Surface Doping Quantum Dots with Chemically Active Native Ligands: Controlling Valence without Ligand Exchange

TitleSurface Doping Quantum Dots with Chemically Active Native Ligands: Controlling Valence without Ligand Exchange
Publication TypeJournal Article
Year of Publication2012
AuthorsTavasoli E, Guo YJ, Kunal P, Grajeda J, Gerber A, Vela J
Journal TitleChemistry of Materials
Volume24
Pages4231-4241
Date Published11
Type of ArticleArticle
ISBN Number0897-4756
Accession NumberWOS:000311239300029
Keywordsblinking, CDSE NANOCRYSTALS, chemical surface modification, click chemistry, colloidal, loading, magnetic-resonance-spectroscopy, METAL NANOPARTICLES, nanocrystals, nmr, optical-properties, paramagnetic-susceptibility, quantum dot, SEMICONDUCTOR NANOCRYSTALS, valence
Abstract

One remaining challenge in the field of colloidal semiconductor nanocrystal quantum dots is learning to control the degree of functionalization or "Valence" per nanocrystal. Current quantum dot surface modification strategies rely heavily on ligand exchange, which consists of replacing the nanocrystal's native ligands with carboxylate- or amine-terminated thiols, usually added in excess. Removing the nanocrystal's native ligands can cause etching and introduce surface defects, thus affecting the nanocrystal's optical properties. More importantly, ligand exchange methods fail to control the extent of surface modification or number of functional groups introduced per nanocrystal Here, we report a fundamentally new surface ligand modification or "doping" approach aimed at controlling the degree of functionalization or valence per nanocrystal while retaining the nanocrystal's original colloidal and photostability. We show that surface-doped quantum dots capped with chemically active native ligands can be prepared. directly from a mixture of ligands with similar chain lengths. Specifically, vinyl and azide-terminated carboxylic acid ligands survive, the high temperatures needed for nanocrystal synthesis. The ratio between chemically active and inactive terminated ligands is maintained on the nanocrystal surface, allowing to control the extent of surface modification by straightforward organic reactions. Using a combination of optical and structural characterization tools, including IR and 2D NMR; We show that carboxylates bind in a bidentate chelate fashion, forming a single monolayer of ligands that are perpendicular to the nanocrystal surface. Moreover, we show that mixtures of ligands with similar chain lengths homogeneously distribute themselves on the nanocrystal surface. We expect this new surface doping approach will be widely applicable to other nanocrystal compositions and morphologies, as well as to many specific applications in biology and materials science.

URL<Go to ISI>://WOS:000311239300029
DOI10.1021/cm3026957
Alternate JournalChem. Mat.