Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-018-07395-4
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dc.titleHydrodynamic assembly of two-dimensional layered double hydroxide nanostructures
dc.contributor.authorJose, N.A
dc.contributor.authorZeng, H.C
dc.contributor.authorLapkin, A.A
dc.date.accessioned2020-10-20T09:38:07Z
dc.date.available2020-10-20T09:38:07Z
dc.date.issued2018
dc.identifier.citationJose, N.A, Zeng, H.C, Lapkin, A.A (2018). Hydrodynamic assembly of two-dimensional layered double hydroxide nanostructures. Nature Communications 9 (1) : 4913. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-018-07395-4
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178381
dc.description.abstractFormation mechanisms of two-dimensional nanostructures in wet syntheses are poorly understood. Even more enigmatic is the influence of hydrodynamic forces. Here we use liquid flow cell transmission electron microscopy to show that layered double hydroxide, as a model material, may form via the oriented attachment of hexagonal nanoparticles; under hydrodynamic shear, oriented attachment is accelerated. To hydrodynamically manipulate the kinetics of particle growth and oriented attachment, we develop a microreactor with high and tunable shear rates, enabling control over particle size, crystallinity and aspect ratio. This work offers new insights in the formation of two-dimensional materials, provides a scalable yet precise synthesis method, and proposes new avenues for the rational engineering and scalable production of highly anisotropic nanostructures. © 2018, The Author(s).
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjecthydroxide
dc.subjectnanoparticle
dc.subjectanisotropy
dc.subjectArticle
dc.subjectchemical structure
dc.subjectcrystallization
dc.subjecthydrodynamics
dc.subjectnanoengineering
dc.subjectparticle size
dc.subjectshear rate
dc.subjecttransmission electron microscopy
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1038/s41467-018-07395-4
dc.description.sourcetitleNature Communications
dc.description.volume9
dc.description.issue1
dc.description.page4913
dc.published.statepublished
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