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dc.contributor.authorHuang, Ching-Maoen_US
dc.contributor.authorWei, Kung-Hwaen_US
dc.contributor.authorJeng, U-Seren_US
dc.contributor.authorLiang, Keng S.en_US
dc.date.accessioned2014-12-08T15:13:40Z-
dc.date.available2014-12-08T15:13:40Z-
dc.date.issued2007-07-10en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma0704764en_US
dc.identifier.urihttp://hdl.handle.net/11536/10563-
dc.description.abstractWe used in situ annealing small-angle X-ray scattering to monitor the structural evolution of a spherical poly(styrene-b-4-vinylpyridine) diblock copolymer (PS-b-P4VP)/2-phenylethanethiol-coated Au nanoparticle (AuSC2Ph) mixture in the solid state during its thermal annealing. We found that the Au nanoparticles (NPs) that existed initially in a random state with some cluster packing in the PS domain diffused to the interface of the amphiphilic PS-b-P4VP diblock copolymer within 4 h at 170 degrees C under vacuum to form NP-filled shell-like assemblies, as further evidenced from transmission electron microscopy imaging. From the X-ray photoelectron spectroscopy data, we speculate that this interfacial activity of AuSC2Ph results from the fact that the initially hydrophobic Au NP surfaces became increasingly hydrophilic as most of the 2-phenylethanethiol ligands had evaporated off. The Au NP nanoshell assemblies located at the interface between PS and P4VP were quite stable even after redissolving in toluene; they remained in the form of PS-Au-P4VP core/shell/corona onion micelles, as evidenced from solution state small-angle X-ray scattering data.en_US
dc.language.isoen_USen_US
dc.titleStructural evolution of poly(styrene-b-4-vinylpyridine) diblock copolymer/gold nanoparticle mixtures from solution to solid stateen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma0704764en_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume40en_US
dc.citation.issue14en_US
dc.citation.spage5067en_US
dc.citation.epage5074en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000247678300045-
dc.citation.woscount20-
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