File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

김병수

Kim, Byeong-Su
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 323 -
dc.citation.number 2 -
dc.citation.startPage 316 -
dc.citation.title POLYMER -
dc.citation.volume 53 -
dc.contributor.author Bak, Jae Min -
dc.contributor.author Lee, Taemin -
dc.contributor.author Seo, Eunyong -
dc.contributor.author Lee, Youngil -
dc.contributor.author Jeong, Han Mo -
dc.contributor.author Kim, Byeong-Su -
dc.contributor.author Lee, Hyung-il -
dc.date.accessioned 2023-12-22T05:37:22Z -
dc.date.available 2023-12-22T05:37:22Z -
dc.date.created 2013-07-05 -
dc.date.issued 2012-01 -
dc.description.abstract We report the preparation of thermoresponsive graphene nanosheets functionalized by the polymer brushes. This approach involves the direct growth of thermoresponsive polymer brushes from functional graphene sheets (FGSs) by chemical modification with initiators followed by extension with poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) through surface-initiated atom transfer radical polymerization. The highly controllable polymerization method affords the hybrid FGS-PDMAEMA with tailorable length of PDMAEMA brushes possessing the average molecular weight (M n) ranging from 7.4 × 10 3 to 6.0 × 10 4 with low molecular weight distributions (M w/M n = 1.09-1.22). The resulting FGS-PDMAEMA was carefully characterized with a number of techniques, including elemental analysis, thermogravimetric analysis, differential scanning calorimetry, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy, all supporting the successful integration of polymer brushes onto the surface of FGS. Most importantly, we accomplished the reversible phase transfer of this hybrid FGS-PDMAEMA between aqueous and organic phases via temperature control by taking advantage of the thermoresponsive nature of PDMAEMA brushes. Moreover, the composite film prepared by depositing the suspensions of FGS-PDMAEMA demonstrated the facile control over the wettability upon temperature changes. This tailored control over dispersion in water, selective solubilization between aqueous and organic solvents, and wettability control upon temperature variation have a significant impact on the ability to improve properties of hybrid graphene-based materials. Because of the highly versatile and tunable properties of surface-initiated atom transfer polymerization, we anticipate that the general concept presented here offers a unique potential platform for integrating responsive polymers for graphene nanosheets for advanced electronic, energy, and sensor applications. -
dc.identifier.bibliographicCitation POLYMER, v.53, no.2, pp.316 - 323 -
dc.identifier.doi 10.1016/j.polymer.2011.11.057 -
dc.identifier.issn 0032-3861 -
dc.identifier.scopusid 2-s2.0-84855822825 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/3420 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84855822825 -
dc.identifier.wosid 000299607400008 -
dc.language 영어 -
dc.publisher ELSEVIER SCI LTD -
dc.title Thermoresponsive graphene nanosheets by functionalization with polymer brushes -
dc.type Article -
dc.relation.journalWebOfScienceCategory Polymer Science -
dc.relation.journalResearchArea Polymer Science -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Thermoresponsive polymer brushes -
dc.subject.keywordAuthor FGSs -
dc.subject.keywordAuthor PDMAEMA -
dc.subject.keywordPlus TRANSFER RADICAL POLYMERIZATION -
dc.subject.keywordPlus EXFOLIATED GRAPHITE OXIDE -
dc.subject.keywordPlus EPITAXIAL GRAPHENE -
dc.subject.keywordPlus NANOCOMPOSITES -
dc.subject.keywordPlus SHEETS -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.