Continuous In-Flight Synthesis for On-Demand Delivery of Ligand-Free Colloidal Gold Nanoparticles

dc.bibliographicCitation.firstPage1336
dc.bibliographicCitation.issue3
dc.bibliographicCitation.journalTitleNano Letters
dc.bibliographicCitation.lastPage1343
dc.bibliographicCitation.volume17
dc.contributor.authorMaguire, Paul
dc.contributor.authorRutherford, David
dc.contributor.authorMacias-Montero, Manuel
dc.contributor.authorMahony, Charles
dc.contributor.authorKelsey, Colin
dc.contributor.authorTweedie, Mark
dc.contributor.authorPérez-Martin, Fátima
dc.contributor.authorMcQuaid, Harold
dc.contributor.authorDiver, Declan
dc.contributor.authorMariotti, Davide
dc.date.accessioned2025-02-27T12:55:45Z
dc.date.available2025-02-27T12:55:45Z
dc.date.issued2017
dc.description.abstractWe demonstrate an entirely new method of nanoparticle chemical synthesis based on liquid droplet irradiation with ultralow (<0.1 eV) energy electrons. While nanoparticle formation via high energy radiolysis or transmission electron microscopy-based electron bombardment is well-understood, we have developed a source of electrons with energies close to thermal which leads to a number of important and unique benefits. The charged species, including the growing nanoparticles, are held in an ultrathin surface reaction zone which enables extremely rapid precursor reduction. In a proof-of-principle demonstration, we obtain small-diameter Au nanoparticles (∼4 nm) with tight control of polydispersity, in under 150 μs. The precursor was almost completely reduced in this period, and the resultant nanoparticles were water-soluble and free of surfactant or additional ligand chemistry. Nanoparticle synthesis rates within the droplets were many orders of magnitude greater than equivalent rates reported for radiolysis, electron beam irradiation, or colloidal chemical synthesis where reaction times vary from seconds to hours. In our device, a stream of precursor loaded microdroplets, ∼15 μm in diameter, were transported rapidly through a cold atmospheric pressure plasma with a high charge concentration. A high electron flux, electron and nanoparticle confinement at the surface of the droplet, and the picoliter reactor volume are thought to be responsible for the remarkable enhancement in nanoparticle synthesis rates. While this approach exhibits considerable potential for scale-up of synthesis rates, it also offers the more immediate prospect of continuous on-demand delivery of high-quality nanomaterials directly to their point of use by avoiding the necessity of collection, recovery, and purification. A range of new applications can be envisaged, from theranostics and biomedical imaging in tissue to inline catalyst production for pollution remediation in automobiles.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/18642
dc.identifier.urihttps://doi.org/10.34657/17661
dc.language.isoeng
dc.publisherWashington, DC : ACS Publ.
dc.relation.doihttps://doi.org/10.1021/acs.nanolett.6b03440
dc.relation.essn1530-6992
dc.relation.issn1530-6984
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540
dc.subject.ddc660
dc.subject.otherColloidal nanoparticleseng
dc.subject.otherdroplet microreactorseng
dc.subject.otherplasmaseng
dc.subject.othersegmented floweng
dc.subject.othersolvated electroneng
dc.titleContinuous In-Flight Synthesis for On-Demand Delivery of Ligand-Free Colloidal Gold Nanoparticleseng
dc.typeArticle
dc.typeText
tib.accessRightsopenAccess
wgl.contributorINP
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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