Please use this identifier to cite or link to this item: https://doi.org/10.1039/b002167i
DC FieldValue
dc.titleChemical deposition of palladium on leucoemeraldine from solutions: State and distribution of palladium species
dc.contributor.authorWang, J.
dc.contributor.authorNeoh, K.G.
dc.contributor.authorKang, E.T.
dc.contributor.authorTan, K.L.
dc.date.accessioned2014-10-09T09:52:03Z
dc.date.available2014-10-09T09:52:03Z
dc.date.issued2000
dc.identifier.citationWang, J., Neoh, K.G., Kang, E.T., Tan, K.L. (2000). Chemical deposition of palladium on leucoemeraldine from solutions: State and distribution of palladium species. Journal of Materials Chemistry 10 (8) : 1933-1938. ScholarBank@NUS Repository. https://doi.org/10.1039/b002167i
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91896
dc.description.abstractThe reactions of polyaniline in its lowest oxidation state, leucoemeraldine (LM), with palladium ions in PdCl2, Pd(NO3)2, mixed solutions of PdCl2 and Pd(NO3)2 and mixed solutions of PdCl2 and AuCl3 were investigated. The amount of Pd deposited on the leucoemeraldine film was calculated from the decrease in Pd ion concentration in solution as determined by inductively coupled plasma emission spectroscopy. The state and distribution of the Pd species on the film surface was analysed using X-ray photoelectron spectroscopy and atomic force microscopy, respectively. The results showed that a much faster and more complete reduction of Pd ions to Pd0 occurred in the Pd(NO3)2 solution as compared to the PdCl2 solution and the explanation for this difference in reactivity has been offered from an electrochemical and coordination chemistry point of view. The mixing of Pd(NO3)2 with PdCl2 appears to affect the Pd coordination states in solution which in turn affects the Pd uptake rate and the manner in which the Pd is deposited on the LM surface. In mixed solutions of PdCl2 and AuCl3, it was clearly seen that the presence of a small amount of AuCl3 (molar ratio of AuCl3/ PdCl2 of 0.1) can greatly accelerate the uptake of Pd and complete removal of Pd ions from PdCl2 can be accomplished.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b002167i
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & ENVIRONMENTAL ENGINEERING
dc.contributor.departmentPHYSICS
dc.description.doi10.1039/b002167i
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume10
dc.description.issue8
dc.description.page1933-1938
dc.description.codenJMACE
dc.identifier.isiut000088552000029
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