Technologies
dc.description.volume5
dc.description.issue3
dc.description.page171-177
dc.description.codenPADTE
dc.identifier.isiutNOT_IN_WOS
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