Please use this identifier to cite or link to this item: https://doi.org/10.1021/la703431j
DC FieldValue
dc.titleModified ligand-exchange for efficient solubilization of CdSe/ZnS quantum dots in water: A procedure guided by computational studies
dc.contributor.authorPong, B.-K.
dc.contributor.authorTrout, B.L.
dc.contributor.authorLee, J.-Y.
dc.date.accessioned2014-10-09T06:54:01Z
dc.date.available2014-10-09T06:54:01Z
dc.date.issued2008-05-20
dc.identifier.citationPong, B.-K., Trout, B.L., Lee, J.-Y. (2008-05-20). Modified ligand-exchange for efficient solubilization of CdSe/ZnS quantum dots in water: A procedure guided by computational studies. Langmuir 24 (10) : 5270-5276. ScholarBank@NUS Repository. https://doi.org/10.1021/la703431j
dc.identifier.issn07437463
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/89460
dc.description.abstractOne of the methods to render CdSe/ZnS core-shell quantum dots(QDots) water-soluble is to functionalize the surface with carboxylate groups by the use of heterobifunctional ligands such as 3-mercaptopropionic acid, where the thiolic end binds onto the outer ZnS shell. However, currently available ligand-exchange procedures starting with TOPO-capped quantum dots often lead to significant loss of quantum yields and poor stability of the colloids in water. As part of our efforts to overcome these problems, we used computational methods to understand the nature of binding between alkyl thiols and ZnS wurtzite surfaces. Guided by the computational results, we modified the ligand-exchange method and increased the reactivity of 3-mercaptopropionic acid toward the ZnS surface in chloroform. The functionlization reaction required only mild reaction conditions and led to QDot nanoparticles that were individually dispersed in water with good colloidal stability. Importantly, the photoluminescence performance of the QDots was highly preserved. © 2008 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/la703431j
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/la703431j
dc.description.sourcetitleLangmuir
dc.description.volume24
dc.description.issue10
dc.description.page5270-5276
dc.description.codenLANGD
dc.identifier.isiut000255856100016
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