| Literature DB >> 28719199 |
Christina J Hanson1, Nicolai F Hartmann1, Ajay Singh1, Xuedan Ma1, William J I DeBenedetti2, Joanna L Casson3, John K Grey4, Yves J Chabal5, Anton V Malko2, Milan Sykora3, Andrei Piryatinski6, Han Htoon1, Jennifer A Hollingsworth1.
Abstract
Toward a truly photostable PbSe quantum dot (QD), we apply the thick-shell or "giant" QD structural motif to this notoriously environmentally sensitive nanocrystal system. Namely, using a sequential application of two shell-growth techniques-partial-cation exchange and successive ionic layer adsorption and reaction (SILAR)-we are able to overcoat the PbSe QDs with sufficiently thick CdSe shells to impart new single-QD-level photostability, as evidenced by suppression of both photobleaching and blinking behavior. We further reveal that the crystal structure of the CdSe shell (cubic zinc-blende or hexagonal wurtzite) plays a key role in determining the photoluminescence properties of these giant QDs, with only cubic nanocrystals sufficiently bright and stable to be observed as single emitters. Moreover, we demonstrate that crystal structure and particle shape (cubic, spherical, or tetrapodal) and, thereby, emission properties can be synthetically tuned by either withholding or including the coordinating ligand, trioctylphosphine, in the SILAR component of the shell-growth process.Entities:
Year: 2017 PMID: 28719199 DOI: 10.1021/jacs.7b03705
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419