Controlled morphology and dimensionality evolution of NiPd bimetallic nanostructures

dc.contributor.authorMaize, Mai
dc.contributor.authorEl-Boraey, Hanaa A.
dc.contributor.authorAyad, Mohamed I.
dc.contributor.authorHolmes, Justin D.
dc.contributor.authorCollins, Gillian
dc.contributor.funderMinistry of Higher Education, Egypten
dc.contributor.funderEgyptian Governmenten
dc.contributor.funderEgyptian Bureau for Cultural & Educational Affairsen
dc.contributor.funderEgyptian Embassy in London, UKen
dc.date.accessioned2021-01-12T14:06:10Z
dc.date.available2021-01-12T14:06:10Z
dc.date.issued2020-10-13
dc.date.updated2021-01-04T15:20:37Z
dc.description.abstractControlling the morphology of noble metal-based nanostructures is a powerful strategy for optimizing their catalytic performance. Here, we report a one-pot aqueous synthesis of versatile NiPd nanostructures at room temperature without employing organic solvents or surfactants. The synthesis can be tuned to form zero-dimensional (0D) architectures, such as core–shell and hollow nanoparticles (NPs), as well as nanostructures with higher dimensionality, such as extended nanowire networks and three-dimensional (3D) nanodendrites. The diverse morphologies were successfully obtained through modification of the HCl concentration in the Pd precursor solution, and the reaction aging time. An in-depth understanding of the formation mechanism and morphology evolution are described in detail. A key factor in the structural evolution of the nanostructures was the ability to tune the reduction rate and to protonate the citrate stabiliser by adding HCl. Spherical core–shell NPs were formed by the galvanic replacement-free deposition of Pd on Ni NPs which can be transformed to hollow NPs via a corrosion process. High concentrations of HCl led to the transition of isotropic spherical NPs into anisotropic wormlike nanowire networks, created through an oriented attachment process. Aging of these nanowire networks resulted in the formation of 3D porous nanodendrites via a corrosion process. The diverse structures of NiPd NPs were anchored onto acid treated-activated carbon (AC) and exhibited improved catalytic efficiency towards the hydrogenation of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP).en
dc.description.statusPeer revieweden
dc.description.versionPublished Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationMaize, M., El-Boraey, H. A., Ayad, M. I., Holmes, J. D. and Collins, G. (2021) 'Controlled morphology and dimensionality evolution of NiPd bimetallic nanostructures', Journal of Colloid and Interface Science, 585, pp. 480-489. doi: 10.1016/j.jcis.2020.10.030en
dc.identifier.doi10.1016/j.jcis.2020.10.030en
dc.identifier.endpage489en
dc.identifier.issn0021-9797
dc.identifier.journaltitleJournal of Colloid and Interface Scienceen
dc.identifier.startpage480en
dc.identifier.urihttps://hdl.handle.net/10468/10900
dc.identifier.volume585en
dc.language.isoenen
dc.publisherElsevieren
dc.relation.projectinfo:eu-repo/grantAgreement/SFI/SFI Research Centres/12/RC/2278/IE/Advanced Materials and BioEngineering Research Centre (AMBER)/en
dc.relation.urihttps://www.sciencedirect.com/science/article/pii/S0021979720313539
dc.rights© 2020 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subject4-nitrophenolen
dc.subjectCatalystsen
dc.subjectCore-shell structureen
dc.subjectDendritic structureen
dc.subjectHollow structureen
dc.subjectNanowire network structureen
dc.subjectNiPd bimetallic nanoparticlesen
dc.subjectReaction mechanismen
dc.subjectShape controlen
dc.subjectStructural evolutionen
dc.titleControlled morphology and dimensionality evolution of NiPd bimetallic nanostructuresen
dc.typeArticle (peer-reviewed)en
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