Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/89951
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorMeng, Z-
dc.creatorWei, Z-
dc.creatorFu, K-
dc.creatorLv, L-
dc.creatorYu, ZQ-
dc.creatorWong, WY-
dc.date.accessioned2021-05-13T08:32:57Z-
dc.date.available2021-05-13T08:32:57Z-
dc.identifier.issn0022-328X-
dc.identifier.urihttp://hdl.handle.net/10397/89951-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2019 Elsevier B.V. All rights reserved.en_US
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/.en_US
dc.rightsThe following publication Meng, Z., Wei, Z., Fu, K., Lv, L., Yu, Z.-Q., & Wong, W.-Y. (2019). Amphiphilic bimetallic polymer as single-source precursors for the one-pot synthesis of L10-phase FePt nanoparticles. Journal of Organometallic Chemistry, 892, 83-88 is available at https://doi.org/10.1016/j.jorganchem.2019.04.015.en_US
dc.subjectAmphiphilic polymeren_US
dc.subjectFePt nanoparticlesen_US
dc.subjectSelf-assemblyen_US
dc.subjectSingle-source precursoren_US
dc.subjectSize effecten_US
dc.titleAmphiphilic bimetallic polymer as single-source precursors for the one-pot synthesis of L10-phase FePt nanoparticlesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage83-
dc.identifier.epage88-
dc.identifier.volume892-
dc.identifier.doi10.1016/j.jorganchem.2019.04.015-
dcterms.abstractAmphiphilic polymers have attracted extensive research attention in constructing various nanostructures by self-assembly. Here we designed and synthesized two amphiphilic bimetallic polymers with different length of the tails P1 and P2, in which Fe,Pt-containing conjugated complex acted as the hydrophobic block and hydrophilic poly(ethylene glycol)(PEG)was bonded to the bimetallic core as the flexible tails. P1 and P2 were used as the single-source precursors to prepare FePt nanoparticles (NPs)by one-pot pyrolysis. The resultant NPs were fully characterized and had a chemically ordered face-centered tetragonal (fct)phase with high crystallinity. The size of NPs pyrolyzed from P1 and P2 was 24.7 and 8.2 nm with the relative coercivity of 9.6 and 1.3 kOe, respectively. The difference was preliminarily explained by the discrepancy of their degrees of crystallinity, and also analyzed by the precursors’ structural effect. The amphiphilic design showed a good potential in preparing monodisperse ferromagnetic FePt NPs, and the possible favorable properties of self-assembly might provide a bright venue for future magnetic recording media.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of organometallic chemistry, 15 Aug. 2019, v. 892, p. 83-88-
dcterms.isPartOfJournal of organometallic chemistry-
dcterms.issued2019-08-
dc.identifier.scopus2-s2.0-85065171470-
dc.description.validate202105 bcvc-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera0847-n04-
dc.identifier.SubFormID1819-
dc.description.fundingSourceRGCen_US
dc.description.fundingTextPolyU153062/18Pen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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