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Self-assembly of like-charged nanoparticles into microscopic crystals

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dc.contributor.author PILLAI, PRAMOD P. en_US
dc.contributor.author Kowalczyk, Bartlomiej en_US
dc.contributor.author Grzybowski, Bartosz A. en_US
dc.date.accessioned 2019-04-29T09:25:03Z
dc.date.available 2019-04-29T09:25:03Z
dc.date.issued 2015-11 en_US
dc.identifier.citation Nanoscale, 8(1), 157-161. en_US
dc.identifier.issn 2040-3364 en_US
dc.identifier.issn 2040-3372 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2657
dc.identifier.uri https://doi.org/10.1039/C5NR06983A en_US
dc.description.abstract Like-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.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Self-assembly en_US
dc.subject Microscopic crystals en_US
dc.subject Oppositely charged ligands en_US
dc.subject COOH terminated thiols en_US
dc.subject 2015 en_US
dc.title Self-assembly of like-charged nanoparticles into microscopic crystals en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Nanoscale en_US
dc.publication.originofpublisher Foreign en_US


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