Handle URI:
http://hdl.handle.net/10754/597720
Title:
Canopy Dynamics in Nanoscale Ionic Materials
Authors:
Jespersen, Michael L.; Mirau, Peter A.; Meerwall, Ernst von; Vaia, Richard A.; Rodriguez, Robert; Giannelis, Emmanuel P.
Abstract:
Nanoscale ionic materials (NIMS) are organic - inorganic hybrids in which a core nanostructure is functionalized with a covalently attached corona and an ionically tethered organic canopy. NIMS are engineered to be liquids under ambient conditions in the absence of solvent and are of interest for a variety of applications. We have used nuclear magnetic resonance (NMR) relaxation and pulse-field gradient (PFG) diffusion experiments to measure the canopy dynamics of NIMS prepared from 18-nm silica cores modified by an alkylsilane monolayer possessing terminal sulfonic acid functionality, paired with an amine-terminated ethylene oxide/propylene oxide block copolymer canopy. Carbon NMR studies show that the block copolymer canopy is mobile both in the bulk and in the NIMS and that the fast (ns) dynamics are insensitive to the presence of the silica nanoparticles. Canopy diffusion in the NIMS is slowed relative to the neat canopy, but not to the degree predicted from the diffusion of hard-sphere particles. Canopy diffusion is not restricted to the surface of the nanoparticles and shows unexpected behavior upon addition of excess canopy. Taken together, these data indicate that the liquid-like behavior in NIMS is due to rapid exchange of the block copolymer canopy between the ionically modified nanoparticles. © 2010 American Chemical Society.
Citation:
Jespersen ML, Mirau PA, Meerwall E von, Vaia RA, Rodriguez R, et al. (2010) Canopy Dynamics in Nanoscale Ionic Materials. ACS Nano 4: 3735–3742. Available: http://dx.doi.org/10.1021/nn100112h.
Publisher:
American Chemical Society (ACS)
Journal:
ACS Nano
KAUST Grant Number:
KUS-C1-018-02
Issue Date:
27-Jul-2010
DOI:
10.1021/nn100112h
PubMed ID:
20536222
Type:
Article
ISSN:
1936-0851; 1936-086X
Sponsors:
Funding provided by the Air Force Office of Scientific Research is gratefully acknowledged. The diffusion portion of this work was supported by the National Science Foundation under Grant No. DMR 04 55117. This publication is based on work supported by Award No. KUS-C1-018-02, made by King Abdullah University of Science and Technology (KAUST). This research was carried out while M. Jespersen was an NRC Postdoctoral Fellow at the Air Force Research Laboratories. We thank H. Koerner and M. Tchoul for assistance with SAXS experiments and GPC experiments, respectively, as well as for productive discussions regarding this research.
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Full metadata record

DC FieldValue Language
dc.contributor.authorJespersen, Michael L.en
dc.contributor.authorMirau, Peter A.en
dc.contributor.authorMeerwall, Ernst vonen
dc.contributor.authorVaia, Richard A.en
dc.contributor.authorRodriguez, Roberten
dc.contributor.authorGiannelis, Emmanuel P.en
dc.date.accessioned2016-02-25T12:55:30Zen
dc.date.available2016-02-25T12:55:30Zen
dc.date.issued2010-07-27en
dc.identifier.citationJespersen ML, Mirau PA, Meerwall E von, Vaia RA, Rodriguez R, et al. (2010) Canopy Dynamics in Nanoscale Ionic Materials. ACS Nano 4: 3735–3742. Available: http://dx.doi.org/10.1021/nn100112h.en
dc.identifier.issn1936-0851en
dc.identifier.issn1936-086Xen
dc.identifier.pmid20536222en
dc.identifier.doi10.1021/nn100112hen
dc.identifier.urihttp://hdl.handle.net/10754/597720en
dc.description.abstractNanoscale ionic materials (NIMS) are organic - inorganic hybrids in which a core nanostructure is functionalized with a covalently attached corona and an ionically tethered organic canopy. NIMS are engineered to be liquids under ambient conditions in the absence of solvent and are of interest for a variety of applications. We have used nuclear magnetic resonance (NMR) relaxation and pulse-field gradient (PFG) diffusion experiments to measure the canopy dynamics of NIMS prepared from 18-nm silica cores modified by an alkylsilane monolayer possessing terminal sulfonic acid functionality, paired with an amine-terminated ethylene oxide/propylene oxide block copolymer canopy. Carbon NMR studies show that the block copolymer canopy is mobile both in the bulk and in the NIMS and that the fast (ns) dynamics are insensitive to the presence of the silica nanoparticles. Canopy diffusion in the NIMS is slowed relative to the neat canopy, but not to the degree predicted from the diffusion of hard-sphere particles. Canopy diffusion is not restricted to the surface of the nanoparticles and shows unexpected behavior upon addition of excess canopy. Taken together, these data indicate that the liquid-like behavior in NIMS is due to rapid exchange of the block copolymer canopy between the ionically modified nanoparticles. © 2010 American Chemical Society.en
dc.description.sponsorshipFunding provided by the Air Force Office of Scientific Research is gratefully acknowledged. The diffusion portion of this work was supported by the National Science Foundation under Grant No. DMR 04 55117. This publication is based on work supported by Award No. KUS-C1-018-02, made by King Abdullah University of Science and Technology (KAUST). This research was carried out while M. Jespersen was an NRC Postdoctoral Fellow at the Air Force Research Laboratories. We thank H. Koerner and M. Tchoul for assistance with SAXS experiments and GPC experiments, respectively, as well as for productive discussions regarding this research.en
dc.publisherAmerican Chemical Society (ACS)en
dc.subjectionic liquidsen
dc.subjectnanoparticle liquidsen
dc.subjectnanoscale ionic materialsen
dc.subjectnuclear magnetic resonanceen
dc.subjectsilica nanoparticlesen
dc.titleCanopy Dynamics in Nanoscale Ionic Materialsen
dc.typeArticleen
dc.identifier.journalACS Nanoen
dc.contributor.institutionWright-Patterson AFB, Dayton, United Statesen
dc.contributor.institutionNational Research Council, Washington, United Statesen
dc.contributor.institutionUniversity of Akron, Akron, United Statesen
dc.contributor.institutionCornell University, Ithaca, United Statesen
kaust.grant.numberKUS-C1-018-02en
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