Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2657
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dc.contributor.authorPILLAI, PRAMOD P.en_US
dc.contributor.authorKowalczyk, Bartlomiejen_US
dc.contributor.authorGrzybowski, Bartosz A.en_US
dc.date.accessioned2019-04-29T09:25:03Z
dc.date.available2019-04-29T09:25:03Z
dc.date.issued2015-11en_US
dc.identifier.citationNanoscale, 8(1), 157-161.en_US
dc.identifier.issn2040-3364en_US
dc.identifier.issn2040-3372en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2657-
dc.identifier.urihttps://doi.org/10.1039/C5NR06983Aen_US
dc.description.abstractLike-charged nanoparticles, NPs, can assemble in water into large, faceted crystals, each made of several million particles. These NPs are functionalized with mixed monolayers comprising ligands terminating in carboxylic acid group ligands as well as positively charged quaternary ammonium ligands. The latter groups give rise to electrostatic interparticle repulsions which partly offset the hydrogen bonding between the carboxylic acids. It is the balance between these two interactions that ultimately enables self-assembly. Depending on the pH, the particles can crystallize, form aggregates, remain unaggregated or even – in mixtures of two particle types – can “choose” whether to crystallize with like-charged or oppositely charged particles.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectSelf-assemblyen_US
dc.subjectMicroscopic crystalsen_US
dc.subjectOppositely charged ligandsen_US
dc.subjectCOOH terminated thiolsen_US
dc.subject2015en_US
dc.titleSelf-assembly of like-charged nanoparticles into microscopic crystalsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleNanoscaleen_US
dc.publication.originofpublisherForeignen_US
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